Syntheses, hydrogen-bonded assembly structures, and spin crossover properties of [FeIII(Him)2(n-MeOhapen)]PF6 (Him = imidazole and n-MeOhapen = N,N'-bis(n-methoxy-2-oxyacetophenylidene)ethylenediamine); n = 4, 5, 6)
Syntheses, hydrogen-bonded assembly structures, and spin crossover properties of [FeIII(Him)2(n-MeOhapen)]PF6 (Him = imidazole and n-MeOhapen = N,N'-bis(n-methoxy-2-oxyacetophenylidene)ethylenediamine); n = 4, 5, 6)
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[FeIII(Him)2(n-MeOhapen)]PF6 的合成、氢键组装结构和自旋交叉特性(Him = 咪唑和 n-MeOhapen = N,N-双(n-甲氧基-2-氧基乙酰亚苯基)
DOI:
10.1016/j.ica.2015.03.034
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发表时间:
2015
影响因子:
2.8
通讯作者:
Yukinari Sunatsuki
中科院分区:
文献类型:
--
作者:
Takeshi Fujinami;Mizuki Ikeda;Masataka Koike;Naohide Matsumoto;Tomohiro Oishi;Yukinari Sunatsuki
Three iron(III) complexes, [FeIII(Him)2(n-MeOhapen)]PF6(1:n= 4,2:n= 5,3:n= 6), where Him = imidazole and n-MeOhapen =N,N′-bis(n-methoxy-2-oxyacetophenylidene)ethylenediamine, were synthesized. Each FeIIIion was coordinated by N4O2donor atoms of equatorial n-MeOhapen and two axial Him. The saturated FeC2N2chelate ring involving the ethylenediamine moiety adopted a gauche conformation and the two phenylidene planes of [FeIII(Him)2(n-MeOhapen)]+were oriented opposite to the FeO2N2coordination plane. Two adjacent [FeIII(Him)2(4-MeOhapen)]+cations in1were connected via PF6−ions by hydrogen bonds between the imidazole group and PF6−to give a one-dimensional chain. Two adjacent cations in2were connected via hydrogen bonds between the phenylidene oxygen and imidazole atoms to form a cyclic dimer structure. Two EtOH molecules were involved in a hydrogen-bonded cyclic dimer structure in3. Compounds1and2showed spin crossover behavior, but3showed incomplete spin crossover.