Abstract
Novel, highly functionalized polysiloxanes were prepared in which each repeat unit bears, on average, one charge transporting and one to two second-order nonlinear optical chromophores. Covalent attachment of charge-transporting carbazole or diphenylamine derivatives was realized through efficient Pt-catalyzed hydrosilylation. Poly(hydrogen methylsiloxane) was reacted with 9-(2-propenyl)carbazole or (N-phenyl-N-2-propenylamino)benzene, affording poly[methyl-3-(9-carbazolyl)propylsiloxane] and poly[methyl-3-(N,N-diphenylamino)propylsiloxane], respectively. Rather remarkable regiospecific bromination of the two arylamine-containing siloxane polymers was achieved using benzyltrimethylammonium chlorobromate, resulting in the formation of poly[methyl-3-(N-(3,6-dibromocarbazolyl))propylsiloxane] and poly[methyl-3-(N,N-bis(4-bromophenyl)amino)propylsiloxane]. Pd-catalyzed Heck-type coupling of the arylbromide-bearing polysiloxanes with either vinylbenzenephosphonic acid diethyl ester or 4-nitrostyrene afforded stilbene-containing polymers bearing phosphonate ester or nitro moieties as electron-withdrawing functionalities, respectively. These fully functionalized polymers were readily soluble in several common organic solvents.
Original language | English (US) |
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Pages (from-to) | 2918-2924 |
Number of pages | 7 |
Journal | Macromolecules |
Volume | 31 |
Issue number | 9 |
DOIs | |
State | Published - May 5 1998 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry
- Materials Chemistry