Park Yoonsu, Semproni Scott P, Zhong Hongyu, Chirik Paul J
Department of Chemistry, Princeton University, Frick Laboratory 292, Princeton, NJ, 08544, USA.
Angew Chem Int Ed Engl. 2021 Jun 21;60(26):14376-14380. doi: 10.1002/anie.202104320. Epub 2021 May 24.
A four-coordinate cobalt-imido complex, ( mPNP)Co=NMes ( mPNP=modified PNP pincer ligand) has been synthesized from addition of 2,4,6-trimethylphenylazide (Mes-N ) to the corresponding dinitrogen complex. The solid-state structure determined by X-ray diffraction established a rare, idealized planar geometry with a Co=N bond distance of 1.716(2) Å. Magnetic measurements revealed an S=1 ground state with CAS-SCF calculations supporting radical character on the imide nitrogen. Thermolysis of the cobalt-imido compound induced selective insertion of the imido group into a Co-P bond and yielded a three-coordinate cobalt complex with a distorted T-shaped geometry. Transition state analysis conducted with DFT calculations established the thermodynamic stability of the P-N coupled product and provided insight into the exclusive selectivity.
通过向相应的二氮配合物中加入2,4,6-三甲基苯基叠氮化物(Mes-N₃),合成了一种四配位钴亚胺配合物(mPNP)Co=NMes(mPNP = 修饰的PNP钳形配体)。通过X射线衍射确定的固态结构建立了一种罕见的、理想化的平面几何结构,Co=N键长为1.716(2) Å。磁性测量揭示了一个S = 1的基态,CAS-SCF计算支持亚胺氮上的自由基特征。钴亚胺化合物的热解诱导亚胺基团选择性插入Co-P键,并产生了一种具有扭曲T形几何结构的三配位钴配合物。用DFT计算进行的过渡态分析确定了P-N偶联产物的热力学稳定性,并深入了解了排他性选择性。