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  • 101
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 377-384 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: N-Substituted carbonimidodithioic acid dimethyl esters, when reacted with an active methylene compound such as nitromethane, undergo carbon-carbon bond formation followed by carbon-sulphur bond cleavage in the presence of zeolite catalysts to give 1-substituted amino-1-methylthio-2-nitroethenes. This carbon-sulphur bond cleavage is facilitated by the presence of rare earth cations in the zeolite-Y framework. The shape selectivity of the zeolite also plays an important role in this cleavage reaction. Force field calculations adopted for the molecules involved in the reaction indicate the geometry and conformational flexibility of these molecules. The computer-simulated model for the zeolite-Y is correlated with the conformation and shape of the reactant and product molecules to explain the variation in yields obtained in the conversion of substituted dimethyl esters.
    Additional Material: 2 Ill.
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  • 102
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 403-411 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A means for determining the stabilization energies, Ec(X), resulting from σ-π and n-π interactions in vinyl and phenyl compounds is described. It is based on extensions of the additivity principle for thermochemical data for organic compounds. The results also provide a method for predicting heats of formation of unsaturated compounds from those of (known) saturated analogues. It is shown that there is a linear relationship between the stabilization energies Ec(X) and the Hammett substituent constants σp+(X). The new results have been used to predict the heats of formation of a number of saturated and unsaturated Si-, Ge-, Sn-, P-, As-, Se-, Zn-, Cd- and Hg-containing species.
    Additional Material: 2 Ill.
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  • 103
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 412-419 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of the concentrations of LiCl, NaCl, KCl, CsCl, Na2CO3 and BaCl2 on the rates of reactions of hydroxide ion with ionized N-hydroxyphthalimide (NHP-) at 30°C and in H2O-MeCN solvents containing 10, 50, 60, 66, 70, 76 and 80% (v/v) MeCN reveal the formation of ion-pair complexes between cations of the salts, which probably exist in solvent-separated loose ion-pair forms (Mn+⃛Xk-) and NHP-. An increase in MeCN content from 2 to 76% (v/v) causes an increase in the association constants (K) by factors of 40, 21 and 9 for LiCl, NaCl and KCl, respectively, while the respective increase in the rate constants (k′s1) for the collapse of the ion-pair complexes to product is ca two-fold. The values of k′s1 remain almost unchanged whereas the values of K increase 7·5-fold with an increase in MeCN content from 2 to 70% (v/v) for CsCl. Ion-pair complex formation was not detected in the presence of Me4NCl at 70% (v/v) MeCN. The observed pseudo-first-order rate constants are highly sensitive to the valence state of cations and almost insensitive to the valence state of the anions of the salts.
    Additional Material: 5 Ill.
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  • 104
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 448-454 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A characteristic feature in the bimolecular nucleophilic substitution reactions at a resonance-stabilized carbenium ion has been shown to be an imbalanced transition state resulting in an elevated value of the cross-interaction constant, which in turn leads to a non-interactive phenomenon. Examples of the reactions of ring-substituted phenylethyl and benzhydryl cations are given.
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  • 105
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 106
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates and products of solvolyses of 4-methylene-2ax- and -2eq-adamantyl p-toluenesulphonates (tosylates) (4a-OTs and 4e-OTs, respectively) were studied. Compound 4a-OTs solvolysed more slowly than 2-adamantyl tosylate (1) in methanol and 2,2,2-trifluoroethanol (TFE) by factors of 2·3 and 2·5, respectively, at 25°C. However, by taking the inductive decelerating effect of a β-methylene substituent into account, the rates were revealed to be enhanced by α-participation by a factor of 50. The products of solvolyses of 4a-OTs in methanol, 80% acetone and TFE at 100°C were 2ax- and 2eq-alkoxy(or hydroxy)-4-methyleneadamantanes (4a-OR and 4e-OR, respectively), exo-4-alkoxy(or hydroxy)-5-methyleneprotoadamantane (exo-5-OR) and 5-[alkoxy(or hydroxy)methyl]-4-protoadamantene (6-OR) with adamantyl to protoadamantyl product ratio of 39:61 (in methanol), 56:44 (in 80% acetone) and 71:29 (in TFE). Despite the nearly symmetric nature of the intermediate cation, the 4a-OR: 4e-OR product ratio was essentially constant with 83:17 (in methanol), 85:15 (in 80% acetone) and 82:18 (in TFE). The formation of considerable amounts of 4e-OR was interpreted as showing the intermediacy of a pair of rapidly equilibrating classical ions. The rates of 4e-OTs were 2300-4300 times faster than those expected from inductive electron-withdrawing effect of a β-methylene substituent. The major product (84·5% in methanolysis and 98·7% in trifluoroethanolysis) was 4e-OR accompanied by small amounts of 2-alkoxy-2,4-methanoadamantane (9-OR) and 2-(alkoxymethyl)-2,4-didehydroadamantane (10-OR), no formation of 4a-OR having been observed. These results suggested that 4e-OTs solvolyses via a π-bridged intermediate cation.
    Additional Material: 2 Ill.
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  • 107
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 479-484 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The determination of stability constants by measuring the increase in solubility of a nearly insoluble host molecule due to complex formation with a soluble guest is discussed. If the host molecule absorbs in the UV-visible region, spectrophotometric measurements are easily performed to obtain the stability constants. The solubilities of the crown ether dibenzo-18-crown-6 and of the cryptand (222BB) in aqueous solutions and the molar absorptivities of these ligands and their complexes with alkali and alkaline earth metal cations were determined. The increase in solubility of these ligands due to complex formation with cations was used to calculate the stabilities of the complexes formed. Even under the assumption that neither the molar absorptivities nor the solubilities are known, the calculated stability constants agree very well with those obtained using the measured values of the molar absorptivities and solubilities. The accuracy of the stability constants even increases with decreasing solubility of the ligands.
    Additional Material: 5 Ill.
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  • 108
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 511-517 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gas-phase acidity and basicity of thioacetamide and the basicity of N,N-dimethylthioformamide were measured by Fourier transform ion cyclotron resonance (FT-ICR) mass sectrometry under conditions which minimized the extent of their decomposition. Thiocarboxamides are both much stronger acids and stronger bases than carboxamides. The relative stabilities of individual neutral and ionic species were assessed in terms of isodesmic reactions, using the published or estimated enthalpies of formation. The neutral molecules of carboxamides and thiocarboxamides are stabilized by interaction between the C = X and NH2 functional groups. This interaction is of a similar magnitude in the corresponding protonated forms but it is of greater strength in the deprotonated forms. With regard to the difference between thiocarboxamides and carboxamides, the most significant factor is probably the Ione pair-Ione pair repulsion operating in the anions.
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  • 109
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 110
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    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 525-533 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of a number of factors, i.e. amine basicity, substrate structure, temperature and deuterium isotope effect, on the rate of phenyl β-bromoethyl sulphone and aryl β-chloroethyl sulphone 1,2-elimination by reaction with amines in acetonitrile was investigated. On the basis of a comparative analysis of the ρ0, β, kH/kD, ΔH
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  • 111
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 534-544 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The bisporphyria N,N′-bis[4″-(meso-triphenylporphyrinyl)benzyl]-4,13-diaza-18-crown-6 and its mono- and dizinc derivatives were synthesized in 66%, 46% and 53% yields, respectively, from 5-(4′-bromomethylphenyl)-10,15,20-triphenylporphyrin or its zinc derivative and 4,13-diaza-18-crown-6. The zinc-containing bisporphyrins form dimers in solution at low temperature or at high concentration. The unsymmetrical bisporphyrin; monozinc N,N′-bis[4″-(meso-triphenylporphyrinyl)benzyl]-4,13-diaza-18-crown-6 shows singlet-singlet energy transfer from the zinc porphyrin moiety to the free base moiety in both the monomeric and the dimeric form. The energy transfer rates were determined using time-resolved fluorescence spectroscopy and were found to be 1·26 × 109 and 2·29 × 109 s-1 for the monomeric and dimeric form, respectively. The difference in energy transfer rates between the two forms can be rationalized by the difference in overlap between the donor fluorescence spectrum and acceptor absorption spectrum, donor-acceptor distance and donor-acceptor orientation.
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  • 112
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 551-554 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Molecular mechanics (MM3) calculations were carried out on the title compounds. Comparison between the MM3 results and those of semi-empirical and ab initio calculations and experiment indicates that the MM3 results are at least as good as results of much more expensive calculations. The MM3 calculations predict that unlike corannulene and cyclopentacorannulene, the transition state of the bowl-to-bowl inversion of the related C30H10 is non-planar, and the activation barrier is too high for this motion to occur.
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  • 113
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 561-566 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The enthalpic contribution to the anomeric effect in r-2-carboethoxy-trans-4,trans-6- and r-2-carboethoxy-cis-4,cis-6-dimethyl-1,3-dithianes was determined by reaction-solution calorimetry. The enthalpy of solution of both isomers in pure p-dioxane and the enthalpy of solution and isomerization in the same solvent and in the presence of trifluoroacetic acid were experimentally measured. From these results the corresponding enthalpies of isomerization in solution were calculated, and were found to be ΔHax→eq = -0·16 ± 0·04 kcal mol-1 (-0·67 ± 0·18 kJ mol-1) and ΔSax→eq = -2·68 ± 0·1 cal K-1 mol-1 (-11·2 ± 0·4 J K-1 mol-1). The slightly negative ΔH term nevertheless reflects a substantial anomeric effect owing to the countervailing steric effects in the axial isomer. The significant entropy loss in the equatorial isomer was explained in terms of intramolecular electrostatic effects. The results are in agreement with those obtained from NMR studies of the conformational behaviour of 2-carboethoxy-5-methyl-5-aza-1,3-dithiacyclohexane.
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  • 114
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 115
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Reactions of benzo-, naphtho- and anthraquinone derivatives (unsubstituted and substituted) with aryliminodimagnesium [ArN(MgBr)2] and aryloxymagnesium of a weak electron-donating ability were studied. In addition to the reduction products (quinhydrones and hydroquinones), nuclear substitution and condensation products were formed. The efficiency of single electron transfer (SET) from ArN(MgBr)2, evaluated by the relative values of the difference between the oxidation and reduction potentials of the reactants (ΔE = Eox - Ered), varies with the electron-accepting power of quinones. ΔE governs the modes of semiquinone appearance (ESR signals) and the relative amounts of the heat of reactions, reflecting the types and yields of the products. It is concluded that condensation products of both components are produced in the reactions of quinones with the lower SET efficiency by the presence of a fused benzene ring or MeO substituent. The structure-reactivity relationship proposed previously for reactions of various magnesium reagents is extended in the reactions with a variety of quinones even in cases of higher SET efficiency.
    Additional Material: 6 Ill.
