A 1H and 13C nuclear magnetic resonance study of silicon and germanium chalcogenide derivatives

1979 ◽  
Vol 57 (24) ◽  
pp. 3253-3256 ◽  
Author(s):  
John E. Drake ◽  
Boris M. Glavinćevski ◽  
Robyn Humphries ◽  
Abdul Majid
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
General Pattern ◽  
Nuclear Magnetic Resonance Study ◽  
Magnetic Resonance Study ◽  
Methyl Substitution ◽  
Nmr Parameters ◽  
13C Nuclear Magnetic Resonance ◽  
Silicon And Germanium ◽  
C Nmr

This paper reports the 1H and 13C nmr parameters of the disilyl- and digermyl-chalcogenide species (MenH3−nM)2E, where M = Si, Ge; E = O, S, Se, Te and n = 0 to 3. The general pattern of changing shifts is markedly influenced by methyl substitution.

1H and 13C nuclear magnetic resonance study of the complexation of uranyl ion with malic acid

1982 ◽  
Vol 60 (8) ◽  
pp. 1007-1018 ◽  
Author(s):  
M. Teresa Nunes ◽  
Victor M. S. Gil ◽  
António V. Xavier
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Malic Acid ◽  
Nuclear Magnetic Resonance Study ◽  
Magnetic Resonance Study ◽  
Molar Ratios ◽  
Nmr Study ◽  
13C Nuclear Magnetic Resonance ◽  
Ph Range ◽  
C Nmr

A full pH range 1H and 13C nmr study was performed of the complexation of UO22+ with malic acid, for variable concentrations and molar ratios. Spectral evidence for the existence of at least five complexes was found, and their stoichiometry and dependence on pH were investigated. Information on the conformation of the bound ligand molecules was also obtained.

Hindered Rotation in Poly(N-acyl)iminoalkylenes - A 13C Nuclear Magnetic Resonance Study

1995 ◽  
Vol 50 (9) ◽  
pp. 1404-1411 ◽  
Author(s):  
Bernabé L. Rivas ◽  
Klaus Albert ◽  
Kurt E. Geckeler ◽  
Ernst Bayer
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Cationic Polymerization ◽  
Nmr Spectra ◽  
Nuclear Magnetic Resonance Study ◽  
Side Chain ◽  
Magnetic Resonance Study ◽  
Hindered Rotation ◽  
13C Nuclear Magnetic Resonance ◽  
C Nmr

AbstractPoly(N-acetyl)iminoethylene. poly(N-propionyl)iminoethylene and poly(N-acetyl)-2,2-dimethyliminoethylene were prepared by cationic polymerization in solution of 2-methyl- 2-oxazoline, 2-ethyl-2-oxazoline, and 2,4,4-trimethyl-2-oxazoline respectively. The 13C NMR spectra of the polymers obtained showed different sets of shifts for the carbon atoms of the backbone as well as for the N-acylimino side chain due to the restricted rotation of the Nacylimino group. The temperature dependence of the N-acylimino side chain signals showed a different coalescence behaviour depending on the substituents at both the main and the side chain.

scholarly journals Cryopreservation Effects on Intermediary Metabolism in a Pancreatic Substitute: A 13C Nuclear Magnetic Resonance Study

2012 ◽  
Vol 18 (21-22) ◽  
pp. 2323-2331 ◽  
Author(s):  
Hajira F. Ahmad ◽  
Nicholas E. Simpson ◽  
Alison N. Lawson ◽  
Athanassios Sambanis
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nuclear Magnetic Resonance Study ◽  
Intermediary Metabolism ◽  
Magnetic Resonance Study ◽  
13C Nuclear Magnetic Resonance ◽  
Nuclear Magnetic ◽  
Pancreatic Substitute
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