Coordination-driven self-assembly of Cp*Rh-based rectangles in novel families of hetero-bimetallic metal-organic frameworks

被引:1
|
作者
Lin, Lin [1 ]
Lin, Yue-jian [2 ]
Jin, Guo-xin [2 ]
机构
[1] Shenyang Med Coll, Key Lab Res Pathogenesis Allergen Provoked Allerg, Dept Translat Med, Res Ctr, Shenyang 110034, Liaoning, Peoples R China
[2] Fudan Univ, State Key Lab Mol Engn Polymers, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai 200433, Peoples R China
基金
美国国家科学基金会;
关键词
coordination-driven; half-sandwich; homometallic; metal-organic; self-assembly; DEHYDROGENATIVE ALKYNE-INSERTION; HOST-GUEST SYSTEMS; ORGANOMETALLIC MACROCYCLES; MOLECULAR BOAT; O-CARBORANE; INCLUSION; SELECTIVITY; DECABORANE; CAGE; ENCAPSULATION;
D O I
10.1002/aoc.4759
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The crystal and molecular structures of a series of structurally related 1,2,3-triazole-4,5-dicarboxylate (LHtzdc = 1,2,3-triazole-4,5-dicarboxylate) ligands for second metal ions were established via single-crystal X-ray structural analysis. [Cu (en)](2+) (en = ethylenediamine) was selected as a second metal ion, the two spare sites of the O atom from LHtzdc are coordinated to a single [Cu (en)](2+), and the [Cu (en)](2+) metal centres act as two outer pockets, which is an effective and innovative method of controlling the assembly of heterometallic cages.
引用
收藏
页数:8
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