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  • 116
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 625-628 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Over the H0 acidity range from + 2 to -8, four different mechanistic variations occur in the Fischer indole reaction, leading to an unusual parabolic dependence of the rate constants on the acidity of the medium. In strongly acidic media kinetic isotope effects indicate that the rate-determining step is deprotonation to form the ene-hydrazine tautomer, whereas in weakly acidic media the tautomerization is so rapid that [3,3]-rearrangement becomes rate limiting. At an intermediate acidity, the deprotonation is rate determining, with the rate being strongly dependent on the concentration of the anionic counter ion.
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  • 117
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    Journal of Physical Organic Chemistry 7 (1994), S. 629-633 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Kinetic studies were carried out on the aminolysis of propargly and 1-methylpropargyl arenesulphonates in acetonitrile at 45·0°C. The cross-interaction constants, ρxz and βxz, are similar to, but smaller than, those for the SN2 processes at other primary and secondary carbon centers. Compared with the allyl series, the smaller magnitude of ρxz and βxz reflects a looser transition state, which in turn leads to a lower rate despite the greater Taft's σ* value and the lower intrinsic (ΔE0≠) and thermodynamic barriers (ΔE0).
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  • 118
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 7 (1994), S. 615-624 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Substitutent effects of acceptor groups were measured for the gas-phase basicities of some substituted benzonitriles, methyl benzoates and acetophenones, and for gas-phase acidities of some substituted benzoic acids. Substitutents considered were NO2, CN, SO2CH3, SO2F, CF3, CH2Cl, COCH3 and COOCH3, always in the meta and para positions. By combination with the literature data, a general conclusion is drawn that the substituent effects are proportional in the two positions and almost equal (the para:meta ratio is 1·06). No sign of any resonance effect was detected within the accuracy of the approach. The substituent effects in solution were recalculated statistically and the result was similar with a higher ratio, 1·09-1·19. It follows that the conjugation of acceptor groups, particularly of NO2 as a typical example, has been overestimated by current theories when compared with the much stronger conjugation of typical donors. Moreover, the inductive effect is propagated more effectively from the para than from the meta position. Many correlations in the literature, neglecting this situation, have been in fact controlled by the more complex, and more striking, behaviour of donors, which has obscured the simpler and more monotonous effect of acceptors, usually less represented in the sample.
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  • 119
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The label incorporation and Z → E isomerization in the reaction of 3-azidomethylenedihydro-(3H)-furan-2-one with Na15NN2 in 1:1 water-acetone were measured as a probe for internal clockwise vs anticlockwise rotation in the intermediate carbanion.
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  • 120
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The gas-phase basicities of eight pyrazoles substituted only at position 4 (R4 = H, NO2, F, Cl, CO2C2H5, CH3, NH2, 1-adamantyl) were measured by Fourier transform ion cyclotron resonance. The experimental values were treated in two ways, first by comparing these values with the AM1-calculated proton affinities. Since the correlation was reasonably good [PA(calc.) = -11·3 + 1·063PA(exp.), n = 8, r = 0·984], a set of 17 further 4-substituted pyrazoles and their cations were calculated using the AM1 approximation and their gas-phase basicities were estimated. Second, both the experimental and the AM1-calculated values were considered within the framework of the Taft-Topsom analysis of substituent effects. Comparison of the analyses for pyrazoles and pyridines led to the unexpected result that, in spite of differences in ring size and number of heteroatoms, both systems behave remarkably alike.
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  • 121
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A calorimetric method is described for the determination of the hydride affinities, ΔHH-(R+) of seven dioxolenium ions from the title compounds and also tropylium, trityl and 9-phenyl xanthylium cations by hydride transfer to the carbocations from BH3CN-. Cyclic voltammetric methods yield free energies for reduction of the cations to the conjugate radicals and to the carbanions. The ΔHH-(R+) values correlate well with the first reduction potentials of the cations.
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  • 122
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 15 (1994), S. 12-22 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The suitability of the two most widely used strategies to compute semiempirical MEPs is examined. For this purpose, MEP minima, electrostatic charges, and dipoles for a large number of molecules were computed at the AM1, MNDO, and PM3 levels using both the NDDO strategy developed by Ferenczy, Reynolds, and Richards and our own quasi-ab initio method. Results demonstrate that the quasi-ab initio is preferred over the NDDO method for the computation of MEP minima. It is also found that the best set of semiempirical charges and dipoles are obtained using either the AM1 NDDO or the MNDO quasi-ab initio methods. In these two cases, the quality of the results is fully comparable with 6-31G* values. © 1994 by John Wiley & Sons, Inc.
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  • 123
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    Journal of Computational Chemistry 15 (1994), S. 54-60 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Explicitly correlated Gaussian functions have been used in variational calculations on the ground state of the helium atom. The major problem of this application, as well as in other applications of the explicitly correlated Gaussian functions to compute electronic energies of atoms and molecules, is the optimization of the nonlinear parameters involved in the variational wave function. An effective Newton-Raphson optimization procedure is proposed based on analytic first and second derivatives of the variational functional with respect to the Gaussian exponents. The algorithm of the method and its computational implementation is described. The application of the method to the helium atom shows that the Newton-Raphson procedure leads to a good convergence of the optimization process. © 1994 by John Wiley & Sons, Inc.
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  • 124
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    Journal of Computational Chemistry 15 (1994), S. 90-104 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: We described various technical aspects in applying reaction field theories using continuum models to practical problems. It was investigated how solvent-dependent properties of solute molecules are influenced by the following factors: difference in quantum-chemical description of solute-solvent (continuum dielectric) interaction, difference in values of empirically determinable parameters such as atomic radii to define a size of a cavity created in a dielectric to accommodate a solute, and difference in the sophistication level of molecular orbital calculation, including electron correlation and different parameter sets (MNDO, AM1, and PM3). Through these investigations, the better parameter sets were found to evaluate accurately physicochemically important parameters such as hydration enthalpy. © 1994 by John Wiley & Sons, Inc.
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  • 125
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    Journal of Computational Chemistry 15 (1994), S. 132-143 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Ab initio MP2/6-31G*//MP2/6-31G* and semiempirical AM1 and PM3 calculations on a series of differently substituted α-oxo-ketenes are used to investigate E/Z-isomerism and rotational barriers in these molecules. Sterically crowded derivatives are found to exist solely as s-E conformers. The unusual stability of these derivatives thus can be attributed to their inability to adopt the s-Z conformation required for the normal α-oxo-ketene reactions. With respect to structures and energies, the PM3 method (especially in the case of highly crowded molecules) is found to be less reliable than AM1. Ab initio HF/3-21G and PM3 vibrational frequencies appear to be of sufficient accuracy for a distinction between s-Z and s-E conformers. In this respect, the AM1 method appears less reliable. © 1994 by John Wiley & Sons, Inc.
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  • 126
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 15 (1994), S. 200-207 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Atomic charges derived from a recently described approach to the very rapid computation of AM1 electrostatic potentials (ESP) accurately parallel, but are ca. 20% smaller than, the corresponding HF/6-31G* values. The dipole moments computed from the AM1 charges are virtually identical to those derived directly from the wave function and in rather better agreement with the experimental values than those computed using the HF/6-31G* charges. Unlike other approaches to the semiempirical calculation of ESP-derived charges, the present method also yields near HF/6-31G* quality potentials close to the molecular periphery. For medium-sized organic molecules (40-100 basis functions), the method is approximately two orders of magnitude faster than those involving prior deorthogonalization of AM1 wave function and explicit computation of the full ESP integral matrix. © 1994 by John Wiley & Sons, Inc.
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  • 127
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    Journal of Computational Chemistry 15 (1994), S. 233-240 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Rigid inhibitors suffer a smaller loss of conformational entropy when they bind to a macromolecular receptor than their acyclic counterparts. They can also be useful for elucidating pharmacophores due to their reduced conformational space and may be more amenable to synthesis. Computational approaches to rational drug design should therefore take these factors into consideration when suggesting possible compounds. We describe how an acyclic chain which links two parts of a receptor site can be ‘braced’ using ring templates. The acyclic chains may be produced from a number of sources, including lattices or the structures of known inhibitors. The resulting structures contain a rich variety of isolated and fused ring systems, which provide many useful molecular skeletons for subsequent inhibitor design. © 1994 by John Wiley & Sons, Inc.
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  • 128
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    Journal of Computational Chemistry 15 (1994), S. 251-268 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A general force field type of calculation has been devised in connection with MM3 to treat 1,2- and 1,4-diketones, both when they are not conjugated (as in derivatives of glyoxal) and when they are conjugated (as in derivatives of ortho- and para-benzoquinone). The molecular structures, moments of inertia, dipole moments, and vibrational spectra have been examined for about 15 compounds, some in several conformations. Ab initio calculations (6-31G*) have been used to determine quantities that have not been previously defined by experiment. In general, the force field permits the calculation of the structures with high accuracy, and the spectroscopic and conformational energy data with fair accuracy. © 1994 by John Wiley & Sons, Inc.
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  • 129
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    Journal of Computational Chemistry 15 (1994), S. 313-321 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Effective core potential (ECP) and full-electron (FE) calculations for MoS4-2, MoO4-2, and MoOCl4 compounds were analyzed. Geometry parameters, binding energies, charge distributions, and topological properties of the electronic density were studied for Mo—L bonds (L = S, O, Cl). Results clearly indicate that those approaches that include valence plus 4s and 4p electrons (ECP2 methods) are able to reproduce the topological properties of Mo—L bonds, charge distributions, and geometries with respect to those obtained by FE methods. ECP methods that consider only the 4d and 5s valence electrons (ECP1) fail in the calculation of molecular properties. The use of 5p functions in ECP1 approaches produces a negative Mulliken charge on Mo. Bader's charges give more consistent results than Mulliken's ones. A new parameter for measuring the degree of ionicity is proposed. © 1994 by John Wiley & Sons, Inc.
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  • 130
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    Journal of Computational Chemistry 15 (1994), S. 346-350 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The equilibrium geometries, excitation energies, force constants, and vibrational frequencies of the low-lying electronic states X2B1, 2A1, 2B2, and 2A2 of the PF2 radical have been calculated at the MRSDCI level with a double zeta plus polarization basis set. Our calculated geometry, force constants, and vibrational frequencies for the X2B1 state are in good agreement with experimental data. The electronic transition moments, oscillator strengths for the 2A1 → X2B1 and 2A2 → X2B1 transitions, and radiative lifetimes for the 2A1 and 2A2 states are calculated based on the MRSDCI wave functions. © 1994 by John Wiley & Sons, Inc.
