Solvent Effects and Hydrogen Bonding

1980 ◽  
pp. 253-258
Author(s):  
EDWIN D. BECKER
1960 ◽  
Vol 38 (12) ◽  
pp. 2508-2513 ◽  
Author(s):  
C. N. R. Rao ◽  
G. K. Goldman ◽  
A. Balasubramanian

The n → π* transition of the carbonyl group has been studied in solvents of varying degree of polarity and hydrogen-bonding ability, in a number of aliphatic carbonyl derivatives. Evidence for hyperconjugation of the alkyl groups in the electronically excited states of molecules has been presented.


1969 ◽  
Vol 72 (11) ◽  
pp. 2430-2436 ◽  
Author(s):  
Takehide TANAKA ◽  
Tetsuo YOKOYAMA ◽  
Yukio YAMAGUCHI ◽  
Seikou NAGANUMA

1968 ◽  
Vol 46 (15) ◽  
pp. 2593-2600 ◽  
Author(s):  
James R. Bartels-Keith ◽  
Ronald F. W. Cieciuch

Certain ortho-substituted acetanilides exhibit proton magnetic resonance signals at unusually low field for the amido proton and the aromatic proton adjacent to the acetamido group. This effect, explicable in terms of intramolecular hydrogen-bonding, has been observed for nitro, carbonyl, sulfamoyl, and sulfonyl substituents. Solvent effects are discussed.


Author(s):  
Patricia P�rez ◽  
Gerald Zapata-Torres ◽  
Julia Parra-Mouchet ◽  
Renato Contreras

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