Conformational Studies of the Benzophenone and Thiobenzophenone Radical Anions
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A conformational energy map is calculated for the anions of benzophenone and thiobenzophenone, using a Bartell repulsion potential. A low energy configuration is obtained in which the phenyl rings are counterrotated by 30° from the planar form. The energy barrier to concerted rotation is also calculated and found to be in reasonable agreement with the findings of Takeshita and Hirota for the oxyketyl. Spin density distributions are also given.
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1979 ◽
Vol 75
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pp. 494
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2009 ◽
Vol 2009
(5)
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pp. 283-286
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1969 ◽
Vol 3
(5)
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pp. 261-263
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