CONFORMATION OF BIPROTONIC PHOTOTAUTOMERISM IN 7-AZAINDOLE HYDROGEN-BONDED DIMERS

CONFORMATION OF BIPROTONIC PHOTOTAUTOMERISM IN 7-AZAINDOLE HYDROGEN-BONDED DIMERS
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DOI:
10.1021/ja00749a007
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发表时间:
1971-01-01
影响因子:
15
通讯作者:
ELBAYOUM.MA
ELBAYOUM.MA
中科院分区:
化学1区
文献类型:
--
作者:
INGHAM, KC;ABUELGHE.M;ELBAYOUM.MA

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The spectral properties of 7-azaindole are compared with those of its A-methyl derivatives. The effect of temperature on the fluorescence of a concentrated solution of 7-azaindole is alsoinvestigated. The results offer strong support for the occurrence of an intermolecular double proton-transfer reaction in the lowest excited singlet electronic state of 7-azaindole hydrogen-bonded dimers. It appears that, at very low temperatures, proton tunneling may be an important mechanism for the reaction.