About: Synthesis and rearrangements of aminosubstituted ferra- and ruthenatricarbaboranes     Goto   Sponge   NotDistinct   Permalink

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  • A room-temperature reaction between the [7-(BuNH)-Bu-t-nido-7,8,9-C3B8H10](-) anion (1a) and [Cp*RUCl](4) leads to the ruthenatricarbollide [1-Cp*-12-(BuNH)-Bu-t-1,2,4,12-RUC3B8H10] (2) (yield 85%). Analogously, the room-temperature photochemical reaction of la with [CpFe(C6H6)]PF6 gives the previously reported iron complex [1-Cp-12-(BuNH)-Bu-t-1,2,4,12-FeC3B8H10] (3) (yield 82%). Both reactions are associated with extensive polyhedral rearrangement, which occurs under very mild conditions and brings the carbon atoms to positions of maximum separation within the framework. Density functional theory calculations at the B3LYP/SDD level were used to estimate relative stabilities of these metallacarborane isomers. The structure of 2 was established by an X-ray diffraction study, and the constitution of all compounds was determined unambiguously by multinuclear NMR spectroscopy, mass spectrometry, and elemental analyses.
  • A room-temperature reaction between the [7-(BuNH)-Bu-t-nido-7,8,9-C3B8H10](-) anion (1a) and [Cp*RUCl](4) leads to the ruthenatricarbollide [1-Cp*-12-(BuNH)-Bu-t-1,2,4,12-RUC3B8H10] (2) (yield 85%). Analogously, the room-temperature photochemical reaction of la with [CpFe(C6H6)]PF6 gives the previously reported iron complex [1-Cp-12-(BuNH)-Bu-t-1,2,4,12-FeC3B8H10] (3) (yield 82%). Both reactions are associated with extensive polyhedral rearrangement, which occurs under very mild conditions and brings the carbon atoms to positions of maximum separation within the framework. Density functional theory calculations at the B3LYP/SDD level were used to estimate relative stabilities of these metallacarborane isomers. The structure of 2 was established by an X-ray diffraction study, and the constitution of all compounds was determined unambiguously by multinuclear NMR spectroscopy, mass spectrometry, and elemental analyses. (en)
  • Jsou popsány výhodné reakce vedoucí k 12- a 11-vrcholovým aminosubstituovaným ruthena- a ferratrikarbaboranovým komplexům a na základě dsd mechanismu jsou vysvětleny jevy spojené s přesmykem trikarbaboranového klastru. (cs)
Title
  • Synthesis and rearrangements of aminosubstituted ferra- and ruthenatricarbaboranes
  • Synthesis and rearrangements of aminosubstituted ferra- and ruthenatricarbaboranes (en)
  • Syntéza a přesmyky aminosubstituovaných ferra- a ruthenatrikarbaboranů (cs)
skos:prefLabel
  • Synthesis and rearrangements of aminosubstituted ferra- and ruthenatricarbaboranes
  • Synthesis and rearrangements of aminosubstituted ferra- and ruthenatricarbaboranes (en)
  • Syntéza a přesmyky aminosubstituovaných ferra- a ruthenatrikarbaboranů (cs)
skos:notation
  • RIV/61388980:_____/05:00029900!RIV06-AV0-61388980
http://linked.open.../vavai/riv/strany
  • 1655;1659
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA203/05/2646), Z(AV0Z40320502)
http://linked.open...iv/cisloPeriodika
  • 6
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
  • 545723
http://linked.open...ai/riv/idVysledku
  • RIV/61388980:_____/05:00029900
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • magnetic-resonance spectrometry (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [9746DCA5CAC9]
http://linked.open...i/riv/nazevZdroje
  • Inorganic Chemistry
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
  • 44
http://linked.open...iv/tvurceVysledku
  • Grüner, Bohumír
  • Holub, Josef
  • Štíbr, Bohumil
  • Kudinov, A. R.
  • Petrovskii, P. V.
  • Perelakin, D. S.
  • Golovanov, D. G.
  • Lyssenko, K. A.
http://linked.open...n/vavai/riv/zamer
issn
  • 0020-1669
number of pages
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