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Linear Dimerization of Terminal Alkynes by Bis( tetramethylphenylcyclopentadienyl) Titanium-Magnesium Hydride and Acetylide Complexes

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    SYSNO ASEP0181733
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleLinear Dimerization of Terminal Alkynes by Bis( tetramethylphenylcyclopentadienyl) Titanium-Magnesium Hydride and Acetylide Complexes
    Author(s) Mach, Karel (UFCH-W) ORCID, RID
    Gyepes, R. (CZ)
    Horáček, Michal (UFCH-W) RID, ORCID
    Petrusová, Lidmila (UFCH-W)
    Kubišta, Jiří (UFCH-W) RID, ORCID
    Source TitleCollection of Czechoslovak Chemical Communications. - : Ústav organické chemie a biochemie AV ČR, v. v. i. - ISSN 0010-0765
    Roč. 68, č. 10 (2003), s. 1877-1896
    Number of pages20 s.
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordstitanium ; alkynes ; hydrides
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA203/02/0774 GA ČR - Czech Science Foundation (CSF)
    GA203/02/0436 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z4040901 - UFCH-W
    AnnotationNew phenyltetramethylcyclopentadienyl trinuclear titanocene hydride - magnesium hydride complexes [{Ti(.eta.5-C5Me4R)2(.mu.-H)2}2Mg], where R = Ph (1) or 4-fluorophenyl (FPh, 2), the dinuclear [Ti(.eta.5-C5Me4Ph)[.eta.5:.eta.1{Ti:Mg}-C5Me4(o-C6H4)](.mu.-H)2Mg(THF)2] (3) and [Ti(.eta.5-C5Me4Ph)2(.mu.-H)2MgC(Me)=CHMe] (4) complexes, and the [{Ti(.eta.5-C5Me4Ph)2(.eta.1-CCSiMe3)2}-{MgCl(THF)}+] (5) tweezer complex initiated the dimerization of (trimethylsilyl)ethyne (TMSE) or 1-hexyne (HXNY) to exclusively head-to-tail dimers at 60 C with the turnover number ranging 300 - 500 mol of the alkyne per one mol of the Ti complex. In contrast, all of them were inactive in the dimerization of tert.-butylethyne (TBUE). Monitoring of reactions of the 1 - 5 complexes with the alkynes by electron spin resonance (ESR) method revealed a decay of the initial complexes 1 - 5 in the dimerizing systems with TMSE and HXYN or a conversion of complexes 3,4 and 5.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2004

Number of the records: 1  

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