五羰基钨(0)配体交换反应动力学及机理

L. Rivera-Rivera, Frisia D. Colón-Padilla, Yessenia Ocasio-Delgado, Jomary Martínez-Rivera, Samirah Mercado-Feliciano, C. Ramos, J. E. Cortés-Figueroa
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引用次数: 6

摘要

路易斯碱三苯基膦和三乙基亚磷酸酯(L)从(m2 - c60)W(CO) 5中置换c60,生成配合物(m1 -L)W(CO) 5。在c60和L的浓度至少为(m2 - c60)W(CO) 5浓度的50倍的条件下,研究了这些置换反应。不同溶剂中对(m2 -C - 60)W(CO) 5的反应均为一级反应。在[c60]/[L], 0和0的条件下,伪一级速率常数值与L的浓度和性质无关,而取决于溶剂的配位能力。在0 h [c60]/[L] h 1条件下,伪一阶速率常数随[c60]/[L]的增大而减小。c60从(m2 - c60)W(CO) 5交换位移的两种极限情况,其对整个机制的相对贡献取决于溶剂的性质,提出了溶剂辅助c60 -W(CO) 5键位移和解离位移. ...
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Kinetics and Mechanisms of Ligand Exchange Reactions on (Dihapto-Buckminsterfullerene) Pentacarbonyl Tungsten(0)
The Lewis bases triphenyl phosphine and triethyl phosphite (L) displace C 60 from ( m 2 -C 60 )W(CO) 5 to produce the complexes ( m 1 -L)W(CO) 5 . These displacement reactions were studied under conditions where the concentrations of C 60 and L were at least 50 times the concentration of ( m 2 -C 60 )W(CO) 5 . The reactions in various solvents were first order with respect to ( m 2 -C 60 )W(CO) 5 . The pseudo first order rate constant values were independent of the concentration and of the nature of L but dependent on the coordinating ability of the solvent under conditions where [C 60 ]/[L] , 0. Under conditions where 0 h [C 60 ]/[L] h 1, the pseudo first order rate constant values decrease as the values of [C 60 ]/[L] increase. Two limiting cases of an interchange displacement of C 60 from ( m 2 -C 60 )W(CO) 5 , whose relative contributions to the overall mechanism depend on the nature of the solvent, are proposed to be a solvent-assisted C 60 -W(CO) 5 bond displacement and a dissociative displacement. ...
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