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Title: Effect of substituents on the /sup 35/Cl NQR frequencies of atoms in conditions of hyperconjugation

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00956084· OSTI ID:5057829

The authors studied the mechanisms of the change in the NOR spectra in a series of alpha-chloro-substituted dialkyl ethers, organonitrogen compounds, and benzyl and benzylidene chlorides. The NQR spectra were made on a pulsed IS-3 spectrometer at a temperature of 77 degrees K. There are n-o and ..pi..-o interactions which decrease the Cl 35 and Br 79 NQR frequencies in the series of alpha-chloro ethers, alpha-chloroalkylamides, and benzyl halides. The introduction of a geminal halogen atom (dichloromethyl ethers, benzylidene halides) decreases the effect of hyperconjugation.

Research Organization:
A.E. Arbuzov Institute of Organic and Physical Chemistry
OSTI ID:
5057829
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Vol. 34:6, PT. 1
Country of Publication:
United States
Language:
English