Structural chemistry of organically templated transition metal phosphite chlorides, [BH2][M(H2PO3)2Cl2] (B = diamine, M = Mn–Ni, Cd) as new analogs of “hydroselenite halides”
Dmitri O. Charkin, Vadim E. Kireev, Dmitri N. Dmitriev, Alexander M. Banaru, Dina V. Deyneko, Sergey M. Aksenov
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引用次数: 0
Abstract
Following the previously reported (enH2)[Co(H2PO3)2Cl2] (enH2 = ethylenediammonium cation), we successfully prepared its analogs with other divalent transition metal cations: Mn2+, Fe2+, Ni2+, and Cd2+. These compounds are isostructural to each other and the archetypic hydroselenites, (enH2)[M(HSeO3)2X2]. Despite evident similarities, some essential differences are observed between hydroselenites and hydrophosphites, both in chemistry and in structural details. Due to smaller size of H2PO3− relative to HSeO3−, only chloride phosphites could be prepared; the reducing capacity of H2PO3− permits preparation of FeII compound but not that of CuII. A single attempt to introduce piperazinediium cation instead of ethylenediammonium results in formation of (pipH2)[Co(H2PO3)2Cl2] with a structure different from (pipH2)[Cd(HSeO3)2Cl2]. Another serendipitous product is the 1-methylpiperazinediium derivative, (mpipH2)2[Co(H2PO3)2I3][H(H2PO3)2], which features a yet unique complex hydrogen-bonded network.
期刊介绍:
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