Library

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1980-1984
  • 1970-1974  (332)
  • 1972  (332)
  • Analytical Chemistry and Spectroscopy  (332)
  • Nuclear reactions
  • 101
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The behaviour of compounds I to XII under electron-impact (electron voltages 30 and 12 eV) was investigated. The abundance of the ions characteristic of amines was shown to decrease drastically with an increase of chain branching in alkylphosphines. Comparison of the spectra of VII and X led to the conclusion that the unshared electron pair of phosphorus does not affect the fragmentation. The main peaks in the spectra of phosphines corresponded to hydrocarbon fragments. The origins of the main fragment ions were confirmed by metastable peaks.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 102
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1225-1237 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectra of 2,6-dimethoxynaphthalene and 14 of its derivatives are reported. The fragmentation patterns proposed to account for the main peaks observed are frequently based on the presence of the appropriate metastable peaks. The fragmentation is initiated by the cleavage of an O—CH3 bond. The molecular ion is the most intense ion in each case and it does not appear to directly eliminate a methoxy group or a substituent directly attached to the naphthalene ring. With NO2 as a substituent the elimination of nitric oxide from the molecular ion has been observed and confirmed by peak matching.
    Notes: On rapporte les spectres de masse du diméthoxy-2,6 naphtaléne et de 14 de ses dérivés. La rationalisation du mode de decomposition par impact électronique qui est proposée, est confirmée la plupart du temps par des pics dûs aux transitions métastables appropriées. L'ion moléculaire, qui est le plus intense des ions dans chacun des spectres enregistrés ne semble pas subir d'élimination directe d'un group méthoxy ou de tout autre substituant directement relié au noyau naphtalénique. La dégradation semble plutot amorcée par l'élimination d'un radical méthyle à partir de l'ion moléculaire. Pour les dérivés nitrés, on a pu mettre en évidence la perte d'une molécule d'oxyde nitrique de l'ion moléculaire. Ce processus est confirmé par une mesure précise de masse du fragment résultant.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 103
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1288-1288 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 104
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1303-1312 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of diphenyl, dibenzyl and six dialkyl phosphoramidates have been recorded and interpreted with the aid of high resolution measurements and the metastable defocusing technique.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 105
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1321-1331 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectra of benzisothiazole, three benzoselenazoles and three benzisoselenazoles have been determined and compared with those of the corresponding benzothiazoles. The elimination of CS known to occur from these latter substances is confirmed in the case of benzisothiazole, but a different mechanism is proposed.The fragmentation of the selenium analogues led to ions of the same type as the benzothiazoles and benzisothiazole, through extrusion of molecules of the type CN - R, but loss of the heteroatom was not accompanied by loss of carbon. Furthermore, the isoselenazole structure seems to be more sensitive to electronolysis than its isomer.All six selenium heterocyclics investigated gave rise to two ions (130 and 132) resulting from a recombination of various fragments, suggesting that this is a characteristic feature of the electron-impact fragmentation of compounds of this type.
    Notes: Les spectres de masse du benzisothiazole, de trois benzosélénzoles et de trois benzisoséléazoles not été mesurés et comparés à ceux des benzothiazoles correspondants. La perte de CS mise en évidence chez ces derniers est confirmée dans le cas du benzisothiazole, mais un mécanisme différent est proposé.La fragmentation des analogues séléniés conduit à des ions du même type que dans le cas des benzothiazoles et du benzisothiazole par perte de molécules du type CN - R, cependant, la perte de l'hétéroatome ne s'accompagne pas de perte de carbone. En outre, il semble que la structure isosélénazole soit plus sensible à l'electronolyse que son isomére.Les six hétérocycles séléniés étudiés ont tous donné naissance à deux ions (130 et 132) provenant d'une recombinaison de divers fragments. Ce phénomène laisse à penser qu'il s'agit là d'un élément caractéristique dans la fragmentation électronique de tels composés.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 106
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of isomeric 2′-hydroxy-chalcones and flavanones (i.e. 2-phenyl-chroman-4-ones) are essentially identical. Thermal isomerisation prior to ionisation was ruled out. A study of metastable transitions (first and second field free region of a double focusing instrument), as well as low energy spectra of both isomers, pointed towards completely identical fragmentation pathways for the two compounds. Five deuterated compounds were then investigated. The heats of formation of the most important ions were determined. It was concluded that an intramolecular equilibrium exists between a chalcone type and a flavanone type molecular ion.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 107
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1377-1382 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of substituents on the activation energy for primary dissociation processes in the molecular ions of mono- and para and meta di-substituted benzenes has been examined. Where the daughter ion retains the substituent group, variation of the energy of activation derives from a combination of the effects of substituents on the ionisation potential of the molecular ion and the appearance potential of the daughter ion. An equation relating the energy of activation for the fragmentation of the molecular ion of a mono-substituted benzene to that of related para and meta di-substituted benzenes is presented.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 108
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 31-37 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 109
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 39-52 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The PMR spectra of cyclopentadine endo-dimer, its 1y-acetoxy-derivative and the dimer of spiro-heptadiene have been thoroughly studied. The assignment is proved by the use of spindecoupling experiments and the INDOR-technique. The relative signs of several coupling constants were found and used for the assignment. General trends in the proton chemical shifts and coupling constants are discussed for the derivatives of the cyclopentadiene dimer and for the substituted cyclopentadiene dimers.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 110
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 195-196 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4J(H—H) couplings and magnetic nonequivalent methylenic protons in some 1,3-oxathiolan-5-one derivatives were studied in several solvents.
