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9
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0001336545
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10
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0001094109
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18
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0011591273
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Under the same conditions, the treatment of the acetone solutions of 1 with 1.0 equiv of T1PF6 leads to the dimer cation, P iPr32H2Os(μ-Cl) 3OsH2(PiPr3)2, which has been previously prepared by protonation of 1 with CF3SO3H in diethyl ether. See: Kuhlman, R, Streib, W. E, Caulton, K. G. Inorg. Chem. 1995, 34, 1788
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3H in diethyl ether. See: Kuhlman, R.; Streib, W. E.; Caulton, K. G. Inorg. Chem. 1995, 34, 1788.
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19
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64749099937
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The BF4 salt of 4 has been previously prepared via [OSH(η2-H2)(CH3CN)2(P i)2]BF4 by protonation in acetonitrile of OsH6(PiPr3)2 with HBF4. See: Smith, K.-T, filset. M, Kuhlman, R, Caulton, K. G. J. Am. Chem. Soc. 1995, 117, 9473
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4. See: Smith, K.-T.; filset. M.; Kuhlman, R.; Caulton, K. G. J. Am. Chem. Soc. 1995, 117, 9473.
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21
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64749086521
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Although the acetonitrile ligands of 5 exchange with the solvent10 and unsaturated species could be proposed as intermediates of the exchange, solvent coordination appears to be faster than diene coordination
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10 and unsaturated species could be proposed as intermediates of the exchange, solvent coordination appears to be faster than diene coordination.
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22
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0041936278
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