Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes
Light induced addition of diphenylphosphine (DPP) to methylvinylcyclotetrasiloxane (MVS) yielded poly(2‐diphenylphosphinoethyl) cyclotetrasiloxane (DPPS). Similar treatment of allyldiphenylphosphine (ADPP) with linear poly(methylhydrogenosiloxane)‐co‐hexamethyldisiloxane (PMS) led to formation of po...
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Veröffentlicht in: | Journal of applied polymer science 1989-07, Vol.38 (2), p.271-280 |
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description | Light induced addition of diphenylphosphine (DPP) to methylvinylcyclotetrasiloxane (MVS) yielded poly(2‐diphenylphosphinoethyl) cyclotetrasiloxane (DPPS). Similar treatment of allyldiphenylphosphine (ADPP) with linear poly(methylhydrogenosiloxane)‐co‐hexamethyldisiloxane (PMS) led to formation of poly(3‐diphenylphosphinopropyl)methylsiloxane‐co‐hexamethyldisiloxane (PPMS). DPPS and PPMS were condensed by acid treatment to give insoluble rubbery phosphine bearing materials P1 and P2, respectively. Iridium and rhodium complexes were immobilized on P1 and P2. The ability of a high molecular weight substrate (PMS) to migrate to active catalytic centers within support matrix was examined. The effect of varying metal: phosphine ratio and total percentage metal on the support were examined during catalysis of O‐silylation of ethanol with PMS and triethoxysilane (TES). |
doi_str_mv | 10.1002/app.1989.070380208 |
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N. ; Parish, R. V. ; Jideonwo, A.</creator><creatorcontrib>Ejike, E. N. ; Parish, R. V. ; Jideonwo, A.</creatorcontrib><description>Light induced addition of diphenylphosphine (DPP) to methylvinylcyclotetrasiloxane (MVS) yielded poly(2‐diphenylphosphinoethyl) cyclotetrasiloxane (DPPS). Similar treatment of allyldiphenylphosphine (ADPP) with linear poly(methylhydrogenosiloxane)‐co‐hexamethyldisiloxane (PMS) led to formation of poly(3‐diphenylphosphinopropyl)methylsiloxane‐co‐hexamethyldisiloxane (PPMS). DPPS and PPMS were condensed by acid treatment to give insoluble rubbery phosphine bearing materials P1 and P2, respectively. Iridium and rhodium complexes were immobilized on P1 and P2. The ability of a high molecular weight substrate (PMS) to migrate to active catalytic centers within support matrix was examined. 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N.</creatorcontrib><creatorcontrib>Parish, R. V.</creatorcontrib><creatorcontrib>Jideonwo, A.</creatorcontrib><title>Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Light induced addition of diphenylphosphine (DPP) to methylvinylcyclotetrasiloxane (MVS) yielded poly(2‐diphenylphosphinoethyl) cyclotetrasiloxane (DPPS). Similar treatment of allyldiphenylphosphine (ADPP) with linear poly(methylhydrogenosiloxane)‐co‐hexamethyldisiloxane (PMS) led to formation of poly(3‐diphenylphosphinopropyl)methylsiloxane‐co‐hexamethyldisiloxane (PPMS). DPPS and PPMS were condensed by acid treatment to give insoluble rubbery phosphine bearing materials P1 and P2, respectively. Iridium and rhodium complexes were immobilized on P1 and P2. The ability of a high molecular weight substrate (PMS) to migrate to active catalytic centers within support matrix was examined. The effect of varying metal: phosphine ratio and total percentage metal on the support were examined during catalysis of O‐silylation of ethanol with PMS and triethoxysilane (TES).</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Inorganic and organomineral polymers</subject><subject>Physicochemistry of polymers</subject><subject>Preparation</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNqNkE9vEzEQxS0EEqHwBTj5wAEOG_xn7V1LXKoK0kpVm0Mrjtas11ZMnbVlb0T22-MoKOLIaaTR-72Z9xD6SMmaEsK-Qkprqnq1Jh3hPWGkf4VWlKiuaSXrX6NVFdGmV0q8Re9K-UUIpYLIFTrcTSWGwxAsTjEsn-FlCZCXkHaxpJ2f7JfiQzzCZAuGacTzzvqM67ngDcw-ThgKLoeUYp4LdjHjuoawzN7gOcNU_EnU7G1dYhP3KdijLe_RGweh2A9_5xV6_vH96ea2uX_c3N1c3zeGS9E3VrqhFYMcRiEG55SzLXFi6KVh4GAcOHft6Lhp2Wgk6Vqr5GgBBIyjYy3j_Aqxs6_JsZRsnU7Z72s-TYk-FadrEn0qTl-Kq9CnM5SgGAiupjC-XMj6mFKcVNm3s-y3D3b5D2N9vd3-e6U5477M9njBIb9o2fFO6J8PG93x7YZR1elb_gfenJR2</recordid><startdate>19890720</startdate><enddate>19890720</enddate><creator>Ejike, E. 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V. ; Jideonwo, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3658-e6fb45b6bd55bff9fe40f5b86c2afadb33f4df3c42dc6074e96deaa5addf24233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Inorganic and organomineral polymers</topic><topic>Physicochemistry of polymers</topic><topic>Preparation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ejike, E. N.</creatorcontrib><creatorcontrib>Parish, R. V.</creatorcontrib><creatorcontrib>Jideonwo, A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ejike, E. 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DPPS and PPMS were condensed by acid treatment to give insoluble rubbery phosphine bearing materials P1 and P2, respectively. Iridium and rhodium complexes were immobilized on P1 and P2. The ability of a high molecular weight substrate (PMS) to migrate to active catalytic centers within support matrix was examined. The effect of varying metal: phosphine ratio and total percentage metal on the support were examined during catalysis of O‐silylation of ethanol with PMS and triethoxysilane (TES).</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.1989.070380208</doi><tpages>10</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Inorganic and organomineral polymers Physicochemistry of polymers Preparation |
title | Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes |
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