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Fischer mono- and biscarbene complexes of tungsten with mono- and dimeric heteroaromatic substituents

机译:带有单和二聚杂芳族取代基的钨的Fischer单和双卡宾配合物

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An electrochemical study of a series of mono- and biscarbene complexes of tungsten pentacarbonyl with mono- and dimeric heteroarene substituents are reported and compared in CH3CN and DCM. Results revealed that the order of oxidation (reduction) depends largely on the aryl substituent attached to the carbene carbon (2-thienyl, 2-fulyl or 2-(N-methylpyrrolyI)). The order of oxidation (reduction) for monocarbene complexes containing a monomeric heteroarene substituent ((1)-(3)), a dimeric heteroarene substituent ((4)-(6)) or biscarbene complexes connected with a heteroarene substituent ((7)-(9)) is the same, namely 2-thienyl > 2-furyl > 2-(N-methylpyrrolyl). Carbene complexes containing a larger conjugated heteroarene substituent attached to the carbene carbon reduce more easily than the monomeric analogues. Tungsten biscarbene complexes exhibit two separate oxidation potentials for the two metal centres or one large oxidation peak, consistent with the simultaneous oxidation of the two W metal centres. (C) 2014 Elsevier B.V. All rights reserved.
机译:报告了一系列五羰基钨与单和二聚杂芳烃取代基的单和双卡宾配合物的电化学研究,并在CH3CN和DCM中进行了比较。结果表明,氧化(还原)的顺序主要取决于连接在卡宾碳原子上的芳基取代基(2-噻吩基,2-富酰基或2-(N-甲基吡咯基))。含有单体杂芳烃取代基((1)-(3)),二聚杂芳烃取代基((4)-(6))或与杂芳烃取代基连接的双卡宾络合物((7))的氧化(还原)顺序-(9))相同,即2-噻吩基> 2-呋喃基> 2-(N-甲基吡咯基)。含有较大的连接到卡宾碳上的共轭杂芳烃取代基的卡宾络合物比单体类似物更容易还原。钨双卡宾配合物对两个金属中心显示两个单独的氧化电位或一个大的氧化峰,这与两个W金属中心的同时氧化相一致。 (C)2014 Elsevier B.V.保留所有权利。

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