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P单元与过渡金属羰基化合物的逐步配位及可逆P-P键活化

Gradual Coordination and Reversible P-P Bond Activation of a P -Unit with Transition Metal Carbonyls.

作者信息

Franz Roman, Gál Dalma, Bruhn Clemens, Kelemen Zsolt, Pietschnig Rudolf

机构信息

Institute for Chemistry and CINSaT, University of Kassel, Heinrich-Plett-Straße 40, 34132, Kassel, Germany.

Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, Műegyetem Rkp 3., Budapest, 1111, Hungary.

出版信息

Adv Sci (Weinh). 2024 Mar;11(11):e2306805. doi: 10.1002/advs.202306805. Epub 2023 Dec 31.

Abstract

Coordination of a stereochemically defined P -chain to a series of transition metal carbonyls [M(CO) ] (M = Mn (x = 5, z = 1), Fe (x = 4, z = 2) or Co (x = 4, z = 1)) is explored using a [3]ferrocenophane scaffold. A gradual transition from η -, η - to η -coordination is observed where in the η -mode the terminal positions of the phosphorus chain are bridged. With an excess of cobalt carbonyl successive P-P bond activation and gradual separation of the central phosphorus atoms from the phosphorus chain has been observed. This process is reversible and with suitable reagents such as methyl lithium, the P -unit is regenerated in stereospecific manner. The bonding situation and steps of the gradual P-P bond activation are investigated by DFT calculations as well as experimental methods (e.g., NMR spectroscopy, X-ray crystallography).

摘要

利用[3]二茂铁撑环骨架研究了立体化学定义的P链与一系列过渡金属羰基化合物[M(CO)ₓ](M = Mn(x = 5,z = 1)、Fe(x = 4,z = 2)或Co(x = 4,z = 1))的配位情况。观察到从η¹-、η²-到η³-配位的逐渐转变,其中在η³-模式下磷链的末端位置被桥连。在过量的羰基钴存在下,观察到连续的P-P键活化以及中心磷原子与磷链的逐渐分离。这个过程是可逆的,使用合适的试剂如甲基锂,P单元以立体专一的方式再生。通过密度泛函理论计算以及实验方法(如核磁共振光谱、X射线晶体学)研究了P-P键逐渐活化的键合情况和步骤。

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