Srinivas Katam, Prabusankar Ganesan
Department of Chemistry, Indian Institute of Technology Hyderabad Kandi, Sangareddy Telangana India-502 285
RSC Adv. 2018 Sep 18;8(56):32269-32282. doi: 10.1039/c8ra06057f. eCollection 2018 Sep 12.
The first comparative study of C, S, Se and P donor ligands-supported copper(i) complexes for C-N and C-Si bond formation reactions are described. The syntheses and characterization of eight mononuclear copper(i) chalcogenone complexes, two polynuclear copper(i) chalcogenone complexes and one tetranuclear copper(i) phosphine complex are reported. All these new complexes were characterized by CHN analysis, FT-IR, UV-vis, multinuclear NMR and single crystal X-ray diffraction techniques. The single crystal X-ray structures of these complexes depict the existence of a wide range of coordination environments for the copper(i) center. This is the first comparative study of metal-phosphine, metal-NHC and metal-imidazolin-2-chalcogenones in C-N and C-Si bond formation reactions. Among all the catalysts, mononuclear copper(i) thione, mononuclear copper(i) N-heterocyclic carbene and tetranuclear copper(i) phosphine are exceedingly active towards the synthesis of 1,2,3-triazoles as well as for the cross-dehydrogenative coupling of alkynes with silanes. The cross-dehydrogenative coupling of terminal alkynes with silanes represents the first report of a catalytic process mediated by metal-imidazolin-2-chalcogenones.
描述了关于用于C-N和C-Si键形成反应的C、S、Se和P供体配体支撑的铜(I)配合物的首次比较研究。报道了八种单核铜(I)硫属酮配合物、两种多核铜(I)硫属酮配合物和一种四核铜(I)膦配合物的合成与表征。所有这些新配合物均通过CHN分析、傅里叶变换红外光谱(FT-IR)、紫外可见光谱(UV-vis)、多核核磁共振(NMR)和单晶X射线衍射技术进行了表征。这些配合物的单晶X射线结构描绘了铜(I)中心存在广泛的配位环境。这是金属膦、金属-N-杂环卡宾和金属咪唑啉-2-硫属酮在C-N和C-Si键形成反应中的首次比较研究。在所有催化剂中,单核铜(I)硫酮、单核铜(I)N-杂环卡宾和四核铜(I)膦对1,2,3-三唑的合成以及炔烃与硅烷的交叉脱氢偶联反应极具活性。末端炔烃与硅烷的交叉脱氢偶联反应代表了由金属咪唑啉-2-硫属酮介导的催化过程的首次报道。