Homeotropic alignment through chargetransfer-induced columnar mesophase formation in an unsymmetrically substituted triphenylene derivative

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Abstract

An unsymmetrically substituted triphenylene, with two adjacent chloroethoxyethyl lateral flexible chains, was synthesized and characterized. Although this compound showed no mesomorphic behavior, it formed a donor-acceptor charge-transfer complex with 2,4,7-trinitrofluorenone (TNF). The resulting 1:1 complex has been investigated using UV-vis and IR spectroscopy, optical microscopy, thermal analysis, and X-ray diffraction. A columnar mesophase with hexagonal symmetry was found. More interestingly, this chargetransfer complex can be easily aligned on a glass surface in a homeotropic orientation, which is stable at room temperature (RT) and over a wide temperature range. Copyright © 2010 IUPAC, Publication date (Web): 6 August 2010.

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Li, J., He, Z., Zhao, H., Gopee, H., Kong, X., Xu, M., … Cammidge, A. N. (2010). Homeotropic alignment through chargetransfer-induced columnar mesophase formation in an unsymmetrically substituted triphenylene derivative. In Pure and Applied Chemistry (Vol. 82, pp. 1993–2003). https://doi.org/10.1351/PAC-CON-09-12-17

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