Skip to Content
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
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
7,7,8,8-Tetracyanoquinodimethane, 98%
Sigma-Aldrich
Tetracyanoethylene, 96%
Sigma-Aldrich
Tetrachloro-1,4-benzoquinone, 99%