Magnetic and Photochromic Properties of a Manganese(II) Metal-Zwitterionic Coordination Polymer

被引:122
|
作者
Gong, Teng [1 ]
Yang, Xiao [1 ]
Sui, Qi [1 ]
Qi, Yan [1 ]
Xi, Fu-Gui [1 ]
Gao, En-Qing [1 ]
机构
[1] E China Normal Univ, Coll Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
END-ON AZIDO; SPIN-CROSSOVER; ORGANIC FRAMEWORKS; ELECTRON-TRANSFER; SLOW RELAXATION; VALENCE TAUTOMERISM; MIXED CARBOXYLATE; MOLECULAR SHUTTLE; CHARGE-TRANSFER; MN-II;
D O I
10.1021/acs.inorgchem.5b01888
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The solvothermal reaction of Mn(ClO4)(2), NaN3, and a rigid viologen-tethered tetracarboxylic acid (1,1'-bis(3,5dicarboxypheny1)-4,4'-bipyridinium chloride, [H4L]Cl-2) led to a coordination polymer of formula [Mn-4(L)(N-3)(6)(H2O)(2)](n).X-ray analysis revealed a 3D coordination structure. The Mn(II) ions are connected by mixed azide and carboxylate bridges to give 2D layers, which are pillared by the viologen tether of the zwitterionic ligand. Magnetic analyses suggested that the compound features antiferromagnetism and field-induced metamagnetism. The compound also shows photochromic and photomagnetic properties. The long-range magnetic ordering is owed to the spin-canting structure of the Mn(II)-azide-carboxylate layer; the photochromism involves the formation of viologen radicals via photoinduced electron transfer, and the photomagnetism is related to the interactions between the metal ion and the photogenerated radicals. The study demonstrates a strategy for the design of new multifunctional materials with photoresponsive properties.
引用
收藏
页码:96 / 103
页数:8
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