Chadwick F Mark, Ashley Andrew E, Cooper Robert T, Bennett Luke A, Green Jennifer C, O'Hare Dermot M
Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, UK.
Dalton Trans. 2015 Dec 14;44(46):20147-53. doi: 10.1039/c5dt03747f.
We describe the synthesis, structure and bonding of the first iridium and rhodium permethylpentalene complexes, syn-[M(CO)2]2(μ:η(5):η(5)-Pn*) (M = Rh, Ir). In fact, [Ir(CO)2]2(μ:η(5):η(5)-Pn*) is the first iridium pentalene complex. An interesting preference for the isolation of the sterically more demanding syn-isomer is observed and substantiated by DFT analysis. Upon photolysis, the rhodium analogue yields an unusual tetrameric species Rh4(CO)6(μ:η(3):η(5)-Pn*)2 with bridging carbonyls and Rh-Rh bonds, which has been characterised by single crystal X-ray diffraction and by solution NMR spectroscopy.
我们描述了首例铱和铑的全甲基戊搭烯配合物syn-[M(CO)₂]₂(μ:η⁵:η⁵-Pn*)(M = Rh,Ir)的合成、结构及键合情况。事实上,[Ir(CO)₂]₂(μ:η⁵:η⁵-Pn*)是首例铱戊搭烯配合物。通过DFT分析观察并证实了在分离过程中对空间位阻更大的顺式异构体存在有趣的偏好。光解后,铑类似物生成了一种不寻常的四聚体物种Rh₄(CO)₆(μ:η³:η⁵-Pn*)₂,其具有桥连羰基和Rh-Rh键,已通过单晶X射线衍射和溶液核磁共振光谱进行了表征。