    Notes: 4J(H—H)-Kopplungen und magnetisch nichtäquivalente Methylenprotonen in einigen 1,3-Oxathiolan-5-on- Derivaten wurden in vershiedenen Lösungsmitteln studiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 111
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972) 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 112
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Changes in 13C and 14N chemical shifts of the nitro derivatives of nitrogen heterocycles upon ionization (anion or cation formation) are twofold - first a uniform paramagnetic or in the case of protonation, a uniform diamagnetic shift of all the ring resonances that parallels the changes in the respective ultraviolet spectra and must be caused by changes in the molecular excited states, and second - the influence of the conjugated nitro group. About one third of the total negative anion charge may be localized on the nitro group, which causes unusually large shifts of the ring 13C resonances in this case.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 113
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The s-cis ⇌ s-trans equilibrium of several enamino ketones and aldehydes, has been evaluated based on the results of aromatic solvent induced shift measurements and of protonation of the title compounds. In contrast to α,β-unsaturated ketones bearing no heteroatom, the Δδ3,cis value but not the Δδ3,trans, proved to be useful in conformational assignments. Protonation, which occurs mainly on oxygen, enhances the rotational barrier, thus enabling the observation of both rotamers at room temperature. Steric hindrance to conjugation enhances the rate of protonation at the carbon C2.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 114
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 309-319 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A 220 MHz NMR spectrometer has been used to identify the structure of polychlorinated biphenyls (PCBs). The proton chemical shifts and approximate coupling constants of PCBs fractionated from Aroclor 1254 are given in the text. The spectra of model compounds are included in the supplement. The chemical shifts are also tabulated according to the ring substitution pattern, when it can be seen that the shifts change systematically with the degree of both the total ring substitution and the substitution in the positions ‘ortho’ to the bridging bond between the rings.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 115
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. i 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 116
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 377-390 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proton decoupled 13C NMR spectra have been measured for the cyclopentadienyl compounds C5H5Si(CH3)nCl3-n(n = 1, 2, 3), C5H5Ge(CH3)3, CH3C5H4Ge(CH3)3, C5H5Sn(CH3)3, σ-C5H5Fe(CO)2-π-C5H5 and C5H5HgCH3. A fast metallotropic rearrangement occurring in the compounds causes the spectra to be temperature dependent for the Si, Ge, Sn and Fe derivatives. For the derivatives of silicon or germanium, the olefinic signals are unsymmetrically broadened by the 1,2-shift at lower migration rates. Line widths of the ring carbon signals have been measured to give an estimate for the activation parameters of the rearrangement in C5H5Ge(CH3)3 (Ea = 10·7 ± 0·9 kcal/mole, ΔG
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 117
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 421-425 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enamino -thial and -thiones R1C(S)CH=CHNR22 (R1 = H or alkyl; R2 = Me or Et) have been shown by NMR spectra to exist in two rotational forms, s-cis and s-trans, the populations of the latter being approximately the same as in the case of the parent oxa analogues. An increase of the order of 2 to 4 Kcal/mole in the heights of C—C and C—N rotation barriers (ΔG*) was found on comparing the title compounds with their oxa analogues. IR spectra failed as a tool to establish the rotational equilibrium. IR absorption bands of the νC—C, νC—H (in the NMe2 group) and γHC=CH vibrations have been found, but the νC=S band could not be assigned unambiguously. Anomalies concerning the frequency and intensity of the νC=C band are discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 118
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The 1H-220 MHz spectra of several alkylpiperidines are reported. Almost complete assignments for all ring protons are possible. The effects of N-methyl and C-methyl groups on adjacent ring protons are discussed in detail.
    Notes: Es werden die 1H-220 MHz-Spektren von verschiedenen Alkylpiperidinen beschrieben. Alle Protonen des Ringes Können weitgehend zugeordnet werden. Die Effekte von N-Methyl- und C-Methylgruppen auf benachbarte Ringprotonen werden eingehend diskutiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 119
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. ii 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 120
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 443-447 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The role of steric factors in magnetic non-equivalence anisochronism of complex geminal groups and of their fragments in compounds of the general formula RCH(Ph)CH(COOR′)2 has been investigated. CMR anisochronism is more sensitive to conformational and other steric changes than is PMR.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 121
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: PMR parameters of some methylene substituted oxiranes are obtained from INDOR experiments on the ABXMN spin systems. Compounds investigated include safrol- and bromosafrol epoxide and β-phenoxypropylene oxide. For the latter compound all the relative signs (except for some long range couplings) were obtained and certain of these are in contradiction with those reported 2 in β-chloropropylene oxide. ‘Non-classical’ long range coupling is also noted and differs in pathway from that reported previously.2.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 122
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of substituted hexahydropyrido [2,1-c] [1,4] oxazin-3(4H)-ones has been synthesised, and the configurations of these bicyclic lactones assigned utilising chemical and spectral data. All the compounds adopt trans-fused conformations and the conformation of the lactone ring is discussed with reference to the magnitude of the geminal coupling constant of the N—CH2—C(O)—O protons, and the vicinal couplings between the angular proton and the methylene protons adjacent to the ring oxygen atom. The lactone ring conformation is shown to differ slightly from the half chair conformation described for some monocyclic δ -lactones. The synthesis and NMR spectra of some related compounds possessing the bridgehead N—CH2—C(O)—O system are discussed and these compounds are also shown to adopt a trans-fused ring conformation.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 123
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 19F NMR spectra of mono- and difluoroacetamide are used to derive the activation parameters for rotation about the C—N bond; it is not possible to obtain useful results for trifluoroacetamide. A total line shape analysis is used.Unusually large deuterium isotope effects upon the shielding of the 19F nucleus are observed for N-deuterated derivatives. The magnitude of the isotope effect is different for mono-, di- and trifluoroacetamides, and in the mono-deuterated species the isotope effect is different for cis and trans rotational isomers.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 124
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The sum of coupling constants of proton H-6 for conformations H1 and 1H of the 6-substituted 5,6-dihydro-α-pyran derivatives have been determined with the aid of appropriate, conformationally biased compounds. With the use of these values and the PMR spectra of the title compounds, thermodynamic values of their conformational equilibria and the conformational preferences of the carbomethoxy, hydroxymethyl and acetoxymethyl groups, have been evaluated.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 125
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 551-555 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The analysis of the PMR spectrum of 1,4-naphthoquinone dissolved in the nematic phase of pp′-di-n-hexyloxyazoxybenzene showed that the naphthoquinone molecule is planar. The ratios of the various interprotonic distances were determined.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 126
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The 13chemical shifts of simple polymethines (cyanines and merocyanines) show the very pronounced charge alternation in these compounds. The 13C shifts of polar merocyanines are also susceptible to solvent polarity, which in this case has a strong influence upon the electron structure.
