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Merck
CN
  • Effects of methyl substituent on the charge-transfer complexations of dicarbazolylalkanes with p-chloranil, tetracyanoethylene and tetracyanoquinodimethane.

Effects of methyl substituent on the charge-transfer complexations of dicarbazolylalkanes with p-chloranil, tetracyanoethylene and tetracyanoquinodimethane.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy (2011-06-28)
Erol Asker, Ece Uzkara, Orhan Zeybek
摘要

Series of 1,n-dicarbazolylalkanes and 1,n-di(3-methylcarbazolyl)alkanes (where n=1-5) were synthesized and the molar extinction coefficients, equilibrium constants, enthalpies, and entropies of their charge-transfer (CT) complexes with the π-acceptors p-chloranil, tetracyanoethylene, and tetracyanoquinodimethane were investigated. 1,n-Di(3-methylcarbazolyl)alkanes formed CT complexes with higher equilibrium constants, more negative enthalpies and entropies than 1,n-dicarbazolylalkanes. Vibrational spectra of CT complexes of one of the donor molecules (1,4-dicarbazolylbutane) with all three acceptors were compared.

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Sigma-Aldrich
四氯-1,4-苯醌, 99%
Sigma-Aldrich
7,7,8,8-四氰基对苯二醌二甲烷, 98%
Sigma-Aldrich
四氰乙烯, 96%