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  • 2020-2022
  • 1990-1994  (353)
  • 1985-1989
  • 1993  (353)
  • Physical Chemistry  (218)
  • crystal structure  (135)
  • 1
    ISSN: 1572-8862
    Keywords: Platinum ; ruthenium ; crystal structure ; heteronuclear cluster
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract From the reaction of Ru(CO)5 and Pt(COD)2, COD = 1, 5-cyclooctadiene, the new platinum-ruthenium heteronuclear cluster complex Pt2Ru4(CO)18,1, was obtained in 60% yield.1 has a folded ladder-like structure with alternating pairs of ruthenium atoms and platinum atoms. The cluster of1 can be split to yield the known compound PtRu2(CO)8(η2-dppe),2, (54% yield) by reaction with 1, 2-bis(diphenylphosphino)ethane, dppe, at 25°C. When1 was treated with excess dppe at 40°C, thebis-diphos compound3, PtRu2(CO)6(μ-η2-dppe)2 was obtained (39% yield). Under the similar reaction conditions,2 was converted to3 in 44% yield. All these complexes were characterized by single crystal X-ray diffraction analyses. Compounds2 and3 both contain a triangular cluster of one platinum and two ruthenium atoms, but in2 the bidentate ligand, dppe, chelates the platinum atom and in3 the two dppe ligands bridge the two Pt-Ru metal-metal bonds. Crystal data for1: space group C2/c,a=12.542(2)Å,b=15.350(4)Å,c=15.252(3)Å, β=105.32(2)°,Z=4, 2192 reflections,R=0.025. For2: space group P21/c,a=14.351(2)Å,b=13.486(3)Å,c=19.218(3)Å, β=108.48(1)°,Z=4, 3029 reflections,R=0.027. For3: space group P21/c,a=18.836(6)Å,b=15.559(5)Å,c=23.259(7)Å, β=111.26(2)°,Z=4, 4204 reflections,R=0.038.
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  • 2
    ISSN: 1572-8862
    Keywords: Tungsten ; chloride ; hexatungsten ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The hexanuclear tungsten cluster complex [W6(μ3-Cl)8Cl6]2−,1 was isolated as a salt of the cation (MeO2CCH2)2N(H)CH2CH2N(CH2CO2Me)2+, EDTEH+, by crystallization from methanol solvent of the product obtained from the reaction of (H3O)2[W6(μ3-Cl)8Cl3] with the disodium salt of ethylenediaminetetraacetic acid. The compound was charcterized by single-crystal X-ray diffraction analysis. The cluster anion contains an octahedral arrangement of six tungsten atoms with chloride ligands bridging the eight triangular faces of the cluster and one chloride ligand terminally coordinated to each of the six tungsten atoms. The cation (EDTEH)+ achieves its positive charge by protonation of one of the nitrogen atoms. Crystal data: space group = P21/a,a=10.689(2) Å,b=22.931(6) Å,c=12.093(3) Å, β=98.41(2)°,Z=2, 2476 reflections,R=0.028.
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  • 3
    ISSN: 1572-8862
    Keywords: Molybdenum ; acetate, carboxylate ; hexamolybdenum ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The hexamolybdenum cluster complex [Mo6(μ3-Cl)8(O2CMe)6]2−, 1 was isolated as the Bu4N+ salt in 71% yield from the reaction of (Bu4N)2[Mo6(μ3-Cl)8Cl6] with AgO2CMe in CH2Cl2 solvent. The compound was characterized by single crystal X-ray diffraction analysis. The cluster contains an octahedral arrangement of six molybdenum atoms with eight chloride ligands bridging the eight trianglar faces and six carboxylate ligands terminally coordinated through one oxygen atom to each of the six molybdenum atoms. Crystal data: space group =P21/n,a=10.713(3)Å,b=14.43(1)Å,c=21.919(4)Å, β=94.37(2)°,Z=2, 1965 reflections,R=0.036.
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  • 4
    ISSN: 1572-8862
    Keywords: Vanadium ; phenylhydrazine ; nitrogenase ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Addition of phenylhydrazine to a mixture of VCl3 · THF/N,N-propyl-bis (salicyladimine) and sodium hydride yielded a trinuclear vanadium complex, V3(μ3-O)(μ-Cl)Cl6(μ-η1-η1PhNHNH2)2(PhNHN H2)2(THF), containing two bridging and two terminal phenylhydrazine ligands. The product has been crystallographically characterized (P21/n, a=12.949(2) Å,b=24.061(4) Å,c=22.504(4) Å, β=107.22(1) deg.,V=6697(2) Å3 withZ=4) and was found to contain the first example of bridging monosubstituted hydrazine (phenylhydrazine) ligands.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymers and the environment 1 (1993), S. 65-80 
    ISSN: 1572-8900
    Keywords: Biodegradable plastic ; microbial degradation ; bacterial poly(d-(−)-3-hydroxybutyrate) ; crystal structure ; physiological behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract As one of a series of studies concerning the relationship between the higher-order structure and the biodegradability of a biodegradable plastic, the effects of the crystal structure of the plastic on microbial degradation were investigated. Bacterial poly(d-(−)-3-hydroxybutyrate) (PHB) films which had a wide range of crystallinity were prepared by the melt-quenching method. Results of the microbial degradation indicated that the development of crystallinity evidently depressed the microbial degradability. From scanning electron microscopy (SEM) observations, it is suggested that the microbial degradation proceeded in at least two manners. One was preferential degradation of the amorphous region leaving the crystalline lamellae intact, which was considered to be a homogeneous enzymatic degradation over the surface. The other was nonpreferential spherical degradation on the surface. The SEMs indicate that the spherical holes were the result of colonization by degrading bacteria. The holes varied in size and number with the change of crystal structure. Therefore, it is considered that the crystal structure of PHB also influenced the physiological behavior of the degrading bacteria on the PHB surface.
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  • 6
    ISSN: 1572-9001
    Keywords: Atomic displacement ; molecular motion ; vibrational analysis ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Atomic displacement parameters determined from a single-crystal X-ray-diffraction study on K2Ru(SO4)2 * 6H2O are analyzed in the molecular mean field approximation. The motion of SO2 2− can be described with a rigid-body model, whereas for [Ru(H2O)6]2+ internal stretching motion and coupling between stretching motion and overall translation are found to be necessary for explaining the observed atomic displacement parameters. Frequencies and force constants of internal motion are not significantly affected by such couplings. K2Ru(SO4)2 * 6H2O crystallizes in the monoclinic space groupP21/c (No. 14), witha = 6.1211(7)Å,b = 12.226(2) Å,c = 8.916(2)Å,β = 105.11(1)°,Z = 2 at 160 K anda = 6.1402(7)Å,b = 12.274(2)Å,c = 8.957(1)Å,β = 105.25(1)°,Z = 2 at 295 K. The structure was refined to a finalR(F) of 0.017 at 160 K and of 0.019 at 295 K for 1438 and 1299 observed reflections withF 0 〉 6σ(F0) and sin θ/λ 〉 0.617 Å1−.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Molecular engineering 3 (1993), S. 43-59 
    ISSN: 1572-8951
    Keywords: Heteropolymolybdates ; heteropolytungstates ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The chemistry of polynuclear oxometalate anions is dominated by molybdenum and tungsten in their highest oxidation state. During the past twenty years this class of compounds has attracted much attention because of their variable applications, e.g. as reagents in analytical procedures, as industrial catalysts and as potential anticancer drugs. In order to obtain model systems for the investigation of the catalytic activity of heteropolyanions we have synthesized and structurally characterized some organo derivatives of polyoxoanions. We secondly focus on Sb(III) and Bi(III) heteropolytungstates to examine the important influence of the unshared electron pair on the resulting structures and properties. Some of these compounds may be regarded as supramolecular aggregates showing inclusion phenomena. In 9 two [SbW9O33]9− anions are linked by a set of six sodium ions forming a nearly planar hexagon. The sodium ions are enveloped by an oxygen cage formed by terminal oxygen atoms of the polyanions and by water molecules. Furthermore, the four anions [Sb2W22O74(OH)2]12−, [Sb2W20Fe2O70(H2O)6]8−, [Sb2W20Co2O70(H2O)6]10− and [Bi2W20Fe2O68(OH)2(H2O)6]6− (in10, 11, 12, 13) may be regarded as transition metal complexes of novel [Sb2W20O70]14− or [Bi2W20O70]14− anions which are serving as ligands. The octahedral coordination sphere of each transition metal is formed by three oxygen atoms of the anion and completed by three water molecules. The Sb(III) heteropolyanion, [Na2Sb8W36O132(H2O)4]22− in (14) includes two sodium and four antimony ions besides four water molecules. Each anion consists of four β-B-SbW9-Keggin fragments linked together by four SbO4-groups, incorporating two sodium and four water molecules effecting an additional connection of the subunits.
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  • 8
    ISSN: 1572-9001
    Keywords: Cobaltocene ; molecular geometry ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molecular and crystal structures of the monoclinic modification of cobaltocene Cp2Co (P21/n, Z=2) was determined at 100 K and 297 K with new sets of X-ray diffraction data (MoKα radiation, 3995 and 6534 reflections, refinement toR = 0.026 and 0.030 using 1061 and 1299 independent observable reflections, respectively). At 297 K the structure is disordered (similar to the isomorphous ferrocene and nickelocene) with two distinct orientations of the ring, differing in occupancy factors (80% and 20%) and by a rotation angle in the ring plane of approximately 34°. Just as for nickelocene but in contrast to ferrocene, no sharp phase transition was found on cooling Cp2Co to 100 K, but an essential ordering of the Cp-ring position was detected with a decrease of the contribution of the second minor orientation to nearly 10%. On the basis of a careful analysis of the molecular geometry, crystal packing, and anisotropic atomic displacement parameters, a dynamic temperature-dependent nature of the disorder in Cp2Co is assumed.
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  • 9
    ISSN: 1573-9171
    Keywords: iron(II) and ruthenium(II) complexes ; synthesis ; carbonyl, cyclopentadienyl, benzoate ligands ; crystal structure ; X-ray diffraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Complexes of Fe(II) and Ru(II) of the general formula Cp(OC)2MOC(O)C6H4X-p, where M=Fe, X=H, F (1, 2) or M=Ru, X=H, F (3, 4) have been prepared by reactingp-XC6H4COOAg with [CpFe(CO)2]2 or CpRu(CO)2I. The crystal structures of complexes1–3 have been determined using X-ray diffraction. Compounds1 and3 are isomorphous. The COO group in1–3 is coordinated as a monodentate ligand. As the latter and the CO ligands are electronically non-equivalent, the coordination of the Cp ligand to the metal is slightly asymmetric.
