Cationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cations

dc.contributor.authorBaldwin, Steven M.deu
dc.contributor.authorBercaw, John E.deu
dc.contributor.authorHenling, Lawrence M.deu
dc.contributor.authorDay, Michael W.deu
dc.contributor.authorBrintzinger, Hans-Herbert
dc.date.accessioned2013-06-17T13:39:13Zdeu
dc.date.available2013-06-17T13:39:13Zdeu
dc.date.issued2011-02-16
dc.description.abstractThe ansa-zirconocene complex rac-Me2Si(1-indenyl)2ZrCl2 ((SBI)ZrCl2) reacts with diisobutylaluminum hydride and trityl tetrakis(perfluorophenyl)borate in hydrocarbon solutions to give the cation [(SBI)Zr(μ-H)3(AliBu2)2]+, the identity of which is derived from NMR data and supported by a crystallographic structure determination. Analogous reactions proceed with many other zirconocene dichloride complexes. [(SBI)Zr(μ-H)3(AliBu2)2]+ reacts reversibly with ClAliBu2 to give the dichloro-bridged cation [(SBI)Zr(μ-Cl)2AliBu2]+. Reaction with AlMe3 first leads to mixed-alkyl species [(SBI)Zr(μ-H)3(AlMexiBu2−x)2]+ by exchange of alkyl groups between aluminum centers. At higher AlMe3/Zr ratios, [(SBI)Zr(μ-Me)2AlMe2]+, a constituent of methylalumoxane-activated catalyst systems, is formed in an equilibrium, in which the hydride cation [(SBI)Zr(μ-H)3(AlR2)2]+ strongly predominates at comparable HAliBu2 and AlMe3 concentrations, thus implicating the presence of this hydride cation in olefin polymerization catalyst systems.eng
dc.description.versionpublished
dc.identifier.citationJournal of American Chemical Society ; 133 (2011), 6. - S. 1805-1813deu
dc.identifier.doi10.1021/ja1050428deu
dc.identifier.pmid21244016
dc.identifier.urihttp://kops.uni-konstanz.de/handle/123456789/23661
dc.language.isoengdeu
dc.legacy.dateIssued2013-06-17deu
dc.rightsterms-of-usedeu
dc.rights.urihttps://rightsstatements.org/page/InC/1.0/deu
dc.subject.ddc540deu
dc.titleCationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cationseng
dc.typeJOURNAL_ARTICLEdeu
dspace.entity.typePublication
kops.citation.bibtex
@article{Baldwin2011-02-16Catio-23661,
  year={2011},
  doi={10.1021/ja1050428},
  title={Cationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cations},
  number={6},
  volume={133},
  issn={0002-7863},
  journal={Journal of the American Chemical Society},
  pages={1805--1813},
  author={Baldwin, Steven M. and Bercaw, John E. and Henling, Lawrence M. and Day, Michael W. and Brintzinger, Hans-Herbert}
}
kops.citation.iso690BALDWIN, Steven M., John E. BERCAW, Lawrence M. HENLING, Michael W. DAY, Hans-Herbert BRINTZINGER, 2011. Cationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cations. In: Journal of the American Chemical Society. 2011, 133(6), pp. 1805-1813. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja1050428deu
kops.citation.iso690BALDWIN, Steven M., John E. BERCAW, Lawrence M. HENLING, Michael W. DAY, Hans-Herbert BRINTZINGER, 2011. Cationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cations. In: Journal of the American Chemical Society. 2011, 133(6), pp. 1805-1813. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja1050428eng
kops.citation.rdf
<rdf:RDF
    xmlns:dcterms="http://purl.org/dc/terms/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
    xmlns:bibo="http://purl.org/ontology/bibo/"
    xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
    xmlns:foaf="http://xmlns.com/foaf/0.1/"
    xmlns:void="http://rdfs.org/ns/void#"
    xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > 
  <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/23661">
    <dc:creator>Bercaw, John E.</dc:creator>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-06-17T13:39:13Z</dcterms:available>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2013-06-17T13:39:13Z</dc:date>
    <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/23661"/>
    <dcterms:title>Cationic alkylaluminum-complexed zirconocene hydrides : NMR-spectroscopic identification, crystallographic structure determination, and interconversion with other zirconocene cations</dcterms:title>