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  • 131
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    Journal of Computational Chemistry 15 (1994), S. 351-373 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A coarse-grain parallel implementation of the free energy perturbation (FEP) module of the AMBER molecular dynamics program is described and then demonstrated using five different molecular systems. The difference in the free energy of (aqueous) solvation is calculated for two monovalent cations ΔΔGaq(Li+ Δ Cs+), and for the zero-sum ethane-to-ethane′ perturbation ΔΔGaq(CH3—methyl—X → X—methyl—CH3), where X is a ghost methyl. The difference in binding free energy for a docked HIV-1 protease inhibitor into its ethylene mimetic is examined by mutating its fifth peptide bond, ΔG(CO—NH → CH=CH). A potassium ion (K+) is driven outward from the center of mass of ionophore salinomycin (SAL-) in a potential of mean force calculation ΔGMeOH(SAL- · K+) carried out in methanol solvent. Parallel speedup obtained is linearly proportional to the number of parallel processors applied. Finally, the difference in free energy of solvation of phenol versus benzene, ΔΔGoct(phenol → benzene), is determined in water-saturated octanol and then expressed in terms of relative partition coefficients, Δ log(Po/w). Because no interprocessor communication is required, this approach is scalable and applicable in general for any parallel architecture or network of machines. FEP calculations run on the nCUBE/2 using 50 or 100 parallel processors were completed in clock times equivalent to or twice as fast as a Cray Y-MP. The difficulty of ensuring adequate system equilibrium when agradual configurational reorientation follows the mutation of the Hamiltonian is discussed and analyzed. The results of a successful protocol for overcoming this equilibration problem are presented. The types of molecular perturbations for which this method is expected to perform most efficiently are described. © 1994 by John Wiley & Sons, Inc.
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  • 132
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    Journal of Computational Chemistry 15 (1994), S. 405-423 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The vibrational spectra of oligomers of thiophene are treated theoretically with the main purpose of deriving information for the interpretation of the infrared and Raman spectra of the polymer and isotopic derivatives. We report the results of a series of semiempirical MNDO calculations on the structure and vibrational properties of oligothiophenes, and we compare the calculated MNDO Pulay scaled force field of the monomer with an empirical harmonic force field that we have obtained by least squares refinement on nine isotopic derivatives. The scaling factors obtained were transferred from thiophene for the computation of the vibrational spectrum and the phonon dispersion curves of the polymer. © 1994 by John Wiley & Sons, Inc.
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  • 133
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    Journal of Computational Chemistry 15 (1994), S. 475-475 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
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  • 134
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    Journal of Computational Chemistry 15 (1994), S. 507-523 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A fast computer algorithm is presented for complete analytical calculation of van der Waals surfaces and volumes. Connolly's analytical algorithms, computing second- and third-order atomic spheres overlaps, are shown to give insufficient numerical approximations of the exact van der Waals surfaces and volumes. The presented algorithm computes overlaps of any order. Practical situations frequently involve six-order overlaps. Analytical computed surfaces and volumes of 63 chemicals are compared with Monte Carlo measured values. © 1994 by John Wiley & Sons, Inc.
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  • 135
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    Journal of Computational Chemistry 15 (1994), S. 488-506 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: An efficient methodology, further referred to as ICM, for versatile modeling operations and global energy optimization on arbitrarily fixed multimolecular systems is described. It is aimed at protein structure prediction, homology modeling, molecular docking, nuclear magnetic resonance (NMR) structure determination, and protein design. The method uses and further develops a previously introduced approach to model biomolecular structures in which bond lengths, bond angles, and torsion angles are considered as independent variables, any subset of them being fixed. Here we simplify and generalize the basic description of the system, introduce the variable dihedral phase angle, and allow arbitrary connections of the molecules and conventional definition of the torsion angles. Algorithms for calculation of energy derivatives with respect to internal variables in the topological tree of the system and for rapid evaluation of accessible surface are presented. Multidimensional variable restraints are proposed to represent the statistical information about the torsion angle distributions in proteins. To incorporate complex energy terms as solvation energy and electrostatics into a structure prediction procedure, a “double-energy” Monte Carlo minimization procedure in which these terms are omitted during the minimization stage of the random step and included for the comparison with the previous conformation in a Markov chain is proposed and justified. The ICM method is applied successfully to a molecular docking problem. The procedure finds the correct parallel arrangement of two rigid helixes from a leucine zipper domain as the lowest-energy conformation (0.5 Å root mean square, rms, deviation from the native structure) starting from completely random configuration. Structures with antiparallel helixes or helixes staggered by one helix turn had energies higher by about 7 or 9 kcal/mol, respectively. Soft docking was also attempted. A docking procedure allowing side-chain flexibility also converged to the parallel configuration starting from the helixes optimized individually. To justdy an internal coordinate approach to the structure prediction as opposed to a Cartesian one, energy hypersurfaces around the native structure of the squash seeds trypsin inhibitor were studied. Torsion angle minimization from the optimal conformation randomly distorted up to the rms deviation of 2.2 Å or angular rms deviation of l0° restored the native conformation in most cases. In contrast, Cartesian coordinate minimization did not reach the minimum from deviations as small as 0.3 Å or 2°. We conclude that the most promising detailed approach to the protein-folding problem would consist of some coarse global sampling strategy combined with the local energy minimization in the torsion coordinate space. © 1994 by John Wiley & Sons, Inc.
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  • 136
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    Journal of Computational Chemistry 15 (1994) 
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    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
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  • 137
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    Journal of Computational Chemistry 15 (1994), S. 627-632 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: An important area of research in computational biochemistry is the design of molecules for specific applications. The design of these molecules, which depends on the accurate determination of their three-dimensional structure, can be formulated as a global optimization problem. In this article, we present results from the application of a new conformation searching method based on direct search methods. We compare these results to some earlier results using genetic algorithms and simulated annealing. © 1994 by John Wiley & Sons, Inc.
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  • 138
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    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
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    Notes: The consistency of three density functional computational implementations (DMol, DGauss, and deMon) are compared with high-level Hartree-Fock and Møller-Plesset (MP) calculations for triazene (HN=NNH2) and formyl triazene (HN=NNHCOH). Proton affinities on all electronegative sites are investigated as well as the geometries of the neutral and protonated species. Density functional calculations employing the nonlocal gradient corrections show agreement with MP calculations for both proton affinities and geometries of neutral and protonated triazenes. Local spin density approximation DMol calculations using numerical basis sets must employ an extended basis to agree with other density functional codes using analytic Gaussian basis sets. The lowest energy conformation of triazene was found to be nonplanar; however, the degree of nonplanarity, as well as some bond lengths, is dependent on the basis set, electron correlation treatment, and methods used for the calculation. © 1994 by John Wiley & Sons, Inc.This article is a U.S. Government work and, as such, is in the public domain in the United States of America.
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  • 139
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    Journal of Computational Chemistry 15 (1994), S. 899-916 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: We describe a method for locating clusters of geometrically similar conformers in ensembles of chemical conformations. We first calculate the pairwise interconformational distance matrix in either torsional or Cartesian space and then use an agglomerative, single-link clustering method to define a hierarchy of clusterings in the same space. Especially good clusterings are distinguished by high values of the separation ratio: the ratio of the shortest intercluster distance to the characteristic threshold distance defining the clustering. We also discuss other statistics. The method has been embodied in a program called XCluster, which can display the distance matrix, the hierarchy of clusterings, and the clustering statistics in a variety of formats. XCluster can also write out the clustered conformations for subsequent or simultaneous viewing with a molecular visualization program. We demonstrate the sorts of insight that this approach affords with examples obtained from conformational search and molecular dynamics procedures. © 1994 by John Wiley & Sons, Inc.
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  • 140
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    Journal of Computational Chemistry 15 (1994), S. 937-946 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The methodology of conformational potential energy (hyper)surface (PES) elucidation is the subject of this article. The decomposition of the recently developed software CICADA and its implementation in the distributed environment using PVM (parallel virtual machine) is presented. CICADA has been chosen for the parallelization because of its ability to elucidate systematically the low-energy areas of PES in polynomial time. This makes the method applicable on larger systems which are beyond the scope of the grid search. To show the level of parallelization, conformational PES of two molecules, cyclohexane and terminally blocked alanine, have been studied by the distributed version, D-CICADA, and results have been compared to those of the sequential version. D-CICADA was tested on several virtual machines composed of DEC and Sun workstations. The timing shows good efficiency for both the decomposition of the original algorithm and the PVM environment. © 1994 by John Wiley & Sons, Inc.
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  • 141
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    Journal of Computational Chemistry 15 (1994), S. 997-1012 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: We present a novel algorithm of constrained, overdamped dynamics to study the long-time properties of peptides, proteins, and related molecules. The constraints are applied to an all-atom model of the molecule by projecting out all components of the nonbonding interactions which tend to alter fixed bond lengths and angles. Because the overdamped dynamical equations are first order in time, the constraints are satisfied by inversion of a banded matrix at each timestep, which is computationally efficient. Thermal effects are included through a Langevin noise term in the equation of motion. Because high-frequency components of the motion have been eliminated, the timestep of the algorithm is determined by the nonbonding forces, which are two to three orders of magnitude weaker than the bonding forces. Using polyalanine as a test example, we demonstrate that trajectories simulating a microsecond of motion can be run about 103 times faster than an equivalent molecular dynamics simulation. © 1994 by John Wiley & Sons, Inc.
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  • 142
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    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Although there is a similarity in the orbital interaction scheme between quinhydrone and N,N,N′,N′-tetramethyl-p-diaminobenzene-chloranil complex, the stacking conformations are different from each other. The former prefers the half-stacked conformation, whereas the latter prefers the completely stacked conformation. We have done ab initio molecular orbital calculations and decomposition analyses of the intermolecular interaction energies to clarify the origin of the different stacking conformations. It was concluded that the main origin is the difference in the steric part of the interaction energies. © 1994 by John Wiley & Sons, Inc.
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  • 143
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    Journal of Computational Chemistry 15 (1994), S. 1019-1040 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A force field for monosaccharides that can be extended to (1 → 4) linked polysaccharides has been developed for the AMBER potential function. The resulting force field is consistent with the existing AMBER force field for proteins and nucleic acids. Modifications to the standard AMBER OH force constant and to the Lennard-Jones parameters were made. Furthermore, a 10-12 nonbonded term was included between the hydroxyl hydrogen of the saccharide and the water oxygen (TIP3P, SPC/E, etc.) to reproduce better the water-saccharide intermolecular distances. STO-3G electrostatic potential (ESP) charges were used to represent the electrostatic interactions between the saccharide and its surrounding environment. To obtain charges for polysaccharides, a scheme was developed to piece together saccharide residues through 1 → 4 connections while still retaining a net neutral charge on the molecule as a whole. Free energy perturbation (FEP) simulations of D-glucose and D-mannose in water were performed to test the resulting force field. The FEP simulations demonstrate that AMBER overestimates intramolecular interaction energies, suggesting that further improvements are needed in this part of the force field. To test further the reliability of the parameters, a molecular dynamics (MD) simulation of α-D-glucose in water was also performed. The MD simulation was able to produce structural and conformational results that are in accord with experimental evidence and previous theoretical results. Finally, a relaxed conformational map of β-maltose was assembled and it was found that the present force field is consistent with available theoretical and experimental results. © 1994 by John Wiley & Sons, Inc.