    Notes: Die 13C-NMR-chemischen Verschiebungen von einfachsten Polymethinen bestätigen die alternierende Elektronendichteverteilung bei diesen Verbindungen. Die Verschiebungen polarer Merocyanine sind von der Polarität des Lösungsmittels abhängig und beweisen damit eine lösungsmittelinduzierte Veränderung der Elektronenstruktur.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 127
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phosphorus nuclear magnetic resonance spectra of pyridine coenzymes show that the reduced and the oxidized coenzymes exhibit different spectral patterns and chemical shifts. The 31P—{1H} NMR spectrum of β-TPN taken as a function pH indicates that the pKa value for the 2′ phosphate group is 6·0. It was further found that in β-TPN, the protonation of the 2′ phosphate group selectively perturbs one 31P resonance of the pyrophosphate backbone.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 128
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 591-594 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrogen exchange process in benzamidoximes (1 and 2) was studied over a range of temperature and a determination of the activation parameter ΔG
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 129
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. i 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 130
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 599-606 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Br79 NQR frequencies of a number of bromothiophene derivatives have been measured at 77°K. The frequencies correlate with Hammett δ values and this correlation demonstrates the importance of the inductive effect. The influences of more than one substituent on the thiophene ring are additive.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 131
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 607-623 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fluorine chemical shifts and spin-spin coupling constants of 65 pentafluorophenyl derivatives with widely varying organic substituents were examined. Useful correlations of the three meta coupling constants with the chemical shifts of the para fluorine were found. It is suggested that these relationships be extended to all compounds of the type considered in order to determine the signs and approximate values of meta coupling constants.Equations for correlation of the fluorine chemical shifts with the Taft constants are presented. The possibility of calculating the Taft constants from the 19F NMR spectra of pentafluorophenyl compounds is being discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 132
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 651-665 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The deprotonation of N-methylpiperidinium salts BHa⊕, observed by means of the coalescence of the N-methyl doublet, is operated either by OH⊖, or by the conjugate base B. The action of OH⊖ is predominant as the steric hindrance increases around Ha and is twice as fast in the axial direction.
    Notes: La déprotonation de sels de N-méthylpipéridinium BHa⊕, observé par la coalescence du doublet N-méthylique en RMN, s'effecute soit par OH⊖ (k1 ∼ 1010 M-1 s-1), soit par la base conjugée B (k2 ∼ 108 M-1 s-1). L'action de OH⊖ est prédominante lorsque croi' l'encombrement stérique autour de Ha, et a lieu 2 fois plus facilement en direction axiale.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 133
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 683-693 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Data for 30 hydrogen bonding pairs taken from the alkanethiols, i-C3H7SH, nC3H9SH and t-C4H9SH, and 16 bases have been obtained by a PMR method. Representative data for i-C3H7SH at 304 ± 2°K are (base, 102K in M-1, -ΔH° in kcal/mole): (CH2)4S, 3·1, 0·8; (CH3)2S, 3·0, 0·9; (CH3)2S2, 3·7, 0·5; (CH3)2CO, 4·7, 0·9; CH3COOC2H5, 5·7, 1·1; (CH2)4O, 6·1, 1·0; HCON(CH3)2, 12, 0·9; (CH3 O)2 SO, 12, 0·9; (C2 H5O)3PO, 6·5, 1·0; CH3 (CH3 O)2PO, 18, 1·0; ((CH3)2N)2 CO, 5·9, 1·1; CH3 CN, 13, 0·6. In essence, the problems and errors involved in obtaining equilibrium data for weak complexes stem from the limited concentration rangethat is accessible. This leads to large uncertainties in the quantities K, ΔH° and ΔS°. Structural effects on hydrogen bonding at the sulfur site, both as Lewis acid or base, are discussed. Two erroneous PMR methods in the literature used for assessing the strength of hydrogen bonds are pointed out.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 134
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 703-707 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: From the ASIS effect on chemical shifts and from solvent and temperature dependence of the vicinal spin-spin coupling constant of 1-tertiobutyl 2-formyl aziridine, the following conclusion is reached: the less polar rotamer is the s-trans rotamer, which is of lower energy than the s-cis rotamer.
    Notes: L'étude de l'isomérie de rotation de la tertiobutyl-1 formyl-2 aziridine est abordée en RMN par examen de l'effet ASIS sur les déplacements chimiques, par examen de l'effet de solvant sur la constante de couplage du proton aldéhydique, enfin par étude de l'effet de la température sur ce couplage. L'isomère s-trans qui est le moins polaire est largement privilégié.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 135
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 733-735 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 136
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972) 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 137
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 1-25 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method is described which permits the analysis of many substituted benzene compounds. The method is useful for mono-through tetra- substituted aromatics. In ideal cases, the number and disposition of the substituents and the chemical shifts of the residual protons can be accurately determined. The method assumes approximate first order couplings and is useful for roughly 50% of all aromatics. Frequently observed anomalous spectra are also discussed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 138
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 27-30 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reversible 1,2-shifts of the ethyl group in the 9-ethyl-9, 10-dimethylphenanthrenonium ion lead to a reversible change of the ring hydrogen states (A′B′C′D′ ⇄ A″B″C″D″). Line shape analysis for the determination of the exchange rate was performed for this case of intramolecular exchange between the two multi-spin systems. The calculations are based on density matrix formalism.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 139
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 53-62 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proton-decoupled carbon-13 magnetic resonance spectra of a series of cyclopropane derivatives have been studied. For stereoisomeric substituted 2-phenylcyclopropanes a difference between the isomers has been found in the shieldings of the three-membered cyclic carbons as well as in the shieldings of the carbons of the substituents. The chemical shifts have been interpreted on the basis of an additive approach worked out in a study of the spectra of monosubstituted cyclopropanes and substituted 2,2-diphenylcyclopropanes. Some simple rules have been proposed, which are useful in distinguishing stereoisomeric 1,2-disubstiuted cyclopropanes.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 140
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 67-72 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Labelling problems associated with the choice of bounds for the angle θ in the trigonometric forms of the co-factor expressions for levels in AB-based NMR spectra have been investigated. It has been shown that any pair of octants within the 0 → 2π range can be specified as bounds, provided that appropriate linear combinations of wave functions are chosen. The range 0 ≤ θ ≤ π/2 is preferred for simplicity in calculation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 141
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 77-93 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The computer analysis of the PMR spectra of several partially deuterated benzocycloheptene derivatives at -120° provides values for all the coupling constants about the C3—C4 bond. An interpretaion using the Karplus equation shows unambiguously that the seven-membered ring exists as a chair conformation. The relationship between the coupling constants determined shows that the form of the Karplus equation established empirically for cyclohexane is applicable to this seven-membered ring. A comparison of coupling constants shows that the benzocycloheptene chair is more puckered than the cyclohexane chair.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 142
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The temperature dependence of the three different methylene AB spectra due to the 1-, 3- and 5-neopentyl groups in 2-chloro-4-iodo, 2-bromo-4-iodo and 2-bromo-4-chloro-1,3,5-trineopentyl-benzene was studied by proton magenetic resonance measurements at 60 MHz. The identification of the lines of the AB quartets at low temperature was carried out on an HA-100 spectrometer by means of the INDOR technique. The activation parameters for all three barriers in each compound were found to be approximately the same, which perhaps reflects the interdependence of the rotations, with the smaller of the two halogens determining the size of the barrier. An explanation in terms of magnetic nonequivalence induced in the 1- and 5-methylenes by the 3-neopentyl group is considered to be most plausible.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 143
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The ΔG* values for the barrier to rotation around the P—N bond have been determined in some aminophosphines and are dependent on the substituents bound to the phosphorus atom. The comparison between 3J(P—N—C—H) and ΔG* values indicates that pπ - dπ overlapping between nitrogen and phosphorus is the main effect.The nucleophilic behaviour of the nitrogen atom has been measured by the rate of the chemical exchange between methyl-trifluoroacetate and various aminophosphines: the results of this kinetic study are in good agreement with the NMR conclusions.
