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Updated: Aug 13, 2026

Patterning via Optical Saturable Transitions - Fabrication and Characterization
Published on: December 11, 2014
Stereocontrolled synthesis and optical properties of all-cis poly(phenylene vinylenes) (PPVs): a method for direct
Hiroyuki Katayama1, Masato Nagao, Tatsuro Nishimura
1International Research Center for Elements Science (IRCELS), Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan. hiroyuki@scl.kyoto-u.ac.jp
Abstract:
Geometrically pure, all-cis poly(phenylene vinylenes) (PPVs) are synthesized by Suzuki-Miyaura-type polycondensation of 2,5-dioctyloxy-1,4-benzenediboronic acid with (Z,Z)-bis(2-bromoethenyl)benzenes, which are prepared by ruthenium-catalyzed (Z)-selective double hydrosilylation of diethynylbenzenes, followed by bromodesilylation of the resulting (Z,Z)-bis(2-silylethenyl)benzenes with N-bromosuccinimide. The all-cis PPVs thus obtained undergo one-way photoisomerization to the corresponding trans-PPVs both in solution and in the solid. This phenomenon is applied to direct microscale patterning of PPVs onto a quartz substrate.
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