Wei Rong-Min, Kong Ming, Cao Fan, Li Jing, Pu Tian-Cheng, Yang Li, Zhang Xiu-Ling, Song You
State Key Laboratory of Coordination Chemistry, Collaborative Innovation Center of Advanced Microstructures, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Department of Chemical and Biomolecular Engineering, John Hopkins University, Baltimore, Maryland 21218, USA.
Dalton Trans. 2016 Nov 22;45(46):18643-18652. doi: 10.1039/c6dt03421g.
A series of octacyanotungstate(iv)-based iron(ii) complexes with the general formula Fe(L)[W(CN)]·nHO [L = (3-pyridyl)methanol (1, 2), 3-methylpyridine (3), (4-pyridyl)methanol (4), and 4-methylpyridine (5); n = 4 for 1, and n = 0 for 2-5] have been synthesized and characterized. Single crystal X-ray diffraction analysis reveals that the Fe ions lie in the centre of the compressed [FeN] octahedron in all complexes. Fe and W ions are alternately bridged by cyano groups forming a three-dimensional (3D) bimetallic framework. Magnetic investigation shows that 1 displays a gradual spin-crossover (SCO) phenomenon with a spin transition temperature (T) of 200 K, and such SCO behaviour is obviously correlated with the lattice water content of the sample. The magnetic measurements of dehydrated samples show that the fractional conversion from the high-spin (HS) to the low-spin (LS) state is reduced with the increasing of dehydration temperature. Complexes 2-5 are in the HS state and do not exhibit SCO properties in the range of 2-300 K. Comparing the octahedral geometry of [FeN] of five complexes, quantified by using continuous shape measures, the distortion of complex 1 is the highest as a result of the intermolecular hydrogen bonds, which shorten the Fe-N bond distances and thus increase the ligand field strength at the Fe sites. The analysis of correlations between the structural characteristics and magnetic behaviour of 1-5 suggests that the SCO is mainly tuned by the octahedral distortion of the [FeN] core caused by intermolecular hydrogen bonds. There is an exact correlation between SCO behaviour and the amount of lattice water molecules existing in the crystal. The spin crossover behaviour of these complexes has been computationally studied using the DFT method. The results of the calculations are consistent with the experiments, which prove that complex 1 with severe distortion of the coordination sphere of Fe is prone to exhibit SCO in theory.
一系列通式为Fe(L)[W(CN)]·nHO的基于八氰钨酸盐(IV)的铁(II)配合物[L = (3 - 吡啶基)甲醇(1, 2)、3 - 甲基吡啶(3)、(4 - 吡啶基)甲醇(4)和4 - 甲基吡啶(5);1中n = 4,2 - 5中n = 0]已被合成并表征。单晶X射线衍射分析表明,在所有配合物中Fe离子位于压缩的[FeN]八面体中心。Fe和W离子通过氰基交替桥连形成三维(3D)双金属框架。磁性研究表明,1表现出逐渐的自旋交叉(SCO)现象,自旋转变温度(T)为200 K,且这种SCO行为明显与样品的晶格水含量相关。脱水样品的磁性测量表明,随着脱水温度升高,从高自旋(HS)态到低自旋(LS)态的分数转化率降低。配合物2 - 5处于HS态,在2 - 300 K范围内不表现出SCO性质。通过使用连续形状测量对五个配合物的[FeN]八面体几何结构进行量化比较,由于分子间氢键的作用,配合物1的畸变最高,这缩短了Fe - N键距,从而增加了Fe位点的配体场强度。对1 - 5的结构特征与磁性行为之间的相关性分析表明,SCO主要由分子间氢键引起的[FeN]核的八面体畸变调节。SCO行为与晶体中存在的晶格水分子数量之间存在确切的相关性。使用密度泛函理论(DFT)方法对这些配合物的自旋交叉行为进行了计算研究。计算结果与实验一致,证明了Fe配位球严重畸变的配合物1在理论上易于表现出SCO。