Novel cyclic molecules, the cyclic phenylazomethine trimers (CPAs), were synthesized via the dehydration of the 4-aminobenzophenone derivatives. The yields of the CPAs were enhanced to over 90% by induction of the bulky α-substituent to the substrate. The UV−vis spectra of the CPAs show a nonconjugated structure and Z conformation compared to the linear oligophenylazomethines (OPAs).
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Higuchi et al. (1999) studied this question.
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