Stereochemistry of metal tetramethylcyclam complexes directed by an unexpected anion effect

被引:11
作者
Derrick, Jeffrey S. [1 ]
Kim, Yujeong [2 ,3 ]
Tak, Hyeonwoo [4 ]
Park, Kiyoung [5 ]
Cho, Jaeheung [4 ]
Kim, Sun Hee [2 ,3 ]
Lim, Mi Hee [1 ]
机构
[1] UNIST, Dept Chem, Ulsan 44919, South Korea
[2] KBSI, Western Seoul Ctr, Seoul 03759, South Korea
[3] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 03760, South Korea
[4] DGIST, Dept Emerging Mat Sci, Daegu 42988, South Korea
[5] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
CRYSTAL-STRUCTURE; CYCLAM LIGANDS; COORDINATING SOLVENTS; NICKEL(II) COMPLEXES; OXOIRON(IV) COMPLEX; ELECTRON-TRANSFER; AMINE COMPLEXES; PERCHLORATE; REACTIVITY; 1,4,8,11-TETRAMETHYL-1,4,8,11-TETRAAZACYCLOTETRADECANE;
D O I
10.1039/c7dt01489a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Metal(TMC) complexes (TMC = tetramethylcyclam) exclusively form trans-I diastereoisomers; thus, little is known about the trans-III isomers. Herein, we report a new method to prepare the trans-III-[Cu(TMC)](2+) complex via an anion effect. Our crystallo-graphic, spectroscopic, and computational analyses validated that [Cu(TMC)](NO3)(2) produced the trans-III complex, different from the trans-I structure of [Cu(TMC)](ClO4)(2).
引用
收藏
页码:13166 / 13170
页数:5
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