首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >Photochromic diarylethene ligands featuring 2-(imidazol-2-yl)pyridine coordination site and their iron(II) complexes
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Photochromic diarylethene ligands featuring 2-(imidazol-2-yl)pyridine coordination site and their iron(II) complexes

机译:具有2-(咪唑-2-基)吡啶配位点的光致变色二芳基乙烯配体及其铁(II)配合物

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摘要

A new family of photochromic diarylethene-based ligands bearing a 2-(imidazol-2-yl)pyridine coordination unit has been developed. Four members of the new family have been synthesized. The photoactive ligands feature non-aromatic ethene bridges (cyclopentene, cyclopentenone, and cyclohexenone), as well as closely spaced photoactive and metal coordination sites aiming a strong impact of photocyclization on the electronic structure of the coordinated metal ion. The ligands with cyclopentenone and cyclohexenone bridges show good cycloreversion quantum yields of 0.20–0.32. The thermal stability of closed-ring isomers reveals half-lives of up to 20 days in solution at room temperature. The ligands were used to explore coordination chemistry with iron(II) targeting photoswitchable spin-crossover complexes. Unexpectedly, dinuclear and tetranuclear iron(II) complexes were obtained, which were thoroughly characterized by X-ray crystallography, magnetic measurements, and Mössbauer spectroscopy. The formation of multinuclear complexes is facilitated by two coordination sites of the diarylethene, acting as a bridging ligand. The bridging nature of the diarylethene in the complexes prevents photocyclization.
机译:已经开发了带有2-(咪唑-2-基)吡啶配位单元的基于光致变色二芳基乙烯的配体新家族。新家族的四个成员已经合成。光活性配体具有非芳族乙烯桥(环戊烯,环戊烯酮和环己烯酮),以及间隔很近的光活性和金属配位点,这些位点旨在使光环化对配位金属离子的电子结构产生强烈影响。带有环戊烯酮桥和环己烯酮桥的配体显示出良好的环回复量子产率,为0.20–0.32。闭环异构体的热稳定性表明,在室温下溶液的半衰期可达20天。配体用于探索与铁(II)靶向配位的光可开关自旋交联配合物的配位化学。出乎意料的是,获得了双核和四核铁(II)配合物,这些配合物通过X射线晶体学,磁性测量和Mössbauer光谱进行了全面表征。多核配合物的形成是通过作为桥连配体的二芳基乙烯的两个配位点促进的。二芳基乙烯在配合物中的桥连性质阻止了光环化。

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