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  • 144
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    Journal of Computational Chemistry 15 (1994), S. 1302-1310 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Although Monte Carlo and molecular dynamics are the primary methods used for free energy simulations of molecular systems, their application to molecules that have multiple conformations separated by energy barriers of ≥ 3 kcal/mol is problematic because of slow rates of convergence. In this article we introduce a hybrid simulation method termed MC-SD which mixes Monte Carlo (MC) and stochastic dynamics (SD). This new method generates a canonical ensemble via alternating MC and SD steps and combines the local exploration strengths of dynamics with the barrier-crossing ability of large-step Monte Carlo. Using calculations on double-well potentials and long simulations (108 steps of MC and 1 μs of SD) of the simple, conformationally flexible molecule n-pentane, we find that MC-SD simulations converage faster than either MC or SD alone and generate ensembles which are equivalent to those created by classical MC or SD. Using pure SD at 300 K, the conformational populations of n-pentane are shown to be poorly converged even after a full microsecond of simulation. © 1994 by John Wiley & Sons, Inc.
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  • 145
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    Journal of Computational Chemistry 15 (1994), S. 1321-1330 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The MM2 and MM3 force fields have been extended to cover this class of compounds. Structures, vibrational spectra, and other data for 13 compounds were examined and can be reproduced satisfactorily by MM3. Except for the spectra, the other data can be reproduced somewhat less well by MM2. © 1994 by John Wiley & Sons, Inc.
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  • 146
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    Journal of Computational Chemistry 15 (1994), S. 1357-1364 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The details of a simple and efficient scheme for performing variational biorthogonal valence bond calculations are presented. A variational bound on the energy functional is obtained through the use of a complete configuration expansion in a well-chosen subset of orbitals. The resultant wave functions are clearly dominated by the covalent (spin-coupled) structures, with a negligible contribution from ionic structures. The orbitals obtained compare favorably with overlap enhanced atomic orbitals obtained by other valence bond approaches. The method is illustrated by calculations on water and dioxygen difluoride. © 1994 by John Wiley & Sons, Inc.
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  • 147
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    Journal of Computational Chemistry 15 (1994), S. 1278-1290 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Two-dimensional protein (ferritin) aggregates with a square lattice symmetry, which were formed within a thin liquid layer on a mercury surface, were studied by molecular dynamics (MD) simulation. For the simulation, the ferritin molecule was modeled by an assembly of 49 spheres, and the intermolecular interactions were given by simple formulae. During the simulation, molecules were confined within a layer, which corresponds to the thin liquid layer. An annealing MD simulation was done starting from a random molecular configuration within the layer, and aggregates with the square lattice symmetry were also obtained. To study the stability of aggregates, dissociation processes of the aggregates were analyzed using MD simulations at room temperature. Interactions between the nearest-neighbor molecules were regarded as bonds. Mean bond energies and correlation coefficients between the bond energies were calculated from the MD trajectories. A decay profile according to the dissociation was obtained, yielding a dissociation rate constant. Buried bonds were stronger than peripheral bonds. The larger the aggregate size, the stronger the bond for each of the buried and peripheral bonds. A simple theoretical account, which is applicable to a general bonded network, was introduced to analyze the dynamics of the aggregates. © 1994 by John Wiley & Sons, Inc.
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    Journal of Computational Chemistry 15 (1994), S. 1291-1301 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The Jacobian method in the refinement of force constants is studied. Theoretical and experimental frequencies and other observables, νs, are matched by minimizing ΣsWs(νsexp - νsth)2, where s = 1, 2, 3,…, proceeds over all normal modes and isotopes, and Ws are weighting factors. Modification of the theoretical frequencies is accomplished with the Jacobian matrix, J, with elements Jsi = ∂νs/∂ki involving each force constant or associated parameter, ki, i = 1, 2, 3,…, by Δν = JΔk. The parameters are adjusted directly with Δk = (JTWJ)-1(JW) Δν, where W is a diagonal matrix which weights the frequencies. The linear dependence problem must be addressed prior to inversion of JTWJ. The approach entails diagonalization of JT WJ, analysis of the components of the eigenvectors associated with zero and small eigenvalues, identification of the linearly dependent parameters, successive elimination of selective parameters, and a repeat of this procedure until linear dependency is removed. The Jacobian matrices are obtained by differencing the frequencies when the parameters are varied and by numerical and analytical evaluation of the derivative of the potential. The unitary transformation, U, used to calculate J = UT (∂F/∂k)U or J = UT (ΔF/Δk)U, is obtained from the diagonalization of the Hessian, Fmn = ∂2ν/∂pm∂qn, where p, q = x, y, z are the Cartesian coordinates for atoms m, n = 1, 2, 3,…, at the initial value of ki, i = 1, 2, 3,⃜ The accuracy of and the ability to evaluate the Jacobian matrix by these methods are discussed. Applications to CH4, H2CO, C2H4, and C2H6 are presented. Linearly dependent and ill-conditioned parameters are identified and removed. The procedure is general for any observable quantity. © 1994 by John Wiley & Sons, Inc.
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    Journal of Computational Chemistry 15 (1994), S. 1331-1340 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Two traditional clustering algorithms are applied to configurations from a long molecular dynamics trajectory and compared using two sets of test data. First, a subset of atoms was chosen to present conformations which naturally fall into a number of clusters. Second, a subset of atoms was selected to span a relatively continuous region of conformational space rather than form discrete conformational classes. Of the two algorithms used, the single linkage method is inappropriate for this kind of data. The divisive hierarchical method, based on minimizing the difference between cluster centroids and extrema, is successful but also prone to imposing clustering hierarchy where none can be justified. © 1994 by John Wiley & Sons, Inc.
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  • 150
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    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
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    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The special-purpose computer GRAPE-2A accelerates the calculation of pairwise interactions in many-body systems. This computer is a back-end processor connected to a host computer through a Versa Module Europe (VME) bus. GRAPE-2A receives coordinates and other physical data for particles from the host and then calculates the pairwise interactions. The host then integrates an equation of motion by using these interactions. We did molecular dynamics simulations for two systems of liquid water: System 1 (1000 molecules), and System 2 (1728 molecules). The time spent for one step of molecular dynamics was 3.9 s (System l), and 10.2 s (System 2). The larger the molecular system, the higher the performance. The speed of GRAPE-2A did not depend on the formula describing the pairwise interaction. The cost performance was about 20 times better than that of the fastest workstations available today, and GRAPE-2A cost only $22,000. © 1994 by John Wiley & Sons, Inc.
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    Journal of Computational Chemistry 15 (1994), S. 23-27 
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    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A scheme for generating water coordinates, whose proton orientations are random, and simultaneously generating side chain coordinates of peptides, preparatory to studying solvation of peptides using molecular dynamics schemes is presented in an X-PLOR context. Examples from the Integrin and Tropomyosin systems are used to illustrate the procedure. © 1994 by John Wiley & Sons, Inc.
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  • 152
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    Journal of Computational Chemistry 15 (1994), S. 61-71 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: Zinc ions have been shown to inhibit human immunodeficiency virus type 1 (HIV-1) protease in vitro at neutral pH [Zhang et al. Biochemistry, 36, 8717 (1991)]. Kinetic data from this study support a reversible binding mechanism of zinc in the active site. Preliminary calculations of the ion-protein potential energy based on the geometry of the crystallographic structure [Wlodawer et al. Science, 245, 616 (1989)] are consistent with this proposed mechanism. To examine the structure of HIV-1 protease with zinc bound in the active site, molecular dynamics simulations in the presence and absence of zinc at this site have been carried out to 200 ps. These simulations suggest zinc remains stably bound to the catalytic aspartate residues without disruption of the dimer or significant alteration of the active site structure. These data are consistent with those observed by Zhang et al. (1991), and together give strong evidence that this is the binding site that leads to inactivation. A proposed model of zinc binding at the active site based on quantum mechanical calculations indicates Zn+2 coordination is monodentate with each catalytic aspartate, leaving at least two ligand positions potentially free (occupied by water molecules in the calculations). © 1994 by John Wiley & Sons, Inc.
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  • 153
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    Journal of Computational Chemistry 15 (1994) 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
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  • 154
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    Journal of Computational Chemistry 15 (1994), S. 144-148 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: In this article, we develop and implement an algorithm for calculating the rovbrational states of diatomic molecules optimized for multiple instructions multiple data computers of distributed memory. The method is based upon the p-version of the finite element method and has been implemented on an INTEL iPSC/2 machine with 16 processors. © 1994 by John Wiley & Sons, Inc.
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  • 155
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: A new method for deriving force fields for molecular simulations has been developed. It is based on the derivation and parameterization of analytic representations of the ab initio potential energy surfaces. The general method is presented here and used to derive a quantum mechanical force field (QMFF) for alkanes. It is based on sampling the energy surfaces of 16 representative alkane species. For hydrocarbons, this force field contains 66 force constants and reference values. These were fit to 128,376 quantum mechanical energies and energy derivatives describing the energy surface. The detailed form of the analytic force field expression and the values of all resulting parameters are given. A series of computations is then performed to test the ability of this force field to reproduce the features of the ab initio energy surface in terms of energies as well as the first and second derivatives of the energies with respect to molecular deformations. The fit is shown to be good, with rms energy deviations of less than 7% for all molecules. Also, although only two atom types are employed, the force field accounts for the properties of both highly strained species, such as cyclopropane and methylcyclopropanes, as well as unstrained systems. The information contained in the quantum energy surface indicates that it is significantly anharmonic and that important intramolecular coupling interactions exist between internals. The representation of the nature of these interactions, not present in diagonal, quadratic force fields (Class I force fields), is shown to be important in accounting accurately for molecular energy surfaces. The Class II force field derived from the quantum energy surface is characterized by accounting for these important intramolecular forces. The importance of each 4.2 to 18.2%. This fourfold increase in the second derivative error dramatically demonstrates the importance of bond anharmonicity in the ab initio potential energy surface. The Class II force field derived from the quantum energy surface is characterized by accounting for these important intramolecular forces. The importance of each of the interaction terms of the potential energy function has also been assessed. Bond anharmonicity, angle anharmonicity, and bond/angle, bond/torsion, and angle/angle/ torsion cross-term interactions result in the most significant overall improvement in distorted structure energies and energy derivatives. The implications of each energy term for the development of advanced force fields is discussed. Finally, it is shown that the techniques introduced here for exploring the quantum energy surface can be used to determine the extent of transferability and range of validity of the force field. The latter is of crucial importance in meeting the objective of deriving a force field for use in molecular mechanics and dynamics calculations of a wide range of molecules often containing functional groups in novel environments. © 1994 by John Wiley & Sons, Inc.
