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- W814586385 abstract "The proton affinities of substituted imidazoles, relevant to the binding of lexitropsins that contain imidazole ring to the base pair (G-C sequence) of minor groove of DNA, are studied with the aid of EHT calculations. It is shown that proton affinity of imidazole substituted at position to the basic nitrogen is slightly larger than that of imidazole substituted at N for the methylimidazole. Proton affinities of N-substituted imidazoles are found to be larger than those of imidazoles substituted at position for a selected set of the other derivatives. As predicted the proton affinity increases when electron-donating group is attached at position N of imidazole." @default.
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- W814586385 date "1994-01-01" @default.
- W814586385 modified "2023-09-23" @default.
- W814586385 title "Theoretical Study for the Substituent Effect on Proton Affinity of Imidazoles" @default.
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