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  • 10
    ISSN: 1573-9171
    Keywords: synthesis ; crystal structure ; azepinethiones ; trimethylsilyl derivative
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title compounds were prepared and X-ray analysis was performed (R = 0.064 and 0.035 for 1309 and 1637 reflections, respectively). In the former the intramolecular S→Si coordination interactions are absent and the Si atom has undistorted tetrahedral coordination with an S...Si distance of 4.034 Å. Crystals of the latter are built of centrosymmetric dimeric H-complexes (S...H(N) 2.58 Å, the S...HN angle 168°).
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  • 11
    ISSN: 1573-9171
    Keywords: peroxosolvates ; potassium fluoride ; monoperoxosolvate ; thermal stability ; crystal structure ; hydrogen bond
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Potassium fluoride peroxosolvate KF-H2O2 was obtained upon action of a 30% aqueous solution of hydrogen peroxide on solid potassium fluoride dihydrate. As compared to other peroxosolvates, KF-H2O2 is characterized by the highest thermal stability: the decomposition rate constantk 1, at 120°C is 1.4 10−3 min−1, the enthalpy of H2O2 addition to KF is 8.1 kcal/ mol. The correlation between the high stability of KF-H2O2 and the absence of catalytic properties of KF towards H2O2, and the formation of strong intermolecular O-H...F and intramolecular O-H...O hydrogen bonds in the crystal is discussed.
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  • 12
    ISSN: 1573-9171
    Keywords: synthesis ; crystal structure ; pentacoordinated silicon ; chelate cycle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The X-ray diffraction structural study of the (N-Si)-chelate of 2-(chlorodimethyl-silylmethylthio)-1-pyrroline was carried out (R = 0.033 for 1894 reflections). The Si atom has a somewhat distorted trigonal bipyramidal coordination with the Cl and N atoms in axial positions. The Si-Cl and Si-N distances (2.423(1) and 1.945(1) Å) belong, respectively, to the longest and shortest known Si-Cl and Si-N distances in pentacoordinated silicon derivatives with an axial N-Si-Cl moiety.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 42 (1993), S. 1149-1151 
    ISSN: 1573-9171
    Keywords: Pt(dddt)2 ; organic conductors ; 5,6-dihydro-1,4-dithiin-2,3-dithiolate((dddt)2−) ; sulfur-containing platinum complexes ; crystal structure ; synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A neutral metal complex, [Pt(dddt)2]° (1), has been obtained by oxidation of the [Pt(dddt)2]− anion with excess (Bu4N)AuBr4 in nitrobenzene. Crystallographic data for 1∶a=17.854(9) Å,b=18.409(9) Å,c=4.717(5) Å, γ=68.83(2)°, space group P21/n,Z=4,d calc=2.55 g/cm3. In1 two independent centrosymmetric [Pt(dddt)2]° molecules are packed in stacks that form layers parallel to the (110) plane. The molecules of1 in the layers have shortened S...S contacts 3.491(9) Å, and 3.594(10) Å. The average bond lengths Pt-S 2.242(7) Å, S-C 1.71(2) Å and C=C 1.40(3) Å, together with the square-planar coordination of Pt in PtS4, suggest considerable conjugation in the metal cycles.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 42 (1993), S. 1415-1417 
    ISSN: 1573-9171
    Keywords: vanadatrane ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An X-ray diffraction study of a substituted vanadatrane-1-one (space groupPna21,R= 0.019 for 1394 reflections, the absolute structure was determined) showed that the geometry of its atrane framework is similar to that of the Si- and Ge-analogs. The bond lengths are: V=O, 1.614(2) Å; V←N, 2.329(2) Å; V-O, 1.800–1.806(2) Å. The deviation of the V atom having distorted trigonal bipyramidal coordination from the equatorial plane of the O atoms is 0.35 Å, the 0=V←N bond angle is 179.4(1)°.
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  • 15
    ISSN: 1573-9171
    Keywords: titanasilanes ; titanasilazanes ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An X-ray structural study of two titanium-containing organosilicon compounds, (Me3Si)3SiTi(NEt2)3 (1) and ClTi[N(SiMe3)2]3 (2), has been performed. The conformation of molecule1 in a crystal is staggered (approximate inherentC 3 symmetry), the Ti-Si and Ti-N bond lengths are 2.671(2) and 1.874–1.890(5) Å, respectively. A crystal of1 consists of one type of enantiomers (the space group is P41212; the absolute configuration has been determined). The structure of2 studied previously has been refined to the value of R=0.029 on the basis of 3442 reflections (the absolute structure has been determined), the Ti-Cl and Ti-N bond lengths are 2.260(1) and 1.926(1) Å, respectively. The strong distortions in the symmetry of the valence environment of the N atoms in the molecules of1, 2, and related structures are caused by electronic effects, in which the conformation of the relevant molecular fragments plays a determining role.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 271 (1993), S. 50-55 
    ISSN: 1435-1536
    Keywords: Polytetrafluoroethylene ; copolymer ; crystal structure ; chain folding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Molecular-mechanics calculations are performed on model folds proposed in the literature for single crystals of polytetrafluoroethylene crystallized in the phase stable below 19°C, in order to evaluate how they are modified when a fluorine atom is substituted by a bulky group, as occurs in fluorinated copolymers of tetrafluoroethylene. Only intramolecular effects are taken into account (isolated-chain model). An exhaustive analysis has been carried out of tetrafluoroethylene-hexafluoropropylene copolymer. Moreover, the lower energy folds found for such a copolymer have been examined for copolymers with chlorotrifluoroethylene and perfluoroalkylvinylethers, as comonomers. Our calculations show that all the considered comonomers can be arranged in the model folds proposed for the homopolymer, according to the imposed geometric constraints.
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  • 17
    ISSN: 0887-3585
    Keywords: thrombin ; bifunctional inhibitor ; crystal structure ; hirutonis ; drugdesing ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The crystal structure of the complexes of hirutonin-2 and hirutonin-6 with human α-thrombin have been solved and refined to R-factors of 0.169 (2.0 Å resolution) and 0.162 (201Å), respectively. Hirutonins belong to a family of bifunctional inhibitors bearing a noncleavable moiety mimicking the scissile bond. Hirutonin-2 is an analog of (D)Phe-Pro-Arg-Gly-hirudin49-65; hirutonin-6 has the same N-terminal tripeptide connected to a shortened fibrinogen exosite-binding part by a short, non-peptidyl linker. The hirutonin-6 molecule is well defined in the electron density with the exception of the C-terminal Leu-h61. The linker follows near the bottom of the canyon connecting the active site with the exosite, forms a short antiparallel β-sheet-like arrangement with Leu-40-Leu41 and makes van der Waals contacts with Glu39-Leu40-Leu41 of thrombin. In the thrombin-hirutonin-2 complex, the N- and C-terminal parts of the inhibitor are well or dered (except the C-terminal Gln-h65) while the central portion of the linker is partially disordered. The glycine analog in the P1′ position of hirutonin-2 assumes a conformation similar to that of the canonical form (Bode and Huber (1992) Eur. J. Biochem. 204 : 433-451) and supports the identification of the S1′ site as restricted by His57, Trp60D, Lys60F, and the Cys42-Cys58 disulfide bridge. The carbonyl oxygen of the P1 arginine residue is located in the oxyanion hole formed by the NH groups of Gly193 and Ser195, while the carbonyl carbon is positioned within a short distance, 2.8 Å, from the Oγ of Ser195. This resembles the conformation of the substrate-like inhibitors bound to other serine proteases. The N-terminal (D)Phe-pro-Arg fragment common to both inhibitors binds to thrombin in a fashion very similar to that of other inhibitors having this motif. The binding of the C-terminus of hirutonins to the fibrinogen-binding exosite is similar to that observed in hirudin and hirulog complexes. © 1993 Wiley-Liss, Inc.
    Additional Material: 9 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 16 (1993), S. 205-213 
    ISSN: 0887-3585
    Keywords: calcium binding ; crystal structure ; protein stability ; site-directed mutagenesis ; subtilisin ; X-ray crystallography ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A version of subtilisin BPN′ lacking the high affinity calcium site (site A) has been produced through genetic engineering methods, and its crystal structure refined at 1.8 Å resolution. This protein and the corresponding version containing the calcium A site are describedand compared. The deletion of residues 75-83 was made in the context of four site-specific replacements previously shown to stabilize subtilisin. The helix that in wild type is interrupted by the calcium binding loop, is continuous in the deletion mutant, with normal geometry. A few residues adjacent to the loop, principally those that were involved in calcium coordination, are repositioned and/or destabilized by the deletion. Because refolding is greatly facilitated by the absence of the Caloop, this proteinoffers a new vehicle for analysis and dissection of the folding reaction. This is among the largest internal changes to a protein to be described at atomic resolution. © Wiley-Liss, Inc.
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  • 19
    ISSN: 1573-1111
    Keywords: 12-membered crown ethers ; crystal structure ; conformation peculiarities ; X-ray analysis ; CH...O contacts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal structures of two 12-membered crown ethers, benzo-12-crown-4 (1) and naphtho-12-crown-4 (2), have been determined by X-ray analysis. Both structures are molecular. Compound1 is monoclonic,P21/b,a=8.466(3),b=8.019(3),c=33.590(10) Å, γ=90.99(3)o. The unit cell contains two crystallographically independent molecules of1 with similar conformations. Compound2 is also monoclinic,P21/a,a=24.148(8),b=14.535(4),c=7.987(5) Å, γ=102.87(2)o. Two independent molecules in the unit cell have significantly different conformations.
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 159-165 
    ISSN: 1573-1111
    Keywords: Dibenzo-30-crown-10 ; crystal structure ; complexation ; dysprosium isothiocyanate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Crystalline [Dy(NCS)3(dibenzo-30-crown-10)(H2O)2]·H2O·MeCN can be obtained by slowly evaporating a reaction mixture of Dy(NCS)3·nH2O with dibenzo-30-crown-10 in a solution of acetonitrile. The material crystallizes in the monoclinic space groupP21/n, the cell parameters area=11.450(5),b=23.284(4),c=18.424(6)Å, β=106.28(4)°,V=4715Å3,M=968.47,D x=1.36 g cm−1, μ=17.80 cm−1,F(000)=1972,Z=4.2740 independently observed [I≥3σI] reflections were used in the final least-squares refinement leading to an agreement index ofR=0.085. The Dy(III) ion coordination geometry approximates a square antiprism, involving two water oxygens and three dibenzo-30-crown-10 oxygen atoms and three isthiocyanate nitrogens. Hydrogen bonds are formed between the two water molecules and four uncoordinated crown ether oxygen atoms.
