๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Volume of mixing effect on solvent shifts in fluorine magnetic resonance spectra

โœ Scribed by Norbert Muller


Publisher
Elsevier Science
Year
1976
Weight
420 KB
Volume
22
Category
Article
ISSN
0022-2364

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Solvent effects on the proton magnetic r
โœ J. A. Lepoivre; H. O. Desseyn; F. C. Alderweireldt ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 426 KB

## Abstract The chemical shifts of the __N__โ€methyl signals for a number of thioโ€oxamide and oxamide derivatives are unambiguously determined in the solvents chloroform, carbon tetrachloride, benzene, chlorobenzene, __o__โ€dichlorobenzene and nitrobenzene. The ASIS effect is discussed. The temperatu

Solvent effects on the proton magnetic r
โœ Gen-Etsu Matsubayashi; Hiroshi Koezuka; Toshio Tanaka ๐Ÿ“‚ Article ๐Ÿ“… 1973 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 365 KB

## Abstract A PMR study of solvent effects on some __p__โ€substituted phenyltin chlorides (substituents = CH~3~, (CH~3~)~3~C, CH~3~O) is reported. Coโ€ordination of solvent molecules to the tin atom leads to an unusual low field shift of the __o__โ€ring protons. The results for __p__โ€tolytin trichlori

Carbon-13 nuclear magnetic resonance spe
โœ E. Kiehlmann; A. S. Tracey ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 736 KB

The "C NMR spectra of 21 catechin derivatives substituted at C-6/C-S by bromine and/or hydrogen and at oxygen by methyl, acetyl and/or hydrogen have been analysed in deuteriated acetone and chloroform. When a methoxy group is flanked by two bulky orrho substituents (6-Br and C4), the M e 0 and ortho