    Notes: L'étude par RMN de la rotation autour de la liaison P—N dans diverses aminophosphines permet de mettre en évidence l';influence des substituants liés au phosphore sur les valeurs de ΔG*. Le parallélisme observé entre la barrière à la rotation et la grandeur des couplages 3J(P—N—C—H) montre que les variations de ΔG* reflètent principalement l'importance du recouvrement pπ - dπ.Une étude de la nucléophilie de l'azote, par réaction d'échange aprotique entre le trifluoroacétate de méthyle et diverses aminophosphines, confirme ces conclusions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 144
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rotational barriers of the dimethylamino group in different enamino aldehydes and ketones have been applied for evaluation of their conformation. It has been maintained that repulsion between bulky substituents causes twisting of the molecule rather than planar deformations. Arguments for and against these alternative concepts based on the analysis of JHH and J(13CH) coupling constants in different fragments of the molecule have been discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 145
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 171-183 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Seven phospholes were prepared by a two-step synthesis as previously described. On the basis of H and 31P NMR data, these phospholes were tentatively classified by their degree of aromaticity. Two of these were reacted with n-butyl lithium. Nucleophilic attacks were observed on the phosphorus atom and on the double bonds. These facts are explained by enhanced p - π and pπ - dπ conjugations between the phosphorus atom and the dienic system by comparison with vinyl phosphines. NMR data seem to support this view. The influence on δ 31P of substitution and cyclic delocalization of the lone pair of electrons on phosphorus is interpreted within the Letcher-Van Wazer formalism.
    Notes: Sept phospholes ont été préparés par une méthode en deux étapes précédemment décrite. Sur la base de données de RMN du proton et du phosphore, on a essayé de classer ces phospholes suivant leur degré d'aromaticité. On a fait réagir deux d'entre eux avec le n-butyl lithium. On a observé une attaque nucléophile sur le phosphore et sur les doubles liaisons. Ces faits sont expliqués par un accroissement des conjugaisons p - π et pπ - dπ entre le phosphore et le système diénique par comparaison avec les vinyl phosphines.Les données RMN semblent en accord avec cette façon de voir. Les influences de la substitution et de la délocalisation du doublet du phosphore sur le δ 31P ont été interprétées dans le cadre du formalisme de Letcher et Van Wazer.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 146
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 229-235 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proton chemical shifts as well as solvent shifts induced by benzene in several amidoximes are examined with respect to their configuration and are compared to the solvent shifts induced in benzalanilines. The geometry of the benzene-solute ‘collision-complex’ is also discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 147
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 237-246 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 13C NMR spectra of antibiotic Viomycin sulphate and its constituent aminoacids in H2O and D2O were examined in a wide range of pH values. The spectra were analysed by proton spin-spin decoupling experiments and measurements of the relative intensities of the resonance and chemical shift values. Exchange experiments were also carried out and an almost complete assignment of the resonances of the spectra was possible. The data obtained are discussed in terms of possible structures for Viomycin and the presence of intramolecular hydrogen bonds. Some information about the conformation of the molecule is also given. A tentative assignment of the 13C spectrum of Viomycin is given and the experimental 13C chemical shift values compare well with the theoretical ones evaluated by Grant's rule.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 148
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of substituted hexahydroindolizin-2(3H)-ones and some related ketones have been prepared by Dieckmann condensation of the appropriate diesters. Utilising spectral data, the configurations of these compounds have been assigned, and their conformations discussed with particular reference to the magnitude of the geminal coupling constant (Jgem) for the N—CH2—C(O) protons. With the exception of tetrahydropyrrolizin-2(3H)-one, all the ketones in this study are shown to exist in predominantly trans-fused conformations. In the case of hexahydroindolizin-2(3H) one and hexahydro-2H-quinolizin-3 (4H)-one, the separate contributions to Jgem from the adjacent N lone pair and the carbonyl π electrons are discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 149
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The utility of C-13 NMR in detecting transannular interactions of a carbonyl group with —O—, —S— and —N— in eight-membered ring compounds has been studied. The C-13 carbonyl chemical shifts were determined in two solvents, employing frequency-sweep and pulse/Fourier transform techniques. The results confirm earlier conclusions based upon other physical methods and indicate that C-13 NMR should prove useful in studies of such interactions.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 150
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 335-342 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Due to hindered rotation about the central C—N bond in N,N-disubstituted trifluoroacetamides, CF3CONR1R2, two resonance peaks are usually observed for each proton in R1 and R2. Chemical shift assignments are made for the following amides: 1, R1 = R2 = Me; 2, R1 = R2 = Et; 3, R1 = Me, R2 = 2-Propyl; 4, R1 = Me, R2 = 1-Butyl; 5, R1 = Me, R2 = Cyclohexyl; 6, R1 = R2 = 2-Propyl; 7, R1 = 2-Propyl, R2 = Cyclohexyl. Amides 6 and 7 show an inversion of the relative chemical shift for both the methine and methyl protons of the 2-propyl group as compared with 3. For non-fluorinated amides, aromatic solvents shift the trans alkyl peaks to higher field faster than those cis (to the carbonyl oxygen atom); however, this generalization does not apply to all trifluoroacetamide proton peaks.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 151
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 353-360 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The natural abundance 13C NMR spectra of bromobenzene and ten derivatives have been obtained using the technique of noise modulated decoupling of the proton resonances. Assignments have been made for all 13C resonance signals using an additivity rule. The chemical shifts of the aromatic carbon nuclei in the para-substituted compounds are discussed in terms of the Taft parameters (σR, σI) and the electronegativity of the substituent.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 152
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 779-781 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The isomer-pairs of the 2-arylamino-2-thiazolines and -thiazines, carrying a methyl substituent on the nitrogen atom of the ring and outside the ring were synthesised by unambiguous routes. An IR and NMR investigation of these compounds revealed the fact that the NMR signal of the 2,6-symmetrically substituted aryl group can be used advantageously for the determination of the isomeric structures. The AB2 multiplet of the aromatic protons is shifted towards the AX2 pattern in the b isomer - containing a conjugated C=N bond outside the ring - as compared to the a isomers. The structure of this multiplet does not depend on the size of the hetero-ring.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 153
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1, 1-Bis-dimethylaminoethylenes with electron attracting substituents on C2 show rotations around the C=C and C—N bonds, the rates of which are in most cases measurable by the NMR line shape method. The temperature-dependent four-and eight-site NMR spectra have been analysed and the barriers to rotation around the different bonds have been evaluated by a complete line shape treatment based on the Bloch formalism. Assignment of sites to methyl groups has been made with the aid of aromatic solvent induced shifts and anisotropy effects.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 154