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  • 21
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 341-349 
    ISSN: 1573-1111
    Keywords: Molecular asymmetry ; calixarene ; acetone ; clathrate ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal and molecular structure of the 1:1 clathrate of the asymmetric calix[4]arene,1, and acetone has been determined by X-ray analysis. The crystal data are: tetragonal, space groupP4/n,a=b=12.574(6),c=12.572(6) Å,V=1988(2) Å3,Z=2,D x =1.111 g cm−3,D m =1.108 g cm−3. Least-squares refinement based on 1131 observed reflections withF 0〉3σ(F 0) and anisotropic temperature factors led toR=0.096. In spite of the molecular asymmetric calixarene1 the crystal structure has high symmetry, because a part of the host and guest molecules are in disordered states.
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  • 22
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 385-398 
    ISSN: 1573-1111
    Keywords: Hydrogen bonding ; alicyclic diol ; helical tubulate ; crystal structure ; ferrocene ; squalene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The inclusion compounds of 2,8-dimethyltricyclo[5.3.1.13,9]dodecane-syn-2,syn-8-diol,3, with ferrocene and with squalene have been prepared. The crystal structures of these helical tubulate compounds: (3)3·(ferrocene)0.75 [P3121,a=b=13.7480(6),c=7.0312(5) Å,Z=1,R=0.038] and (3)3·(squalene)0.23 [P3121,a=b=13.677(1),c=7.0533(9) Å,Z=1,R=0.042] are described.
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  • 23
    ISSN: 1573-1111
    Keywords: Werner clathrate ; nickel octahedral complex ; tetrahydrofuran ; crystal structure ; NMR ; molecular recognition ; hydrocarbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract This paper addresses the general question: what are the significant guest properties selected by this host when interacting with guest molecules in the liquid phase, resulting in cocrystallization of the host and guest? In particular, to what extent do π electrons in a guest molecule effect its potential as a guest? Werner clathrates of the host [Ni(NCS)2(4-ViPy)4] with mixtures of tetrahydrofuran (THF) and cyclic hydrocarbons as guests have been synthesised and their structures elucidated. Clathrate (1): [Ni(NCS)2(4-ViPy)4](1.78 THF)(0.22 cyclohexane), crystallizes in the orthorhombic space groupP bcn a=9.976(6),b=20.630(25),c=19.861 (4) Å,V=4087Å3,Z=4,R=0.087 for 1461 reflections; (2): [Ni(NCS)2(4-ViPy)4](1.76 THF)(0.24 cyclohexene),P bcn ,a=9.987(7),b=20.614(4),c=19.898(4)Å,V=4096Å3,Z=4,R=0.084 for 1304 reflections; (3): [Ni(NCS)2(4-ViPy)4](0.48 THF)(0.52 1,3-cyclohexadiene), tetragonalI41/a,a=16.898(3),b=16.898(3),c=26.463(6)Å,V=7556Å3,Z=8,R=0.120 for 1698 reflections; (4): [Ni(NCS)2(4-ViPy)4](0.36 THF)(1.04 1,4-cyclohexadiene),I41/a,a=16.986(4),b=16.986(4),c=25.896(15)Å,V=7472Å3,Z=8,R=0.103 for 2025 reflections; (5): [Ni(NCS)2(4-ViPy)4](0.35 THF)(1.05 benzene),I41/a,a=17.102(10),b=17.102(10),c=25.498(8)Å,V=7458Å3,Z=8,R=0.118 for 2200 reflections; (6): [Ni(NCS)2(4-ViPy)4](3 benzene), triclinicP1,a=10.432(24),b=11.155(9),c=21.581(7)Å, α=78.70(5), β=82.60(7), γ=74.09(13)°,V=2361Å3,Z=2,R=0.078 for 3427 reflections. Host-guest ratios and, for mixtures of guests, guest1/guest2 ratios, were elucidated by density and NMR. We show that the conformational freedom of the substituted pyridines is not the primary reason for the clathrating ability of Werner hosts. All six structures show no host-guest interaction at the level of van der Waals interactions. As non-bonding interactions are not observed between the host and guest, this study shows that the above host's selectivity by enclathration of particular guest molecules cannot be accounted for by solid state structural analysis.
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  • 24
    ISSN: 1573-1111
    Keywords: Iminophosphoranes ; amine inclusion compounds ; 13C CPMAS NMR spectroscopy ; salt-like crystalline aggregates ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal and molecular structure is reported for the inclusion compound 2-[o-(triphenylphosphoranylidenamino)benzyliden]amino-1H-2,3-dihydroindazol-3-one/isopropylamine/water3b. The crystal structure consists of discrete dimeric salt-like aggregates joined together by strong N+−H...−O−C hydrogen bonds between pairs of centrosymmetrically-related indazolonate anions and isopropylammonium cations. Six other inclusion compounds have been prepared and characterized by NMR [with propylamine (3a), withtert-butylamine (3c), withsec-butylamine (3d), withtert-pentylamine (3e), with 1-methylbutylamine (3f) and withiso-pentylamine (3g)]. Two different arrangements are found, both with the host being in the anionic form. The guests are either: (i) one protonated amine and one water molecule (3b and3f); or (ii) one protonated amine and the corresponding neutral amine (3a, 3c, 3d, 3e and3g).
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  • 25
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    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 16 (1993), S. 267-272 
    ISSN: 1573-1111
    Keywords: Crown ether ; ytterbium nitrate ; phen ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title complex was prepared by reacting Yb(NO3)3 (12-crown-4) with 1,10-phenanthroline (hereafter phen) in acetone. It crystallized in the triclinic space group $$P\bar 1$$ witha=10.095(5),b=17.415(4),c=8.710(2) Å α=92.45(2), β=115.83(3), γ=74.08(3)0 andD c=1.85 g cm−3;Z=2. The metal ion in this complex is nine-coordinated to three bidentate nitrate ions, two nitrogen atoms of a phen and a water molecule. The crown ligand is hydrogen bonded to the coordination water molecule. The symmetry change of the crown ether is also discussed.
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  • 26
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1713-1723 
    ISSN: 0887-6266
    Keywords: phthalocyanine siloxane ; crystal structure ; epitaxial growth ; high-resolution electron microscopy ; molecular imaging ; polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thin films of SiPc(OH)2 (Pc = phthalocyanine) were formed epitaxially on the (001) surface of mica by vacuum deposition and were then polymerized by heat treatment. The molecular packing of the SiPc(OH)2 was determined by electron diffraction and high-resolution electron microscopy as triclinic\documentclass{article}\pagestyle{empty}\begin{document}${\rm P\bar 1} $\end{document} having dimensions a = 0.727, b = 1.307, c = 0.688 nm, α = 102.5, β = 104.2, and γ = 97.4°. This monomer crystal grows with its c-axis parallel to the a-axis of the substrate mica and its bc-plane parallel to the (001) surface of mica. By heat treatment at 320°C, the SiPc(OH)2 polymerized with the c-axis of the polymer parallel to the c-axis of the monomer. At 420°C, the c-axis of the polymer became parallel to the a*-axis of the monomer (i.e., perpendicular to the film surface). From high-resolution electron microscopy of partially polymerized specimens, the polymerization was shown to start at the edges of small monomer crystals. This may be considered to be due to the volume expansion during the polymerization. © 1993 John Wiley & Sons, Inc.
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  • 27
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1923-1940 
    ISSN: 0887-6266
    Keywords: poly(4,4′-oxybibenzoate) ; polymerization ; morphology ; transitions ; crystal structure ; disclination domains ; Iamellae ; single crystals ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 4-Acetoxy 4′-carboxy biphenyl has been polymerized from solution, the bulk melt, and in constrained thin films, all below the melting point of the monomer as measured by differential scanning calorimetry (DSC). An isothermal sublimation-recrystallization-melting (and chemical change)-polymerization-crystallization process is proposed. From solution and in the thin films, single crystals consisting of ca. 100 Å thick lamellae are observed, with evidence for monomer addition-reaction on the end (top and bottom) surfaces. The bulk samples are fibrous, the “fibers” consisting of whisker-like single crystals. The polymer is highly heat and radiation (electron beam) resistant, with numerous successive electron diffraction (ED) patterns from the same crystal or sheared sample permitting comparison of the changes in ED patterns with transitions seen by DSC at ca. 350, 530, and 590°C. Phase I (a = 7.8, b = 5.5, c = 10.8 Å), a possible phase II (a = 15.6, b = 3.6 Å c = unknown), and a phase III (a = 9.0, b = 5.2 = √3a, c = 10.8 Å). Phases I and II are seen in samples polymerized at temperatures at and below 310°C; phase III is observed in samples polymerized at and above 350°C and in sheared samples. © 1993 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
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  • 28
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1759-1767 
    ISSN: 0887-6266
    Keywords: rigid rod polymer ; thermotropic ; aromatic polyester ; fiber ; modulus ; crystal structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fiber spinning and mechanical properties of four rigid polyesters with alkoxy substituents of different length and placement were evaluated. Properties of oriented fibers from the polymer with dodecyloxy substituents on the terephthalate moiety, PTA12HQ, were significantly affected by the crystal modification. At room temperature the following properties (tensile modulus E, tensile strength σb, and strain at break εb) could be obtained: E = 9.5 GPa, σb = 85 MPa and εb = 1.1% for phase Lf (the “frozen in layered mesophase”); E = 10.4 GPa, σb = 59 MPa and εb = 0.6% for modification A; E = 17.3 GPa, σb = 158 MPa and εb = 1.2% for modification B. Because of the higher amount of main chains per cross sectional area the polymer with hexyloxy side chains, PTA6HQ, showed better properties at a comparable degree of molecular orientation: E = 24 GPa, σb = 270 MPa, εb = 1.4%. Fibers obtained from the polyester with dodecyloxy substituents on the hydroquinone moiety, PTAHQ12, were too brittle to handle. The polyester with dodecyloxy substituents on both moieties, PTA12HQ12, was spun from the isotropic melt. Because of the obtained low degree of orientation, properties (E = 1 GPa, σb = 40 MPa, and εb = 6.3%) were governed by interactions between the chains (the main chains are not load-bearing). © 1993 John Wiley & Sons, Inc.
