Unprecedented encapsulation of a [FeIIICl4]- anion in a cationic [Fe4IIL6]8+ tetrahedral cage derived from 5,5′"-dimethyl-2,2′:5′,5":2",2′"-quaterpyridine

被引:68
作者
Glasson, Christopher R. K. [1 ]
Clegg, Jack K. [2 ,3 ]
McMurtrie, John C. [4 ]
Meehan, George V. [1 ]
Lindoy, Leonard F. [1 ,2 ]
Motti, Cherie A. [5 ]
Moubaraki, Boujemaa [6 ]
Murray, Keith S. [6 ]
Cashion, John D. [7 ]
机构
[1] James Cook Univ, Sch Pharm & Mol Sci, Townsville, Qld 4814, Australia
[2] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[3] Univ Cambridge, Dept Chem, Cambridge CB12 1EW, England
[4] Queensland Univ Technol, Brisbane, Qld 4001, Australia
[5] Australian Inst Marine Sci, Townsville, Qld 4810, Australia
[6] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[7] Monash Univ, Sch Phys, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
ELECTROSPRAY EMITTER; THERMAL-ANALYSIS; IRON COMPLEXES; FE-II; DESIGN; ION; RECOGNITION; CHEMISTRY; HOST;
D O I
10.1039/c0sc00523a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A unique example of incorporation of a tetrahalometalate anion in a small supramolecular cage is described in which a tetrahedral cage of type [Fe4L6](8+) selectively encapsulates a [FeIIICl4](-) anion over a [(FeCl4)-Cl-II](2-) anion in its central cavity to yield a discrete, mixed oxidation state, Fe(II)/Fe(III) supramolecular assembly. This unusual outcome has been achieved using two alternative synthetic strategies.
引用
收藏
页码:540 / 543
页数:4
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