Anion-dependent formation of helicates versus mesocates of triple-stranded M 2L 3 (M = Fe 2+, Cu 2+) complexes

Fengjuan Cui, Shaoguang Li, Chuandong Jia, Jennifer S. Mathieson, Leroy Cronin, Xiao Juan Yang, Biao Wu*

*此作品的通讯作者

科研成果: 期刊稿件文章同行评审

80 引用 (Scopus)

摘要

A series of dinuclear triple-stranded complexes, [Fe 2L 3⊃X]X 6 [X = BF 4 - (1), ClO 4 - (2)], [Fe 2L 3⊃SO 4] 2(SO 4) 5 (3), [Fe 2L 3⊃Br](BPh 4) 6 (4), Fe 2L 3(NO 3)Br 6 (5), and [Cu 2L 3⊃NO 3](NO 3) 6 (6), which incorporate a central cavity to encapsulate different anions, have been synthesized via the self-assembly of iron(II) or copper(II) salts with the N,N′-bis[5-(2,2′-bipyridyl)methyl]imidazolium bromide (LBr) ligand. X-ray crystallographic studies (for 1-4 and 6) and elemental analyses confirmed the cagelike triple-stranded structure. The anionic guest is bound in the cage and shows remarkable influence on the outcome of the self-assembly process with regard to the configuration at the metal centers. The mesocates (with different configurations at the two metal centers) have formed in the presence of large tetrahedral anions, while helicates (with the same configuration at both metal centers) were obtained when using the relatively smaller spherical or trigonal-planar anions Br - or NO 3 -.

源语言英语
页(从-至)179-187
页数9
期刊Inorganic Chemistry
51
1
DOI
出版状态已出版 - 2 1月 2012
已对外发布

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