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  • 29
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    Journal of Physical Organic Chemistry 6 (1993) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 30
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    Journal of Physical Organic Chemistry 6 (1993), S. 601-608 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Exhaustive methylation of 1-phenylurazole (1), using ethereal diazomethane as the methylating agent, results in the formation of three products: 1-phenyl-3,5-dimethoxy-1,2,4-triazole (2), 1-phenyl-3-methoxy-4-methyl-Δ2-1,2,4-triazolinev5-one (3) and 1-phenyl-2,4-dimethylurazole (4). Based on the amounts of 2-4 isolated, the overall yields in these reactions are typically 〉90%. When 1 and diazomethane were allowed to react in a fashion that resulted in the formation of monomethylated analogues of 1, 1-phenyl-3-methoxy-Δ2-1,2,4-triazoline-5-one (5) and 1-phenylv2-methylurazole (6) were formed. In separate experiments, the monomethylated species 5 and 6 were allowed to react with diazomethane in efforts to develop a sequence of reactions that reasonably accounts for the formation of 2-4. Whereas N- and O-methylated products were obtained when 5 was treated with ethereal diazomethane, the reaction of 6 and diazomethane produced only the N-alkylated product 1-phenyl-2,4-dimethylurazole (in quantitative yield). The outcomes of these experiments are consistent with a sequence of reactions in which the treatment of 1 with diazomethane results, initially, in the formation of the monomethylated species 5 and 6. In the presence of sufficient diazomethane, 5 and 6 then undergo further mothylation, forming the dimethylated species 2-4.
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  • 31
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    Journal of Physical Organic Chemistry 6 (1993), S. 615-620 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The potential for C—S rotation in ethyl hydrodisulphide, CH3CH2SSH, has been studied with ab initio methods. All stationary point structures were fully optimized at the HF/6-31G* and MP2/6-31G* levels. MP2/6-31G* molecular geometries were used in subsequent single-point energy calculations with several basis sets and including various amounts of electron correlation up to the MP4SDQ/6-311+G(2d,p) level of theory. Zero-point vibrational energies and thermal corrections were calculated and used to obtain relative values for ΔH0 and ΔH298. The stability order for the three energy minima is gauche - ≥ gauche + 〈 trans (positive disulphide chirality, C—S—S—H torsion ≈ 89°). The results have implications for force field calculations on disulphide bridge conformations in peptides and proteins.
    Additional Material: 1 Ill.
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  • 32
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates of elimination of several alkyl methanesulphonates were determined in a seasoned, static reaction vessel over the temperature range 300-420°C and the pressure range 28-163 Torr. The reactions are homogeneous, unimolecular and follow a first-order rate law. The overall rate coefficients are given by the following equations: for isobutyl methanesulphonate, log k1 (s-1) = (12·51 ± 0·38) - (177·0 ± 2·1) kJ mol-1 (2·303RT)-1; for 2-phenyl-1-propyl methanesulphonate, log k1(s-1) = (12·62 ± 0·04) - (176·2 ± 0·5) kJ mol-1 (2·303RT)-1; for neopentyl methane-sulphonate, log k1(s-1) = (13·35 ± 0·42) - (198·2 ± 5·2) kJ mol-1 (2·303RT)-1; and for 3-chloro-2,2-dimethyl-1-propyl methanesulphonate, log k1(s-1) = (13·87 ± 0·42) - (218·2 ± 5·4) kJ mol-1 (2·303RT)-1. Rearrangements in these methanesulphonate pyrolyses may proceed via an intimate ion-pair type of mechanism. Consequently, the results appear to confirm that intramolecular migration through autosolvation is possible in gas-phase elimination reactions of certain types of organic molecules.
    Additional Material: 11 Tab.
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  • 33
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    Journal of Physical Organic Chemistry 6 (1993), S. 126-131 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The photolysis of cyclobutylchlorodiazirine affords chlorocyclopentene and chloromethylenecyclobutane by direct rearrangements from the diazirine's excited state (65%) and by competitive formation and subsequent rearrangement of cyclobutylchlorocarbene. The involvement of excited diazirine in the analogous cyclobutylfluorodiazirine photolysis is much reduced (12%).
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  • 34
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    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 35
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    Journal of Physical Organic Chemistry 6 (1993), S. 145-152 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibria and kinetics of acid-base reactions in toluene between a carboxylic acid (m-toluic, salicylic acid) and a set of carbinol bases (derived from basic triarylmethane dyes) were studied spectrophotometrically. The results for the equilibrium and kinetic parameters were critically analysed. The rate constant of the forward step of the acid-carbinol base equilbrium was found to provide a suitable scale of basicities in toluene. The basicities of the dye carbinols chosen decrease in the order Ethyl Violet- 〉Crystal Violet- 〉Methyl Violet- ≈ Victoria Pure Blue BO- ≫ Brilliant Green- 〉Malachite Green-carbinol. This is fairly consistent with the order observed in water. A fairly good correlation between base strengths of the carbinols and σR+ parameters of their para-alkylamino substituents was obtained.
    Additional Material: 6 Tab.
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  • 36
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    Journal of Physical Organic Chemistry 6 (1993), S. 333-340 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rate of intramolecular photoinduced electron transfer (PET) between a naphthacene electron donor (D) and a sulfonium electron acceptor (A) was found to be dependent on the thermodynamics for PET and distance between D and A. The slopes of In kET vs through-bond and through-space distance plots was found to be -0·60 and -0·91 Å-1, respectively. The product distribution obtained from the photolysis of regioisomeric naphthacenyl sulfonium salt derivatives was found to be independent of distance. Photolysis of three regioisomeric naphthacenyl phenylmethyl-p-cyanobenzylsulfonium salts produced unsubstituted thiomethylphenylnaphthacene and mono-, di- and tri-p-cyanobenzyl-substituted thiomethylphenylnaphthacene. The appearance of the out-of-cage di- and trisubstituted photoproducts suggests that secondary photochemistry and intermolecular electron transfer bond-cleavage reactions are occurring when the concentration of the sulfonium salt in acetonitrile is 10-2 and 10-3 M and the degree of conversion is high. The primary photoproduct is the mono-substituted naphthacene derivative.
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  • 37
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    Journal of Physical Organic Chemistry 6 (1993), S. 15-22 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Zinc(II) complexes of N-pyridylcinnamides (H, m-OCH3, p-OCH3 and p-OH derivatives) were studied by spectrophotometric methods in aprotic media, and represent a chemical model inhibition by cinnamides of coniferyl alcohol dehydrogenase (CAD), a zinc enzyme involved in the lignification process. The complexation of N-pyridylcinnamide and m-methoxy-N-pyridylcinnamide with zinc ion is effected according to a 1 : 1 stoichiometry (ML), whereas a two-step equilibrium (M + L ⇌ ML \documentclass{article}\pagestyle{empty}\begin{document}$ V_{\rm m} = 4 \cdot 45C_0 + 6 \cdot 44C_1 - 3 \cdot 33C_2 + 0 \cdot 46C_4 + 52 \cdot 9{\rm (}n = 300,r = 0 \cdot 999,s = 0 \cdot 81) $\end{document} ML2) is preferred with p-methoxy and p-hydroxy compounds. These ligands are mainly bonded through the carbonyl oxygen atom and the nitrogen of the pyridyl ring. Molar absorptivities for these complexes, not directly available, were calculated from analysis of the experiemental data. The UV complexation results are also supported by the stoichiometry of the complexes, which were synthesized and characterized.
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  • 38
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction of monosilylated imines and a disilylated enamine with nitrosyl salts in dichloromethane at -78°C is shown to proceed via intermediate vinyl diazonium salts and vinyl cations.
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  • 39
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    Journal of Physical Organic Chemistry 6 (1993) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 40
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ambident reactivity of phenoxide ion towards 1,3,5-trinitrobenzene (TNB) was re-examined by means of a novel reaction system(CD3CN-glyme-d10) which allows the investigation of species formed at low temperatures (-40°C), contrasting with previous studies in dimethyl sulfoxide (DMSO) at ambient temperature. The new method coupled with 400 MHz NMR spectroscopy has allowed the definitive observation of both O- and C-bonded phenoxide σ-complex adducts for the first time, confirming the formation of the former through kinetic control and of the latter through thermodynamic control. The corresponding O-bonded σ-adduct in the TNB-mesitoxide system (whereC-bonded σ-adduct formation is not possible but where there is competing nitro group displacement) has also been characterized by 1H and 13C NBR. Another O-bonded aryloxide adduct characterized is that from the reaction of TNB with3,5-di-tert-butylphenoxide; in this system there is also competing NO2 displacement. Stereoelectronic factors in the O-bonded σ-adducts and aryl ethers are discussed.
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  • 41
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    Journal of Physical Organic Chemistry 6 (1993), S. 95-100 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The (2 + 2) cycloaddtion reactions of 1-tert-butyl-3-methylallene (tBMA) with radicophiles were investigated. The attempted cycloaddition reactions with N-phenylmaleimide, acrylonitrile and methyl acrylate produce only (4 + 2) cycloadducts of 1-tert-butyl-1,3-butadiene which is formed by the more rapid [1.3] hydrogen sigmatropic rearrangement of the tBMA. The (2 × 2) cycloaddition of tBMA with 1,1-dichloro-2,2-difluoroethene (1122) occurs more rapidly than does the sigmatropic rearrangement, and produces a mixture of the four cycloadducts 1-4. The cycloaddition of 1122 with enantioenriched tBMA produces one cycloadduct (3) in which ca 91% of the enantiomeric excess (ee) of the tBMA is transferred to the cycloadduct. The other three cycloadducts are formed retaining much less of the ee of the starting tBMA. The results are interpreted on the basis of molecular modeling calculations carried out on the 1122-1,3-dimethylallene system reported previously. It is suggested that cycloadduct 3 is formed by essentially only one continuous minimum-energy reaction pathway, while cycloadducts 2 and 4 are formed by two competitive minimum-energy reaction pathways which result in the formation of cycloadducts possessing opposite absolute configurations. The combined contributions of the two competitive pathways result in much lower overall degrees of transfer of the ee of the tBMA to the diradical intermediates and cycloadducts.
