Substituent effects on the phosphorus-31, nitrogen-15, and carbon-13 NMR spectra of N-(arylsulfonyl)-P,P,P-triphenylphospha-.lambda.5-azenes and on the nitrogen-15 and carbon-13 NMR spectra of the corresponding arenesulfonamides

1987 ◽  
Vol 52 (1) ◽  
pp. 159-163 ◽  
Author(s):  
Martin Pomerantz ◽  
Whe Narn Chou ◽  
Malgorzata K. Witczak ◽  
Christina G. Smith
1986 ◽  
Vol 51 (3) ◽  
pp. 670-676 ◽  
Author(s):  
Eva Solčániová ◽  
Štefan Toma ◽  
Tibor Liptaj

13C NMR spectra of 18 ferrocene analogues of trans stilbenes (1-aryl-2-ferrocenylethylenes) were measured. It was found that bridge group weakens the transfer of the substituent electron effects into ferrocene nucleus, especially distinctly into 3',4'positions of cyclopentadienyl ring. The transfer of substituent effects into β-position of the bridge -CH=CH- is greater in derivatives studied by us than in stilbenes. Synthesis of 1-(4-dimethylaminophenyl)-2-ferrocenylethylene is described.


1982 ◽  
Vol 20 (3) ◽  
pp. 159-161 ◽  
Author(s):  
Yoshiaki Kusuyama ◽  
Satoru Inoshita ◽  
Ginjiro Okada ◽  
Minoru Yanagi ◽  
Kenjiro Tokami ◽  
...  

1975 ◽  
Vol 7 (1) ◽  
pp. 51-53 ◽  
Author(s):  
Ernest Wenkert ◽  
Miroslav J. Gašić ◽  
Edward W. Hagaman ◽  
L. D. Kwart

1975 ◽  
Vol 30 (9-10) ◽  
pp. 794-799 ◽  
Author(s):  
Ludger Ernst

The 13C NMR spectra of twelve amino-, dimethylamino-, diamino-, and bis(dimethylamino)naphthalenes are completely assigned by selective 13C{1H} double resonance and by interpretation of proton-coupled spectra. Strong substituent effects (Δδ) upon chemical shifts are observed and can largely be accounted for by mesomerism. The pronounced high-field shifts of C-6 in the 2-amino- and 2-dimethylaminonaphthalenes coincide with the enhanced reactivity of this position towards electrophilic reagents. In 1-dimethylaminonaphthalene and even more so in 1-dimethylamino-2-methylnaphthalene, conjugation is inhibited for steric reasons and Δδ’s are greatly diminished, thus giving an estimate for the contribution of resonance to substituent-induced shifts in the unhindered compounds. In two 1,8-disubstituted naphthalenes there are large deviations from additivity of substituent effects.


1980 ◽  
Vol 14 (2) ◽  
pp. 138-140 ◽  
Author(s):  
E. Solčániová ◽  
S. Toma

1975 ◽  
Vol 30 (9-10) ◽  
pp. 788-793 ◽  
Author(s):  
Ludger Ernst

During a reinvestigation of the 13C NMR spectra of 1-fluoronaphthalene (1) and of 2-fluoronaphthalene (2) at 20 and 25.16 MHz, uncertainties that existed in the literature about signal assignments for 1 could be cleared. In the spectral analyses for 2 given so far, five out of ten signals were incorrectly assigned. The corrected assignment is supported by extensive 13C{1H} double resonance experiments, by recording of proton-coupled 13C and 13C{19F} spectra and by off-resonance 13C{1H} noise-decoupling. The results show a strong + M-effect of the fluorine substituents on 13C chemical shifts similar to the effects of OH and OCH3 groups. 1H NMR spectra of 1 and 2 could be partially assigned by decoupling of the 19F resonances and by iterative analysis.


1980 ◽  
Vol 58 (15) ◽  
pp. 1503-1511 ◽  
Author(s):  
Pierre Metzger ◽  
Eliette Casadevall ◽  
André Casadevall ◽  
Marie-José Pouet

The 13C nmr spectra of α, αα, and αα′ substituted trans-fused bicyclo [4,n,0]alkan-3 ones, are described. Substituent effects are discussed in terms of their electron withdrawing character, axial or equatorial configuration, and cyclohexane deformation. 13C=O chemical shifts are shown to be based on the polarization of π bond and on C=O/X non-bonded interactions. As in ir and uv spectroscopy, 13C nmr is a convenient method for detecting an a substituent configuration in fixed ring ketones.


2008 ◽  
Vol 46 (2) ◽  
pp. 182-185 ◽  
Author(s):  
Andrzej Maślankiewicz ◽  
Maria J. Maślankiewicz ◽  
Krzysztof Marciniec

2005 ◽  
Vol 18 (8) ◽  
pp. 818-824 ◽  
Author(s):  
Janusz Oszczapowicz ◽  
Irena Oszczapowicz

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