Loading…

Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts

The role of the ketimide ligand geometry in Ti half‐sandwich complexes and the consequent effects in olefin polymerization catalysis (ethylene, styrene, 1‐hexene polymerization, and ethylene/1‐hexene copolymerization) were investigated under various conditions. [CpTiCl2(N=CtBu2)] (1; Cp=η5‐cyclopent...

Full description

Saved in:
Bibliographic Details
Published in:ChemCatChem 2017-08, Vol.9 (16), p.3160-3172
Main Authors: Varga, Vojtech, Večeřa, Miloš, Gyepes, Róbert, Pinkas, Jiří, Horáček, Michal, Merna, Jan, Lamač, Martin
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53
cites cdi_FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53
container_end_page 3172
container_issue 16
container_start_page 3160
container_title ChemCatChem
container_volume 9
creator Varga, Vojtech
Večeřa, Miloš
Gyepes, Róbert
Pinkas, Jiří
Horáček, Michal
Merna, Jan
Lamač, Martin
description The role of the ketimide ligand geometry in Ti half‐sandwich complexes and the consequent effects in olefin polymerization catalysis (ethylene, styrene, 1‐hexene polymerization, and ethylene/1‐hexene copolymerization) were investigated under various conditions. [CpTiCl2(N=CtBu2)] (1; Cp=η5‐cyclopentadienyl) was used as a reference compound for comparison with the recently described complex [{η5‐C5H4CMe2CMe2C(tBu)=N‐κN}TiCl2] (2 a) and a new derivative that has a longer linker between Cp and the ketimide, [{η5‐C5H4CH2CH2CMe2C(tBu)=N‐κN}TiCl2] (9). The presence of a distorted intramolecularly tethered ketimide moiety reduces the polymerization activity significantly in systems that contain Al‐based cocatalysts (methylaluminoxane, triisobutylaluminum). However, in Al‐free systems both types of compounds provided active polymerization catalysts. Notably, the recently reported activation system Et3SiH/B(C6F5)3 was for the first time demonstrated to activate Ti complexes for ethylene and 1‐hexene (co)polymerization catalysis by hydride transfer. Unleashed activity: Effects of ketimide ligand distortion that result from its intramolecular tethering in Ti half‐sandwich complexes are investigated with respect to the olefin polymerization activity. The role of the cocatalyst on the catalytic performance is decisive. Huge differences between the studied complexes are found if Al‐based cocatalysts are used, whereas the activating system in which hydrosilane and B(C6F5)3 are used performs well for both types.
doi_str_mv 10.1002/cctc.201700498
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1931121690</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1931121690</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53</originalsourceid><addsrcrecordid>eNqFkMFOwzAMhisEEmNw5RyJc0eSrk1zRNVgiElDYpwrL3W2jDYdTSZUuPAIPCNPQquhceRkW__32_IfBJeMjhil_Fopr0acMkHpWKZHwYCliQijVMrjQ5_S0-DMuQ2liYxEPAg-Jlqj8o7Umvg1kpmxL8au-jFrVVlv0XooDNq2JGAL8oDeVKbowVU3O2IsWRgP1uwqMoVSf39-PXXCm1FrMi9Rd_pjXbYVNuYdvKktycBD2TrvzoMTDaXDi986DJ5vJ4tsGs7md_fZzSxUERNp2D0TJ0vQqUwgQY4UgI4ZasWBx4iR4Cgk8ELwRClAQcciFsCpiLRaoo6jYXC137tt6tcdOp9v6l1ju5M5kxFjnCWSdtRoT6mmdq5BnW8bU0HT5ozmfcB5H3B-CLgzyL3hzZTY_kPnWbbI_rw_BTuCdA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1931121690</pqid></control><display><type>article</type><title>Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Varga, Vojtech ; Večeřa, Miloš ; Gyepes, Róbert ; Pinkas, Jiří ; Horáček, Michal ; Merna, Jan ; Lamač, Martin</creator><creatorcontrib>Varga, Vojtech ; Večeřa, Miloš ; Gyepes, Róbert ; Pinkas, Jiří ; Horáček, Michal ; Merna, Jan ; Lamač, Martin</creatorcontrib><description>The role of the ketimide ligand geometry in Ti half‐sandwich complexes and the consequent effects in olefin polymerization catalysis (ethylene, styrene, 1‐hexene polymerization, and ethylene/1‐hexene copolymerization) were investigated under various conditions. [CpTiCl2(N=CtBu2)] (1; Cp=η5‐cyclopentadienyl) was used as a reference compound for comparison with the recently described complex [{η5‐C5H4CMe2CMe2C(tBu)=N‐κN}TiCl2] (2 a) and a new derivative that has a longer linker between Cp and the ketimide, [{η5‐C5H4CH2CH2CMe2C(tBu)=N‐κN}TiCl2] (9). The presence of a distorted intramolecularly tethered ketimide moiety reduces the polymerization activity significantly in systems that contain Al‐based cocatalysts (methylaluminoxane, triisobutylaluminum). However, in Al‐free systems both types of compounds provided active polymerization catalysts. Notably, the recently reported activation system Et3SiH/B(C6F5)3 was for the first time demonstrated to activate Ti complexes for ethylene and 1‐hexene (co)polymerization catalysis by hydride transfer. Unleashed activity: Effects of ketimide ligand distortion that result from its intramolecular tethering in Ti half‐sandwich complexes are investigated with respect to the olefin polymerization activity. The role of the cocatalyst on the catalytic performance is decisive. Huge differences between the studied complexes are found if Al‐based cocatalysts are used, whereas the activating system in which hydrosilane and B(C6F5)3 are used performs well for both types.