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  • 42
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    Journal of Physical Organic Chemistry 6 (1993), S. 132-132 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 43
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The advantage of using the YBnCl scale over the YCl scale in Grunwald-Winstein-type correlation analysis was demonstrated by the kinetic evidence of a significant nucleophilic solvent intervention in the solvolysis of 2-aryl-2-chloropropanes. A depression of log k values measured in ethanol-trifluoroethanol mixtures and a positive azide salt effect were observed.
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  • 44
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    Journal of Physical Organic Chemistry 6 (1993), S. 139-144 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The contribution of the polarized resonance structures to 7-methyl-7H-pyrrolo[2,3,-b]pyridine and 4-methyl-4H-pyrrolo [3,2-b] pyridine, which have recently attracted much attention in physico-chemical studies, was considered based on multinuclear (1H, 13C and 15N) NMR spectroscopy and MO calculation. Comparison of the chemical shifts of the compounds with those of other relevant compounds and the effects of concentration and solvents observed by multinuclear NMR suggested that the contribution of the non-polarized structures to both compounds predominates over that of the polarized structures. This result was also supported by ab initio MO calculations using the 6-31G basis set.
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  • 45
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    Journal of Physical Organic Chemistry 6 (1993), S. 160-162 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Stern-Volmer quenching equation for use of a dualistic quencher, which serves not only as the quencher for an excited starting molecule but also as the promoting agent for product formation, was obtained by applying the steady-state approximation to the photoreaction system. The equation was applied to the kinetic analysis of the Norrish type II photoreaction of valerophenone using triethylamine, which serves as the excited-state quencher and as the promoting agent for product formation.
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  • 46
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The four studied semi-rigid fluorenol derivatives differ only in the size of the 9-substituents. All four compounds crystallize with two molecules per asymmetric unit and with relatively low crystallographic symmetry [P1 for the 9-methyl derivative (1) and P21/n for the 9-(1-naphthyl) (3) and 9-(2-biphenylyl) (4) derivatives]. Crystal data: 1, a = 8·779(1), b = 11·570(1), c = 11·747(1), α = 91·197(5), β = 104·345(4), γ = 105·848(6)° 2, a = 8·425(1), b = 13·819(1), c = 23·902(2)Å, β = 95·87(1)° 3, a = 15·679(4), b = 8·567(2); c = 23·884(17)Å, β = 92·60(6)° 4, a = 7·770(6), b = 33·766(10), c = 13·649(4)Å, β = 95·30(1)°. Nevertheless, the packing modes are different. The 9-methylfluoren-9-ol molecules, forming H-bonded tetramers with full H-bond saturation, give rise to the lowest packing coefficient among the four compounds. The crystals of the 9-phenyl derivative are built up of H-bonded dimers, whereas those of the bulky 9-naphthyl and 9-diphenylyl derivatives consist of single molecules only. The latter two compounds, however, have a denser packing than the two that contain H-bonded aggregates. The crystal structures are held together mainly by ordinary Van der Waals forces. In the case of 9-biphenylyfluoren-9-ol, the structure seems to be stabilized also by weak H-bond-type interactions from the alcoholic hydroxyl group to the π-electron cloud of an aromatic ring in the neighbouring molecule the O…centroid distances are 3·182(3) and 3·248(4)Å, and in the 9-naphthyl derivative the OH groups are involved in some short (˜3·3Å) intermolecular approach, possibly indicating an electrostatically favourable packing for the compound.
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  • 47
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    Journal of Physical Organic Chemistry 6 (1993), S. 187-192 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reactivity ratio between the three- and four-membered cyclic ammonium ions in ring-opening elimination reactions was measured. The comparison with the analogous ratio obtained in a previous study on ring-opening substitution reactions suggests a substantial difference in the effect of the stereochemical factors governing the two ring-opening reactions and confirms the anomalous behaviour of small rings in the ring-opening substitution reaction.
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  • 48
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Hammett type plot of kinetic solvent isotope effect (KSIE = kSOH/kSOD), log(KSIE) vs σ, can be a useful mechanistic tool for solvoltic reactions. The slopes of such straight line plots for para-substituted benzenesulphonyl chlorides in methanol (0·15), water (0·05) and methanol-water (0·05) are interpreted in terms of different reaction channels (general base-catalysed and SN2), in contrast to simple Hammett plots, log kSOH (or log kSOD) vs σ, invariably exhibiting non-linear concave curves.
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  • 49
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    Journal of Physical Organic Chemistry 6 (1993), S. 243-250 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ab initio calculations, using the 6-31G* basis set, were performed in order to study the energetics of the electrophilic attack on water by such diazonium ions as methyl-, ethyl- and fluroethyldiazonium. For the first case, an indication of a transition state appears at the Hartree-Fock level, whereas for the other two, the energy is continuously decreasing from reactants to products. When correlation energy was taken into account via single-point MP2/6-31G* calculations, a deep ion-dipole energy minimum was observed for the methyldiazonium ion followed by a low transition state, whereas the other two did not change their energy pattern. On performing the MP2/6-31G* optimization for the methyl species, the Hartree-Fock results were confirmed, with a slight displacement of the transition state toward a shorter CO distance.
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  • 50
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 10-Methylacridine dimer [(AcrH)2] dissociates into a pair of 10-methylacridyl radicals (AcrH·) on laser excitation (308 nm) in solvents of various polarities. Exposure of (AcrH)2 in methylcyclohexane glass at 77 K to γ-rays of 60Co generates the radical cation (AcrH)2+·. Thermal annealing of the matrix to 90 K results in dissociation of (AcrH)2+· into AcrH· and 10-methylacridinium cation (AcrH+).
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  • 51
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The longest wavelength absorption band of substituted anilines containing electron-accepting groups is characterized as an intramolecular charge-transfer (ICT) transition. Dual absorption peaks observed for the ICT transition of some para-substituted anilines in a strongly hydrogen-bonding solvent, hexafluoropropan-2-ol (HFP) can be attributed to two inequivalently hydrogen-bonded species with differently hybridized aniline nitrogens in HFP. The hydrogen bond-induced rehybridization causes appreciable changes in the ICT absorption spectra of highly polar aromatic amines. Rehybridization of aromatic amino nitrogens depends on the OH acidity in the solvent molecule and the basicity of the substituted anilines. The geometry of trivalent nitrogens in aryl amines is critically dependent upon the ionization potential of the amino group, the electron affinity of the electron-accepting substituent and the substitution site of the electron-withdrawing group with respect to the amino moiety.
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  • 52
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    Journal of Physical Organic Chemistry 6 (1993), S. 287-292 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The acid-catalysed solvolysis of (R)-1-phenyl-1-methoxyethane was studied in mixtures of dilute aqueous perchloric acid and acetonitrile at 50°C. The rate of loss of optical activity (kα) was found to be the same as the rate of solvolysis (ksolv) at both low and high water contents of the solvent. These results are not in accord with literature data on racemization and oxygen exchange of 1-phenylethanol in water, which has been discussed in terms of interconversion of chiral ion-dipole pair intermediates. The mechanistic implications of the results are discussed.
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  • 53
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    Journal of Physical Organic Chemistry 6 (1993), S. 307-315 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 13C NMR spectra of 45 vicinally substituted 2-, 3- and 4-aminopyridines were investigated. The substituent effects are evidently sensitive to the position of both the substituent and the fixed amino group. In the para position with respect to the substituent, long-range electronic effects are expressed by the dual substituent parameter treatment (DSP), and the resonance contribution is more important than the inductive contribution. Correlation results for the ipso and ortho carbon atoms using the more sophisticated extended DSP equation suggest non-electronic effects of unknown origin.
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  • 54
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been established that the product of the reaction of N-pentafluorophenylcarbonimidoyl dichloride (1) with dibenzylamine, viz. N2-pentafluorophenyl-N1,N1-dibenzylchloroformamidine (4a) is a Z-isomer, whereas according to the concept of stereoelectronic control one might have expected a product with E-configuration. The heat of formation and the geometry of Z- and E isomer of N2-pentafluorophenyl-N1,N1-diethylchloroformamidine (4b) (the latter is a product of the reaction of 1 with diethylamine) were calculated with the semi-empirical MNDO method. The calculated geometry of (Z)-4b was found to be in a good agreement with the experimentally determined structure of 4a. The formation of (Z)-4b is more preferable energetically than that of (E)-4b; the calculated difference in the heats of formation is 2·8 kcal mol-1. Thermodynamic control of the reaction stereochemistry is proposed.
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  • 55
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    Journal of Physical Organic Chemistry 6 (1993), S. 326-332 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The 13C NMR spectra of most of the substituted perhydro-1,2-oxazolo[3,2-c] [1,4]oxazines (3) at low temperature showed the presence of two isomers of unequal populations. The major isomer is shown to be the cis isomer {except in 2-hydroxymethyl-2-methylperhydro-1,2-oxazolo[3,2-c] [1,4] oxazine (3e)}, which is in equilibrium with the minor isomer (trans conformer) by a relatively slow nitrogen inversion. Intramolecular hydrogen bonding in oxazines, having 2-hydroxymethyl substituents, is shown to be an important factor in determining the population ratio of the two isomers. The barrier to nitrogen inversion was determined by detailed band-shape analysis of proton and carbon NMR spectra and were in the range 66·3-72·9 kJ mol-1. The chair inversion had been slowed down, in one case, trans-dimethylperhydro-1,2-oxazol[3,2-c] [1,4]oxazine-2,3-dicarboxylate (3j), to show the presence of the two forms of the cis isomers. The barrier to chair inversion is 41·5 kJ mol-1 as determined by proton NMR band-shape analysis of 3j.
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  • 56
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    Journal of Physical Organic Chemistry 6 (1993), S. 478-482 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solvent and pressure effects were examined for the isomerization rates of N-phenyl- and N-methylrhodaminelactams (RL-Ph and RL-CH3) from their zwitterionic to the spiro forms. From the pressure dependence of the reaction rate, the activation volumes were estimated to be about 5 cm3 mol-1 for RL-Ph and 3-10 cm3 mol-1 for RL-CH3. It is proposed that there are two rotameric isomers for the coloured zwitterionic forms, and the role of these rotamers in the kinetic effects of solvent and pressure is discussed. The results are consistent with a reaction mechanism involving heterolytic ring closure on activation.
