Hard and Soft Metal Complexes of Calix[4]-bis-monothiacrown-5: X-ray and NMR Studies of Discrete Homodinuclear Complexes and a Heteromultinuclear Network

被引:21
|
作者
Kim, Ja-Yeon [1 ,2 ]
Park, In-Hyeok [1 ,2 ]
Lee, Jai Young [3 ]
Lee, Joon-Hwa [1 ,2 ]
Park, Ki-Min [1 ,2 ]
Lee, Shim Sung [1 ,2 ]
机构
[1] Gyeongsang Natl Univ, Dept Chem, Jinju 660701, South Korea
[2] Gyeongsang Natl Univ, Res Inst Nat Sci, Jinju 660701, South Korea
[3] Konyang Univ, Dept Chem, Nonsan 320711, South Korea
关键词
SUPRAMOLECULAR SILVER(I); COORDINATION POLYMERS; CYCLIC POLYETHERS; EXO-COORDINATION; LIGAND ISOMERISM; CROWN; 1,3-ALTERNATE; MACROCYCLES; CADMIUM(II); MERCURY(II);
D O I
10.1021/ic401648b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Endocyclic homodinuclear complexation and endo/exocydic heteronuclear networking of calix[4]-bis-monothiacrown-5 (L) are reported. First, dipotassium(I) and disilver(I) complexes of L were isolated and their solid state structures characterized. To probe the complexation behavior for these same systems in solution, the competition between potassium(I) and silver(I) for L was monitored by H-1 NMR Potassium(1) showed a higher affinity to L than silver(l) both in the solid and solution states. The reaction of L with KI in the presence of HgI2 afforded a two-dimensional coordination polymer with the endocyclic dipotassium(I) complex linked by an exocyclic mercury(II) iodide cluster backbone.
引用
收藏
页码:10176 / 10182
页数:7
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