Novel Polyselenidoarsenate and Selenidoarsenate: Solvothermal Synthesis and Characterization of [Co(phen)<sub>3</sub>][As<sub>2</sub>Se<sub>2</sub>(μ-Se<sub>3</sub>)(μ-Se<sub>5</sub>)] and [Co(phen)<sub>3</sub>]<sub>2</sub>[As<sub>8</sub>Se<sub>14</sub>]
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Novel cobalt polyselenidoarsenate [Co(phen)3][As2Se2(μ-Se3)(μ-Se5)] (1; phen = 1,10-phenanthroline) was methanolothermally synthesized by the reaction of CoCl2, As2O3, and Se templated by phen in a CH3OH solvent at 130 °C. The same reaction in a H2O solvent yielded cobalt selenidoarsenate [Co(phen)3]2[As8Se14] (2). In 1, the AsSe+ units are alternately joined by the μ-Se32− and μ-Se52− bridging ligands to form a novel helical polyselenidoarsenate chain [As2Se2(μ-Se3)(μ-Se5)2−]∞. In 2, eight pyramidal AsSe3 units are connected via corner sharing into the new member of the selenidoarsenate aggregate [As8Se14]4− with a condensation grade of 0.571, which represents the first discrete selenidoarsenate(III) with a condensation grade of above 0.50. The octahedral complex [Co(phen)3]2+ is formed in situ to act as a countercation in compounds 1 and 2. 1 and 2 exhibit steep absorption band gaps at 2.09 and 2.16 eV, respectively.