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  • 57
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    Journal of Physical Organic Chemistry 6 (1993), S. 483-487 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Triplet zero-field splitting parameters were obtained in 2-methyltetrahydrofuran glass at 77 K for phenylene-1,4-dinitrene (1), biphenyl-4,4′-dinitrene (2), (E)-1,2-bis(4′-nitrenophenyl)ethene (3), 1,4-bis(4′-nitrenophenyl)buta-1,3-diene (4) and 1,8-bis(4′-nitrenophenyl)octa-1,3,5,7-tetraene (5). The results were (1) |D/hc| = 0·169 cm-1 |E/hc| = 0·004 cm-1, (2) |D/hc| = 0·189 cm-1, |E/hc| = 0·00 cm-1, (3) |D/hc| = 0·122 cm-1, |E/hc| = 0·00 cm-1, (4) |D/hc| = 0·0865 cm-1, |E/hc| = 0·00 cm-1 and (5) |D/hc| = 0·0442 cm-1, |E/hc| = 0·00 cm-1. All these biradicals are ground-state singlets. Based on the observed decrease in triplet signal intensities as temperature decreases. The substantial magnitudes of |D/hc| for 3-5, despite the large distance between localized nitrene electrons, is much more than can be explained by a simple dipolar interaction between localized electrons, and is attributed at least partly to spin polarization effects on the π-electron clouds of these systems.
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  • 58
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    Journal of Physical Organic Chemistry 6 (1993), S. 523-530 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: NMR spectroscopic and conformation analyses ware carried out for five dimethyl β,γ-disubstituted propylphosphonates, YCH2CHXCH2PO3Me2, in five solvents and in acetone containing sodium and magnesium ions. Conformational preferences observed for the rotation about the C1—C2 bond are determined by the attractive interactions between the oxygen containing substituents X (X = OH, OMe) and the phosphoryl group, and are enhanced by the metal ions, presumably via chelation effects. The rotation about the C2—C3 bond yields statistical distribution of the rotamers. For Y = benzoyl, there was no evidence for a competition of the carbonyl group for the intramolecular interactions with X or with a metal ion.
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  • 59
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In many reactions of magnesium reagents, including Grignard and aryliminodimagnesium [ArN(MgBr)2, IDMg], the formation of abnormal products via reactions such as radical dimerization, hydrogen abstraction and conjugate 1,4-addition orginating from efficient single electron transfer (SET) is not excluded. In IDMg reactions with benzonitrile and N,N-dimethylformamide in tetrahydrofuran, however, clean reactions took place affording N-arylbenzamidine and N,N′-diarylformamidine via exclusive 1,2-addition and condensation plus replacement, respectively. Some alkyl and arylvinyl cyanides gave the corresponding amidines without 1,4-addition or hydrogen abstraction. These results are the first observation of such reactions of magnesium reagents, and are attributed to a combination of the weak electron-donating ability (EDA) of IDMg with the weak electron-accepting ability (EAA) of nitriles. Although ESR is therefore inapplicable, factors governing the product yields were studied on the basis of effects caused by the addition of strongly coordinating hexamethylphosphoramide and pyridine to the reagent solution, and by addition of nitrobenzenes having a strong EAA. From the results, a large participation of σ-complexation followed by implicit SET in the inner sphere of the complex is proposed.
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  • 60
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    Journal of Physical Organic Chemistry 6 (1993) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 61
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    Journal of Physical Organic Chemistry 6 (1993), S. 539-544 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The use of quantitative structure-activity relationships (QSAR) in correlating biological phenomena to chemical structure, and the use of linear free energy relationships (LFER) and linear solvation energy relationships (LSER) for correlating physical phenomena are becoming standard occurrences. In this work the empirical LSER solvatochromic descriptors were replaced with a computationally derived set to aid in a priori property prediction. This paper deals with the application of this descriptor set to correlating the solubilities of 22 compounds in super critical CO2. A reasonable correlation, consistent with previous correlations by other researchers, was found.
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  • 62
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    Journal of Physical Organic Chemistry 6 (1993), S. 555-560 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Deoxymercuration was examined in the antiperiplanar stereochemistry of trans-2-acetoxycyclohexylmercury(II) acetate (6). The presence of the mercury group accelerates the departure of the beta leaving group by a factor of about 1010. This beta effect is larger than that of silicon and comparable to that of germanium. In contrast to these latter cases, the rate for 6 was found to increase with the nucleophilicity of the solvent. It is concluded that a molecule of solvent is coordinated with mercury in the transition state. This nucleophilic assistance raises the polarizability and nucleophilicity of the mercury group, enhancing its ability to stabilize the developing positive charge or to form a bridged intermediate.
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  • 63
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    Journal of Physical Organic Chemistry 6 (1993), S. 567-573 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1-Alkoxycarbonylbenzotriazoles on thermolysis lose carbon dioxide; the decarboxylation is accompanied by the formation of a mixture of 1- and 2-alkylbenzotriazoles, with the N-1 isomer predominating over the N-2 isomer in all cases. A cross-over experiment, in which heating equimolar amounts of 1-benzyloxycarbonylbenzotriazole and 1-(4-methylbenzyloxycarbonyl)-5,6-dimethylbenzotriazole gave almost all the cross-over products, supports the proposed intermolecular mechanism for this decarboxylation and the formation of 1- and 2-alkylbenzotriazoles. No decarboxylation was observed for 1-phenoxycarbonylbenzotriazole.
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  • 64
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cyclopentannulation of 4-tert-butyldimethylsilyloxy-2-cyclopenten-1-one from a β-metallated dioxolane-type orthoester affords 4-tert-butyldimethylsilyloxy-8,8-ethylenedioxy-6-phenylsuiphonyl-2-oxobicyclo [3·3·0] octanes as a mixture of two diastereoisomers. Their stereochemical structures were established by NMR and x-ray analysis. The minor product possesses a cis ring fusion, the sulphonyl and the tert-butyldimethylsilyloxy groups being endo and exo, respectively. The major isomer also has a cis ring fusion but an exo position for both dimethylsilyloxy and sulphonyl groups. Both cyclopentannulation products result from an anti addition with respect to the 4-tert-butyldimethylsilyloxy group on the enone.
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  • 65
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: NMR measurements of associations between simple organic host and guest molecules bearing alternatively negatively charged groups and electroneutral π-moieties show in aqueous solutions weak but distinct attractions reaching approximately 2 kJ mol-1 and X-/arene unit. A similar value is observed for the complex between a calixarene with 4-sulfonato groups and toluene, for which the NMR shifts indicate an orientation with the guest methyl substituent upwards. The conformational fit of the selected complexes is checked by molecular mechanics simulations.
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  • 66
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ab initio theoretical calculations have been carried out on directly bonded donor-acceptor (Ẍ-Y) species and on variously substituted E-1,2-disubstituted ethanes, and π interaction energies have been estimated. In conjunction with the previously calculated radical stabilization energies of mono- and disubstituted methyl radicals, a comparison is made of the relative magnitudes of the π interaction energies between groups with zero, one and two intervening 2p AOs on carbon atoms. It is concluded that the stabilizing effect of the π interaction between directly bonded donor Ẍ and acceptor Y groups (zero intervening 2p AOs) is approximately 2·1 times that in the disubstituted methyl radicals (one intervening 2p AO), while in the E-1,2-disubstituted ethenes (two intervening 2p AOs) the stabilizing effect is ˜ 0·7 of that calculated for the disubstituted methyl radicals for both acceptor-donor and acceptor-acceptor disubstituted systems. No correlation is observed with the π stabilization energies of the ‘cross-conjugated’ 1,1-disubstituted ethenes.
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  • 67
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    Journal of Physical Organic Chemistry 6 (1993), S. 634-636 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Physical-chemical properties can be correlated and predicted using linear free energy or linear solvation energy relationships (LSER). Procedures to obtain theoretical parameters from calculated molecular structures that can be used in LSER have recently been evaluated [G R. Famini, C. A. Penski and L. Y. Wilson, J. Phys. Org. Chem. 5, 395-408 (1992)]. Among other applications, these procedures were applied to correlate octanol-water partition coefficients and pKa values for two groups of structurally diverse solutes with very good reported results. In this paper, the statistical results of those studies are re-examined. The corrected statistical parameters do not provide tenability for the appropriateness of the methodology in these applications. However, valid multilinear relationships of the theoretical LSER parameters with the experimental properties are found which do substantiate the original conclusions of Famini et al.
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  • 68
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    Journal of Physical Organic Chemistry 6 (1993) 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 69
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    Journal of Physical Organic Chemistry 6 (1993), S. 642-644 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Contrary to a recent report, the specific rates of solvolyses of five 2-aryl-2-chloropropanes give only marginally (not significantly) better correlations with use of the YBnCl scale rather than the YCl scale. With the use of the extended (two-term) Grunwald-Winstein equation, some evidence for a weak nucleophilic solvation is obtained, but at a low confidence level. The specific rates of 2-bromo-2(p-trifluoromethylphenyl)propane solvolysis are significantly better correlated using YBr (rather than YBnBr) values and, indeed, the use of NT values in conjunction with YBr values leads to an l value of 0·17 ± 0·06 and evidence for a weak nucleophilic participation at a 98·7% confidence level.
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  • 70
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    Journal of Physical Organic Chemistry 6 (1993), S. 645-650 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The recently developed σ-π energy separation technique was applied to substituted monocyclic ring systems. Modified correlation diagrams are presented which allow the influence of the substituent on the σ and π energies to be assessed. The slopes of the σ and π electron energy curves can be used to classify aromatic, non-aromatic and anti-aromatic compounds. A two-dimensional resonance coordinate representation shows a clustering of compounds of the three classes in distinctly different regions of this plane.
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  • 71
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    Journal of Physical Organic Chemistry 6 (1993), S. 651-659 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The solubility behaviour of β-cyclodextrin in aqueous mixtures was studied by determining the interactions between the co-solvent and water. Three clear classes of co-solvent are evident. In the first, including ethanol, tetrahydrofuran and acetone, there is formation of clathrate hydrates by the co-solvent. In these systems the solubilization is a maximum at the mole fraction corresponding to the minimum in the partial excess molar volume. The second class, including such solvents as dimethyl sulphoxide and pyridine, forms strong molecular complexes with water, and here a valley and a plateau region occur in the solubility values. In the third class, including formamide and urea, a steady increase in the solubility is observed. For these highly polar solvents no maxima are observed in intrinsic solvent properties such as the partial excess molar volume.
