|
11. |
Long‐range deuterium isotope effects on13C NMR shifts of intramolecularly hydrogen‐bonded 9‐hydroxyphenalen‐1‐ones |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 54-62
Carin Engdahl,
Adolf Gogoll,
Ulf Edlund,
Preview
|
PDF (780KB)
|
|
摘要:
AbstractThe1H and13C NMR spectra of 9‐hydroxyphenalenone (1) and 9‐hydroxy‐2‐methylphenalenone (2) have been completely assigned. Primary and secondary deuterium isotope effects were determined in three solvents (chloroform, acetone and dimethyl sulphoxide), including the effect of temperature on the secondary isotope effects. Both negative and large long‐range secondary isotope effects were found for both 1 and 2. The average secondary isotope effects for corresponding carbons follow the same sign and magnitude pattern in both
ISSN:0749-1581
DOI:10.1002/mrc.1260290112
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
12. |
1H NMR structural analysis of isomeric tetrazole‐substituted spirostan steroids: Shielding effects and conformational study |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 63-72
Christopher J. L. Silwood,
David B. Davies,
Preview
|
PDF (660KB)
|
|
摘要:
AbstractThe structures of two pairs of tetrazole‐substituted spirostan steroids were characterized by the use of one‐ and two‐dimensional1H NMR measurements. The conformation of the seven‐membered spirostan ring A of the steroid was determined by analysis of proton spin coupling constants and confirmed by 1D and 2D NOE experiments showing interactions between the methyl group and ring protons. The conformation of the tetrazole‐substituted ring A was found to be the same for the four isomers, allowing them to be differentiated by the analysis of the effect of tetrazole‐ring isomerization on the chemical shifts of neighbour
ISSN:0749-1581
DOI:10.1002/mrc.1260290113
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
13. |
Selenium—selenium bond order in diselenides.77Se–77Se and77Se–13C coupling constants and77Se chemical shifts of symmetrical and unsymmetrical diselenides |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 73-77
Willy Gombler,
Preview
|
PDF (465KB)
|
|
摘要:
Abstract77Se–77Se spin‐spin coupling constants of unsymmetrically and, for the first time, of symmetrically substituted diselenides have been measured for CF3SeSeCH3, CF3SeSeCF3, CF3SeSeCF2Cl and CF2ClSeSeCF2Cl. A correlation of the1J(SeSe) values with the average77Se shielding is found for perhalomethyl diselenides and organyl diselenides.77Se–13C coupling constants are also reported for the perhalomethyl diselenides. The coupling constants are much larger than in organyl diselenides. NMR data for the thioselenides CF3SeSR (R = CF3, CF2Cl, CFCl2, CCl3) are reported for comparison. It can be concluded that π‐type interactions occur in the SeSe or SeS bonds of diselenides and thioselenides, respectively, containing perhalom
ISSN:0749-1581
DOI:10.1002/mrc.1260290114
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
14. |
Influence of the phosphorus lone pair on coupling constants in vinylphosphines |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 78-82
Terence N. Mitchell,
Kerstin Heesche‐Wagner,
Heinz‐Joachim Belt,
Preview
|
PDF (398KB)
|
|
摘要:
AbstractMultinuclear NMR data are presented and discussed for a variety of vinylphosphines in which the vinyl group bears one, two or three substituents; these include organic and trimethylstannyl residues. The orientation of the phosphorus lone pair can be determined from two‐bond phosphorus‐carbon coupling constant values. The magnitudes of the3J(PCCSn),4J(PCCSnC) and5J(PCCSnCH) coupling constants are clearly determined by a throughspace interaction when P and C are in acisconf
ISSN:0749-1581
DOI:10.1002/mrc.1260290115
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
15. |
Long‐range heteronuclear correlation 2D NMR by MLEV‐16 isotropic mixing |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 83-87
Gareth A. Morris,
Andrew Gibbs,
Preview
|
PDF (327KB)
|
|
摘要:
AbstractCoherence transfer by MLEV‐16 isotropic mixing is shown to be an efficient way of obtaining phase‐sensitive heteronuclear chemical shift correlation 2D spectra. Both long‐ and short‐range correlations are possible by appropriate choice of mixing time. At long mixing times, the contribution of coherence transfer pathways through multiple couplings extends the range of correlation. Long mixing time experiments may therefore be useful for structure determination in total unknowns. Results are presented for a13C‐detected isotropic mixing experiment o
ISSN:0749-1581
DOI:10.1002/mrc.1260290116
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
16. |
Complete1H and13C assignment of some cubane derivatives by 2D NMR spectroscopy |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 88-91
T. Axenrod,
B. Liang,
A. Bashir‐Hashemi,
P. R. Dave,
D. S. Reddy,
Preview
|
PDF (227KB)
|
|
摘要:
AbstractThe13C and1H chemical shift values of 31 cubanes ranging from mono‐ to hexa‐substituted derivatives were recorded in CDCl3solution and the spectra were fully assigned using, where necessary, 2D13C–H shift correlated spectra optimized for either one‐bond or long‐range13C–H couplings. The one‐bond13C–H coupling constants for the cubyl carbon resonances were also measure
ISSN:0749-1581
DOI:10.1002/mrc.1260290117
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
17. |
News and events |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page 92-92
Preview
|
PDF (83KB)
|
|
ISSN:0749-1581
DOI:10.1002/mrc.1260290119
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
18. |
Masthead |
|
Magnetic Resonance in Chemistry,
Volume 29,
Issue 1,
1991,
Page -
Preview
|
PDF (101KB)
|
|
ISSN:0749-1581
DOI:10.1002/mrc.1260290101
出版商:John Wiley&Sons, Ltd.
年代:1991
数据来源: WILEY
|
|