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The INDOR homonuclear PMR spectra of three quinolizidine alkaloids - pachycarpine (d-sparteine), lupanine and 13-hydroxylupanine - have been studied. The molecular conformations including the boat-structure of the ring C have been established.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 155
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 105-111 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High resolution mass measurements, defocused metastable ion detection and deuterium labeling experiments have been employed in an investigation of the electron-impact induced decomposition of a series of carbocyclic amino acids, which varied in ring size from three to eight carbon atoms. About 50 per cent of the total ion current is carried by [M — COOH]+ ions in the spectra obtained from compounds with five to eight carbon atoms in the ring. This is analogous to the fragmentation of the open chain naturally occurring amino acids. The behavior of the compounds with the two smallest rings is anomalous, reflecting to a larger extent the influence of the ring itself. Special attention has been given the loss of H2O and NH4 from ionized species of 1-aminocyclopropanecarboxylic acid.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 156
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 141-150 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aryl substituent has been shown to affect the fragmentation and abundance of skeletal rearrangement ions in the spectra of aryl sulphonyl chlorides and sulphonic acids. The spectra of 2-hydroxy and 2-chloroethyl aryl sulphones contain [aryl SO]+ ions, suggesting that alkyl migration has competed successfully with aryl migration to the electron deficient oxygen atom.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 157
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 179-188 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of O-methyloximes of fifteen aliphatic aldehydes and ketones of various molecular weights and degrees of branching have been examined. All give molecular ions, and many of the fragmentations parallel those of aldoximes and ketoximes. The formation of some ions is better explained by the initial production of a novel substituted cyclopropene ion. O-Methyloximes of of the long-chain aldehydes and methyl ketones are readily distinguished by the masses of abundant products of McLafferty rearrangement at m/e 73 and 87, repectively.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 158
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 217-223 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: o-N,N,N-Trimethylanilinium oxide is evaporated structurally unchanged, admixed with the corresponding transalkylated ether. The ionization potential for the anilinium oxide was determined as 6·8 eV which was 0·8 eV lower than for the corresponding ether. An explanation for the unusually low IP value is advanced. In IP measurements in binary mixtures the semi-log plot method showed parallel curves for different compositions in the gas phase, but no linear relationship between the recorded IP and composition was found. Appearance potential measurements show that the energy of the zwitterion in the gas phase is at least 10 kcal/mol higher than in the corresponding ether.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 159
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A combination of a kinetic approach, thermochemical approach and atomic labeling techniques has been employed to demonstrate that several series of allylic and homoallylic bromides undergo Br· expulsion with the aid of remote π-electron density.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 160
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 283-291 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The CI mass spectra of aryl ketones, πCOR, were studied and found to give primarily [M + 29]+, [M + 1]+, [M - 1]+, [πCO]+ and [RCO]+ ions. The major change in the spectra with increasing length of the aliphatic side chain was an increase in the [M - 1]+/[M + 1]+ ratio. Increasing sample size was reflected primarily in the formation of [2M + 1]+ ions and a decrease in [M + 1]+ ions. Small amounts of water in the reactant gas reduced the extent of fragmentation action.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 161
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1-8 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectrometry can be used for amino acid sequence determination in β-lysine-containing peptides and for the identification of α- and β-lysine residues in peptides, as well as for amide bond type determination in β-lysine peptides. The peptide bond in streptothricin D is shown to be formed through the participation of an ε-amino group of the L-β-lysine residue.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 162
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 39-45 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of a number of methyl- and phenylthiohydantoin amino acid derivatives have been obtained. The major metastable transitions occurring in the mass spectra of these derivatives have been identified and measured. The major fragmentation pathways associated with the metastable transitions have been outlined and are discussed for each group of compounds. Inspection of the metastable data has shown that there is at least one unique metastable transition occurring for each thiohydantoin derivative which may be used to uniquely identify that derivative in the presence of a mixture of thiohydantoin derivatives obtained from the Edman degradation of a peptide or protein. The use of metastable ions to uniquely identify thiohydantoin derivatives in mixtures has proven useful in the identification of the MTH and PTH derivatives of glycine whose molecular ions are not unique and for resolving such ambiguities as occur for example in the mixture of leucine and isoleucine.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 163
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of several perfluoroaromatic nitrogen compounds, including primary and secondary amines, diamines, nitriles, hydrazines, azines and azo compounds, are presented. Fragmentation patterns of these compounds are described and the data are discussed in terms of comparisons amongst perfluoroaromatic nitrogen compounds, and with reference to the hydrogen substituted analogs, or to oxygen and sulfur analogs of a particular compound.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 164
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972) 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 165
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 151-166 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact induced fragmentation of staphylomycin S (I) and related cyclodepsipeptides (II to V) is mainly initiated by elimination of an azomethin molecule (R—CH=N—R′), i.e. 1,2-dehydro-4-oxopiperidine for I and II, 1,2-dehydro-4-hydroxy-piperidine for III and IV, and an unknown hydroxy-1,2-dehydro-4-oxopiperidine for VI. Cyclic imino acids, e.g. a pipecolic acid derivative for I to IV and 4-hydroxyproline for etamycin (IX) preferentially trigger this reaction. Clearcut evidence for the amino acid sequence is given by the mass spectra of the linear peptides obtained from I, V and IX by alkaline hydrolysis of the lactone function and esterification of the carboxy group.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 166
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Charge exchange and electron-impact induced cleavages of some N-phenyl benzamides, phenyl benzoates and benzophenones are reported. The data obtained appear to be consistent with energy being lost from ions by photon emission or stored in isolated states of the molecular ions.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 167
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972) 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 168
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: It is shown that in general it is not possible to differentiate between diphenyl methane derivatives (and compounds of analogous structure) substituted in o-position to the CH2-bridge and those carrying an m- or p-substituent by resorting solely to the ‘ortho-effect’ of the former. A rationale for this apparent anomaly is given.