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  • 156
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    International Journal of Chemical Kinetics 26 (1994), S. 705-718 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The multiphoton decomposition of CF3I with a pulsed CO2 laser has been studied at incident fluences of 0.6 and 1.2 J/cm2. The effect of pressure on the reaction probability for dissociation of CF3I was measured in the presence of added isobutane, Ar and CO2. In the experiments with isobutane, the CF3 radicals generated by the decomposition of excited CF3I react to yield CF3H in competition with the recombination to C2F6. The laser absorption cross section was also measured as a function of fluence at a pressure of 0.1 torr of CF3I and with 0.5-2.0 torr of added isobutane. The experimental results were modeled with a master equation in order to obtain information on the energy transferred by collisions of excited CF3I with the bath molecules. An energy dependent value of 〈ΔE〉d produces the best fit to the experimental data. Integration of the rate equations to account for the fractional product yield, [CF3I]/[C2F6], allowed for the calculation of the specific rate constant for hydrogen abstraction from isobutane by CF3 radicals. The value obtained is dependent on the total pressure and higher than expected at room temperature. From these results, an effective temperature for the reaction mixture was calculated. © 1994 John Wiley & Sons, Inc.
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  • 157
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    International Journal of Chemical Kinetics 26 (1994), S. 743-747 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An exceptional kinetic behavior on the reactivity of β-diketones against copper(II) have been found. Some relationship between ligand basicity and unexpected enhancement on the rates of complex formation, which may be useful for predicting rate constants of similar monochelated copper(II) complexes, are established. © 1994 John Wiley & Sons, Inc.
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  • 158
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    International Journal of Chemical Kinetics 26 (1994) 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 159
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    International Journal of Chemical Kinetics 26 (1994), S. 869-886 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In earlier work on the room temperature oxidation of C2H2 by O atoms, two distinct sources of methylene radicals have been identified: (i) direct, primary production via channel 1b of the C2H2 + O reaction, and (ii) delayed formation via the secondary reaction 3 involving the products HCCO and H of the other primary channel 1a: Presently, it was confirmed by a detailed sensitivity analysis that the precise shapes of the resulting total methylene concentration-versus-time profiles in C2H2/O systems depend strongly on the k1a/k1b branching ratio. Along that line, the important parameter k1a/k1b was determined from relative CH2 concentration-versus-time profiles measured in a variety of C2H2/O/H systems using Discharge Flow-Molecular Beam sampling Mass Spectrometry techniques (DF-MBMS). The data analysis was carried out by deductive kinetic modelling; the method, as applied to profile shapes, is discussed at length. Via this novel, independent approach, the CH2(3B1) yield of the two-channel C2H2 + O reaction was determined to be k1b/k1 = 0.17 ± 0.08. The indicated 2σ error includes possible systematic errors due to uncertainties in the rate constants of other reactions that influence the shapes of the CH2 profiles. The present result, which translates to an HCCO yield k1a/k1 = 0.83 ± 0.08, is in excellent agreement with other recent determinations. The above mechanism, with the subsequent reactions that it initiates, also reproduces the measured absolute [C2H2], [O], and [H] profiles with an average accuracy of 5%, thus validating the consistency of the C2H2/O/H reaction model put forward here. © 1994 John Wiley & Sons, Inc.
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  • 160
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    International Journal of Chemical Kinetics 26 (1994), S. 921-928 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition of water vapor has a strong positive effect on the rate of ethane oxidation at 575°C. This effect is attributed to the role of H2O as a third body in the decomposition of H2O2 to OH radicals. Carbon tetrafluoride likewise enhances the rate of ethane conversion, although not to the extent realized with H2O. A kinetic model, based on known elementary reactions, adequately accounts for the conversions and selectivities observed as a function of H2O pressure, temperature, contact time, and O2 pressure. © 1994 John Wiley & Sons, Inc.
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  • 161
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    International Journal of Chemical Kinetics 26 (1994), S. 929-944 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The formation yields of selected products of the OH radical-initiated reactions of toluene, o-xylene, and 1,2,3,-trimethylbenzene have been measured in the absence of NOx and in the presence of varying concentrations of NO and NO2. The formation yield of o-cresol from toluene increased from 0.123 ± 0.022 in the absence of NOx to 0.160 ± 0.008 for an average NO2 concentration of 1.7 × 1014 molecule cm3. The formation yield of 2,3-butanedione from o-xylene was 0.092 ± 0.013 in the absence of NOx, and in the presence of NOx decreased from 0.16 at an average NO2 concentration of (7-8) × 1012 molecule cm-3 to 0.09 at an average NO2 concentration of ca. 7 × 1013 molecule cm-3. The formation yield of 2,3-butanedione from 1,2,3-trimethylbenzene increased from 0.18 in the absence of NOx to 0.444 ± 0.053 in the presence of ca. (0.16-3.6) × 1013 molecule cm-3 of NO2. These product data are consistent with literature kinetic data showing that the hydroxycyclohexadienyl radicals formed by OH radical addition to the aromatic ring react with both O2 and NO2 and with the NO2 reaction rate constants being ca. 105 higher than the O2 reaction rate constants at room temperature. Under typical tropospheric conditions the reactions of the hydroxycyclohexadienyl radicals with O2 will dominate over their reactions with NO2. © 1994 John Wiley & Sons, Inc.
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  • 162
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    International Journal of Chemical Kinetics 26 (1994) 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 163
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    International Journal of Chemical Kinetics 26 (1994), S. 991-996 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experimental and theoretical investigations of bistability occurring in the nitric acid-hydroxylamine CSTR system are presented. Features of the stationary concentration vs. inlet concentration diagram and some mechanistic implications are discussed. © 1994 John Wiley & Sons, Inc.
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  • 164
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    International Journal of Chemical Kinetics 26 (1994), S. 1013-1021 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic data on the esterification of succinic anhydride with methanol catalyzed by sulfuric acid have been obtained using a stirred batch reactor. In addition to get a precise ascertainment of the parameters the esterification of monomethyl succinate with methanol has been studied separately. Several experiments have been carried out with different initial molar ratios and different amounts of sulfuric acid at various temperatures. The conversion to dimethyl succinate at 30-65°C follows a first-order rate expression with respect to each component. A theoretical rate equation is derived by the following reaction mechanism: (1) succinic anhydride is protonated by sulfuric acid to form a reaction intermediate, (2) irreversible esterification to monomethyl succinate, (3) protonation of the monoester, and (4) the esterification to dimethyl succinate proceeds reversibly. The resultant kinetic equation fitted the experimental data quite well and is given by the expression: \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{dc_{{\rm CH}_{\rm 3} {\rm OH}}}}{{dt}} = c_{{\rm H}_2 {\rm SO}_4} \left[{- 4.344*10^8 e^{- 65239/RT} c_{{\rm C}_4 {\rm H}_{\rm 4} {\rm O}_3 {\rm C}_{{\rm CH}_{\rm 3} {\rm OH}}} {\rm - 2}{\rm .457*10}^{\rm 6} e^{- 57732/RT} c_{{\rm C}_{\rm 5} {\rm H}_{\rm 8} {\rm O}_{\rm 4}} c_{{\rm CH}_3 {\rm OH}} + 229e^{- 34361/{\rm RT}} c_{{\rm C}_6 {\rm H}_{{\rm 10}} {\rm O}_{\rm 4} {\rm C}_{{\rm H}_{\rm 2} {\rm O}}}} \right] $$\end{document} © 1994 John Wiley & Sons, Inc. © 1994 John Wiley & Sons, Inc.
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  • 165
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    International Journal of Chemical Kinetics 26 (1994), S. 903-912 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of CO2·- with bilirubin which is not detectable in homogeneous aqueous medium proceeds almost with diffusion controlled rate in CTAB micellar system. This could be explained on the basis of catalysis caused by the possible electrostatic surface potential of cationic CTAB Micelles. The rate constant for the oxidation of bilirubin by haloperoxyl radicals have been shown to increase with increasing solvent polarity. Although the polarity effect was small, it followed a trend in the expected direction. Micellar effect was not observed in the oxidation reactions when alcohol was present in high concentration. But a small increase in the rate constant was observed when alcohol concentration was lower. © 1994 John Wiley & Sons, Inc.
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  • 166
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A regression based model was developed to determine whether highest occupied molecular orbital (HOMO) energies, calculated using Kohn-Sham orbital density functional theory (DFT), could be used to estimate the OH rate constants of hydrofluorocarbons (HFCs) and hydrofluoroethers (HFEs), proposed substitutes for stratospheric O3 depleting chlorofluorocarbons. The goodness of fit of the DFT model was compared with a second regression model, derived using recently reported HOMO energies obtained from Hartree Fock theory (HFT). Both models were employed to predict OH rate constants for a number of HFCs and HFEs whose OH rate constants have not been measured, thus providing data on the types of chemical structures that may increase the OH reactivity of the substitute and hence decrease its contribution to global warming. The estimated percent standard errors in the OH rate constant HFT and DFT regression models were 72% and 78%, respectively. The goodness of fits were such that the models can differentiate between two rate constants only when their ratio exceeds about a factor of four. Model results suggest that (1) only a limited number of HFEs will have OH rate constants that are more than an order of magnitude greater than the value for their corresponding HFCs and (2) the strategy of introducing an ether linkage into an HFC to dramatically enhance its reactivity will be most effective for the least fluorinated HFCs. © 1994 John Wiley & Sons, Inc.This article is a US Government work and, as such, is in the public domain in the United States of America.
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  • 167
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    International Journal of Chemical Kinetics 26 (1994), S. 951-954 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gas-phase elimination reactions of number of N-substituted diacetamides have been studied. The rates of N-phenyl, 4-methoxyphenyl, 4-nitrophenyl, and benzyl diacetamide have been measured between 643-683, 642-693, 673-725, and 555-610 K, respectively. They undergo unimolecular first-order elimination reactions, for which log A = 12.8, 12.9, 12.8, and 11.0 s-1 and Ea = 185.7, 191.4, 193.4, and 143.6 kJ mol-1, respectively. The reactivity of these compounds has been compared with the unsubstituted diacetamide at 600 K. The kinetic data reveals that each of the N-aryldiacetamides is less reactive than the parent molecule. We attribute this observation to the resonance of the lone pair of electrons on the nitrogen with either the two carbonyl oxygen atoms or with the 6π electrons in the aromatic ring which will result in the stabilization of the N-aryldiacetamides related to the parent molecules. © 1994 John Wiley & Sons, Inc.
