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Redox-Active 1D Coordination Polymers of Iron–Sulfur Clusters
Author(s) -
Noah E. Horwitz,
Jiaze Xie,
Alexander S. Filatov,
R. Papoular,
William Shepard,
David Z. Zee,
Mia P. Grahn,
Chloe Gilder,
John S. Anderson
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b12339
Subject(s) - chemistry , redox , reagent , crystallography , polymer , rietveld refinement , coordination polymer , crystal structure , cluster (spacecraft) , inorganic chemistry , organic chemistry , computer science , programming language
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.

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