    Notes: Es ist i.a. nicht möglich, zwischen Diphenylmethan-Derivaten (und analogen Verbindungen), die in o-Stellung zur CH2-Brücke substituiert sind, und inren m- und P-Isomeren nur auf Grund des ‘ortho-Effektes’ zu unterscheiden. Eine Erklärung für dieses scheinbar anomale Verhalten wird gegeben.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 169
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 293-300 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectral fragmentations of several naturally-occurring 3,4-dialkoxy furocoumarins from the Halfordia species and their nor-derivatives have been studied using deuterium labelling and metastable analysis. Halfordin (I), isohalfordin (VI) and halkendin (X) show a common major breakdown pathway involving initial loss of a methyl radical from the 3-methoxy group followed by expulsion of CO, then loss of C2H3O, the latter fragment containing the methyl group from the 4-position.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 170
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 341-343 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 171
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectrum of N,N′,N″-triacetyl spermidine (I) is characterised by signals at m/e 143, 157 and 169. The degradation reactions which lead to the corresponding ions cannot be explained by known sequences. By examination of the mass spectra of derivatives of I, fragmentation mechanisms have been deduced.It is interesting to note that it is mainly the 1,3-diamino propane part of the spermidine molecule which participates in the mass spectral degradation to give the previously mentioned, characteristic ions.The two tertiary nitrogen atoms of the diamino propane part are the main promoters of these fragmentation reactions, as can be seen Schemes 2 to 7. Hence the mode of mass spectral degradation of the trifunctional spermidine derivative proceeds in a similar way to that of the bifunctional alkanes.
    Notes: Das Massenspektrum von N,N′,N″-Triacetylspermidin (I) zeichnet sich durch charakteristische Signale bei m/e 143, 157 und 169 aus. De Reaktionen, die zu den entsprecenden Ionen führen, lassen sich nicht durch Anweding einfacher Fragmentierungsreaktionen erklären. Auf der Bzasis der Massenspektren deuterierter Derivate von I werden Fragmentierungsmechanismen vorgeschlagen. Interessanterweise ist hauptsächlich der 1, 3-Diaminopropan-Teil und weiniger der 1, 4-Diamino-butan-Teil (Putrescin) des Spermidin-Moleküls an den Abbaureaktionen zu den erwänten Ionen beteilligt. Die beiden teriären Sticktoffatome des Diaminopropanteiles sind im wesentlichen die Promotoren der Fragmentierung, wie aus den Schematatas 2 bis 7 hervorgeht. Dieser Verlauf des massenspektrometrischen Zerfalls des trifunktionellen Spermidin-Derivates verläuft ser ähnlich dem Zerfall bifunktioneller Alkane.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 172
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 647-653 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: In order to determine the relationship between elementary ion-molecule reactions in the gas phase and certain steps of chemical reactions in the liquid phase, we have tried to model the formation of σ-complexes as part of the electrophilic aromatic substitution reaction by means of a proton transfer reaction to aromatic molecules. The Hammett equation should provide the necessary criteria for such a relationship.The comparison of the Hammett σ-constants with the cross section ratios for the proton transfer reaction of unsubstituted and substituted aromatics - the latter being representative of the corresponding reaction rate constants - does not yield a linear relationship and therefore suggests that the Hammett equation is not valid in the domain of gas phase reactions. If, on the other hand, the σ-constants are set in relation with the proton affinity PA, i.e. with the energy released during the formation of a σ-complex, a linear or otherwise well-defined relationship results. This observation was taken to be an indication of the fact that the Hammett equation is also valid in the case of ion-molecule reactions.