    <dc:creator>Brintzinger, Hans-Herbert</dc:creator>
    <dc:creator>Baldwin, Steven M.</dc:creator>
    <dc:language>eng</dc:language>
    <dc:creator>Henling, Lawrence M.</dc:creator>
    <dc:contributor>Henling, Lawrence M.</dc:contributor>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/29"/>
    <dc:contributor>Bercaw, John E.</dc:contributor>
    <dc:creator>Day, Michael W.</dc:creator>
    <dcterms:abstract xml:lang="eng">The ansa-zirconocene complex rac-Me&lt;sub&gt;2&lt;/sub&gt;Si(1-indenyl)&lt;sub&gt;2&lt;/sub&gt;ZrCl&lt;sub&gt;2&lt;/sub&gt; ((SBI)ZrCl&lt;sub&gt;2&lt;/sub&gt;) reacts with diisobutylaluminum hydride and trityl tetrakis(perfluorophenyl)borate in hydrocarbon solutions to give the cation [(SBI)Zr(μ-H)&lt;sub&gt;3&lt;/sub&gt;(AliBu&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt;, the identity of which is derived from NMR data and supported by a crystallographic structure determination. Analogous reactions proceed with many other zirconocene dichloride complexes. [(SBI)Zr(μ-H)&lt;sup&gt;3&lt;/sup&gt;(AliBu&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt; reacts reversibly with ClAliBu&lt;sub&gt;2&lt;/sub&gt; to give the dichloro-bridged cation [(SBI)Zr(μ-Cl)&lt;sub&gt;2&lt;/sub&gt;AliBu&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt;. Reaction with AlMe&lt;sub&gt;3&lt;/sub&gt; first leads to mixed-alkyl species [(SBI)Zr(μ-H)&lt;sub&gt;3&lt;/sub&gt;(AlMexiBu&lt;sub&gt;2&lt;/sub&gt;−x)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt; by exchange of alkyl groups between aluminum centers. At higher AlMe&lt;sub&gt;3&lt;/sub&gt;/Zr ratios, [(SBI)Zr(μ-Me)&lt;sub&gt;2&lt;/sub&gt;AlMe&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt;, a constituent of methylalumoxane-activated catalyst systems, is formed in an equilibrium, in which the hydride cation [(SBI)Zr(μ-H)&lt;sub&gt;3&lt;/sub&gt;(AlR&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;]&lt;sup&gt;+&lt;/sup&gt; strongly predominates at comparable HAliBu&lt;sub&gt;2&lt;/sub&gt; and AlMe&lt;sub&gt;3&lt;/sub&gt; concentrations, thus implicating the presence of this hydride cation in olefin polymerization catalyst systems.</dcterms:abstract>
    <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/>
    <dcterms:bibliographicCitation>Journal of American Chemical Society ; 133 (2011), 6. - S. 1805-1813</dcterms:bibliographicCitation>
    <dcterms:issued>2011-02-16</dcterms:issued>
    <dc:rights>terms-of-use</dc:rights>
    <dc:contributor>Day, Michael W.</dc:contributor>
    <dc:contributor>Baldwin, Steven M.</dc:contributor>
    <dc:contributor>Brintzinger, Hans-Herbert</dc:contributor>
  </rdf:Description>
</rdf:RDF>
kops.identifier.nbnurn:nbn:de:bsz:352-236619deu
kops.sourcefieldJournal of the American Chemical Society. 2011, <b>133</b>(6), pp. 1805-1813. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja1050428deu
kops.sourcefield.plainJournal of the American Chemical Society. 2011, 133(6), pp. 1805-1813. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja1050428deu
kops.sourcefield.plainJournal of the American Chemical Society. 2011, 133(6), pp. 1805-1813. ISSN 0002-7863. eISSN 1520-5126. Available under: doi: 10.1021/ja1050428eng
kops.submitter.emailoleg.kozlov@uni-konstanz.dedeu
relation.isAuthorOfPublicationab4c86da-5c57-43c2-83ff-89fe2e461f70
relation.isAuthorOfPublication.latestForDiscoveryab4c86da-5c57-43c2-83ff-89fe2e461f70
source.bibliographicInfo.fromPage1805
source.bibliographicInfo.issue6
source.bibliographicInfo.toPage1813
source.bibliographicInfo.volume133
source.identifier.eissn1520-5126
source.identifier.issn0002-7863
source.periodicalTitleJournal of the American Chemical Society

Dateien

Lizenzbündel

Gerade angezeigt 1 - 1 von 1
Vorschaubild nicht verfügbar
Name:
license.txt
Größe:
1.92 KB
Format:
Plain Text
Beschreibung:
license.txt
license.txtGröße: 1.92 KBDownloads: 0