Redox-Active 1D Coordination Polymers of Iron–Sulfur Clusters

作者：Noah E. Horwitz, Jiaze Xie, Alexander S. Filatov, R. Papoular, William Shepard, David Z. Zee, Mia P. Grahn, Chloe Gilder, John S. Anderson · 发表于：Journal of the American Chemical Society · 年份：2019 · DOI：10.1021/jacs.8b12339 · 被引用次数：68 · 研究领域：Metal-Organic Frameworks: Synthesis and Applications、Magnetism in coordination complexes、Organic and Molecular Conductors Research

Here we describe the combination of an archetypal redox-active metal sulfide cluster, Fe 4 S 4, with an organic linker, 1,4-benzenedithiolate, to prepare coordination polymers containing infinite chains of Fe 4 S 4 clusters. The crystal structures of two solid materials have been solved from synchrotron X-ray powder diffraction data using simulated annealing and refined by a least-squares Rietveld refinement procedure. The electronic properties of these chains have also been characterized by UV–visible and Mössbauer spectroscopies. Additional experiments demonstrated that these chains can be solubilized by variation of the countercation and that the chain structure is maintained in solution. The redox-activity of the Fe 4 S 4 clusters can be accessed with chemical reagents. Introduction of charge carriers by reduction of the Fe 4 S 4 clusters is found to increase the electrical conductivity of the materials by up to 4 orders of magnitude. These results highlight the utility of Fe 4 S 4 clusters as redox-active building blocks in preparing new classes of coordination polymers.