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首页> 外文期刊>Journal of Organometallic Chemistry >Reaction of [M(CO)(4)](-) (M = Ir, Rh) with cyclopropenyl tetrafluoroborate - Ring opening and coupling of cyclopropenyl ligands to form dinuclear metal complexes
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Reaction of [M(CO)(4)](-) (M = Ir, Rh) with cyclopropenyl tetrafluoroborate - Ring opening and coupling of cyclopropenyl ligands to form dinuclear metal complexes

机译:[M(CO)(4)](-)(M = Ir,Rh)与环丙烯基四氟硼酸酯的反应-开环和环丙烯基配体偶联形成双核金属络​​合物

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Reaction of the iridium tetracarbonylate [PPN][Ir(CO)(4)] (1a) with triphenylcyclopropenyl tetrafluoroborate [C3Ph3][BF4] afforded two dinuclear species Ir-2(CO)(4)(mu, eta(1):eta(2)-C3Ph3)(mu, eta(2): eta(3)-C3Ph3) (2) and Ir-2(CO) 4(mu,eta(4): eta(4)-C6Ph6) (3a) resulting from the ring opening and in the latter case, coupling of the resulting acyclic, propenyl ligands. The analogous reaction with [PPN][Rh(CO)(4)] (1b) afforded only the rhodium analogue for 3a. (C) 2008 Elsevier B.V. All rights reserved.
机译:四羰基铱铱[PPN] [Ir(CO)(4)](1a)与三苯基环丙烯基四氟硼酸酯[C3Ph3] [BF4]反应得到两个双核物种Ir-2(CO)(4)(mu,eta(1): eta(2)-C3Ph3)(mu,eta(2):eta(3)-C3Ph3)(2)和Ir-2(CO)4(mu,eta(4):eta(4)-C6Ph6)(3a )是由开环产生的,在后一种情况下,是所得无环丙烯基配体的偶联。与[PPN] [Rh(CO)(4)](1b)的类似反应仅提供3a的铑类似物。 (C)2008 Elsevier B.V.保留所有权利。

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