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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Octahedral metal clusters as building blocks of trimetallic superexpanded Prussian blue analogues
Jian-Jun Zhang1, Abdou Lachgar
1Department of Chemistry, and §Center for Energy, Environment and Sustainability, Wake Forest University , Winston-Salem, North Carolina 27109, United States.
Abstract:
The self-assembly of octahedral metal clusters (diamagnetic [Nb(6)Cl(12)(CN)(6)](4-) or paramagnetic [Ta(6)Cl(12)(CN)(6)](3-)), [Mn(salen)](+) [salen = N,N'-ethylenebis(salicylidene)iminate] and mononuclear {M'(CN)(x)} polycyanometallates ([Fe(CN)(6)](4-), [Cr(CN)(6)](3-), [Fe(CN)(5)(NO)](2-), or [Ni(CN)(4)](2-)) building blocks results in the formation of a series of six cluster-containing 3D heterotrimetallic frameworks: [H(3)O](2)[Nb(6)Cl(12)(CN)(6)[Mn(salen)](6)Fe(CN)(6)]·3H(2)O (1), [H(3)O][Nb(6)Cl(12)(CN)(6)[Mn(salen)](6)Cr(CN)(6)]·4H(2)O (2), [Nb(6)Cl(12)(CN)(6)[Mn(salen)](6)Fe(CN)(5)(NO)]·5H(2)O (3), [Nb(6)Cl(12)(CN)6[Mn(salen)](6)Ni(CN)4]·7H(2)O (4), [H(3)O][Ta(6)Cl(12)(CN)(6)[Mn(salen)](6)Fe(CN)6]·4H(2)O (5), and [Ta(6)Cl(12)(CN)(6)[Mn(salen)](6)Cr(CN)(6)]·7H(2)O (6). Single-crystal X-ray diffraction analyses show that compounds 1, 2, 5, and 6 have distorted face-centered-cubic frameworks that can be considered as superexpanded Prussian blue analogues built of two different hexacyanometallate nodes and expanded by insertion of the [Mn(salen)](+) complex, while 4 features a quasi-superexpanded Prussian blue framework because the structure is based on the hexacyano metal cluster and disordered tetracyano [Ni(CN)(4)](2-) nodes. The powder X-ray diffraction of 3 indicates that it possesses a quasi-superexpanded Prussian blue framework based on the hexacyano cluster and disordered pentacyano [Fe(CN)(5)(NO)](2-) nodes. Compound 6 is the first compound containing three 3d-3d'-M6 cluster (4d) spin centers. Magnetic measurements reveal that the overall magnetic nature can be systematically controlled by the choice of the octahedral metal cluster and polycyanometallate nodes. H(2)/N(2) adsorption and thermal stability of the compounds were investigated.
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