ChemInform Abstract: SOLVENT EFFECTS ON THE BORON-11 AND PROTON NMR SPECTRA OF DECABORANE(14), B10H14

1985 ◽  
Vol 16 (1) ◽  
Author(s):  
D. F. GAINES ◽  
C. K. NELSON ◽  
J. C. KUNZ ◽  
J. H. MORRIS ◽  
D. REED
1984 ◽  
Vol 23 (20) ◽  
pp. 3252-3254 ◽  
Author(s):  
Donald F. Gaines ◽  
Caterina K. Nelson ◽  
Joan C. Kunz ◽  
John H. Morris ◽  
David Reed

2004 ◽  
Vol 82 (12) ◽  
pp. 1707-1711 ◽  
Author(s):  
Keith C Brown ◽  
Muhsin El-Bermani ◽  
John A Weil

In investigating liquid-phase proton NMR spectra of 2,2-dimethyl-1-(2,4,6-trinitrophenyl)hydrazine in various solvents, we have found an interesting correlation, at sufficiently low temperatures T, between the chemical-shift difference (splitting) of the picryl proton peaks, measured as f(T), and the Kamlet–Taft hydrogen-bonding basicity parameter β. The observed solvolytic effect offers a convenient way of determining and checking the value of the empirical parameter β. The phenomenon discloses that the molecular geometric configuration is affected vividly by hydrogen bonding with the surrounding solvent molecules. It follows that the internal conformation interchange taking place (in a higher T range) is not in fact solely a unimolecular property.Key words: picryl proton NMR, chemical shift, solvent effects, hydrogen bonding, Kamlet–Taft β.


1971 ◽  
Vol 4 (1) ◽  
pp. 123-135 ◽  
Author(s):  
D.W White ◽  
G.K McEwen ◽  
R.D Bertrand ◽  
J.G Verkade
Keyword(s):  

1984 ◽  
Vol 15 (43) ◽  
Author(s):  
YU. YU. SAMITOV ◽  
I. N. GONCHAROVA ◽  
N. P. RAMZAEVA ◽  
P. B. TERENT'EV

1980 ◽  
Vol 11 (16) ◽  
Author(s):  
K. A. ANDRIANOV ◽  
A. A. ZHDANOV ◽  
B. A. ASTAPOV ◽  
B. D. LAVRUKHIN ◽  
T. V. STRELKOVA ◽  
...  
Keyword(s):  

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