Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation

The reaction of tris(pentafluorophenyl)borane, B(C6F5)3 with surface silanol (=Si-OH) of silica occurs only in the presence of a Bronsted base (diethylaniline, Et2NPh), which does not form a complex with B(C6F5)3, and affords selectively a well-defined ionic entity [=SiO-B(C6F5)3]-[HNEt2Ph]+. With a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Comptes rendus. Chimie 2004-08, Vol.7 (8-9), p.725-736
Hauptverfasser: Millot, Nicolas, Santini, Catherine C., Lefebvre, Frédéric, Basset, Jean-Marie
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 736
container_issue 8-9
container_start_page 725
container_title Comptes rendus. Chimie
container_volume 7
creator Millot, Nicolas
Santini, Catherine C.
Lefebvre, Frédéric
Basset, Jean-Marie
description The reaction of tris(pentafluorophenyl)borane, B(C6F5)3 with surface silanol (=Si-OH) of silica occurs only in the presence of a Bronsted base (diethylaniline, Et2NPh), which does not form a complex with B(C6F5)3, and affords selectively a well-defined ionic entity [=SiO-B(C6F5)3]-[HNEt2Ph]+. With a strong nucleophile base such as pyridine (C5H5N), the complex (C6F5)3B.NC5H5 is formed and is only physisorbed onto silica surface. Without a base, B(C6F5)3 does not react with (=Si-OH), and is only physisorbed. On the contrary, with any molecular compound ROH, B(C6F5)3 forms a stable complex (C6F5)3BO(H)R.
doi_str_mv 10.1016/j.crci.2004.03.011
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_32671565</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>32671565</sourcerecordid><originalsourceid>FETCH-LOGICAL-c320t-b2acc3075fa0be2eb876f0c814da55cda86d6aee8b0e83813ee5174c8f2c88093</originalsourceid><addsrcrecordid>eNpNkLFOwzAQhi0EEqXwAkye2BLsOE5cNlRBQarEAMyWczm3qZK42I5Q3p6EMjDdDd_9uv8j5JazlDNe3B9S8NCkGWN5ykTKOD8jC65KlXCZi_N_-yW5CuHApqOVLBYkvA_eGkDq_M70rsNo2rYBCnvsmhD9-EAN9W6ISKOj39i2SY226bGmlfOup3uM6N0Oe3RDoOASMFPEGCK1zlPXzjA9unbs0DfBxMb11-TCmjbgzd9cks_np4_1S7J927yuH7cJiIzFpMoMgGCltIZVmGGlysIyUDyvjZRQG1XUhUFUFUMlFBeIkpc5KJuBUmwlluTulHv07mvAEPVUCaYK5vdZLbKi5LKQE5idQPAuBI9WH33TGT9qzvTsVx_07FfPfjUTevIrfgCkk3NN</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>32671565</pqid></control><display><type>article</type><title>Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation</title><source>Elsevier ScienceDirect Journals Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Millot, Nicolas ; Santini, Catherine C. ; Lefebvre, Frédéric ; Basset, Jean-Marie</creator><creatorcontrib>Millot, Nicolas ; Santini, Catherine C. ; Lefebvre, Frédéric ; Basset, Jean-Marie</creatorcontrib><description>The reaction of tris(pentafluorophenyl)borane, B(C6F5)3 with surface silanol (=Si-OH) of silica occurs only in the presence of a Bronsted base (diethylaniline, Et2NPh), which does not form a complex with B(C6F5)3, and affords selectively a well-defined ionic entity [=SiO-B(C6F5)3]-[HNEt2Ph]+. With a strong nucleophile base such as pyridine (C5H5N), the complex (C6F5)3B.NC5H5 is formed and is only physisorbed onto silica surface. Without a base, B(C6F5)3 does not react with (=Si-OH), and is only physisorbed. On the contrary, with any molecular compound ROH, B(C6F5)3 forms a stable complex (C6F5)3BO(H)R.</description><identifier>ISSN: 1878-1543</identifier><identifier>ISSN: 1631-0748</identifier><identifier>EISSN: 1878-1543</identifier><identifier>DOI: 10.1016/j.crci.2004.03.011</identifier><language>eng</language><ispartof>Comptes rendus. Chimie, 2004-08, Vol.7 (8-9), p.725-736</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-b2acc3075fa0be2eb876f0c814da55cda86d6aee8b0e83813ee5174c8f2c88093</citedby><cites>FETCH-LOGICAL-c320t-b2acc3075fa0be2eb876f0c814da55cda86d6aee8b0e83813ee5174c8f2c88093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Millot, Nicolas</creatorcontrib><creatorcontrib>Santini, Catherine C.