the cis isomers are kinetic products. This behavior is different than described in the literature for similar complexes, where the cis isomer is obtained from the trans isomer. Additionally, the catalytic activity of the complexes (1), (2) and (3) was investigated, as pre-catalysts, in the reduction of the acetophenone and 4-methylacetophenone by transfer-hydrogenation.
摘要 反式-[RuCl2(dppb)(cydn)] (1)、反式-[RuCl2(dppb)(opda)] (2) 和顺式-[RuCl2(dppb)(cydn)] (3) 配合物由[RuCl2(dppb)}2-μ-(dppb)] 其中:dppb =
1,4-双(二苯基膦)丁烷;cydn = 顺式和反式 (±)
1,2-二氨基环己烷,以及 opda =
邻苯二胺}。通过
磷的核磁共振 (31P1H} NMR)、循环伏安法 (CV)、红外和紫外/可见光谱 (IR 和 UV/vis) 以及元素分析 (CHN) 对配合物进行了表征。确定了 (1) 和 (3) 的 X 射线结构,并将它们呈现在此处。DFT 计算和实验数据表明,反式异构体是作为热力学产物获得的,而顺式异构体是动力学产物。这种行为与文献中描述的类似复合物不同,其中顺式异构体由反式异构体获得。此外,还研究了作为预催化剂的配合物 (1)、(2)