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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of applied polymer science 1989-07, Vol.38 (2), p.271-280
Hauptverfasser: Ejike, E. N., Parish, R. V., Jideonwo, A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 280
container_issue 2
container_start_page 271
container_title Journal of applied polymer science
container_volume 38
creator Ejike, E. N.
Parish, R. V.
Jideonwo, A.
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
format Article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_app_1989_070380208</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_73PG2197_H</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3658-e6fb45b6bd55bff9fe40f5b86c2afadb33f4df3c42dc6074e96deaa5addf24233</originalsourceid><addsrcrecordid>eNqNkE9vEzEQxS0EEqHwBTj5wAEOG_xn7V1LXKoK0kpVm0Mrjtas11ZMnbVlb0T22-MoKOLIaaTR-72Z9xD6SMmaEsK-Qkprqnq1Jh3hPWGkf4VWlKiuaSXrX6NVFdGmV0q8Re9K-UUIpYLIFTrcTSWGwxAsTjEsn-FlCZCXkHaxpJ2f7JfiQzzCZAuGacTzzvqM67ngDcw-ThgKLoeUYp4LdjHjuoawzN7gOcNU_EnU7G1dYhP3KdijLe_RGweh2A9_5xV6_vH96ea2uX_c3N1c3zeGS9E3VrqhFYMcRiEG55SzLXFi6KVh4GAcOHft6Lhp2Wgk6Vqr5GgBBIyjYy3j_Aqxs6_JsZRsnU7Z72s-TYk-FadrEn0qTl-Kq9CnM5SgGAiupjC-XMj6mFKcVNm3s-y3D3b5D2N9vd3-e6U5477M9njBIb9o2fFO6J8PG93x7YZR1elb_gfenJR2</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Ejike, E. 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. 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><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.1989.070380208</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; Exact sciences and technology ; Inorganic and organomineral polymers ; Physicochemistry of polymers ; Preparation</subject><ispartof>Journal of applied polymer science, 1989-07, Vol.38 (2), p.271-280</ispartof><rights>Copyright © 1989 John Wiley &amp; Sons, Inc.</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3658-e6fb45b6bd55bff9fe40f5b86c2afadb33f4df3c42dc6074e96deaa5addf24233</citedby><cites>FETCH-LOGICAL-c3658-e6fb45b6bd55bff9fe40f5b86c2afadb33f4df3c42dc6074e96deaa5addf24233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fapp.1989.070380208$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.1989.070380208$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6589930$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ejike, E. 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. N.</creator><creator>Parish, R. V.</creator><creator>Jideonwo, A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19890720</creationdate><title>Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes</title><author>Ejike, E. N. ; Parish, R. 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. N.</au><au>Parish, R. V.</au><au>Jideonwo, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insoluble poly(akylarylphosphine)siloxanes and their application as supports for catalytic transition-metal complexes</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>1989-07-20</date><risdate>1989</risdate><volume>38</volume><issue>2</issue><spage>271</spage><epage>280</epage><pages>271-280</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>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).</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>
fulltext fulltext
identifier ISSN: 0021-8995
ispartof Journal of applied polymer science, 1989-07, Vol.38 (2), p.271-280
issn 0021-8995
1097-4628
language eng
recordid cdi_crossref_primary_10_1002_app_1989_070380208
source Wiley Online Library Journals Frontfile Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T02%3A11%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insoluble%20poly(akylarylphosphine)siloxanes%20and%20their%20application%20as%20supports%20for%20catalytic%20transition-metal%20complexes&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Ejike,%20E.%20N.&rft.date=1989-07-20&rft.volume=38&rft.issue=2&rft.spage=271&rft.epage=280&rft.pages=271-280&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.1989.070380208&rft_dat=%3Cistex_cross%3Eark_67375_WNG_73PG2197_H%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true