Počet záznamů: 1  

Displacement of ethene from the decamethyltitanocene-ethene complex with internal alkynes, substituent-dependent alkyne-to-allene rearrangement, and the electronic transition relevant to the back-bonding interaction

  1. 1.
    SYSNO ASEP0443290
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevDisplacement of ethene from the decamethyltitanocene-ethene complex with internal alkynes, substituent-dependent alkyne-to-allene rearrangement, and the electronic transition relevant to the back-bonding interaction
    Tvůrce(i) Pinkas, Jiří (UFCH-W) RID, ORCID
    Gyepes, R. (SK)
    Císařová, I. (CZ)
    Kubišta, Jiří (UFCH-W) RID, ORCID
    Horáček, Michal (UFCH-W) RID, ORCID
    Mach, Karel (UFCH-W) ORCID, RID
    Zdroj.dok.Dalton Transactions. - : Royal Society of Chemistry - ISSN 1477-9226
    Roč. 44, č. 16 (2015), s. 7276-7291
    Poč.str.16 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovatitanocene-ethene complex ; tail dimerization ; molecular structure
    Vědní obor RIVCF - Fyzikální chemie a teoretická chemie
    CEPGAP207/12/2368 GA ČR - Grantová agentura ČR
    Institucionální podporaUFCH-W - RVO:61388955
    UT WOS000352784000026
    EID SCOPUS84927750171
    DOI10.1039/C5DT00351B
    AnotaceThe titanocene-ethene complex [Ti(II)(η2-C2H4)(η5-C5Me5)2] (1) with simple internal alkynes R1C[triple bond, length as m-dash]CR2 gives complexes [Ti(II)(η2-R1C[triple bond, length as m-dash]CR2)(η5-C5Me5)2] {R1, R2: Ph, Ph (3), Ph, Me (4), Me, SiMe3 (5), Ph, SiMe3 (6), t-Bu, SiMe3 (7), and SiMe3, SiMe3 (8). In contrast, alkynes with R1 = Me and R2 = t-Bu or i-Pr afford allene complexes [Ti(II)(η2-CH2[double bond, length as m-dash]C[double bond, length as m-dash]CHR2)(η5-C5Me5)2] (11) and (12), whereas for R2 = Et a mixture of alkyne complex (13A) and minor allene (13) is obtained. Crystal structures of 4, 6, 7 and 11 have been determined; the latter structure proved the back-bonding interaction of the allene terminal double bond. Only the synthesis of 8 from 1 was inefficient because the equilibrium constant for the reaction [1] + [Me3SiC[triple bond, length as m-dash]CSiMe3] [right left harpoons] [8] + [C2H4] approached 1. Compound 9 (R1, R2: Me), not obtainable from 1, together with compounds 3–6 and 10 (R1, R2: Et) were also prepared by alkyne exchange with 8, however this reaction did not take place in attempts to obtain 7. Compounds 1 and 3–9 display the longest-wavelength electronic absorption band in the range 670–940 nm due to the HOMO → LUMO transition. The assignment of the first excitation to be of predominantly a b2 → a1 transition was confirmed by DFT calculations. The calculated first excitation energies for 3–9 followed the order of hypsochromic shifts of the absorption band relative to 8 that were induced by acetylene substituents: Me > Ph > SiMe3. Computational results have also affirmed the back-bonding nature in the alkyne-to-metal coordination.
    PracovištěÚstav fyzikální chemie J.Heyrovského
    KontaktMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Rok sběru2016
Počet záznamů: 1  

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