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  • 168
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    International Journal of Chemical Kinetics 26 (1994), S. 963-972 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic micelles of alkyltrimethylammonium chloride and bromide (alkyl = n—C12H25, n—C14H29, and n—C16H33) catalyze and anionic micelles of sodium dodecyl sulfate inhibit the reaction of hydroxide ion with 2-phenoxyquinoxaline (1). Inert anions such as chloride, nitrate, mesylate, and n-butanosulfonate inhibit the reaction in CTABr by competing with OH- at the micellar surface. The overall micellar effects on rate in cationic micelles and dilute electrolyte can be treated quantitatively in terms of the pseudo-phase ion-exchange model. The determined second-order rate constants in the micellar pseudo-phase are smaller than the second-order constants in water. © 1994 John Wiley & Sons, Inc.
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  • 169
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    International Journal of Chemical Kinetics 26 (1994), S. 681-692 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of base hydrolysis of (αβ S)-(o-methoxy benzoato) (tetraethylenepentamine)cobalt(III) obeyed the rate law: kobs = kOH[OH-], in the range 0.05 ≤ [OH-]T, mol dm-3 ≤ 1.0, I = 1.0 mol dm-3, and 20.0-40.0°C. At 25°C, kOH = 13.4 ± 0.4 dm3 mol-1 s-1, ΔH≠ = 93 ± 2 kJ mol-1 and ΔS≠ = 90 ± 5 JK-1 mol-1. Several anions of varying charge and basicity, CH3CO2-, SO32-, SO42-, CO32-, C2O42-, CH2(CO2)22-, PO43-, and citrate3- had no effect on the rate while phthalate2-, NTA3-, EDTA4-, and DTPA5- accelerated the process via formation of the reactive ion pairs. The anionic (SDS), cationic (CTAB), and neutral (Triton X-100) micelles, however, retarded the reaction, the effect being in the order SDS〉 CTAB 〉 Triton X-100. The importance of electrostatic and hydrophobic effects of the micelles on the selective partitioning of the reactants between the micellar and bulk aqueous pseudo-phases which control the rate are discussed. © 1994 John Wiley & Sons, Inc.
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  • 170
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    International Journal of Chemical Kinetics 26 (1994), S. 729-736 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Classical trajectory calculations on the methyl isocyanide molecule at energies above 25,000 cm-1 confirm that the rate of reaction to methyl cyanide is bimodal, with a very fast rate before 0.1 ps, and a slower rate from then on. We conclude that before 0.1 ps, the reacting molecules are unrandomized, but thereafter, they are essentially randomized, with decay to products being, to a good approximation, pure exponential. We estimate that the time for randomization is roughly 0.3 ps at energies near the reaction threshold of 13,500 cm-1. © 1994 John Wiley & Sons, Inc.
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  • 171
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    International Journal of Chemical Kinetics 26 (1994), S. 749-756 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new flowtube reactor employing dissociative electron attachment to produce radicals and high-pressure photoionization in the mass spectrometric detection of radicals is described. The system has been applied to a study of the association reactions of CHCl2 and CCl3 with O2 in a great excess of helium at total densities below 1017 cm-3 over the temperature range 286 to 332 K. Both reactions display a strong negative temperature coefficient. The results can be parameterized in the form k0(CHCl2 + O2) = (4.3 ± 0.2) × 10-31(T/300)-6.7±0.7 cm6 s-1, k0(CCl3 + O2) = (2.7 ± 0.2) × 10-31(T/300)-8.7±1.0 cm6 s-1. © 1994 John Wiley & Sons, Inc.
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  • 172
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    International Journal of Chemical Kinetics 26 (1994), S. 801-812 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants for the reactions of the DS radical with NO2 (reaction 1) and ClNO (reaction 2) have been measured using the discharge-flow technique at 2 torr total pressure of helium. The DS radical was monitored by laser-induced fluorescence. The reactions were found to have the following bimolecular rate constants (95% confidence level, in units of cm3 molecule-1 s-1): \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k_{\rm 1} = \left({3.4 \pm 0.8} \right) \times 10^{- 11} \exp \left[{{{\left({210 \pm 70} \right)} \mathord{\left/ {\vphantom {{\left({210 \pm 70} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right] \\ k_{\rm 2} = \left({2.2 \pm 0.5} \right) \times 10^{- 11} \exp \left[{{{\left({- 480 \pm 100} \right)} \mathord{\left/ {\vphantom {{\left({- 480 \pm 100} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right] \\ \end{array} $$\end{document} This expression for k1 is found to be in excellent agreement with one of several previous studies. The magnitude of k2 is examined within the framework of a well-established reactivity trend. © 1994 John Wiley & Sons, Inc.
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  • 173
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    International Journal of Chemical Kinetics 26 (1994), S. 757-770 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ignition of propane has been studied in a shock tube and by computational modeling to determine the effect of methyl tert-butyl ether (MTBE) as a fuel additive. MTBE and isobutene were added in amounts up to 25% of the fuel to propane-oxygen-argon mixtures in shock tube experiments covering a range of temperatures between 1450 and 1800 K. Ignition delays were measured from chemiluminescence at 432 nm due to excited CH radicals. The temperature dependence of the ignition rates was analyzed to yield Arrhenius parameters of Ea ca. 40 kcal/mol and A ca. 109 s-1 for the overall propane reaction and Ea ca. 34 kcal/mol and A ca. 108.3 s-1 for the overall propane/MTBE reaction. Reactions involving MTBE and its decomposition products were combined with an established propane mechanism in a numerical model to describe the kinetic interaction of this additive with a typical hydrocarbon fuel. The experiments and the kinetic model both show that MTBE and isobutene retard propane ignition with nearly equal efficiency. The kinetic model demonstrates that isobutene kinetics are responsible for inhibition by both MTBE and isobutene, and the specific elementary reactions that produce this behavior are identified. © 1994 John Wiley & Sons, Inc.
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  • 174
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    International Journal of Chemical Kinetics 26 (1994), S. 779-799 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of the pulsed laser powered homogeneous pyrolysis technique for measuring unimolecular decomposition rate constants under unambiguously homogeneous conditions is investigated by numerical simulation of the experiment. The coupled partial differential equations which govern the gas dynamics and chemical kinetics are solved numerically and the results analyzed. Conditions under which rate constants can be extracted from the experimental data using a simplified analysis are determined. The effects of five sources of error in the simplified analysis are computed. A correlation is presented which may be used to correct for overestimation of the rate constant which is inherent in the simple analysis. Conditions under which the other four sources of error become negligible are presented. Overall, it is expected that this technique will be capable of routinely measuring rate constants within a factor of 2, and will do much better when a high power laser with a uniform beam profile is used and/or a well characterized thermal monitor molecule is available which decomposes with kinetic parameters close to that of the reactant being investigated. © 1994 John Wiley & Sons, Inc.
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  • 175
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    International Journal of Chemical Kinetics 26 (1994), S. 1063-1074 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The OH- ion catalyzed hydrolysis of AOT and sodium mono-methyl succinate in aqueous and aquo-dioxane media has been studied. The second-order rate constant for the former has been found to be nearly ten times slower than that of the latter. At AOT concentrations above CMC, the rate constants become insensitive to the concentration in the studied range of temperature, 25°C-40°C. The activation parameters for the kinetic process have been found to be reasonable, negative entropy of activation has supported a stable transition state complex. A good enthalpy-entropy compensation of the kinetic process has been found both for AOT and sodium monomethyl succinate in aqueous and aquo-dioxane media supporting similar nature of the transition state complexes in the hydrolytic reactions. The enthalpies of hydrolysis of AOT and the half ester of succinic acid in aqueous and aquo-dioxane media have been also reported. © 1994 John Wiley & Sons, Inc.
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  • 176
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    International Journal of Chemical Kinetics 26 (1994), S. 1121-1134 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic studies of the hydrogen peroxide decomposition catalyzed by the dimeric Mn(II)-gluconate complex, in alkaline medium, showed evidence for the oxidative cleavage of the ligand, leading to the formation of formaldehyde as one of the products. In the presence of a large excess of other hydroxylated substrates, such as methanol or ethylene glycol, a significant increase in the yield of formaldehyde was observed, corroborating the observed peroxidase activity in this system, in addition to the catalase activity. Oxygen free radicals were detected as intermediates of reaction, by ESR spectroscopy using the spintrapping method, only under aerobic conditions. Therefore, a nonradical mechanism was proposed for the reaction, based on the formation of a peroxo-Mn(II) complex, and its further reduction to the previous Mn(II) species. © 1994 John Wiley & Sons, Inc.
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  • 177
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    International Journal of Chemical Kinetics 26 (1994), S. 1135-1141 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nitrogenated compounds react with hypochlorous acid yielding N-chloro compounds. In principle, α-amino acids chlorination may take place on the oxygen of the carboxylic group or on the nitrogen of the amino group. In this framework, we discuss the different reactivities of nitrogen and oxygen towards chlorine, and come to the conclusion that the nitrogen is the preferred reaction site in α-amino acids chlorination. © 1994 John Wiley & Sons, Inc.
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  • 178
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    International Journal of Chemical Kinetics 26 (1994), S. 1151-1166 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In many decomposition reactions, the reaction velocity can be described as a product of two functions: a temperature dependent part K(T) and the kinetic function f(1 - α), where T designates the temperature and α the fraction of reactant that has decomposed. The physical interpretation of these functions is discussed for both solid and homogeneous systems. A method is described by which f(1 - α) and K(T) can be determined from kinetic data. The mechanism of decomposition can subsequently be identified which should be consistent with the derived kinetic parameters. The method has been applied to analyze the kinetics of the thermal decomposition of nitromethane. © 1994 John Wiley & Sons, Inc.
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  • 179
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    International Journal of Chemical Kinetics 26 (1994), S. 665-671 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The violet superoxo complex, [(H2O)4(OH)RhIII(O2)RhIII(OH)(H2O)4]3+, formed by treatment of (RhII)24+ with O2 in HClO4, is converted to a le- reduction product, the corresponding μ-peroxo complex, by the reductants I-, IrCl63-, and the trinuclear aquamolybdenum(III) cation, (MoIII)3. Each reaction is first-order in both redox partners, and the le- reduction by IrCl63- is followed by a much slower conversion to a peroxide-free complex. Among the rapid reductions of the superoxo derivative examined here and in a previous study, only that by IrCl63- is accelerated by increases in acidity; the rate law for this reaction features both an acid-independent and a [H+]-proportional component, the latter stemming from partial conversion of the oxidant to its conjugate acid (pKA 〈 -1.0). Rate laws for reductions by other metal-center reagents generally exhibit inverse-[H+] terms, reflecting deprotonation of the reductant. All reductions thus far observed involving this superoxo species appear to be outer-sphere. Treatment of acid-independent rate constants within the framework of the Marcus model, allows estimates of the self-exchange rate, k11, for the (RhIII)2-bound superoxo-peroxo couple. Because values of k11 calculated from the several reductions span a range of 104.5, reductions of the superoxo complex cannot be taken to conform satisfactorily to the Marcus treatment, being in this respect comparable to the systems VO(OH)+/2+, Mn2+/3+, Eu2+/3+, and Ti(OH)2+/3+, each of which exhibits similar divergences. The wide range of calculated self-exchange rates appears to invalidate an earlier suggestion that reduction of the superoxo complex by Fe2+ proceeds primarily through a bridged path. © 1994 John Wiley & Sons, Inc.
