|
1. |
Forthcoming papers |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 6-6
Preview
|
PDF (94KB)
|
|
ISSN:0030-4921
DOI:10.1002/mrc.1270070812
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
2. |
Carbon‐13 NMR spectra of some polychloro hydrocarbons and related compounds |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 361-365
F. K. Velichko,
E. C. Chukovskaya,
V. I. Dostovalova,
N. A. Kuzmina,
R. Kh. Freidlina,
Preview
|
PDF (514KB)
|
|
摘要:
AbstractData derived from the carbon‐13 NMR spectra of 37 organic polychloro compounds allow one to identify readily the CHCl2, CCl2 and CH2Cl groups, the13C signals of which are registered in the shift ranges of 67 to 78 (80), 85 to 96 and 38 to 55 (59) ppm (from TMS), respectively, and have the distinctive one bond spin‐spin coupling constants1J(CH) 170 to 184 Hz (for the CHCl2groups) and 147 to 158 Hz (for the CH2Cl groups). The CCl2CH2CH2Cl fragment features characteristic diamagnetic shieldings of the CCl2 and CH2Cl that may be related to increased electron densit
ISSN:0030-4921
DOI:10.1002/mrc.1270070802
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
3. |
Etudes configurationnelles et conformationnelles de quelques chlorures de désoxy‐6 β‐L‐héxopyrannosyle chlorosulfonyles et de leurs glycosides de méthyle |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 366-371
G. Hajdukovic,
M. L. Martin,
P. Sinaÿ,
J. R. Pougny,
Preview
|
PDF (633KB)
|
|
摘要:
AbstractUne analyse complète des spectres RMN de désoxy‐6 L‐hexopyrannoses de configuration α et des anomères β correspondants est réalisée. L'ensemble des paramètres obtenus confirme l'existence d'une structure chaise 1C (L) présentant une disposition axiale du substituant anomère dans le cas des α‐fuco‐, α‐rhamno‐ et α‐chinovopyrannosides de méthyle et des chlorures de α‐fuco‐ et α‐rhamnopyrannosyle. La structure reste de type chaise 1C (L) dans le cas des β‐fuco‐ et β‐chinovopyrannosides de méthyle. Il en est de même en dépit de I'effect anomère dû à I'atome de chlore, pour les chlorures de β‐fuco‐et β‐rhamnopyrannosyle. Par contre les paramètres RMN du chlorure de β‐chinovopyrannosyle ne semblent interprétables ni sur la base d'une g
ISSN:0030-4921
DOI:10.1002/mrc.1270070803
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
4. |
Carbon‐13 NMR Spectra of some aryl substituted ferrocenes |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 372-375
S. Gronowitz,
I. Johnson,
A. Maholanyiova,
S. Toma,
E. Solcániová,
Preview
|
PDF (336KB)
|
|
摘要:
AbstractThe carbon‐13 spectra of someparaandmetasubstituted phenylferrocenes have been analysed. The substituent‐caused shifts are discussed and compared with similarly substituted biphenyls. Correlations with Hammett parameters and with the reactivity parameters of Swain and Lupton have been attemp
ISSN:0030-4921
DOI:10.1002/mrc.1270070804
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
5. |
Exemple d'une transposition dyotropique à l'état solide Mise en evidence par RMN haute résolution |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 376-378
M. F. Grenier‐Loustalot,
A. Lectard,
F. Metras,
Preview
|
PDF (214KB)
|
|
摘要:
AbstractL'analyse des spectres RMN à 250 MHz de tribromo‐2,3,6 méthyl‐4 cyclohexanones a permis de déterminer avec précision les constantes de couplageJ(HH) de ces composés. La validité des attributions a été contrôlé en reconstituant les spectres par calcul électronique. Les résultats observés ont été interprétés en terme de d
ISSN:0030-4921
DOI:10.1002/mrc.1270070805
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
6. |
NMR study of organosilicon compounds. III—Silicon‐29, nitrogen‐14, carbon‐13 and proton NMR spectra of silylakylamines |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 379-385
J. Schraml,
Nguyen‐Duc‐Chuy,
V. Chvalovský,
M. Mägi,
E. Lippmaa,
Preview
|
PDF (772KB)
|
|
摘要:
Abstract29Si,14N13C and1H NMR data are presented for a series of homologous (methylethoxysilyl)alkylamines of the type (CH3)3−n(C2H5O)nSi(CH2)mNH2(n=o to 3;m= 1 to 4). The measured13C and1H chemical shifts correlate with the total net chargesQAon the corressponding atoms, estimated by the Del Re method.14N and29Si chemical shifts which do not show simple linear relationships to the charges are found to correlate with the relative basicities of the compounds. The influence of the remote substituent (NH2and others) on the29Si chemical shifts is shown to depend on the number and nature of substituents directly on the silicon atom. Argyments for d‐orbital participation in the SiO bounds are given. The chemical shifts of29Si,14N and13C nuclei are not consistent with the fromation of intramolecular ‘long bonds’ between the solicon and nitrogen atoms in aliphatic silym
ISSN:0030-4921
DOI:10.1002/mrc.1270070806
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
7. |
Influence de la substitution sur la structure de la benzophenone. X.—Etude conformationnelle de benzaldehydes, acetophénones et benzophénones substitués par complexation avec les lanthanides |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 386-391
Marcel Grimaud,
Geneviève Pfister‐Guillouzo,
Preview
|
PDF (576KB)
|
|
摘要:
AbstractLa résonance magnétique nucléaire du proton à basse température s'est révélée peu fructueuse dans l'étude conformationnelle des benzophénones substituées. Cependant, l'analyse des déplacements induits par les lanthanides nous a permis de recouper de façon très satisfaisante les résultats obtenus par diffusion Rayleigh dépolarisée et dipolemétrie pour les benzophénonesmetaetorthosubstituées. L'existence en solution d'un équilibre conformationnel pour ces co
ISSN:0030-4921
DOI:10.1002/mrc.1270070807
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
8. |
1H and13C NMR study of α‐acetylenic PIIIand PIVderivatives. Signs and magnitudes ofJ(PC) andJ(PH) |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 392-400
R.‐M. Lequan,
M.‐J. Pouet,
M.‐P. Simonnin,
Preview
|
PDF (781KB)
|
|
摘要:
AbstractAllJ(PH) andJ(PC) values, including signs, have been obtained in acetylenic and propynylic phosphorus derivatives, R2P(X)CCH and R2P(X)CCCH3(X oxygen, lone pair and R C6H5, N(CH3)2, OC2H5, N(C6H5)2, Cl) from1H and13C NMR spectra. In PIVderivatives the following signs are obtained:1J(PC)+,2J(PC)+,3J(PC)+,3J(PH)+,4J(PH). Linear relations are observed between1J(PC),2J(PC) and3J(PC) versus3J(PH), indicating that these coupling constants are mainly dependent on the Fermi contact term, though the other terms of the Ramsey theory do not seem to be negligible for1J(PC) and2J(PC).In PIIIderivatives these signs are:1J(PC)‐ and +,2J(PC)+,3J(PC)‐,3J(PH)‐,4J(PH)+. Only3J(PC) and3J(PH) reflect a small contribution of the Fermi contact term while in1J(PC) and2J(PC) this contribution seems to be negligi
ISSN:0030-4921
DOI:10.1002/mrc.1270070808
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
9. |
An NMR study of someN‐arylaminopropenylylidenearylammonium salts |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 401-404
C. P. Richards,
G. A. Webb,
Preview
|
PDF (315KB)
|
|
摘要:
AbstractThe preparation, characterisation and1H NMR spectra of someN‐arylaminopropenylylidenearylammonium salts are reported. The NMR data show that in DMSO the cations exist as conjugated amino–imines, generally as the ‘all‐trans’ geometrical isomer. An exception is found in the case of the 4‐nitrophenyl derivative which produces a mixture of the ‘all‐trans’ and ‘cis‐trans’ isomers with slow exchange between them at room temperature. The relative stability of the ‘all‐trans’ isomer increases as the salt becomes more ionic. By varying the temperature, pH and nature of the anion it is found that exchange of the NH protons on the cation controls the appearance of spin‐spin coupling betwee
ISSN:0030-4921
DOI:10.1002/mrc.1270070809
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
10. |
Determination of relative signs of13C13C coupling constants in doubly labelled compounds |
|
Organic Magnetic Resonance,
Volume 7,
Issue 8,
1975,
Page 405-406
P. E. Hansen,
O. K. Poulsen,
A. Berg,
Preview
|
PDF (187KB)
|
|
摘要:
AbstractAnalysis of the noise decoupled13C spectra of doubly13C labelled compounds where the two labelled carbons are identical, makes the determination of reltive signs of13C13C coupling constants possible in a very simple way. The involved carbon form AA'X or AA'B spin system
ISSN:0030-4921
DOI:10.1002/mrc.1270070810
出版商:John Wiley&Sons Limited
年代:1975
数据来源: WILEY
|
|