</creatorcontrib><creatorcontrib>Lefebvre, Frédéric</creatorcontrib><creatorcontrib>Basset, Jean-Marie</creatorcontrib><title>Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation</title><title>Comptes rendus. Chimie</title><description>The reaction of tris(pentafluorophenyl)borane, B(C6F5)3 with surface silanol (=Si-OH) of silica occurs only in the presence of a Bronsted base (diethylaniline, Et2NPh), which does not form a complex with B(C6F5)3, and affords selectively a well-defined ionic entity [=SiO-B(C6F5)3]-[HNEt2Ph]+. With a strong nucleophile base such as pyridine (C5H5N), the complex (C6F5)3B.NC5H5 is formed and is only physisorbed onto silica surface. Without a base, B(C6F5)3 does not react with (=Si-OH), and is only physisorbed. On the contrary, with any molecular compound ROH, B(C6F5)3 forms a stable complex (C6F5)3BO(H)R.</description><issn>1878-1543</issn><issn>1631-0748</issn><issn>1878-1543</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpNkLFOwzAQhi0EEqXwAkye2BLsOE5cNlRBQarEAMyWczm3qZK42I5Q3p6EMjDdDd_9uv8j5JazlDNe3B9S8NCkGWN5ykTKOD8jC65KlXCZi_N_-yW5CuHApqOVLBYkvA_eGkDq_M70rsNo2rYBCnvsmhD9-EAN9W6ISKOj39i2SY226bGmlfOup3uM6N0Oe3RDoOASMFPEGCK1zlPXzjA9unbs0DfBxMb11-TCmjbgzd9cks_np4_1S7J927yuH7cJiIzFpMoMgGCltIZVmGGlysIyUDyvjZRQG1XUhUFUFUMlFBeIkpc5KJuBUmwlluTulHv07mvAEPVUCaYK5vdZLbKi5LKQE5idQPAuBI9WH33TGT9qzvTsVx_07FfPfjUTevIrfgCkk3NN</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>Millot, Nicolas</creator><creator>Santini, Catherine C.</creator><creator>Lefebvre, Frédéric</creator><creator>Basset, Jean-Marie</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20040801</creationdate><title>Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation</title><author>Millot, Nicolas ; Santini, Catherine C. ; Lefebvre, Frédéric ; Basset, Jean-Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-b2acc3075fa0be2eb876f0c814da55cda86d6aee8b0e83813ee5174c8f2c88093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Millot, Nicolas</creatorcontrib><creatorcontrib>Santini, Catherine C.</creatorcontrib><creatorcontrib>Lefebvre, Frédéric</creatorcontrib><creatorcontrib>Basset, Jean-Marie</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Comptes rendus. Chimie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Millot, Nicolas</au><au>Santini, Catherine C.</au><au>Lefebvre, Frédéric</au><au>Basset, Jean-Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation</atitle><jtitle>Comptes rendus. Chimie</jtitle><date>2004-08-01</date><risdate>2004</risdate><volume>7</volume><issue>8-9</issue><spage>725</spage><epage>736</epage><pages>725-736</pages><issn>1878-1543</issn><issn>1631-0748</issn><eissn>1878-1543</eissn><abstract>The reaction of tris(pentafluorophenyl)borane, B(C6F5)3 with surface silanol (=Si-OH) of silica occurs only in the presence of a Bronsted base (diethylaniline, Et2NPh), which does not form a complex with B(C6F5)3, and affords selectively a well-defined ionic entity [=SiO-B(C6F5)3]-[HNEt2Ph]+. With a strong nucleophile base such as pyridine (C5H5N), the complex (C6F5)3B.NC5H5 is formed and is only physisorbed onto silica surface. Without a base, B(C6F5)3 does not react with (=Si-OH), and is only physisorbed. On the contrary, with any molecular compound ROH, B(C6F5)3 forms a stable complex (C6F5)3BO(H)R.</abstract><doi>10.1016/j.crci.2004.03.011</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1878-1543
ispartof Comptes rendus. Chimie, 2004-08, Vol.7 (8-9), p.725-736
issn 1878-1543
1631-0748
1878-1543
language eng
recordid cdi_proquest_miscellaneous_32671565
source Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals
title Surface organometallic chemistry: a route to well-defined boron heterogeneous co-catalyst for olefin polymerisation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T03%3A57%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Surface%20organometallic%20chemistry:%20a%20route%20to%20well-defined%20boron%20heterogeneous%20co-catalyst%20for%20olefin%20polymerisation&rft.jtitle=Comptes%20rendus.%20Chimie&rft.au=Millot,%20Nicolas&rft.date=2004-08-01&rft.volume=7&rft.issue=8-9&rft.spage=725&rft.epage=736&rft.pages=725-736&rft.issn=1878-1543&rft.eissn=1878-1543&rft_id=info:doi/10.1016/j.crci.2004.03.011&rft_dat=%3Cproquest_cross%3E32671565%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=32671565&rft_id=info:pmid/&rfr_iscdi=true