Synthesis and molecular structure of tetranuclear Cu4P4 complexes with R2P–O–PR2 ligands
摘要:
The reaction of secondary phosphine oxides R2P(O)H 1 with Cu(OAc)(2) under nitrogen atmosphere produced complexes [(R2P)(2)O(CuOAc)(2)](2) 2. A rapid ligand exchange took place when treating complexes 2 with NH4Cl to generate [(R2P)(2)O(CuCl)(2)](2) 3 in good yields. The structures of 3 were determined by Xray crystallography, showing that the geometries of these tetranuclear copper complexes vary with the R group of the phosphorus units. Compared to complexes 2 which are air sensitive, complexes 3 are stable under air. (C) 2014 Elsevier B. V. All rights reserved.
Synthesis and molecular structure of tetranuclear Cu4P4 complexes with R2P–O–PR2 ligands
摘要:
The reaction of secondary phosphine oxides R2P(O)H 1 with Cu(OAc)(2) under nitrogen atmosphere produced complexes [(R2P)(2)O(CuOAc)(2)](2) 2. A rapid ligand exchange took place when treating complexes 2 with NH4Cl to generate [(R2P)(2)O(CuCl)(2)](2) 3 in good yields. The structures of 3 were determined by Xray crystallography, showing that the geometries of these tetranuclear copper complexes vary with the R group of the phosphorus units. Compared to complexes 2 which are air sensitive, complexes 3 are stable under air. (C) 2014 Elsevier B. V. All rights reserved.
Selective PP and POP Bond Formations through Copper-Catalyzed Aerobic Oxidative Dehydrogenative Couplings of H-Phosphonates
作者:Yongbo Zhou、Shuangfeng Yin、Yuxing Gao、Yufen Zhao、Midori Goto、Li-Biao Han
DOI:10.1002/anie.201003484
日期:2010.9.10
Different copper complexes selectively catalyze the aerobicoxidativecoupling of H‐phosphonates to afford either hypophosphates and pyrophosphates in high yields with high selectivity (see scheme; tmeda=N,N,N′,N′‐tetramethylethylenediamine).