    Notes: Im Rahmen der Untersuchungen über die Analogiebeziehungen zwischen elementaren Ion-Molekül-Reaktionen (IMR) in der Gasphase bestimmten Schritten chemischer Reationen in der Flüssigkeit wurde versucht, den Reaktionsschritt der σ-Komplex-Bildung bei der elektrophilen aromatischen Substitutionsreaktion durch eine Protonenübertragungsreaktion zu modellieren. Als Kriterium für die Modellierbarkeit die Hammett-Gleichung.Eine Gegenüberstellung von Hammett-σ-Kontanten und - Stellvertretend für die entsprechenden Geschwindigkeitskonstanten - dem Verhältnis der Wirkungsquerschnitte von unsubstituierten und substituierten Aromaten führte zu keiner die Gültigkeit der Hammett-Gleicnung voraussetzenden linearen Beziehung. Charakterisiert man demgegenüber die elementare IMR durch die bei der Bildung des σ-Komplexes frei werdende Energie, die Protonenaffinität PA, zeigt sich eine lineare bzw. allgemein eine gesetzmäßige Beziehung zwischen σ-Konstante und PA, was auf eine Gültigkeit der Hammett-Gleichung auch für den Bereich der IMR hindeutet.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 173
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: At an electron energy of 70 eV (nominal) both the [M]+·-ion and the [M—H]+-ion of the title compound expel hydrogen cyanide. 13C labelling in the cyano group shows that these ions lose - within experimental error - only H13CN when decomposing in the ion source, i.e. when possessing a relatively high internal energy. In the first and second field free region, however, as well as in the ion source at low ionizing energies (9 eV, nominal), H12CN is also eliminated. This phenomenon may be explained by ring contraction of the molecular ion to a six membered ring, possibly initiated by the formation of a norcaradiene structure, which may then rearrange further to a species of higher symmetry. This ring contraction is supported by the occurrence of peaks of low intensity at m/e 78 and m/e 77, due to fragments which are generated in one step from the molecular ion.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 174
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Twelve synthetic di- and tripeptides which are related to the thyrotropin releasing hormone (TRH) have been subjected to electron-impact without conversion to more volatile derivatives as background for structural elucidation of unknown peptides isolated on a microgram basis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 175
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 765-783 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical ionization mass spectra of several hydroxy steroids were obtained using methane as the reactant gas. The spectra are much less complex than the electron ionization spectra and little fragmentation of the steroid nucleus is observed. The major fragment ions involve the loss of water from [M + H]+. A 3-keto group in the steroids was characterized by an abundant [M + C2H5]+ ion. 5α- and 5β-Dihydrotestosterone could be distinguished by their spectra, with H2 as the reactant gas by marked differences in amounts of [M + H]+, [M + H - H2O]+ and [M + H - 2H2O]+. Substituted 3α-X-, 17 β-ol compounds, (X = Cl, Br) were also studied to obtain relative amounts of protonation at these sites.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 176
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 805-814 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectra of erythro and threo 2,3-diphenylbutanes are assigned to one rearrangement and one simple cleavage. After calculation of these spectra, it is suggested that their differences are issued essentially from the enthalpy difference of the molecular ions and not from the enthalpy difference between the rearrangement transition states. It is shown that in the gaseous state the threo 2,3-diphenylbutane is more stable than the erythro isomer.
    Notes: Les spectres de masse de 2,3-diphénylbutanes érythro et thréo sont attribués à un réarrangement et à une rupture simple; leur calcul est proposé. II est suggéré que les différences entre les spectres des deux isoméres proviennent essentiellement de al différence d'enthalpie entre les ions moléculaires et non de la différence d'enthalpie entre les états de transition du réarrangement; il en est déduit qu'à l'état gazeux le 2,3-diphénylbutane thréo est plus stable que l'érythro.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 177
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 897-903 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of neopentyl alcohol, bromide and chloride and some 13C and 2H labelled analogues have been studied. Most fragmentations of the molecular ions of these compounds occur by simple bond cleavages and do not involve rearrangement before fragmentation. We propose that in the [M — CH3]+ fragment ions, seven of the eight hydrogen atoms and all four carbon atoms are involved in randomisation when an ethylene molecule is ejected. The eighth hydrogen atom (which comes from a methyl group) is probably associated with the heteroatom. The neopentylcation, observed only in the mass spectrum of the bromide, fragments mainly by loss of an ethylene molecule, also containing randomly selected hydrogen and carbon atoms. The [C4H7]+ ion also was observed to undergo complete atom scrambling.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 178
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 923-930 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Substituent effects in the electron-impact and field ionization mass spectra of acteophenones are compared. No Hammett correlation could be found for the fragments formed on the surface of the field anode. A straight line log z/z0 versus σ+ was observed, however, for the metastable decomposition of para-substituted acetophenones (and also some benzophenones). Meta-substituted compounds did not yield such straight lines.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 179
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 942-942 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 180
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 991-1001 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation and the mass spectra of the trimethylsilyl ethers of six hydroxyporphyrins are reported. In every case the side chain bearing the ether grouping is the most labile on electron-impact and exhibits characteristic ‘benzylic’ cleavage. The presence of a metastable peak allows a definite identification of this cleavage to be made.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 181
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1045-1049 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The negative ion mass spectra of chlorine-containing molecules have been measured using a double focusing mass spectrometer with a photographic plate detector. The formulae of the negative ions not previously assigned using an electron multiplier detector have now been assigned.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 182
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1060-1061 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 183
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 963-970 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ratio [M — D]/{[M-D] + [M — H]} in the 70 eV mass spectra of six deuterated 3-methylthiophenes has been determined. From these values the mole fractions of the molecular ions that lose hydrogen atoms specifically from the various positions of the molecule were calculated, as well as the mole fraction in which the hydrogen atoms are fully scrambled before hydrogen elimination. It appears that hydrogen atoms are mainly lost from a fully scrambled [C5H6S]+· ion and from the α-position of the original molecular ion. A deuterium isotope effect of 1·60 to 1·72 was calculated for the hydrogen elimination. The reaction was also studied at low electron energies. In order to determine the degree of scrambling in the [C5H5S]+ ions, some decomposition reactions of this ion were investigated.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 184
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1003-1009 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the [M — methyl]+ ion in the mass spectra of ring-deuterated tri- and tetramethylbenzenes has confirmed the partial randomisation of hydrogen and deuterium atoms observed by other workers. The results can be explained by postulating randomisation of the peripheral entities, followed by several cycles of ring expansion and contraction, prior to fragmentation.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 185
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1051-1058 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fragmentation patterns by electron-impact of five butyrophenones (neuroleptic drugs) are presented and discussed, with particular emphasis being placed on the anomalous behaviour of azaperone.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 186
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1062-1062 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 187
