SYNTHESES, STRUCTURES, AND PROPERTIES OF 6 NOVEL ALKALI-METAL TIN SULFIDES - K2SN2S8, ALPHA-RB2SN2S8, BETA-RB2SN2S8, K2SN2S5, CS2SN2S6, AND CS2SNS14

Six alkali metal tin polysulfides and one monosulfide, K2Sn2S8 (I), alpha-Rb2Sn2S8 (II), beta-Rb2Sn2S8 (III), K2Sn2S5 (IV), Cs2Sn2S6 (V), and Cs2SnS14 (VI), respectively, were synthesized by a molten salt technique. I and IV were made by heating mixtures of Sn/K2S/S (molar ratio 1/2/8) at 275 and 320-degrees-C, respectively, for 4-6 days. II and III were made by heating mixtures of Sn/Rb2S/S (molar ratio 1/2/12 for II and 1/1/8 for III at 330 and 450-degrees-C, respectively, for 4-6 days. V and VI were made by heating mixtures of Sn/Cs2S/S (molar ratio 1/3/8 for V and 1/2/8-12 for VI at 275-degrees-C for 4-6 days. The crystals form in a K2S(x), Rb2Sx, and Cs2Sx flux, respectively. Orange crystals of I crystallize in the monoclinic space group P2(1)/n with a = 9.580(8) angstrom, b = 10.004(5) angstrom, c = 14.131(7) angstrom, beta = 107.82(6)degrees, and Z = 4. Orange crystals of II and III have the same anionic frameworks as I. II crystallizes also in the monoclinic space group P2(1)/n with a = 9.788(3) angstrom, b = 9.978(3) angstrom, c = 14.360(2) angstrom, and beta = 106.70(2)degrees, and Z = 4. III crystallizes in the orthorhombic space group Pbcn with a = 9.987(5) angstrom, b = 19.635(3) angstrom, c = 13.747(3) angstrom, and Z = 8. The yellow-orange IV crystallizes in the monoclinic space group C2/c with a = 11.804(3) angstrom, b = 7.808(1) angstrom, c = 11.539(1) angstrom, beta = 108.35(1)degrees, and Z = 4. The yellow V crystallizes in the triclinic space group P1BAR with a = 7.289(4) angstrom, b = 7.597(3) angstrom, c = 6.796(3) angstrom, alpha = 114.80(3)degrees, beta = 108.56(4)degrees, gamma = 97.54(4)degrees, and Z = 1. Red crystals of VI are monoclinic, space group P2(1)/n, with a = 6.964(6) angstrom, b = 18.66(1) angstrom, c = 14.80(1) angstrom, beta = 99.39(1)degrees, and Z = 4. The structures of these six compounds have been determined by single-crystal X-ray diffraction analysis. IR and Raman spectra for these compounds are reported. I-III have novel two-dimensional structures. Each [Sn2S8]n2n- layer is composed of [Sn2S4]n parallel chains, which contain octahedral SnS6 and tetrahedral SnS4, cross-linked by S4(2-) ligands. Charge-compensating potassium or rubidium cations are found between the layers. IV has the Tl2Sn2S5 structure type and has a three-dimensional structure, with [SnS3]2n- chains formed by distorted SnS5 trigonal bipyramids sharing two of their common edges with one another. Those chains are then cross-linked by sharing the remaining vertices of the trigonal bipyramids to generate parallel tunnels in which potassium cations are located. The structure of V is closely related to IV. It also comprises [SnS3]n2n- chains which in a different fashion are cross-linked by S2(2-) to form an extended two-dimensional structure. VI contains a molecular [SnS14]2- Complex anion with octahedral Sn4+ ligated by two S42- and one S62- chelating ligands. The UV/vis optical properties of I-V are reported. The optical band gaps are 2.15 eV for I-III, 2.36 eV for IV, and 2.44 eV for V.