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  • 180
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    International Journal of Chemical Kinetics 26 (1994), S. 719-728 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate coefficients for the reactions of Cl atoms with CH3Br, (k1) and CH2Br2, (k2) were measured as functions of temperature by generating Cl atoms via 308 nm laser photolysis of Cl2 and measuring their temporal profiles via resonance fluorescence detection. The measured rate coefficients were: k1 = (1.55 ± 0.18) × 10-11 exp{(-1070 ± 50)/T} and k2 = (6.37 ± 0.55) × 10-12 exp{(-810 ± 50)/T} cm3 molecule-1 s-1. The possible interference of the reaction of CH2Br product with Cl2 in the measurement of k1 was assessed from the temporal profiles of Cl at high concentrations of Cl2 at 298 K. The rate coefficient at 298 K for the CH2Br + Cl2 reaction was derived to be (5.36 ± 0.56) × 10-13 cm3 molecule-1 s-1. Based on the values of k1 and k2, it is deduced that global atmospheric lifetimes for CH3Br and CH2Br2 are unlikely to be affected by loss via reaction with Cl atoms. In the marine boundary layer, the loss via reaction (1) may be significant if the Cl concentrations are high. If found to be true, the contribution from oceans to the overall CH3Br budget may be less than what is currently assumed. © 1994 John Wiley & Sons, Inc.
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  • 181
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    International Journal of Chemical Kinetics 26 (1994), S. 737-742 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissolution and the kinetics of dissolution of cooper(II) oxide in water saturated by sulphur dioxide has been studied. In the experiments, the particle size, the flow rate of the gas, the solid to liquid ratio, and the reaction temperature have been chosen as parameters, while the stirring rate was held constant. As a result of present experiments, it was observed that the decrease of the particle size, the solid to liquid ratio, and an increase of the reaction temperature increased the dissolution rate. It was also observed that the flow rate of sulphur dioxide in the range of its flow rate values did not affect the dissolution rate.The reaction kinetics of copper(II) oxide according to the heterogeneous reaction models was examined and it was found that the dissolution rate was controlled by chemical reaction. The calculated activation energy is 66.50 kJmol-1. © 1994 John Wiley & Sons, Inc.
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  • 182
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    International Journal of Chemical Kinetics 26 (1994) 
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    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 183
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    International Journal of Chemical Kinetics 26 (1994), S. 771-778 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants for the reaction of C6H5 with HBr and DBr have been measured with the cavity-ring-down method in the temperature range of 297 to 523 K and 297 to 500 K, respectively. These rate constants can be effectively represented, in units of cm3/s, by \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k_{{\rm HBr}} = 10^{- 10.40 \pm 0.24} \exp \left[{{{\left({- 554 \pm 208} \right)} \mathord{\left/ {\vphantom {{\left({- 554 \pm 208} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right]{\rm and} \\ k_{{\rm DBr}} = 10^{- 10.36 \pm 0.17} \exp \left[{{{\left({- 662 \pm 151} \right)} \mathord{\left/ {\vphantom {{\left({- 662 \pm 151} \right)} T}} \right. \kern-\nulldelimiterspace} T}} \right]{\rm.} \\ \end{array} $$\end{document} Both activation energies are similar and positive, contrary to those of alkyl radical reactions, all of which exhibit negative temperature dependencies. The difference, as pointed out before [1], could be accounted for by the electron-withdrawing effect of the phenyl vis-à-vis the electron-donating ability of the alkyls. © 1994 John Wiley & Sons, Inc.
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  • 184
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    International Journal of Chemical Kinetics 26 (1994), S. 813-825 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time-resolved vibrational chemiluminescence from HF has been recorded following the production of F atoms by the pulsed laser photolysis (λ = 266 nm) of F2 in the presence of HCl, CH4, and CF3H. In the first two cases, experiments have been conducted by observing emission from HF(ν = 3) at four temperatures from 295 to 139 K. Rate constants have been determined over this range of temperature for the reactions of F atoms with HCl and CH4 and of CH3 radicals with F2, and for the relaxation of HF(ν = 3) by HCl and CH4. The reaction of F atoms with CF3H is slower than those with HCl and CH4 and measurements on the emission from HF(ν = 2) have been used to infer rate constants for reaction and relaxation only at 295 K. © 1994 John Wiley & Sons, Inc.
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  • 185
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    International Journal of Chemical Kinetics 26 (1994), S. 857-867 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The infrared multiphoton excitation of triethylsilane in the gas phase, with a pulsed CO2 laser at high intensities (I 〉 700 MW/cm2), produced an intense luminescence. The spectrum and time profile of this luminescence was studied as a function of pressure, and laser frequency. The radiative lifetime of this emission was 357 ± 10 ns, and the quenching rates by Cl2 and NO were determined from lifetime measurements. A reasonable mechanism for the interpretation of this luminescence involves the initial infrared multiphoton decomposition of triethylsilane, followed by the secondary infrared multiphoton excitation of the primary photofragment diethylsilyl radical, which subsequently undergoes relaxation to an excited electronic state. The addition of O2 resulted in a new chemiluminescence at shorter wavelengths, which corresponds to the SiO* chromophore group. © 1994 John Wiley & Sons, Inc.
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  • 186
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    International Journal of Chemical Kinetics 26 (1994), S. 847-855 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An investigation of the kinetics of oxidation of epimeric piperidin-4-ols, oxan-4-ols, and cyclohexanol by N-chloro-r-2, c-6-diphenyl-t-3-methylpiperidin-4-one (NCP) in aqueous acetic acid in the presence of perchloric acid shows that the reaction is first-order each in substrate and oxidant. Both H3O+ and Cl- which catalyze the reaction, exhibit a fractional order kinetics. While increase in ionic strength increases the rate slightly, an inverse dependence is observed between rate and solvent polarity. Addition of r-2-c-6-diphenyl-t-3-methylpiperidin-4-one, one of the reaction products, did not influence the rate. Also, no kinetic isotope effect has been observed. A plausible mechanism consistent with these observations is proposed and the relative reactivities of the substrates are explained on conformational grounds. © 1994 John Wiley & Sons, Inc.
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  • 187
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    International Journal of Chemical Kinetics 26 (1994), S. 1023-1039 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ultraviolet absorption spectrum of CF3CFClO2 and the kinetics of the self reactions of CF3CFCl and CF3CFClO2 radicals and the reactions of CF3CFClO2 with NO and NO2 have been studied in the gas phase at 295 K by pulse radiolysis/transient UV absorption spectroscopy. The UV absorption cross section of CF3CFCl radicals was measured to be (1.78 ± 0.22) × 10-18 cm2 molecule-1 at 220 nm. The UV spectrum of CF3CFClO2 radicals was quantified from 220 nm to 290 nm. The absorption cross section at 250 nm was determined to be (1.67 ± 0.21) × 10-18 cm2 molecule-1. The rate constants for the self reactions of CF3CFCl and CF3CFClO2 radicals were (2.6 ± 0.4) × 10-12 cm3 molecule-1 s-1 and (2.6 ± 0.5) × 10-12 cm3 molecule-1 s-1, respectively. The reactivity of CF3CFClO2 radicals towards NO and NO2 was determined to (1.5 ± 0.6) × 10-11 cm3 molecule-1 s-1 and (5.9 ± 0.5) × 10-12 cm3 molecule-1 s-1, respectively. Finally, the rate constant for the reaction of F atoms with CF3CFClH was determined to (8 ± 2) × 10-13 cm3 molecule-1 s-1. Results are discussed in the context of the atmospheric chemistry of HCFC-124, CF3CFClH. © 1994 John Wiley & Sons, Inc.
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  • 188
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    International Journal of Chemical Kinetics 26 (1994), S. 1075-1094 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ozonolysis of 1-5 ppm concentrations of trans- and cis-2-C4H8 was carried out in a 580 l spherical glass reaction vessel at 730 ± 5 torr and 296 ± 2 K. The yields of CH3CHO, HCHO, CO, CO2, CH4, and CH3OH were determined by long-path FTIR spectroscopy. About 60% of C4H8 that reacted with O3 decomposed via the formation of the excited CH3CHO2* intermediates into the following pathways: (4a) CO2 + CH4, (4b) CO2 + H + CH3, (4c) CO + OH + CH3, and (4d) CO + CH3OH. The branching ratios for each channel, expressed as the percent of the total pathways, were determined for trans isomer: 20, 30, 40, and 10, and for cis isomer: 29, 35, 24, and 12, respectively. The conversion of C4H8 relative to the reacted O3 was about 1.6 and 1.4 for trans and cis isomers, respectively. These results were explained by the reactions of OH radicals formed in (4c) with C4H8, in which secondary OH radicals were generated: C4H8 + OH + O2 → CH3—CH(OH)—CH(CH3)OO, followed by CH3-CH(OH)-CH(CH3)OO → 2 CH3CHO + OH. About 40% of C4H8 that reacted with O3 yielded a mixture of a carbonyl and a noncarbonyl product, assigned as hydroxyethyl formate, CH3CH(OH)—O—CHO, and secondary butene ozonide, respectively. The addition of HCHO increased the formation of the former while the latter was unaffected. These results were consistent with the mechanism proposed by Cremer et al. [Chem. Phys. Lett., 187, 491 (1991)], where the primary ozonide rearranges, before dissociation, to the carbonyl oxide-aldehyde complex (the dipole complex) which is the precursor of the secondary ozonide. © 1994 John Wiley & Sons, Inc.
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  • 189
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    International Journal of Chemical Kinetics 26 (1994) 
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    Keywords: Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology
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  • 190
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    International Journal of Chemical Kinetics 26 (1994), S. 1143-1150 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The system iodate-peroxide-manganese(II)-butanone is a member of the Briggs-Rauscher set of oscillators. The stoichiometry and variation of the oscillation period with concentration for each component is studied under batch conditions. The system is simulated using the skeleton mechanism of earlier workers and reproduces the observed variation in oscillation period. Examination of the roles of the reaction steps shows that there are significant differences from those found using malonic acid. Iodine is stored during the low iodide regime and utilized during the high iodide regime, and different overall reactions occur during the two regimes. © 1994 John Wiley & Sons, Inc.