</description><identifier>ISSN: 1867-3880</identifier><identifier>EISSN: 1867-3899</identifier><identifier>DOI: 10.1002/cctc.201700498</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Catalysis ; Catalysts ; Chemical industry ; Copolymerization ; cyclopentadienyl ligands ; Ethylene ; ligand effects ; Polymerization ; sandwich complexes ; Titanium</subject><ispartof>ChemCatChem, 2017-08, Vol.9 (16), p.3160-3172</ispartof><rights>2017 Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2017 Wiley-VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53</citedby><cites>FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53</cites><orcidid>0000-0002-9499-9526 ; 0000-0002-6508-0844 ; 0000-0002-2908-0425</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Varga, Vojtech</creatorcontrib><creatorcontrib>Večeřa, Miloš</creatorcontrib><creatorcontrib>Gyepes, Róbert</creatorcontrib><creatorcontrib>Pinkas, Jiří</creatorcontrib><creatorcontrib>Horáček, Michal</creatorcontrib><creatorcontrib>Merna, Jan</creatorcontrib><creatorcontrib>Lamač, Martin</creatorcontrib><title>Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts</title><title>ChemCatChem</title><description>The role of the ketimide ligand geometry in Ti half‐sandwich complexes and the consequent effects in olefin polymerization catalysis (ethylene, styrene, 1‐hexene polymerization, and ethylene/1‐hexene copolymerization) were investigated under various conditions. [CpTiCl2(N=CtBu2)] (1; Cp=η5‐cyclopentadienyl) was used as a reference compound for comparison with the recently described complex [{η5‐C5H4CMe2CMe2C(tBu)=N‐κN}TiCl2] (2 a) and a new derivative that has a longer linker between Cp and the ketimide, [{η5‐C5H4CH2CH2CMe2C(tBu)=N‐κN}TiCl2] (9). The presence of a distorted intramolecularly tethered ketimide moiety reduces the polymerization activity significantly in systems that contain Al‐based cocatalysts (methylaluminoxane, triisobutylaluminum). However, in Al‐free systems both types of compounds provided active polymerization catalysts. Notably, the recently reported activation system Et3SiH/B(C6F5)3 was for the first time demonstrated to activate Ti complexes for ethylene and 1‐hexene (co)polymerization catalysis by hydride transfer. Unleashed activity: Effects of ketimide ligand distortion that result from its intramolecular tethering in Ti half‐sandwich complexes are investigated with respect to the olefin polymerization activity. The role of the cocatalyst on the catalytic performance is decisive. Huge differences between the studied complexes are found if Al‐based cocatalysts are used, whereas the activating system in which hydrosilane and B(C6F5)3 are used performs well for both types.</description><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical industry</subject><subject>Copolymerization</subject><subject>cyclopentadienyl ligands</subject><subject>Ethylene</subject><subject>ligand effects</subject><subject>Polymerization</subject><subject>sandwich complexes</subject><subject>Titanium</subject><issn>1867-3880</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkMFOwzAMhisEEmNw5RyJc0eSrk1zRNVgiElDYpwrL3W2jDYdTSZUuPAIPCNPQquhceRkW__32_IfBJeMjhil_Fopr0acMkHpWKZHwYCliQijVMrjQ5_S0-DMuQ2liYxEPAg-Jlqj8o7Umvg1kpmxL8au-jFrVVlv0XooDNq2JGAL8oDeVKbowVU3O2IsWRgP1uwqMoVSf39-PXXCm1FrMi9Rd_pjXbYVNuYdvKktycBD2TrvzoMTDaXDi986DJ5vJ4tsGs7md_fZzSxUERNp2D0TJ0vQqUwgQY4UgI4ZasWBx4iR4Cgk8ELwRClAQcciFsCpiLRaoo6jYXC137tt6tcdOp9v6l1ju5M5kxFjnCWSdtRoT6mmdq5BnW8bU0HT5ozmfcB5H3B-CLgzyL3hzZTY_kPnWbbI_rw_BTuCdA</recordid><startdate>20170823</startdate><enddate>20170823</enddate><creator>Varga, Vojtech</creator><creator>Večeřa, Miloš</creator><creator>Gyepes, Róbert</creator><creator>Pinkas, Jiří</creator><creator>Horáček, Michal</creator><creator>Merna, Jan</creator><creator>Lamač, Martin</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-9499-9526</orcidid><orcidid>https://orcid.org/0000-0002-6508-0844</orcidid><orcidid>https://orcid.org/0000-0002-2908-0425</orcidid></search><sort><creationdate>20170823</creationdate><title>Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts</title><author>Varga, Vojtech ; Večeřa, Miloš ; Gyepes, Róbert ; Pinkas, Jiří ; Horáček, Michal ; Merna, Jan ; Lamač, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical industry</topic><topic>Copolymerization</topic><topic>cyclopentadienyl ligands</topic><topic>Ethylene</topic><topic>ligand effects</topic><topic>Polymerization</topic><topic>sandwich complexes</topic><topic>Titanium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Varga, Vojtech</creatorcontrib><creatorcontrib>Večeřa, Miloš</creatorcontrib><creatorcontrib>Gyepes, Róbert</creatorcontrib><creatorcontrib>Pinkas, Jiří</creatorcontrib><creatorcontrib>Horáček, Michal</creatorcontrib><creatorcontrib>Merna, Jan</creatorcontrib><creatorcontrib>Lamač, Martin</creatorcontrib><collection>CrossRef</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Varga, Vojtech</au><au>Večeřa, Miloš</au><au>Gyepes, Róbert</au><au>Pinkas, Jiří</au><au>Horáček, Michal</au><au>Merna, Jan</au><au>Lamač, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts</atitle><jtitle>ChemCatChem</jtitle><date>2017-08-23</date><risdate>2017</risdate><volume>9</volume><issue>16</issue><spage>3160</spage><epage>3172</epage><pages>3160-3172</pages><issn>1867-3880</issn><eissn>1867-3899</eissn><abstract>The role of the ketimide ligand geometry in Ti half‐sandwich complexes and the consequent effects in olefin polymerization catalysis (ethylene, styrene, 1‐hexene polymerization, and ethylene/1‐hexene copolymerization) were investigated under various conditions. [CpTiCl2(N=CtBu2)] (1; Cp=η5‐cyclopentadienyl) was used as a reference compound for comparison with the recently described complex [{η5‐C5H4CMe2CMe2C(tBu)=N‐κN}TiCl2] (2 a) and a new derivative that has a longer linker between Cp and the ketimide, [{η5‐C5H4CH2CH2CMe2C(tBu)=N‐κN}TiCl2] (9). The presence of a distorted intramolecularly tethered ketimide moiety reduces the polymerization activity significantly in systems that contain Al‐based cocatalysts (methylaluminoxane, triisobutylaluminum). However, in Al‐free systems both types of compounds provided active polymerization catalysts. Notably, the recently reported activation system Et3SiH/B(C6F5)3 was for the first time demonstrated to activate Ti complexes for ethylene and 1‐hexene (co)polymerization catalysis by hydride transfer. Unleashed activity: Effects of ketimide ligand distortion that result from its intramolecular tethering in Ti half‐sandwich complexes are investigated with respect to the olefin polymerization activity. The role of the cocatalyst on the catalytic performance is decisive. Huge differences between the studied complexes are found if Al‐based cocatalysts are used, whereas the activating system in which hydrosilane and B(C6F5)3 are used performs well for both types.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cctc.201700498</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-9499-9526</orcidid><orcidid>https://orcid.org/0000-0002-6508-0844</orcidid><orcidid>https://orcid.org/0000-0002-2908-0425</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1867-3880
ispartof ChemCatChem, 2017-08, Vol.9 (16), p.3160-3172
issn 1867-3880
1867-3899
language eng
recordid cdi_proquest_journals_1931121690
source Wiley-Blackwell Read & Publish Collection
subjects Catalysis
Catalysts
Chemical industry
Copolymerization
cyclopentadienyl ligands
Ethylene
ligand effects
Polymerization
sandwich complexes
Titanium
title Effects of the Linking of Cyclopentadienyl and Ketimide Ligands in Titanium Half‐Sandwich Olefin Polymerization Catalysts
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T00%3A35%3A39IST&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=Effects%20of%20the%20Linking%20of%20Cyclopentadienyl%20and%20Ketimide%20Ligands%20in%20Titanium%20Half%E2%80%90Sandwich%20Olefin%20Polymerization%20Catalysts&rft.jtitle=ChemCatChem&rft.au=Varga,%20Vojtech&rft.date=2017-08-23&rft.volume=9&rft.issue=16&rft.spage=3160&rft.epage=3172&rft.pages=3160-3172&rft.issn=1867-3880&rft.eissn=1867-3899&rft_id=info:doi/10.1002/cctc.201700498&rft_dat=%3Cproquest_cross%3E1931121690%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3178-49856baf896a6e2e0aa041efc2a25ee372e79a2d726ccae704757a2073fcbef53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1931121690&rft_id=info:pmid/&rfr_iscdi=true