当前位置:
X-MOL 学术
›
Inorg. Chem.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Solvent-dependent SCO Behavior of Dinuclear Iron(II) Complexes with a 1,3,4-Thiadiazole Bridging Ligand
Inorganic Chemistry ( IF 4.3 ) Pub Date : 2016-06-13 00:00:00 , DOI: 10.1021/acs.inorgchem.6b00163 Christian F. Herold 1 , Sergii I. Shylin 1 , Eva Rentschler 1
Inorganic Chemistry ( IF 4.3 ) Pub Date : 2016-06-13 00:00:00 , DOI: 10.1021/acs.inorgchem.6b00163 Christian F. Herold 1 , Sergii I. Shylin 1 , Eva Rentschler 1
Affiliation
Two dinuclear iron(II) complexes [Fe2(μ-L)2]X4*4DMF (X = BF4– (1·4DMF) and ClO4– (2·4DMF)) with a 1,3,4-thiadiazole bridging ligand have been synthesized and show a very distinct solvent-depending SCO behavior. The complexes represent new solvatomorphs of the first dinuclear iron(II) complexes with the ligand L (2,5-bis[(2-pyridylmethyl)amino]methyl-1,3,4-thiadiazole). The incorporated lattice DMF molecules directly affect the spin state of these complexes. This behavior reveals a structural insight into the role of the solvent molecules on the spin transition.
中文翻译:
1,3,4-噻二唑桥联配体的双核铁(II)配合物的溶剂依赖性SCO行为
两个具有1,3,4-的双核铁(II)配合物[Fe 2(μ-L)2 ] X 4 * 4DMF(X = BF 4 –(1·4DMF)和ClO 4 –(2·4DMF))噻二唑桥联配体已经合成,并显示出非常独特的溶剂依赖性SCO行为。该配合物代表具有配体L(2,5-双[(2-吡啶基甲基)氨基]甲基-1,3,4-噻二唑)的第一双核铁(II)配合物的新溶剂化物。掺入的晶格DMF分子直接影响这些络合物的自旋状态。这种行为揭示了对溶剂分子在自旋转变中的作用的结构洞察力。
更新日期:2016-06-13
中文翻译:
1,3,4-噻二唑桥联配体的双核铁(II)配合物的溶剂依赖性SCO行为
两个具有1,3,4-的双核铁(II)配合物[Fe 2(μ-L)2 ] X 4 * 4DMF(X = BF 4 –(1·4DMF)和ClO 4 –(2·4DMF))噻二唑桥联配体已经合成,并显示出非常独特的溶剂依赖性SCO行为。该配合物代表具有配体L(2,5-双[(2-吡啶基甲基)氨基]甲基-1,3,4-噻二唑)的第一双核铁(II)配合物的新溶剂化物。掺入的晶格DMF分子直接影响这些络合物的自旋状态。这种行为揭示了对溶剂分子在自旋转变中的作用的结构洞察力。