Volume 46, Issue 1 pp. 45-49
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Polysilylenes with ethynylphenyl substituents

H. Frey

H. Frey

Centre for Materials Research (CMO) and Department of Chemical Technology, P.O. Box 217, Universiteit Twente, The Netherlands

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E.-J. Schulenburg

E.-J. Schulenburg

Centre for Materials Research (CMO) and Department of Chemical Technology, P.O. Box 217, Universiteit Twente, The Netherlands

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M. Möller

M. Möller

Centre for Materials Research (CMO) and Department of Chemical Technology, P.O. Box 217, Universiteit Twente, The Netherlands

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H. Noorlander-Bunt

H. Noorlander-Bunt

Department of Organic Chemistry, Universiteit Twente, Chemische Technologie, P.O. Box 217, 7500 AE Enschede, The Netherlands

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J. F. J. Engbersen

J. F. J. Engbersen

Department of Organic Chemistry, Universiteit Twente, Chemische Technologie, P.O. Box 217, 7500 AE Enschede, The Netherlands

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D. N. Reinhoudt

D. N. Reinhoudt

Department of Organic Chemistry, Universiteit Twente, Chemische Technologie, P.O. Box 217, 7500 AE Enschede, The Netherlands

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First published: February 1995
Citations: 3

Abstract

Ethynylphenyl-methyldichlorosilane (EPDMS) has been prepared as a new monomer for the synthesis of polysilylenes with triple bonds attached to the catenated Si chain. A series of copolymers with methylphenyldichlorosilane (MPDS) as well as the homopolymer, PEPMS, have been synthesized. The content of ethynylphenyl substituents was quantitatively analyzed by FTIR spectroscopy. The optical properties of the new polymers were studied with respect to potential π−σ interaction. No significant bathochromic shift of the UV-absorption maximum could be detected. Unexpectedly, increasing content of incorporated EPMS units led to a decrease of the (σ−σ*) absorption. The ethynylphenyl-substituted polysilylenes exhibited strong, temperature-dependent fluorescence in solution as well as in films.

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