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  • 72
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    Journal of Physical Organic Chemistry 6 (1993), S. 660-684 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The β2H scale of solute hydrogen-bond basicity, formulated from 1:1 hydrogen-bond complexation constants in tetrachloromethane, has been used to set up a scale of effective or summation hydrogen-bond basicity, appropriate for the situation in which a solute is surrounded by solvent molecules. The method is based on the equation, \documentclass{article}\pagestyle{empty}\begin{document}$$ \log SP = c + rR_2 + s\pi _2^{\rm H} + a\sum {\alpha _2^{\rm H}} + b\sum {\beta _2 + vVx} $$\end{document} where SP is, in this work, a set of solute water-solvent partition coefficients in a given system. The explanatory variables are solute parameters as follows: R2 is an excess molar refraction, π2H is the solute dipolarity/polarizability, Σα2H and Σβ2 are the effective solute hydrogen-bond acidity and basicity and Vx is McGowan's characteristic volume. Various equations are established using β2H in the equation, and then amended β2H values are back-calculated and new Σβ2H values obtained. It is found that for most solutes, the effective basicity Σβ2H is invariant over the systems used to within an experimental error of around 0·03 units. About 350 Σβ2H values obtained from two or more experimental log P values are listed, together with values for homologous series and a number of singly determined values. For some specific solutes, such as sulphoxides, alkylanilines and alkylpyridines, Σβ2 is not constant, and an additional solute basicity denoted as Σβ2O is needed in order to deal with partitions from water to solvents that are partially miscible with water, such as isobutanol and octanol. Values of Σβ2O, and where possible Σβ2H also, are listed for 80 additional solutes.
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  • 73
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    Journal of Physical Organic Chemistry 6 (1993), S. 685-689 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Experimental gas-phase acidities are reported for a series of 4-substituted bicyclo [2.2.2] oct-1-yl carboxylic acids and for a limited number of the corresponding bicyclo [2.2.2] oct-2-enyl carboxylic acids. Similar acidities are also reported for additional 4-substituted benzoic acids, allowing a comparison of field and resonance effects between the three series. Ab initio molecular orbital calculations for these series of acids confirm the conclusion that the aromatic acids display direct field and resonance effects, whereas the acidities in the aliphatic series acids are largely determined by direct field effects.
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  • 74
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    Journal of Physical Organic Chemistry 6 (1993), S. 690-695 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fully optimized transition states for hydrogen transfer from methane and propene to substituted 2-adamantyl radicals were calculated using the AM1 molecular orbital method. Methane and propene were chosen to provide an early (propene) and a late (methane) transition state. For 5-substituted radicals (F, Cl, Ph, CH3, CF3) the enthalpic differences between syn and anti reactions was found to be small [〈0·1 kcal mol-1 (1 kcal = 4·184 kJ)]. Other radicals with nitrogen or boron included directly in the adamantyl fragment showed greater selectivities, with aza substitution favoring syn and bora substitution favouring anti attack, as did the 4,9-difluoro derivative. The calculated selectivities are all in qualitative agreement with experimental results (where available) on bromine atom transfer. PPFMO calculations showed the polarization of the SOMO to be generally in accord with the AM1 results, whereas the polarization of the LUMO's was less indicative. The bond orders for the bonds syn and anti to the incipient C—H bond in the adamantyl fragments indicated that the anti bonds were always weaker than those syn, in agreement with the suggestion by Cieplak that has been used to explain the experimental selectivities. However, the bond lengths of the incipient C—H bonds are always shorter for the side of preferred attack, in apparent agreement with the suggestion by Anh.
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  • 75
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    Journal of Physical Organic Chemistry 6 (1993), S. 696-698 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The first determination of a 1,2-phenyl shift in α,α-dimethylbenzylchlorocarbene was achieved by nanosecond laser flash photolysis, τ = 50 ns.
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  • 76
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    Journal of Physical Organic Chemistry 6 (1993), S. 1-6 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of the oxidation of a number of para- and meta-monosubstituted benzaldehydes by ethyl N-chlorocarbamate (ECC) were studied in aqueous acetic acid solution in the presence of perchloric acid. The main product of the oxidation is the corresponding benzoic acid. The reaction is first order with respect to the aldehyde, ECC and hydrogen ions. The oxidation of benzaldehyde exhibits a substantial primary kinetic isotope effect (kH/kD = 5·20 ± 0·10). Addition of ethyl carbamate has no effect on the rate. [EtOC(OH)NHCI]+ is postulated as the reactive oxidizing species. The rates of oxidation of para-substituted benzaldehydes exhibit an excellent correlation with Taft's σ1 and σR+ values whereas those of the meta-substituted compounds compounds correlate best with σ1 and σR0 values. The reaction constants are large and negative. A mechanism involving transfer of a hydride ion from the aldehyde to the oxidant, in the rate-determining step, is proposed.
    Additional Material: 5 Tab.
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  • 77
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    Journal of Physical Organic Chemistry 6 (1993), S. 23-28 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics and mechanism of the alkaline hydrolysis of both acyl- and aryl-substituted benzyl benzoates were studied in 80% (v/v) aqueous acetone at 20, 34, and 40 °C. Each of the substituted benzyl alcohols generated an independent σ-ρ plot which was correlated well with the Hammett equation (R = 0·996-0·999). The values of ρ for the acyl moiety showed no tendency either to increase or to decrease with the intrinsic reactivity of the parent benzyl alcohol and were all within ±0·098 of the mean of 2·236. However, the Hammett ρ values for the leaving groups decreased from H to p-NO2 substituents of the acyl part, in which the values were smaller than those of acyl moieties and fairly accurately obeyed the σ0 values rather than the σ values. The rate data for benzyl-substituted benzoates were correlated by the Yukawa-Tsuno equation, log k/k0 = 1·72(σ0 + 0·49ΔσR-) - 0·020, R = 0·996. The results suggested that the alkaline hydrolysis of benzyl benzoates showed a greater sensitivity to acyl than aryl activation, and the rates and activation parameters were largely determined by the addition step. The results are attributed to the preferential partitioning of an unstable tetrahedral intermediate to the products.
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  • 78
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It was found that substituted picric acids form slightly soluble 1 : 2 : 2 adducts with several simple crown ethers or with tri-, tetra-, or pentaethylene glycol dimethyl ether (glymes 4, 5 and 6) in water, whereas 2,4,6-trinitrobenzenesulfonic acid forms a 1 : 1 : 1 adduct with dicyclohexano-18-crown-6 (cis-syn-cis). The ability of a crown ether to precipitate a given acid follows the order dicyclohexano-18-crown-6 (cis-syn-cis) 〉 benzo-15-crown-5 〉 dicyclohexano-24-crown-8 〉 18-crown-6 〉 21-crown-7, 15-crown-5 ≫ 12-crown-4, roughly in the order of its base strength. Precipitation can occur even when the concentration(s) of one or more of the components are 〈 10-4 M. The solubility products of the 18-crown-6 complexes with dichloro- or dimethylpicric acids were estimated. In the solid state the 1 : 2 : 2 dicyclohexano-18-crown-6 (cis-anti-cis)-dichloropicric acid-water complex, which reportedly has two pseudohydronium ions lacking C3v symmetry of H3O+, exhibits an IR spectrum in the OH stretching region characteristic of an aqua complex.
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  • 79
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    Journal of Physical Organic Chemistry 6 (1993), S. 54-58 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates of elimination of primary, secondary and tertiary α-hydroxycarboxylic acids were determined in a seasoned, static reaction vessel over the temperature range 280-390°C and the pressure range 30-201 Torr. The reactions, in the presence of a free radical inhibitor, are homogeneous, unimolecular and follow a first-order rate law. The rate coefficients are given by the following equations: for glycolic acid, log k1 (s-1) = (14·03 ± 0·24) - (209·3 ± 1·5) kJ mol-1 (2·303RT)-1; for lactic acid, log k1 (s-1) = (12·24 ± 0·11) - (182·8 ± 1·3) kJ mol-1 (2·303RT)-1; and for 2-hydroxyisobutyric acid, log k1 (s-1) = (12·91 ± 0·13) - (174·7 ± 1·5) kJ mol-1 (2·303RT)-1. The basicity and the ease with which the hydroxy group is removed from primary to tertiary α-hydroxycarboxylic acids are reflected in rate enhancement. The mechanism of these eliminations appears to proceed through a semi-polar five-membered cyclic transition state.
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  • 80
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    Journal of Physical Organic Chemistry 6 (1993), S. 83-84 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The interaction of dichlorocarbene with imines and ketene imines was studied by means of the MNDO method. The results indicate that the lack of ylide cyclization products in the reactions of dichlorocarbene with ketene imines is due to a high reactivity of ketene imine ylides in intermolecular reactions, rather than stereoelectronic factors preventing cyclization. It was shown that the dichlorocarbene reaction with N-benzylideneaniline resulting in gem-dichloraziridine proceeds through transient formation of ylide.
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  • 81
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    Journal of Physical Organic Chemistry 6 (1993), S. 107-112 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A molecular mechanics scheme developed for bridged ferrocene derivatives was applied to study the conformational energy surface of [1.1] ferrocenophane (1). The mechanism of the intramolecular interconversion of 1 is shown to be different from the mechanism of the syn-syn exchange proposed earlier for this ‘molecular acrobat’.
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  • 82
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    Journal of Physical Organic Chemistry 6 (1993), S. 101-106 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acidity constants of benzamide and seven ortho-substituted derivatives were determined. Except for o-nitrobenzamide, all the amides exhibit medium effects. The data were treated by vector analysis. o-Aminobenzamide displays two protonation equilibria. The second acidity constant was determined by vector analysis and by the excess acidity function, since the acid strength provided by perchloric acid is insufficient for complete protonation. Different acidity functions and the ortho substituent effect on ionization of the amide group are compared.
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  • 83
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    Journal of Physical Organic Chemistry 6 (1993), S. 113-121 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A molecular mechanics study of cyclophosphazenic polypodands and of glymes, of their complexes with ion pairs (IPs) M+ I- (M+ = Li+, Na+, K+, Rb+) and IP aggregates (M+ I-)n was carried out to investigate the catalytic activity of these ligands in solid-liquid phase-transfer reaction. This activity is explained by their ability to bind IP aggregates effectively and to activate the anion by increasing the interionic distance in the single IP.
    Additional Material: 5 Ill.
