[TiCl3(η5-C5(CH3)4(Si(CH3)2CH2CHCHCH2Si(CH3)2Cl)] | 443889-18-7

• 英文名称: [TiCl3(η5-C5(CH3)4(Si(CH3)2CH2CHCHCH2Si(CH3)2Cl)]
• CAS: 443889-18-7
• 化学式: C₁₇H₃₀Cl₄Si₂Ti
• 分子量: 480.288
• InChiKey: KZEQRJYYWUQWIS-UHFFFAOYSA-K

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为产物：
  描述：

  盐酸 、 ansa-[Ti(III)(η3:η5:η5-C5(CH3)4(Si(CH3)2CH2CHCHCHSi(CH3)2C5(CH3)4)] 以 正己烷 为溶剂， 以85%的产率得到ansa-[TiCl(η5:η5-C5(CH3)4(Si(CH3)2CH2CHCHCH2Si(CH3)2C5(CH3)4)]
  参考文献：
  名称：

  Reduction-Induced Cyclization and Redox Reactions of Fully Methylated Titanocene Dichlorides Bearing Pendant Alkenyldimethylsilyl Groups, [TiCl₂{η⁵-C₅Me₄(SiMe₂R)}₂] (R = Vinyl and Allyl)

  摘要：

  Reduction of titanocene dichlorides bearing (omega-alkenyl)dimethylsilyl substituents [TiCl2{eta(5)-C5Me5(SiMe2R)}(2)], where R = CH=CH2 (3) and CH2CH=CH2 (4), affords highly reactive Ti(II) intermediates, which immediately undergo intramolecular reactions with the pendant double bonds in a way dependent on the length of the alkenyl chain. The reduction of 4 with magnesium at 60 degreesC affords cleanly the cyclopentadienyl-ring-tethered titanacyclopentane, [Ti(eta(1):eta(1):eta(5):eta(5)-C5Me4SiMe2CH(Ti)CH(Me)CH(Me)CH(Ti)SiMe2C5Me4](5), which can be opened by HCl to an ansa-titanocene dichloride with a six-membered saturated bridging chain, [TiCl2-{eta:(5)eta(5)-C5Me4SiMe2CH2CH(Me)CH(Me)CH2SiMe2C5Me4)(2)}] (6). An analogous reaction of 3 can be accomplished at low temperatures and only to some extent, providing a mixture of titanacyclopentane complex [Ti(eta(1):eta(1):eta(5):eta(5)-C5Me4SiMe2CH(Ti)CH2CH2CH(Ti)SiMe2C5Me4] (10) and the fluxional eta(2)-alkene complex [Ti(eta(5)-C5Me4SiMe2CH=CH2)(eta(2):eta(5)-C5Me4SiMe2CH=CH2)1 (9). At 60 degreesC, the reduction of 3 yields a mixture of ansa-eta(2)-alkene complex [Ti{eta(2):eta(5)-C5Me4SiMe2CH2CH=CHCH2SiMe2C5Me4}] (7) and the product of a hydrogen loss, the doubly tethered; paramagnetic eta(3)-allyl Ti(III) complex [Ti{eta(3):eta(5):eta(5)-C5Me4SiMe2CHCH=CHCH2SiMe2C5Me4}] (8). When the reduction of 3 with magnesium is carried out in the presence of bis(trimethylsilyl)ethyne as the proton acceptor, 8 is obtained as the sole isolated product. Complex 8 reacts with protic reagents such as HCl and methanol under protonation/decomplexation of the allyl system to give the d(1) paramagnetic complexes [TiX{eta:(5)eta(5)-C5Me4SiMe2CH2CH=CHCH2SiMe2C5Me4}] (X = Cl, 12; OMe, 13). Oxidation of 8 with PbCl2 yields eta(1)-alkenyl complex [TiCl{eta(1):eta(5):eta5-C5Me4SiMe2CH(Ti)CH=CHCH2SiMe2C5Me4}] (11). A similar oxidation of 12 to ansa-titanocene dichloride [TiCl2{eta:(5)eta-C5Me4SiMe2CHCH=CHCH2SiMe2C5Me4}] (14) containing a symmetrical unsaturated bridging chain requires a stronger oxidizing agent, AgCl. Compounds 5, 7, 8, and 10-14 have been characterized by X-ray crystallography.

  DOI：

  10.1021/om020150d