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  • 191
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    International Journal of Chemical Kinetics 26 (1994), S. 1207-1227 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation kinetics of NO by O2 in aqueous solution was observed using a stopped flow apparatus. The kinetics follows a third order rate law of the form k · [NO]2 · [O2] in analogy to gas-phase results. The rate constant at 296 K was measured as (6.4 ± 0.8) · 106 M-2 s-1 with an activation energy of 2.3 kcal/mol and a preexponential factor of (4.0 ± 0.5) · 108 M-2 s-1. The rate constant displays a very slight pH dependence corresponding to less than a factor of three over the range 0 to 12. The system NO/O2 in aqueous solution is an efficient nitrosating agent which has been tested using phenol as a substrate over the pH range 0 to 12. The rate limiting step leading to formation of 4-nitrosophenol is the formation of the reactive intermediate whose competitive hydrolysis yields HONO or NO2-. The absence of NO3- in the autoxidation of NO, the exclusive presence of NO2- as a product of the nitrosation reaction of phenol, and the kinetic results of the N3- trapping experiments point towards N2O3 as the reactive intermediate. © 1994 John Wiley & Sons, Inc.
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  • 192
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    International Journal of Chemical Kinetics 26 (1994), S. 1095-1104 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The absolute rate constant for the reaction of phenyl radical with acetylene has been measured at 20 torr total pressure in the temperature range of 297 to 523 K using the cavity-ring-down technique. These new kinetic data could be quantitatively correlated with the data obtained earlier with a relative rate method under low-pressure (10-3-10-2 torr) and high-temperature (1000-1330 K) conditions. These kinetic data were analyzed in terms of the RRKM theory employing the thermochemical and molecular structure data computed with the BAC-MP4 technique.The calculated results reveal that the total rate constant for the C6H5 + C2H2 reaction (kt) is pressure-independent, whereas those for the formation of C6H5C2H (kb) and the C6H5C2H2 adduct (kc) are strongly pressure-dependent. A least-squares analysis of the calculated values for 300-2000 K at the atmospheric pressure of N2 or Ar can be given by \documentclass{article}\pagestyle{empty}\begin{document}$$ k_b = 9.5 \times {\rm 10}^{{\rm - 42}} T^{9.33} \exp \left({- 1,713/T} \right) $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_C = 1.8 \times {\rm 10}^{{\rm - 7}} T^{-1.63} \exp \left({- 2,711/T} \right) $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$ k_t = 4.1 \times {\rm 10}^{{\rm - 18}} T^{1.77} \exp \left({- 1,152/T} \right) $$\end{document} all in units of cm3/s. The latter equation effectively represents the two sets of experimental data. © 1994 John Wiley & Sons, Inc.
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  • 193
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    International Journal of Chemical Kinetics 26 (1994), S. 1105-1119 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetics of manganese(III) oxidation of L-arginine has been studied in the presence of pyrophosphate and acetate ions in acidic media at 328 K and 323 K, respectively. The nature of the oxidizing species formed in manganese(III) solutions was determined by spectrophotometric and redox potential measurements. The reaction shows a first-order dependence on [manganese(III) pyrophosphate] in the pyrophosphate medium, pH 2-3, and a half-order on [manganese(III) acetate] in HOAc-acetate medium. In both media, the kinetic order is one with respect to [arginine]. The dependencies of the rate on the reduction product, manganese(II), concentration are zero- and inverse first-orders in acetate and pyrophosphate media, respectively. Effects of varying dielectric constant of the medium and of added anions such as acetate, pyrophosphate, fluoride, chloride, and perchlorate have been investigated, in both media. There is evidence for the existence of free radicals as transient species. Activation parameters have been evaluated using the Arrhenius and Eyring plots. Mechanisms consistent with the observed kinetic data have been proposed and discussed. Kinetic data for the oxidations of some α-amino acids by manganese(III) species of different forms are summarized and compared. © 1994 John Wiley & Sons, Inc.
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  • 194
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    International Journal of Chemical Kinetics 26 (1994), S. 1179-1184 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nanosecond laser flash photolysis (λ = 355 nm) of an aqueous solution of 3-chloro-3-p-chlorophenyldiazirine in isooctane produces a transient absorption at 310 nm due to the formation of the carbene. In the presence of 2-vinylpyridine, a second transient with a broad absorption band peaking at 520 nm grows in. This absorption is attributed to 2-vinylpyridinium ylide. The ylide decays with a lifetime equal to 33 µs at 25°C independent of the concentration of 2-vinylpyridine. As the ylide decays, there is a concomitant growth of an absorption at 330 nm, attributed to the formation of inodolizine. The activation parameters for the 1,5-dipolar cyclization of the ylide to indolizine were determined; Ea = 12.1 kcal mol-1 and log A = 13.4. © 1994 John Wiley & Sons, Inc.
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  • 195
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    International Journal of Chemical Kinetics 26 (1994), S. 1185-1191 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase reaction of ozone with unsaturated alcohols in air has been investigated at atmospheric pressure and ambient temperature (288-291 K). Cyclohexane was added to scavenge the hydroxyl radical which forms as a product of the ozone-unsaturated alcohol reaction. The reaction rate constants, in units of 10-18 cm3 molecule-1 s-1, are 16.2 ± 0.7 for (±) 3-buten-2-ol, 17.9 ± 1.8 for 1-penten-3-ol, 10.0 ± 0.3 for 2-methyl-3-buten-2-ol, 169 ± 25 for cis-2 penten-1-ol, and 251 ± 41 for 2-buten-1-ol (mixture of isomers). Substituent effects on reactivity are discussed. The reactivity of unsaturated alcohols towards ozone is similar to that of their alkene structural homologues. Implications of these results with respect to the atmospheric persistence of unsaturated alcohols are briefly discussed. © 1994 John Wiley & Sons, Inc.
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  • 196
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    International Journal of Chemical Kinetics 26 (1994), S. 1167-1178 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: With a view to clarifying analogies and differences between the mechanisms involved in the nitrosation of amino acids and secondary amines, we studied the kinetics of the nitrosation of five imino acids (azetidine-2-carboxylic acid, pyrrolidine-2-carboxylic acid, piperidine-2-carboxylic acid, piperidine-3-carboxylic acid, and piperidine-4-carboxylic acid) and of the ethyl esters of three of them. Reaction kinetics were determined by the initial rate method, by spectrophotometric monitoring of the concentration of nitroso amino acid formed. The presence of the —COO- group in the amino acids opens a new mechanistic route for the nitrosation of the secondary amino group: a nitrosyl carboxylate formed initially acts as an internal nitrosating agent, resulting in intramolecular migration of —N = O from the carboxylate group to the secondary amino group. The observed order of the α-, β-, and γ-amino acids as regards the ease of N-nitrosation by this route is explained in terms of the relative energies of (a) the equatorial and axial orientations of the Cring—Ccarboxyl bond, and (b) the chair and boat forms of the piperidine ring. © 1994 John Wiley & Sons, Inc.
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  • 197
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    International Journal of Chemical Kinetics 26 (1994), S. 1193-1205 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the gas-phase reactions of O3 with the sesquiterpenes α-cedrene, α-copaene, β-caryophyllene, α-humulene, and longifolene, and with the monoterpenes limonene, terpinolene, α-phellandrene, and α-terpinene, have been measured using a relative rate technique at 296 ± 2 K and atmospheric pressure of air. The rate constants obtained (in units of 10-17 cm3 molecule-1 s-1) are: limonene, 20.1 ± 5.1; terpinolene, 188 ± 67; α-phellandrene, 298 ± 105; α-terpinene, 2110 ± 770; α-cedrene, 2.78 ± 0.71; α-copaene, 15.8 ± 5.6; β-caryophyllene, 1160 ± 430; α-humulene, 1170 ± 450; and longifolene, 〈0.07, where the indicated errors include the estimated overall uncertainties in the rate constants for the reference organics. Hydroxyl radical formation yields were also determined for the O3 reactions with the sesquiterpenes, of 0.67 for α-cedrene, 0.35 for α-copaene, 0.06 for β-caryophyllene, and 0.22 for α-humulene, all with estimated overall uncertainties of a factor of ca. 1.5. The tropospheric lifetimes of the sesquiterpenes due to reaction with O3 are calculated. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 198
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    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 15 (1994), S. 28-43 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The fast multipole method proposed by Greengard and Rokhlin (GR) is applied to large biomacromolecular systems. In this method, the system is divided into a hierarchy of cells, and electric field exerted on a particle is decomposed into two parts. The first part is a rapidly varying field due to nearby cells, so that it needs rigorous pairwise calculations. The second part is a slowly varying local field due to distant cells; hence, it allows rapid calculations through a multipole expansion technique. In this work, two additional possibilities for improving the performance are numerically examined. The first is an improvement of the convergence of the expansion by increasing the number of nearby cells, without including higher-order multipole moments. The second is an acceleration of the calculations by the particle-particle and particle-mesh/multipole expansion (PPPM/MPE) method, which uses fast Fourier transform instead of the hierarchy. For this purpose, the PPPM/MPE method originally developed by the authors for a periodic system is extended to a nonperiodic isolated system. The advantages and disadvantages of the GR and PPPM/MPE methods are discussed for both periodic and isolated systems. It is numerically shown that these methods with reasonable costs can reduce the error in potential felt by each particle to 0.1-1 kcal/mol, much smaller than the 30-kcal/mol error involved in conventional simple truncations. © 1994 by John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 199
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    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 15 (1994), S. 72-79 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: We consider the application of canonical numerical integrators to molecular dynamics simulations. Computer experiments are done to analyze the relative merits of using canonical integrators against their noncanonical counterparts. These experiments involve the study of the properties of liquid argon utilizing the Lennard-Jones interaction potential. To accomplish this comparative study of canonical and noncanonical integrators, we computed thermodynamic and structural quantities. Our results indicate that noncanonical methods, with one exception, fail miserably to conserve energy and as a consequence give poor estimates of the other quantities. Also, higher-order canonical methods may offer an advantage over the Störmer/Verlet method. © 1994 by John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
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  • 200
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 15 (1994), S. 105-123 
    ISSN: 0192-8651
    Keywords: Computational Chemistry and Molecular Modeling ; Biochemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The convergence behavior of free energy calculations has been explored in more detail than in any previously reported work, using a model system of two neon atoms in a periodic box of water. We find that for thermodynamic integration-type free energy calculations as much as a nanosecond or more molecular dynamics sampling is required to obtain a fully converged value for a single λ point of the integrand. The concept of “free energy derivatives” with respect to the individual parameters of the force field is introduced. This formalism allows the total convergence of the simulation to be deconvoluted into components. A determination of the statistical “sampling ratio” from these simulations indicates that for window-type free energy calculations carried out in a periodic waterbox of typical size at least 0.6 ps of sampling should be performed at each window (0.7 ps if constraint contributions to the free energy are being determined). General methods to estimate and reduce the error in thermodynamic integration and free energy perturbation calculations are discussed. We show that the difficulty in applying such methods is determining a reliable estimate of the correlation length from a short series of data. © 1994 by John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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