Počet záznamů: 1  

Chromocene-Cyclopentadienyltitanium Trichloride Ion Pairs and Their Rearrangement to Titanocene Chloride-Cyclopentadienylchromium Dichlorides Ethylene Polymerization Tests

  1. 1.
    SYSNO ASEP0492078
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevChromocene-Cyclopentadienyltitanium Trichloride Ion Pairs and Their Rearrangement to Titanocene Chloride-Cyclopentadienylchromium Dichlorides Ethylene Polymerization Tests
    Tvůrce(i) Varga, Vojtěch (UFCH-W) RID
    Pinkas, Jiří (UFCH-W) RID, ORCID
    Císařová, I. (CZ)
    Kubišta, Jiří (UFCH-W) RID, ORCID
    Horáček, Michal (UFCH-W) RID, ORCID
    Mach, Karel (UFCH-W) ORCID, RID
    Gyepes, Robert (UFCH-W) RID, ORCID
    Zdroj.dok.European Journal of Inorganic Chemistry. - : Wiley - ISSN 1434-1948
    Roč. 2018, č. 23 (2018), s. 2637-2647
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.DE - Německo
    Klíč. slovatransition-metal-complexes ; arene titanium catalysts ; olefin polymerization ; molecular-structures ; acetylene complexes ; chromium catalysts ; trimerization
    Vědní obor RIVCF - Fyzikální chemie a teoretická chemie
    Obor OECDPhysical chemistry
    CEPGA17-13778S GA ČR - Grantová agentura ČR
    Institucionální podporaUFCH-W - RVO:61388955
    UT WOS000435936400004
    EID SCOPUS85048853813
    DOI10.1002/ejic.201800202
    AnotaceReactions of chromocene [CrCp2] (Cp = (5)-C5H5) with cyclopentadienyltitanium trichlorides [Ti((5)-C5H5-nMen)Cl-3] (n = 0-5) and [Ti(C5Me4Et)TiCl3] in toluene resulted in precipitation of ion pairs of [CrCp2](+)[Ti((5)-C5H5-nMen)Cl-3](-) (1-6) and [CrCp2](+)[Ti((5)-C5Me4Et)Cl-3](-) (7). Heating their toluene solutions to 100 degrees C yielded the titanocene chloride cyclopentadienylchromium dichloride complexes with the metals linked by bridging chloride ligands. For n = 0-3, the purple-violet complexes [CpCpTi(mu-Cl)(2)Cr(Cp)Cl] (Cp cyclopentadienyl ligand of the titanium component) (8-11) were stable at 100 degrees C, and the single-crystal structure of [Cp2Ti(mu-Cl)(2)Cr(Cp)Cl] (8) was determined. The bridging complexes of the same type for n = 4, 5 and the C5Me4Et ligand (12-14) were contaminated with titanocene dichlorides containing mixed auxiliary ligands [TiCp(C5HMe4)Cl-2] (15), [TiCp(C5Me5)Cl-2] (16), and [TiCp(C5Me4Et)Cl-2] (17), respectively. In addition, they contained the hitherto unknown (CpCrCl)(n) (18). Heating of 12-14 to 100 degrees C resulted in their decomposition to 15-17, accompanied with 18 in all cases. The molecular and electronic properties of 1, 4, 5, 8 and both isomers of 13 were investigated by DFT. Complexes 8, 9, and 11 activated with MMAO polymerized ethylene in toluene to very high molecular weights polyethylene (M-n 500 kgmol(-1)). Upon activation with B(C6F5)(3)/Et3SiH in dichloromethane they produced M-n = 9-23 kgmol(-1). The titanium species was the catalytically dominant one in both cases.
    PracovištěÚstav fyzikální chemie J.Heyrovského
    KontaktMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Rok sběru2019
Počet záznamů: 1  

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