Journal of the American Chemical Society p. 3612 - 3618 (1992)
Update date:2022-08-03
Topics:
Michaeli, Shalom
Hugerat, Muhamad
Levanon, Haim
Bernitz, Mazal
Natt, Aliza
Neumann, Ronny
Molecular compatibility of a guest porphyrin in a thermotropic nematic liquid crystalline host phase was shown to control the orientation of the porphyrin chromophore. In this manner, the normal alignment of a porphyrin plane parallel to the director in a nematic phase was inverted to a perpendicular orientation by attachment of mesogenic type appendages orthogonal to a porphyrin ring on one side of the ring plane. This molecular design also leads to a head-to-tail ordering of the porphyrin even in isotropic phases. The conclusions reached are based on detection and analysis of time-resolved EPR spectra of photoexcited triplet states.
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