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1
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0003637198
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Steifel, E. I, Matsumoto K, Eds, American Chemical Society: Washington, DC
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(a) Transition Metal Sulfur Chemistry, Biological and Industrial Significance; Steifel, E. I., Matsumoto K., Eds.; American Chemical Society: Washington, DC, 1996.
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(1996)
Transition Metal Sulfur Chemistry, Biological and Industrial Significance
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2
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0003666155
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Weber, Th, Prons, R, van Santen, R. A, Eds, Kluwer Academic Publishers: Dordrecht, The Netherlands
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(b) Transition Metal Sulphides - Chemistry and Catalysis; Weber, Th., Prons, R., van Santen, R. A., Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1998.
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(1998)
Transition Metal Sulphides - Chemistry and Catalysis
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7
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33749842932
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(c) Matsumoto, T.; Nakaya, Y.; Tatsumi, K. Organometallics 2006, 25, 4835.
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(2006)
Organometallics
, vol.25
, pp. 4835
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Matsumoto, T.1
Nakaya, Y.2
Tatsumi, K.3
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9
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42149155185
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Crystal data for 2: C74H74Ge 2NiP2S4; monoclinic; C2/c (No. 15, a, 30.814(3) Å b, 21.9372(16) Å c, 30.454(3) Å; β, 127.5838(18)°, V, 16311(3) Å Z, 8; T, 193 K; λ, 0.71073 Å; F(000, 5632; μ, 11.363 cm-1; ρcalcd, 1.105 g cm -3; 91 233 reflections (2θ < 55.0°, 18 666 unique (Rint, 0.093, R1, 0.0860 (I > 2σ(I, wR2, 0.2642 (all data, GOF (on F 2, 1.367. Crystal data for 3·1.5toluene: C 94.5H92Ge2NiP2S4; triclinic; P1 (No. 2, a, 14.0364(14) Å b, 18.010(3) Å c, 18.085(3) Å; α, 106.910(6)°, β, 107.7173(13)°, γ, 95.117(2)°, V, 4086.6(9) A
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2. Anisotropic refinement was applied to all non-hydrogen atoms. All the hydrogen atoms were put at calculated positions, except for those of the disordered crystalline solvent molecules, two toluenes for 3 and a dichloromethane for 5.
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10
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0004009372
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6th ed, John Wiley & Sons: New York
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Cotton, F. A.; Wilkinson, G.; Murillo, G. Advanced Inorganic Chemistry, 6th ed.; John Wiley & Sons: New York, 1999; pp 840-842..
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(1999)
Advanced Inorganic Chemistry
, pp. 840-842
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Cotton, F.A.1
Wilkinson, G.2
Murillo, G.3
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11
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42149192874
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-1. The fraction containing 5 was observed at 45 min retention time, while 1 has a significantly longer 49 min retention time.
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-1. The fraction containing 5 was observed at 45 min retention time, while 1 has a significantly longer 49 min retention time.
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12
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42149193435
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Synthesis of [DmpGe(μ-S)3]4Ni6 (5, A toluene solution of 3 (200 mg, 0.135 mmol) was heated for 12 h at 110°C. The crude product was separated by GPC (CHCl3, 3.5 mL/min) to give a fraction of 45 min retention time, which was further crystallized by EtOH/CH2Cl2 to give 5 (27 mg) as a red crystals. The yield calculated on the basis of nickels is 53, 1H NMR (500 MHz, CDCl3, δ, 7.47 (t, J, 7.6 Hz, 4H, p-CH of Dmp, 6.98 (s, 16H, m-CH of Mes, 6.97 (d, J, 7.6 Hz, 8H, m-CH of Dmp, 2.27 (s, 24H, p-CH3 of Mes, 1.83 (s, 48H, o-CH3 of Mes, Elemental analysis calcd, ) for C96H100Ge4Ni6S12: C, 50.55; H, 4.42; S, 16.87. Found: C, 49.98; H, 4.02; S, 16.90
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12: C, 50.55; H, 4.42; S, 16.87. Found: C, 49.98; H, 4.02; S, 16.90.
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13
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42149186734
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McCleverty, J. A, Meyer, T. J, Eds, Elsevier: Amsterdam
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Meyer, F.; Kozlowski, H. In Comprehensive Coordination Chemistry II; McCleverty, J. A., Meyer, T. J., Eds.; Elsevier: Amsterdam, 2004; Vol. 6, pp 322-342..
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(2004)
Comprehensive Coordination Chemistry II
, vol.6
, pp. 322-342
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Meyer, F.1
Kozlowski, H.2
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