Spin-crossover iron(II) coordination polymer with zigzag chain structure

被引:97
作者
Matouzenko, GS
Molnar, G
Bréfuel, N
Perrin, M
Bousseksou, A
Borshch, SA
机构
[1] Ecole Normale Super Lyon, UMR CNRS 5532, Sterochim & Interact Mol, F-69364 Lyon 07, France
[2] CNRS, UPR 8241, Chim Coordinat Lab, F-31077 Toulouse, France
[3] Univ Lyon 1, UMR 5078, Lab Reconnaissance & Organisat Mol, F-69622 Villeurbanne, France
[4] Inst Rech Catalyse, CNRS, UPR 5401, F-69626 Villeurbanne, France
[5] Ecole Normale Super Lyon, Lab Chim Theor & Mat Hybrides, F-69364 Lyon 07, France
关键词
D O I
10.1021/cm021307v
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report on the synthesis and characterization of a first iron(II) spin-crossover coordination polymer of formula [Fe(pyim)(2)(bpy)](ClO4)(2).2C(2)H(5)OH, where pyim = 2-(2-pyridyl)imidazole and bpy = 4,4'-bipyridine, with zigzag chain structure. The chains are linked by 7 stacking into a two-dimensional network. Variable-temperature magnetic susceptibility measurements have revealed the occurrence of the HS <----> LS transition without hysteresis. The spin conversion temperature T-1/2 (temperature for which the HS fraction is equal to 0.5) is found equal to 205 K. The crystal structure was resolved at 293 K (high-spin form) and at 173 K (low-spin form). Both spin-state structures belong to the monoclinic space group C2/c (Z = 4). The complex assumes one-dimensional zigzag chain structure, in which the iron(II) active sites are linked to each other by a chemical bridge as the rigid rodlike 4,4'-bipyridine molecule. The Fe-Fe separation via the bpy ligand equals 11.523(2) and 11.201(2) Angstrom in the high-spin and low-spin structures, respectively. The polymeric chains extended along the c axis are stacked in the b direction forming two-dimensional sheets of bound molecules. The sheets are linked together by several intermolecular H-bonds in the a direction. The ensemble of structural features of the complex, potentially leading to the cooperativity, provides a basis for strong interactions. However, they are not strong enough in comparison with the HS-LS energy gap and result in a relatively gradual spin transition of the complex. The structural features and magnetic properties of the complex have been discussed and compared with those for earlier reported iron(II) spin-crossover coordination polymers.
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页码:550 / 556
页数:7
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