Incorporation of a New Type of Transition Metal Complex into the Thioarsenate Anion: Syntheses, Structures, and Properties of Two Novel Compounds [Mn<sub>3</sub>(2,2‘-bipy)<sub>3</sub>(As<sup>V</sup>S<sub>4</sub>)<sub>2</sub>]<i><sub>n</sub></i>·<i>n</i>H<sub>2</sub>O and Mn<sub>2</sub>(2,2‘-bipy)As<sub>2</sub><sup>III</sup>S<sub>5</sub>
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The incorporation of [Mn(2,2‘-bipy)2]2+ with thioarsenate resulted in the formation of two novel compounds, [Mn3(2,2‘-bipy)3(AsVS4)2]n·nH2O (1) and Mn2(2,2‘-bipy)As2IIIS5 (2), in which the main-group chalcogenide framework is incorporated with a [tm(2,2‘-bipy)m]n+ complex. Meanwhile, the tetrathioarsenate(V) anion acts as a new μ3-1κS:1,2κS‘:2,3κS‘ ‘:3κS‘ ‘‘ ligand in 1, in which all four S atoms of the [AsVS4]3- anion are coordinating to metal. As a result, the two compounds exhibit semiconducting properties (Eg = 2.18 eV (1) and 1.83 eV (2)) and strong blue photoluminescence, with the emission maximum occurring at about 440 nm. Magnetic measurements show that both compounds have AF ordered states with Néel temperatures of 19 and 24 K for 1 and 2, respectively.
