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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.
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