Počet záznamů: 1
Ferra- and ruthenatricarbollides CpFeC3B8H11 and Cp*RuC3B8H11
- 1.0028598 - ÚACH 2006 RIV US eng J - Článek v odborném periodiku
Perelakin, D.S. - Holub, Josef - Golovanov, D.G. - Lyssenko, KA. - Petrovskii, PV. - Štíbr, Bohumil - Kudinov, AR.
Ferra- and ruthenatricarbollides CpFeC3B8H11 and Cp*RuC3B8H11.
[Ferra a ruthenatrikarbollidy CpFeC3B8H11 a Cp*RuC3B8H11.]
Organometallics. Roč. 24, č. 18 (2005), s. 4387-4392. ISSN 0276-7333. E-ISSN 1520-6041
Grant CEP: GA ČR GA203/05/2646
Grant ostatní: INTAS(RU) N04-83-3848
Klíčová slova: magnetic-resonance spectroscopy * metallatricarbadecaboranyl analogs * structural characterizations
Kód oboru RIV: CA - Anorganická chemie
Impakt faktor: 3.473, rok: 2005
The room-temperature photochemical reaction of the tricarbollide anion [nido-7,8,9-C3B8H11](-) (1a) with [CpFe(C6H6)](+) proceeds without cluster rearrangement to form the 12-vertex closo-ferratricarbollide 1-Cp-1,2,3,4-FeC3B8H11 (2a, the metal atom is assigned number 1). 2a rearranges to the isomeric complex 1-Cp-1,2,3,5-FeC3B8H11 (2b) at 110 degrees C and further to 1-Cp-1,2,4,10-FeC3B8H11 (2c) at 165 degrees C. The reaction of 1a with [Cp*RuCl](4) is accompanied by polyhedral rearrangement giving 1-Cp*-1,2,3,5-RuC3B8H11 (3b). The constitution of the compounds prepared was determined by multinuclear NMR spectroscopy and mass spectrometry. The structures of 2a, 2b, and 3c were established by X-ray diffraction.
Ferra a ruthenatrikarbollidy CpFeC3B8H11 a Cp*RuC3B8H11byly připraveny insercí fragmentů CpFe+ a CpRu+ do skeletu trikarbaboranového aniontu [nido-7,8,9- C3B8H11]- . Je popsán i vznik několika isomerů lišících se polohou uhlíkových atomů ve skeletu.
Trvalý link: http://hdl.handle.net/11104/0118523
Počet záznamů: 1