On rhenium(I)-silver(I) cyanide porous macrocyclic clusters

被引:7
|
作者
Krawczyk, Monika K. [1 ,2 ]
Bikas, Rahman [1 ,3 ]
Krawczyk, Marta S. [4 ]
Lis, Tadeusz [1 ]
机构
[1] Univ Wroclaw, Fac Chem, F Joliot Curie 14 St, PL-50383 Wroclaw, Poland
[2] Univ Wroclaw, Inst Expt Phys, M Borna 9, PL-50204 Wroclaw, Poland
[3] Univ Zanjan, Dept Chem, Fac Sci, Zanjan 4537138791, Iran
[4] Wroclaw Med Univ, Dept Analyt Chem, Fac Pharm, Borowska 211A St, PL-50556 Wroclaw, Poland
来源
CRYSTENGCOMM | 2017年 / 19卷 / 23期
关键词
SINGLE-MOLECULE MAGNETISM; METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; TETRAHEDRAL CORNERS; BUILDING-BLOCKS; RE-II; GUEST; HOST; COMPLEXES; SORPTION;
D O I
10.1039/c7ce00646b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first cyanide rhenium(I)-silver(I) clusters were synthesized in the course of simple one-pot high-yielding reactions. This new class of obtained self-assembled, cyclic octanuclear complexes is composed of pseudo-square-shaped {Re4Ag4(mu-CN)(8)} units, which, along with PPh3 ligands, adopt an approximately block-like overall geometry. We discovered that the studied cavity-shaped clusters feature a channeling crystal network capable of hosting smaller molecules and exhibit the ability to undergo reversible guest solvent sorption. Depending on the reaction conditions, the tetranuclear complex [Re2Ag2(mu-CN) (4)(CO)(4)(PPh3)(6)] and the species of the formal motif {ReAg1.5(CN)(2.5)(CO)(2)(PPh3)(2)} can be formed.
引用
收藏
页码:3138 / 3144
页数:7
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