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  • 84
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Notes: The Gibbs energies of activation of the solvolytic reactions of tert-butyl halides (chloride, bromide and iodide) in eight mono-alcohols and eight di-alcohols were dissected into contributions from the initial state and transition state. The unified approach proposed by Abraham was applied and the various factors making up the overall solvent effect in both states were identified and compared. To perform this study, the Gibbs energies of transfer of the initial state were calculated using the infinite dilution activity coefficient values of the solutes in the solvents, γ∞. These values were determined from the UNIFAC group-contribution method, with the modified Flory-Huggins equation in the combinatorial term and with group interaction parameters from the Parameter Table exclusively based on experimental γ∞ data reported in the literature. It is concluded that solvent polarizability and polarity-HBD acidity and cavity effects during the activated process are mainly due to transition-state contributions.
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  • 85
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    Journal of Physical Organic Chemistry 6 (1993), S. 163-170 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular structure of [4] metacyclophane is optimized at the ab initio STO-3G SCF level and a genuine minimum is located. In the STO-3G structure the benzene ring is less bent and geometrically distorted than in the previously reported MNDO structure. Although some bond alternation is calculated for the carbon-carbon bond lengths of the bent benzene ring, their values still fall in the range of highly delocalized compounds. Despite the fact that the STO-3G strain energy [SE(tot.)] is larger than the corresponding MNDO strain energy, the distribution of SE(tot.) over the bent benzene ring [SE(bb.)] and the oligomethylene bridge [SE(br.)] is similar. To facilitate the hitherto unsuccesful identification of [4] metacyclophane, its electronic transition energies were calculated with CNDO/S-CI using the STO-3G geometry as input geometry. The reliability of the CNDO/S-CI results was assessed by a comparison of calculated and experimental electronic transition energies for p- and, m-xylene, [5] para- and [5] metacyclophane and [4] paracyclophane following the same approach.
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  • 86
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The stoichiometry of the reaction of TIIII with ascorbic acid (H2A) in the presence and absence of chloride ion conforms to TIIII + H2A 〉 TII + 2H+ + A. where A is dehydroascorbic acid. The reaction exhibits complex kinetics and the reactivity of various chlorothallium (III) species decreases in the order of [TIOH]2+ 〉 TI3+ 〉 [TICI]2+ 〉 [TICI2]+ 〉 TICI3 〉 [TICI4]-. The mass balance relationship was employed to calculate the equilibrium concentration of the chloride ion for evaluation of the rate constants.
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  • 87
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    Journal of Physical Organic Chemistry 6 (1993), S. 193-194 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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  • 88
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Substituent effects on the thermal elimination reactions of carbonates and thiocarbonates were investigated MO theoretically using the AM1 method. For both substrates, an electron-withdrawing group is found to facilitate the decomposition. A two-step process is favoured by carbonates, whereas one- and two-step processes can compete in the pyrolysis of thiocarbonates. The ability to transmit substituent effect is greater with oxygen (carbonates) than with sulphur (thicarbonates) in contrast to the experimental results of Taylor and co-workers. Modelling studies with replacement of the phenyl ring with a vinyl group are found to be justified in this type of work.
    Additional Material: 9 Tab.
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  • 89
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The erythro-thioimidazole precursor to the cyclopropyloxiranylmethyl radical has been prepared. Treatment with 7-19 equiv. of triphenyltin hydride at 70°C gave only 3-cyclopropylprop-2-en-1-ol, the product of epoxide ring opening. No product in which the cyclopropyl ring had opened was observed. Kinetic analysis allowed the assignment of a lower limit for the rate of oxiranylcarbinyl radical rearrangements of 1 × 1010 s-1 at this temperature.
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  • 90
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    Journal of Physical Organic Chemistry 6 (1993), S. 251-253 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The calorimetric isotherm of water sorption by solid human serum albumin (HSA) was measured in water-dioxane mixtures. This isotherm has been successfully described at low water contents in the solvent within the framework of the presented model. The adsorption equilibrium constant and the monolayer formation energy were estimated from this model. The interaction enthalpies of solid HSA with the solvent in water-rich mixtures do not differ essentially from the solution enthalpy of HSA in water. This means that the solvent water content may be sufficient for the intermolecular interactions of HSA suspended in a water-organic mixture to be similar to those in aqueous protein solution.
    Additional Material: 2 Ill.
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  • 91
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal and molecular structure of N-nitro-N-methyl-p-nitroaniline was solved with good precision: R = 0·058 and average estimated standard deviation for bond lengths = 0·003 Å. Analysis of the geometry reveals that the NO2 attached to the N atom is strongly conjugated. Application of the HOSE model to its geometry and to geometries of 12 other para-substituted nitrobenzenes yields good linear regressions between canonical structure weights and Hammett σ values by interpolation, σ for the N(Me)NO2 group is estimated to 0·36.
    Additional Material: 2 Ill.
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  • 92
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    Journal of Physical Organic Chemistry 6 (1993), S. 281-286 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Marcus cross relation provides a tool to calculate cross rates from the corresponding identity rates and the equilibrium constant. Assumptions made in deriving the Marcus cross relation and conclusions which can be drawn from agreement or disagreement between experimental and calculated cross rates are discussed. For a small variation in identity rate constants, agreement between experimental and calculated cross rates are discussed. For a small variation in identity rate constants, agreement between experimental and calculated cross rates simply means that the rate constant of a hypothetical thermoneutral cross reaction has a value within the range covered by the identity rates. Whether or not this value corresponds to the mean value of logarithmic identity rate constants can only be checked for a large variation in identity rates. Therefore, a newly defined index M is used to relate the difference in experimental and calculated logarithmic rate constants to the variation in the logarithmic identity rates. Provided that the Marcus cross relation is not obeyed, this indicates non-additivity of kinetic parameters. Applying this analysis to protontransfer reactions between different transition metal acids and between 9-alkylflourenes and (9-alkylfluorenyl)lithium shows that claims about agreement or disagreement of experimental rate constants with the rate constants calculated by means of the Marcus cross relation have to be revised in part.
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  • 93
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    Journal of Physical Organic Chemistry 6 (1993), S. 302-306 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A thermodynamic hydrogen-bond basicity scale, pKHB, and a spectroscopic hydrogen-bond basicity scale, Δν(OH), were measured which permitted the construction of the solute hydrogen-bond basicity scale, β2H, for 71 nitriles embracing a wide range of structures from trichloroacetonitrile to cyanamides. Field, resonance, and polarizability contributions of the X substituents to the hydrogen-bond basicity of XCN compounds were established. Steric effects do not contribute to the hydrogen-bond basicity of nitriles.
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  • 94
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    Journal of Physical Organic Chemistry 6 (1993) 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 95
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    Journal of Physical Organic Chemistry 6 (1993), S. 341-346 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The UV spectra of 3,4-diphenyl-1,2,5-thiadiazole 1,1-dioxide (I) and that of its thiadiazoline and thiadiazolidine derivatives were measured in several aprotic and protic solvents. Strong specific interactions of I with protic solvents are observed and the formation of stable carbinolamine type derivatives of I with methanol or ethanol is proposed. Spectroscopic data (UV, 1H and 13C NMR) and electrochemical evidence for their formation are given and a new thiadiazoline derivative of I (3-ethoxy-2-methyl-3,4-diphenyl-1,2,5-thiadiazoline 1,1-dioxide) was synthesized. The equilibrium constant for the reaction of I with ethanol is reported.
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  • 96
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    Journal of Physical Organic Chemistry 6 (1993), S. 361-366 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The negative slope (ΔρY+ 〈 0) of the Hammett-type plot using kinetic solvent isotope effect, log kSOH/kSOD versus σ+, for methanolysis of 1-(Y-phenyl)ethyl chlorides is rationalized by an ion-pair mechanism in which a solvent molecule attacks the relatively stable carbocation formed in the pre-equilibrium.
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  • 97
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    Journal of Physical Organic Chemistry 6 (1993), S. 357-360 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nucleophilic substitution reactions of isopropyl arenesulphonates with anilines and benzylamines in acetonitrile at 65·0°C were investigated. The cross-interaction constants ρxz (and βxz) between substituents in the nucleophile (X) and leaving group (Z) are positive and relatively small. The transition state (TS) variation is consistent with that predicted by the More O'Ferrall-Jencks diagram, as expected from the positive ρxz. The small magnitude of ρxz correctly reflects a relatively loose TS structure, in contrast to the tight TS for ethyl (or methyl) derivatives under similar reaction conditions.
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  • 98
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    Journal of Physical Organic Chemistry 6 (1993) 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 99
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relatively high stability and the structure of the simplest homoaromatic carbocation, the cyclobutenyl cation 1, was established ab initio by using correlated wave functions at HF 6-31G*, MP2(full)/6-31G*, MP2(full)/6-311G** and MP4(SDQ,full)/6-31G* geometries. The stability of 1 was estimated using homodesmotic and isodesmic reactions. The heat of formation of 1 was estimated to be 244 kcal mol-1 (1 kcal = 4·184 kJ). Chemical shift calculations were carried out at correlated levels and are in good agreement with the experimental values. At all levels of theory chemical shift calculations confirm the bent structure of 1. The MP4(SDTQ,fc)/6-311G**//MP2(full)/6-311G** + ZPE(MP2/(full)6-31G*), QCISD(T,fc)/6-31 + G*//MP2(full)/6-31G* + ZPE(MP2(full)/6-31G*) and MP4(SDQ,full)/6-31G*//MP4(SDQ,full)/6-31G* + ZPE(MP2(full)/6-31G*) ring inversion energies of 9·1, 9·3 and 9·0 kcal mol-1, respectively, agree with experiment (8·4 ± 0·5 kcal mol-1). Triplet electronic states are not competitive energetically. The homoaromatic character of the cyclobutenyl cation is shown by the nearly equal charges on C-1, C-2 and C-3, the considerable 1,3-bond order, the short 1·74 Å C-1—C-3 distance and the large stabilization energy relative to the allyl cation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 100
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993), S. 471-477 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 2-(2-Thienyl)pyrrole and its 3-alkyl-1-vinyl derivatives have been shown (1H NMR) to be protonated by HSO3F, CF3COOH, HCl and HBr at the pyrrole C-5 atom. Reaction with the superacid system HSO3F—SbF5-SO2 results in the equilibrium between pyrrolium and thiophenium ions. The heats of formation (ΔH), charges and HOMO partial electron densities for 2-(2-thienyl)pyrrole and its protonated forms have been calculated by the MNDO method. The calculated ΔH values of thienylpyrrolium and pyrrolythiophenium ions are in agreement with the experimentally observed ratio.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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