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• W2004374016 endingPage "107" @default.
• W2004374016 startingPage "86" @default.
• W2004374016 abstract "The closo-[1-M(CO)3(η4-E9)]4- (E = Sn, Pb; M = Mo, W) anions have been obtained by extracting the binary alloys KSn2.05 and KPb2.26 in ethylenediamine (en) in the presence of 2,2,2-crypt or in liquid NH3 followed by reaction with M(CO)3·mes (M = Mo, W) or Cr(CO)3·tol in en or liquid NH3 solution. Crystallization of the molybdenum and tungsten salts was induced by vapor diffusion of tetrahydrofuran into the en solutions. The salts [2,2,2-crypt-K]4[1-M(CO)3(η4-Sn9)]·en (M = Mo, W) crystallize in the triclinic system, space group P1̄, Z = 4, a = 16.187(3) Å, b = 25.832(4) Å, c = 29.855(5) Å, α = 111.46(1)°, β = 102.84(2)°, γ = 92.87(2)° at −95 °C (M = Mo) and a = 17.018(3) Å, b = 27.057(5) Å, c = 28.298(6) Å, α = 66.42(3)°, β = 76.72(3)°, γ = 87.27(3)° at 20 °C (M = W). The salts (CO)3M(en)2[2,2,2-crypt-K]4[1-M(CO)3(η4-Pb9)]·2.5en (M = Mo, W) crystallize in the triclinic system, space group P1̄, Z = 2, a = 16.319(3) Å, b = 17.078(3) Å, c = 24.827(5) Å, α = 71.82(3)°, β = 83.01(3)°, γ = 81.73(3)° at −133 °C (M = Mo) and a = 16.283(4) Å, b = 17.094(3) Å, c = 24.872(6) Å, α = 71.62(2)°, β = 82.91(2)°, γ = 81.35(2)° at −153 °C (M = W). The [1-M(CO)3(η4-Sn9)]4- anions were also characterized in liquid NH3 solution by 119Sn, 117Sn, and 95Mo NMR spectroscopy. Unlike their fluxional precursor, nido-Sn94-, NMR studies show that the [1-M(CO)3(η4-Sn9)]4- anions are rigid on the NMR time scale. All possible inter- and intraenvironmental couplings, J(119,117Sn−119,117Sn), J(119,117Sn−183W), and one J(119,117Sn−95Mo) coupling, have been observed and assigned. Complete spin−spin coupling constant assignments were achieved by detailed analyses and simulations of all spin multiplets that comprise the 119Sn and 117Sn NMR spectra and that arise from natural abundance tin isotopomer distributions and from natural abundance 183W, in the case of [1-W(CO)3(η4-Sn9)]4-. Both the solid state and solution structures of the [1-M(CO)3(η4-Sn9)]4- anions are based on a closo-bicapped square antiprismatic structure in which the transition metal occupies a cap position. The cluster structures are consistent with Wade's rules for 22 (2n + 2) skeletal electron systems. Electron structure calculations at the density functional theory (DFT) level provide fully optimized geometries that are in agreement with the experimental structures. Complete assignment of the NMR spectra was also aided by GIAO calculations. The calculated vibrational frequencies of the E94- and [1-M(CO)3(η4-E9)]4- anions are also reported and are used to assign the solid-state vibrational spectra of the [1-M(CO)3(η4-E9)]4- anions." @default.
• W2004374016 created "2016-06-24" @default.
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• W2004374016 date "2001-12-13" @default.
• W2004374016 modified "2023-10-16" @default.
• W2004374016 title "Syntheses, Crystal Structures, and Density Functional Theory Calculations of the <i>c</i><i>loso</i>-[1-M(CO)₃(η⁴-E₉)]⁴^- (E = Sn, Pb; M = Mo, W) Cluster Anions and Solution NMR Spectroscopic Characterization of [1-M(CO)₃(η⁴-Sn₉)]⁴^- (M = Cr, Mo, W)" @default.
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• W2004374016 doi "https://doi.org/10.1021/ic010695k" @default.
• W2004374016 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11782147" @default.
• W2004374016 hasPublicationYear "2001" @default.
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