Aryl-BIAN-ligated silver(I) trifluoromethoxide complex

被引:60
作者
Chen, Shouxiong [1 ]
Huang, Yangjie [1 ]
Fang, Xin [1 ]
Li, Haohong [1 ]
Zhang, Zhongxing [2 ]
Hor, T. S. Andy [2 ,3 ]
Weng, Zhiqiang [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Peoples R China
[2] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[3] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
ALPHA-FLUORINATED ETHERS; OXIDATIVE DESULFURIZATION-FLUORINATION; BIDENTATE NITROGEN LIGANDS; ORGANOMETALLIC CHEMISTRY; SUBSTITUENT CONSTANTS; HOMOGENEOUS CATALYSIS; COPPER; ALKYNES; TRIFLUOROMETHYLSELENOLATION; DERIVATIVES;
D O I
10.1039/c5dt02078f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A reaction of acetonitrile-solvated AgOCF3 with 1 equiv. of Aryl-BIAN ligand in THF at room-temperature afforded the silver(I) complex (Aryl-BIAN)AgOCF3 (1) in 75% yield. The crystal structure of this silver(I) trifluoromethoxide was determined by single-crystal X-ray crystallography. The molecular structure of 1 shows the metal centre bound to one molecule of BIAN, one trifluoromethoxide and one THF solvate, resulting in a distorted tetrahedral silver. Density functional theory (DFT) calculations and the natural bond orbital (NBO) analysis were conducted to give insights into the electronic structure of 1 and the bonding characters of the OCF3 group. The reactivity of 1 towards trifluoromethoxylation of organic halides was also examined; a reaction with benzyl bromides gave the desired products of benzyl trifluoromethyl ethers in good to excellent yields.
引用
收藏
页码:19682 / 19686
页数:5
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