The concentration dependence of the chemical shift for the fused mobile-proton peak in a fast-exchange system

1984 ◽  
Vol 20 (1) ◽  
pp. 98-100
Author(s):  
V. V. Turov ◽  
V. K. Pogorelyi

1994 ◽  
Vol 67 (4) ◽  
pp. 629-635 ◽  
Author(s):  
K. J. McGrath ◽  
C. M. Roland

Abstract 129Xe NMR spectroscopy is employed to demonstrate that polyepichlorohydrin and poly(vinylmethylether), which have virtually equal glass transition temperatures, form thermodynamically miscible blends. This conclusion is drawn from the appearance of a single resonance in the blend spectrum, at a chemical shift differing from that calculated for the fast exchange regime. 13C NMR results are consistent with thermodynamic miscibility, and reflect the similarity of the component dynamics.



1998 ◽  
Vol 93 (1) ◽  
pp. 145-151 ◽  
Author(s):  
M.A. WENDT ◽  
J. MEILER ◽  
F. WEINHOLD ◽  
T.C. FARRAR


1974 ◽  
Vol 29 (10) ◽  
pp. 1467-1470 ◽  
Author(s):  
O. Lutz ◽  
W. Steinkilberg

Abstract The NMR signals of the nuclei 55Mn and 2H have been investigated in aqueous solutions of permanganates. The concentration dependence of the NMR signals of 55Mn has been determined in potassium permanganate solutions in H2O and D2O and a large solvent isotope effect on the chemical shift of 55Mn has been established. The ratio of the Larmor frequencies of 55Mn relative to 2H has been measured with high accuracy. Using the concentration dependence, the ratio of the Larmor frequencies of 55Mn for infinite dilution relative to 2H in pure D2O is given. From this ratio a magnetic moment for 55Mn in the permanganate ion has been derived.



1998 ◽  
Vol 93 (1) ◽  
pp. 145-152 ◽  
Author(s):  
M. A. WENDT J. MEILER F. WEINHOLD T


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