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首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Rhodium and iridium complexes with thiolate and tertiary phosphine ligands. The synthesis and structures of trans-[Ir(SC6H3Cl2-2,6)(CO)(PPh3)(2)], [Rh-2(mu-SC6H3Pr3i-2,4,6)(2)(CO)(2)-(PPh3)(2)], [Rh2H2(mu-SC6H4PPh2-2)(2)(CO)(2)(PPh3)(2)][BF4](2), and
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Rhodium and iridium complexes with thiolate and tertiary phosphine ligands. The synthesis and structures of trans-[Ir(SC6H3Cl2-2,6)(CO)(PPh3)(2)], [Rh-2(mu-SC6H3Pr3i-2,4,6)(2)(CO)(2)-(PPh3)(2)], [Rh2H2(mu-SC6H4PPh2-2)(2)(CO)(2)(PPh3)(2)][BF4](2), and

机译:铑和铱与硫醇盐和叔膦配体的配合物。反式[Ir(SC6H3Cl2-2,6)(CO)(PPh3)(2)],[Rh-2(mu-SC6H3Pr3i-2,4,6)(2)(CO)(2)的合成和结构)-(PPh3)(2)],[Rh2H2(mu-SC6H4PPh2-2)(2)(CO)(2)(PPh3)(2)] [BF4](2)和

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摘要

Reaction of [MF(CO)(PPh3)(2)] (M=Rh or Ir) with bulky aromatic thiols ArSH gave the binuclear complexes [M-2(mu-SAr)(2)(CO)(2)(PPh3)(2)] (M=Rh, SAr=SC6H2Pr3i-2,4,6 or SC6H3Me2-2,6) and mononuclear complexes [M(SAr)(CO)(PPh3)(2)] (M=Rh or Ir, SAr=SC6H3Cl2-2,6 or SC6H4SiPh3-2; M=Ir, SAr=SC6H2Pr3i-2,4,6 or SC6H3Me2-2,6. The crystal structure of [Rh-2(mu-SC6H3Pr3i-2,4,6)(2)(CO)(2)(PPh3)(2)] showed a binuclear thiolate bridged core while that of [Ir(SC6H3Cl2-2,6)(CO)(PPh3)(2)] revealed a conventional square planar geometry with trans PPh3 ligands. Three rhodium complexes were shown to be efficient catalysts for the hydroformylation of hept-1-ene under mild conditions with good selectivity for linear aldehyde for SAr=SC6H4SiPh3-2. Reaction of [MF(CO)(PPh3)(2)] with phosphinothiolate proligands PSH gave the monomeric complexes [M(PS)(CO)(PPh3)(2)] (M=Rh or Ir; PS=SC6H4PPh2-2 or S(CH2)(3)PPh2; M=Rh, PS=SCH2CH2PPh2 or SCH(CH3)CH2PPh2). The complex [Rh(SC6H4PPh2-2)(CO)(PPh3)] reacted reversibly with protons (HBF4) to give the dimeric dication [Rh-2(mu-SC6H4PPh2-2)(2)(CO)(2)(PPh3)(2)](2+), shown by a crystal structure be a thiolate bridged dimer with an Rh-Rh bond and pseudo-octahedral geometry about each Rh-III. Electrophilic attack by [Me3O][BF4] on [Rh(SC6H4PPh2-2)(CO)(PPh3)] occurred at sulfur to give [Rh(MeSC6H4PPh2-2)(CO)(PPh3)](+) and excess of MeI gave [Rh2I6(MeSC6H4PPh2-2)(2)], with octahedral Rh-III linked by a double iodide bridge. Attack at sulfur also occurred in [Rh(SC6H4PPh2-2)(CO)(PPh3)] with I(CH2)(3)I and ICH2CO2H to give [Rh(2-Ph2PC6H4SCH2CH2CH2)(CO)(PPh3)] and [RhI2(2-Ph2PC6H4SCH2CO2)(PPh3)] respectively. The complex [RhI3(CO)(PPh3)(2)] was a by-product and shown by a crystal structure to have a pseudo-octahedral structure with trans-PPh3 ligands. [References: 44]
机译:[MF(CO)(PPh3)(2)](M = Rh或Ir)与庞大的芳族硫醇ArSH反应生成双核络合物[M-2(mu-SAr)(2)(CO)(2)(PPh3 )(2)](M = Rh,SAr = SC6H2Pr3i-2,4,6或SC6H3Me2-2,6)和单核络合物[M(SAr)(CO)(PPh3)(2)](M = Rh或Ir [Rh-2(mu-SC6H3Pr3i-2,4 ,, SAr = SC6H3Cl2-2,6或SC6H4SiPh3-2; M = Ir,SAr = SC6H2Pr3i-2,4,6或SC6H3Me2-2,6。 6)(2)(CO)(2)(PPh3)(2)]显示了双核硫醇盐桥接核,而[Ir(SC6H3Cl2-2,6)(CO)(PPh3)(2)]则显示了常规正方形具有三个反式PPh3配体的平面几何结构。三种铑配合物被证明是在温和条件下对庚-1-烯进行加氢甲酰化的有效催化剂,对SAr = SC6H4SiPh3-2的线性醛具有良好的选择性。[MF(CO)(PPh3) )(2)]与硫代膦酸酯配体PSH一起生成单体配合物[M(PS)(CO)(PPh3)(2)](M = Rh或Ir; PS = SC6H4PPh2-2或S(CH2)(3)PPh2; M = Rh,PS = SCH2CH2PPh2或SCH(CH3)CH2PPh2)配合物[Rh(SC6H4PPh2-2)(CO)(PPh3)]可逆反应带有质子(HBF4)的二聚体[Rh-2(mu-SC6H4PPh2-2)(2)(CO)(2)(PPh3)(2)](2+),晶体结构表明是硫醇盐每个Rh-III都带有Rh-Rh键的桥连二聚体和伪八面体几何形状。 [Me3O] [BF4]对[Rh(SC6H4PPh2-2)(CO)(PPh3)]的亲电攻击发生在硫原子上,得到[Rh(MeSC6H4PPh2-2)(CO)(PPh3)](+)和过量的MeI得到[Rh2I6(MeSC6H4PPh2-2)(2)],并具有由双碘化物桥连接的八面体Rh-III。 [Rh(SC6H4PPh2-2)(CO)(PPh3)]中也发生了硫的攻击,带有I(CH2)(3)I和ICH2CO2H得到[Rh(2-Ph2PC6H4SCH2CH2CH2)(CO)(PPh3)]和[RhI2 (2-Ph2PC6H4SCH2CO2)(PPh3)]。络合物[RhI3(CO)(PPh3)(2)]是副产物,并通过晶体结构显示为具有带有反式PPh3配体的伪八面体结构。 [参考:44]

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