Electronic, infrared, and resonance-Raman spectroscopic studies of the linear-chain, halogen-bridged, mixed-valence complexes [Pt(NH3)4][Pt(NH3)4X2]Y4(X = Br or I, Y = HSO4, ClO4, or BF4). The X-ray crystal structures of [Pt(NH3)4][Pt(NH3)4Br2][HSO4]4and [Pt(NH3)4][Pt(NH3)4I2][HSO4]3[OH]·H2O

Author(s):  
Robin J. H. Clark ◽  
Mohamedally Kurmoo ◽  
Anita M. R. Galas ◽  
Michael B. Hursthouse
ChemSusChem ◽  
2016 ◽  
Vol 10 (3) ◽  
pp. 551-561 ◽  
Author(s):  
Anke Keidel ◽  
Isidoro López ◽  
Jana Staffa ◽  
Uwe Kuhlmann ◽  
Fernando Bozoglian ◽  
...  

2002 ◽  
Vol 57 (10) ◽  
pp. 1090-1100
Author(s):  
Franziska Emmerling ◽  
Caroline Röhr

AbstractThe title compounds were synthesized at a temperature of 700 °C via oxidation of elemental Bi with the hyperoxides AO2 or via reaction of the elemental alkali metals A with Bi2O3. Their crystal structures have been determined by single crystal x-ray diffraction. They are dominated by two possible surroundings of Bi by O, the ψ-trigonal-bipyramidal three (B) and the ψ-tetrahedral four (T) coordination. Cs6Bi4O9 (triclinic, spacegroup P1̄, a = 813.82(12), b = 991.60(14), c = 1213.83(18) pm, α = 103.658(2), β = 93.694(3), γ = 91.662(3)°, Z = 2) contains centrosymmetric chain segmentes [Bi8O18]12- with six three- (T) and two four-coordinated (B) Bi(III) centers. K9Bi5O13 (monoclinic, spacegroup P21/c, a = 1510.98(14), b = 567.59(5), c = 2685.6(2) pm, β = 111.190(2)°, Z = 4) is a mixed valence compound with isolated [BivO4]3- tetrahedra and chains [BiIII4O9]6- of two T and two B coordinated Bi. In the compounds A2Bi4O7 (A = Rb/Cs: monoclinic, C2/c, a = 2037.0(3) / 2130.6(12), b = 1285.5(2) / 1301.9(7), c = 1566.6(2) / 1605.6(9) pm, β = 94.783(3) / 95.725(9)°, Z = 8) ribbons [Bi4O6O2/2]2- are formed, which are condensed to form a three-dimensional framework.


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