Great framework variation of polymers in the manganese(II) maleate/α,α' -: Diimine system:: Syntheses, structures, and magneto-structural correlation

被引:30
作者
Ma, CB
Chen, CN
Liu, QT [1 ]
Chen, F
Liao, DZ
Li, LC
Sun, LC
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China
[3] Dalian Univ Technol, State Key Lab Fine Chem, Dalian, Peoples R China
[4] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
关键词
crystal structure; maleic acid; magnetic properties; manganese; structural topology;
D O I
10.1002/ejic.200300097
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three novel manganese(II) coordination polymers, [Mn (maleate)(phen)](n) (1; phen = 1,10-phenanthroline), [Mn-(maleate)(phen)](n).nH(2)O (2), and [Mn(maleate)(bpy)](n) (3; bpy = 2,2'-bipyridine), have been synthesized by treatment of Mn2+ with maleic acid with participation of chelate diimine ligands, and have been identified by single-crystal, X-ray diffraction to have either one-dimensional (1D) zigzag chain structures (1 and 2) or a two-dimensional (2D) sinuous layer structure (3). Each maleate dianion coordinates to three Mn centers, in different bridging modes (syn-anti in 1 and 2, syn-syn and anti-anti in 3). These compounds represent an interesting example of structural topology variation from 1D to 2D mediated by chemically similar auxiliary chelate ligands. Variable-temperature magnetic susceptibility measurements show weak anti-ferromagnetic exchange interactions between the adjacent Mn-II ions, with J = -0.06 cm(-1) (2) and J = -1.3 cm(-1), zJ' = -0.27 cm(-1) (3). The differences in the magnitudes of these coupling interactions agree well with the nature of the carb oxylate-bridging coordination of maleate. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.
引用
收藏
页码:2872 / 2879
页数:8
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