Sterically Encumbered Coordination Sites. Iron(II) Complexes of Jager-type ligands with a Terphenyl Backbone

被引:1
作者
Duerrmann, Andreas [1 ]
Hoerner, Gerald [1 ]
Wagner, Stefan [2 ]
Breuning, Matthias [2 ]
Weber, Birgit [1 ]
机构
[1] Univ Bayreuth, Inorgan Chem, Dept Chem, NWI, Univ Str 30, D-95440 Bayreuth, Germany
[2] Univ Bayreuth, Organ Chem, Dept Chem, NWII, Univ Str 30, D-95440 Bayreuth, Germany
来源
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE | 2021年 / 647卷 / 22期
关键词
Schiff base; Iron; Spin crossover; Magnetic properties; Terphenyl; SPIN-CROSSOVER COMPLEXES; HYDROGEN-BOND; ENERGY; STATE; PRESSURE; FLUORESCENCE; FUNCTIONALS;
D O I
10.1002/zaac.202100196
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A Schiff base-like ligand H2LTerPh featuring a para-terphenyl backbone was synthesized and converted in two steps to an octahedral iron(II) coordination polymer with 1,2-bis-(4-pyridyl)-ethylene as bridging ligand. Single crystal X-ray structure analysis was possible for the free ligand and the two octahedral iron(II) complexes. The Schiff base-like ligand features a [N2O2](2-) coordination sphere for the metal center and the para-terphenyl backbone introduces intrinsic steric constraint. Characterization of the coordination polymer with an N4O2 coordination sphere around the iron center via magnetic measurements (SQUID) and room temperature Mossbauer spectroscopy revealed HS character in the entire temperature range investigated. Structure modelling with DFT calculations supports the findings, but support also the possibility of spin crossover in solution.
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页码:2088 / 2097
页数:10
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