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1077-1081 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectrometric fragmentation pattern of phenylboronic acid has been determined and that of triphenylboroxine redetermined and extended, and the origin of some high abundance ions, previously unassigned, have been identified.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 188
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1153-1160 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of a series of βγ-unsaturated cyclic and acyclic carboxylic acids are reported. Metastable ion studies and precise mass measurements have been employed in demonstrating that the ten compounds studied conform to one or other of two generalised fragmentation pathways.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 189
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1239-1242 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several primary nitroalkenes have been shown to undergo migration of oxygen to the carbon-carbon double bond during mass spectrometric fragmentation. The oxocarbonium ion species which result are rationalized as arising through cleavage of ionized epoxide intermediates.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 190
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1279-1281 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mass spectrometric study of five diacetyl[3]ferrocenophanes has been made. The molecular ion was the base peak in these five compounds. Fragment ions with relative intensities greater than 10 percent occurred only in those compounds having an acetyl group in the alpha position to the trimethylene bridge.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 191
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1289-1292 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is demonstrated that the ionisation potentials of mono- and di-substituted benzenes are related to the sum of Brown's σp+ of the substituents for both the meta and para isomers. From this it is concluded that the charge, in substituted arenes, lies predominantly on the aromatic ring rather than on either of the substituents. An empirical equation relating the IP's of mono- and disubstituted benzenes to the sum of σp+ is presented.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 192
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recently, Dougherty et al.1 reported ionisation potentials for the [M]+· and appearance potentials for the [M — CH3]+ ions of 2,7-dimethyl- (I), 4,5-dimethyl- (II), 2,4,5,7-tetramethyl- (III) and 3,4,5,6-tetramethyl-phenanthrenes (IV). For evaluation of strain energies they used the assignments presented by Arnett et al.2 The expression used is shown to be thermodynamically irrelevant and the strain energies of II and IV in comparison to I and III are re-estimated with the aid of thermodynamically relevant assumptions. A close agreement prevails between the present results and those obtained with comparison of heats of formation.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 193
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1347-1351 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact induced fragmentation of 3,5-diphenyl-1,2,4-oxadiazole has been investigated by labelling experiments, defocused metastable ion detections and high resolution mass measurements. The main fragmentation process suggests heterocyclic cleavage at the 1 to 5 and 3 to 4 bonds confirming our previous interpretation. The structure of the major fragment ion [C7H5NO]+· has been interpreted as being represented by the isomeric benzonitrile oxide and phenylisocyanate structures, the latter isomerising irreversibly from the former. The benzonitrile oxide structure is consistent with [C7H5NO]+· formation by cleavage of the 1 to 5 and 3 to 4 bonds.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 194
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972) 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 195
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 9-20 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photo-ionization (PI) mass spectrometry performed with a monochromatic photon beam was applied to a series of peptide derivatives. PI mass spectra of ten N-acylpeptide methyl esters containing two to four residues of glycine, alanine, valine, leucine, proline, tryptophan, tyrosine, phenylalanine, methionine, carboxymethylcysteine, lysine and ornithine were studied. Comparative analysis of PI (10.2 eV) and electron-impact ionization (EI) (70 eV) mass spectra shows the total number of peaks on PI to be much less than that obtained with EI, especially in the low m/e region (〈 250 to 300). At the same time the relative abundance of ‘heavy’ ions, including molecular ions, is much higher in PI. The amino acid fragmentation pattern followed by N-acylpeptide esters in PI was found to be the same as for EI.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 196
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 273-282 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ion kinetic energy (IKE) spectra of pyrazine, pyrimidine, pyridazine, pyrazine-d4, pyrimidine-d4 and pyridazine-d4 have shown that these compounds can more readily be distinguished on the basis of IKE spectra than mass spectra. Studies of the fragmentation of various doublycharged ions have given information about the localization of charge on the heteroatoms and on the structures of the ions themselves. Transition states from which fragmentation occurs for doublycharged ions with loss of either [H]+ or [D]+ have shown large differences of the order 1 Å between the intercharge distances in the two cases.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 197
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 317-324 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 1,3-dithiane, 2-methyl- and 2,2-dimethyl-1,3-dithiane have been studied by 2H labelling and metastable defocusing. The various molecular ions eliminate S2H. to produce the ions [C4H7]+, [C5H9]+ and [C6H11]+ respectively, each of which scramble the hydrogens either before or accompanying further decomposition. Other processes are complex, but parallel those already reported for 2-aryl-1,3-dithianes.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 198
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 349-366 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The results of a mass spectrometric analysis of the series C6Cl6; C6Cl5F; 1,3-F2C6Cl4; 1,3,5-F3C6Cl3; 1,2,3,5-F4C6Cl2; C6F5Cl; C6F6 obtained by successive replacements of chlorine atoms by fluorine atoms, starting with hexachlorobenzene, are presented. Similarly the corresponding series of perfluorochloropyridines are examined. The sequences of degradation observed are quite regular in both series, and correspond to possible simple mechanisms often confirmed by the observations of the corresponding metastable ions.
    Notes: Nous présentons ici les résultats de l'analyse en spectrométrie de maasse des séries C6Cl6; C6Cl5F; 1,3-F4C6Cl2; C6F5Cl; C6F6 obstenues par remplacvement successif des atomes de chlore par des atomes de flour, à partir de l'hexachlorobenzène. De měme, la série correspondante des perchloroflouropyridines est analysée. Les séquences de dégradations observées sont trés réguliéres dans les deux séries, et sont interprétables par des schémas simples, souvent confirmés par l'observation des pics métastables correspondents.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 199
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of the compounds C12F8M2 (M = S, Se), (I), C12F8M (M = S, Se, Te), (II) and C12F8SX2 (X = Br, I), (III), have been measured. Results indicate that sulfur-carbon bonds are more stable under electron bombardment than either selenium-carbon or tellurium-carbon bonds. Numerous metastable-supported transitions are evident, which are incorporated into comprehensive fragmentation schemes for these compounds. Many metastable transitions, not previously reported, were observed for the fluorocarbon fragments and a fragmentation scheme is reported.The bromine and iodine-containing compounds behave remarkably like the heterocyclic systems, I and II, presumably due to initial loss of Br2 or I2 to form a ring system of type II.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 200
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The configuration at C-2 and C-4 in the molecules of 2-methyl- and 1,2-dimethyl-4-vinylethinyl(n-butyl)-4-hydroxyperhydroquinolines was determined by mass spectrometry. The principal conclusions concerning the stereochemistry were made on the basis of differences in the values of the I[M-15]+/I[M]+·, I[M-17]+/I[M]+·, I[M-43]+/I[M]+· and I[M-57]+/I[M]+· ratios in the mass spectra of the epimeric vinylethinylic alcohols, and of the I[M-15]+/I[M]+· and I[M-15]+/I[M]+· ratios in the case of the n-butylic alcohols.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...