Self-assembled Co(II) and Co(III) [M2L3] helicates and [M4L6] tetrahedra from an unsymmetrical quaterpyridine ligand

被引:1
作者
Siddique, Rashid G. [1 ,2 ]
Mcmurtrie, John C. [3 ,4 ]
Clegg, Jack K. [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Adelaide, Sch Phys Chem & Earth Sci, Adelaide, SA 5005, Australia
[3] Queensland Univ Technol QUT, Sch Chem & Phys, Brisbane, Qld 4000, Australia
[4] Queensland Univ Technol QUT, Ctr Mat Sci, Brisbane, Qld 4000, Australia
基金
澳大利亚研究理事会;
关键词
TRIPLE HELICATE; NICKEL(II); CHEMISTRY; CAGES;
D O I
10.1039/d4dt01565g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In order to bind guest molecules with exquisite selectivity, biological host molecules often employ low symmetry binding pockets. The majority of metallosupramolecular assemblies, however, rely on symmetrical ligands to form high-symmetry assemblies that enclosing similarly symmetrical cavities. Here we employ an unsymmetrical quaterpyridine ligand in combination with cobalt(ii) to form a mixture of low-symmetry [M2L3] helicates and [M4L6] tetrahedra and their subsequent oxidation to Co(iii)-containing assemblies.
引用
收藏
页码:11237 / 11241
页数:5
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