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  • 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)
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)
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)
skos:notation
  • RIV/61388955:_____/11:00361646!RIV12-GA0-61388955
http://linked.open...avai/predkladatel
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA203/09/1574), P(GPP207/10/P200), P(LC06070), Z(AV0Z40400503)
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 205560
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/11:00361646
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • ,etallocenes; zirconium; benzyne complexes (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [06E766BAE97B]
http://linked.open...i/riv/nazevZdroje
  • Inorganica chimica acta
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 373
http://linked.open...iv/tvurceVysledku
  • Pinkas, Jiří
  • Horáček, Michal
  • Kubišta, Jiří
  • Lamač, Martin
http://linked.open...ain/vavai/riv/wos
  • 000291244600043
http://linked.open...n/vavai/riv/zamer
issn
  • 0020-1693
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.ica.2011.03.061
is http://linked.open...avai/riv/vysledek of
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