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Yen-Ju Cheng

Publications and source records attributed to Yen-Ju Cheng.

3 recordsLinked to original sources

Alternating divinylarene-silylene copolymers.

A summary of recent advances on the chemistry and photophysics of silylene-spaced divinylarene copolymers is presented. The silicon moieties have been shown to serve as an insulating spacer in these copolymers. The photophysical studies have provided useful insights into how chromophores in polymers interact intramolecularly. Because different chromophores can be regioregularly introduced into the polymeric chain, these copolymers have been extensively used as models for studying energy transfer, light harvesting as well as chiroptical transfer.

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Facile synthesis of highly efficient phenyltetraene-based nonlinear optical chromophores for electrooptics.

[reaction: see text] A facile synthetic route has been developed to convert an electron-rich, sterically hindered dialkylaminodienone into a conjugated dialkylaminotrienal with good yield. The derived dialkylaminotetraene-type nonlinear optical chromophores possess an all-trans conformation and can be functionalized with fluoro-dendron to provide proper shape modification for poling. Polymers doped with two examples of these chromophores in high concentrations have been poled to afford ultra-large electrooptic coefficients (r(33)) of 208 and 262 pm/V, respectively, at the measuring wavelength of 1.31 mum.

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Synthesis, light-harvesting and energy-transfer properties of regioregular silylene-spaced alternating [(donor-SiMe2-)(n=1-3)-(acceptor-SiMe2)] copolymers.

A series of silylene-spaced alternating [(donor-SiMe2)(n=1-3)-(acceptor-SiMe2)] copolymers 4-6 was synthesized by rhodium-catalyzed hydrosilylation of bisalkynes with bissilyl hydrides. Monomeric reference compounds 7-10 with similar chromophore components were prepared for comparison. The ratio of donor to acceptor groups is well-controlled by the precise regiochemistry and nature of the repeat units. The silylene moieties serve as insulating spacers between chromophores. The polymers exhibit light-harvesting abilities, for which the intensity of the emission enhanced with larger donor-to-acceptor ratios. No emission originating from the donors was observed in fluorescence spectra, illustrating that intrachain energy transfer is highly efficient along the polymer chain.

Journal Article↗