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rdf:type
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Description
| - The diphenyl zirconocene [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(2)CH=CH(2)}ZrPh(2)] (2) was readily obtained from the corresponding zirconocene dichloride 1 and two equivalents of phenyllithium. Upon thermal treatment at 80 degrees C, complex 2 released benzene, with concomitant activation of the pendant double bond and formation of intramolecularly alpha-tethered zirconaindane [(eta(5)-C(5)H(5)){eta(5), eta(1), eta(1)-C(5)H(4)CMe(2)(CH(2))(2)CHCH(2)C(6)H(4)}Zr] (3). Both Zr-C sigma-bonds in 3 easily undergo nucleophilic reactions with two equivalents of HCl or one equivalent of Cl(2)PPh giving rise to zirconocene dichlorides with pendant phenyl group [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(4)Ph}ZrCl(2)] (4) or with 1-phenylphosphindolinyl moiety [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(2)cyclo-CHCH(2)C(6)H(4)P(Ph)}ZrCl(2)] (5), respectively.
- The diphenyl zirconocene [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(2)CH=CH(2)}ZrPh(2)] (2) was readily obtained from the corresponding zirconocene dichloride 1 and two equivalents of phenyllithium. Upon thermal treatment at 80 degrees C, complex 2 released benzene, with concomitant activation of the pendant double bond and formation of intramolecularly alpha-tethered zirconaindane [(eta(5)-C(5)H(5)){eta(5), eta(1), eta(1)-C(5)H(4)CMe(2)(CH(2))(2)CHCH(2)C(6)H(4)}Zr] (3). Both Zr-C sigma-bonds in 3 easily undergo nucleophilic reactions with two equivalents of HCl or one equivalent of Cl(2)PPh giving rise to zirconocene dichlorides with pendant phenyl group [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(4)Ph}ZrCl(2)] (4) or with 1-phenylphosphindolinyl moiety [(eta(5)-C(5)H(5)){eta(5)-C(5)H(4)CMe(2)(CH(2))(2)cyclo-CHCH(2)C(6)H(4)P(Ph)}ZrCl(2)] (5), respectively. (en)
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Title
| - Intramolecular activation of pendant alkenyl group as a tool for modification of the zirconocene framework
- Intramolecular activation of pendant alkenyl group as a tool for modification of the zirconocene framework (en)
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skos:prefLabel
| - Intramolecular activation of pendant alkenyl group as a tool for modification of the zirconocene framework
- Intramolecular activation of pendant alkenyl group as a tool for modification of the zirconocene framework (en)
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skos:notation
| - RIV/61388955:_____/11:00361646!RIV12-GA0-61388955
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http://linked.open...avai/predkladatel
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - P(GA203/09/1574), P(GPP207/10/P200), P(LC06070), Z(AV0Z40400503)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61388955:_____/11:00361646
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - ,etallocenes; zirconium; benzyne complexes (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Pinkas, Jiří
- Horáček, Michal
- Kubišta, Jiří
- Lamač, Martin
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http://linked.open...ain/vavai/riv/wos
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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http://bibframe.org/vocab/doi
| - 10.1016/j.ica.2011.03.061
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is http://linked.open...avai/riv/vysledek
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