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1
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1642458769
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Université de Bourgogne
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(a) Université de Bourgogne.
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2
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1642581141
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Université de Sherbrooke
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(b) Université de Sherbrooke.
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4
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0001482221
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(h) Pelagatti, P.; Bacchi, A.; Carelli, M.; Costa, M.; Fochi, A.; Ghidini, P.; Leporati, E.; Masi, M.; Pelizzi, C.; Pelizzi, G. J. Organomet. Chem. 1999, 583, 94.
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Pelizzi, G.10
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0001671703
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Stern and Maples examined the catalytic activity of this complex with respect to homogeneous hydrogenation. Because the complex was handled in air, the true nature of the catalyst may be unknown. Stern, E.; Maples, P. K. J. Catal. 1972, 27, 120.
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Sappa, E.6
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24
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(c) Adams, R. D.; Li, Z.; Swepson, P.; Wu, W.; Yamamoto, J. J. Am. Chem. Soc. 1992, 114, 10657.
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25
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0542367975
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in Russian
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Berenblyum, A. S.; Aseeva, A. P.; Lakham, L. I.; Petrovsky, V. V.; Moiseev, I. I. Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 1227 (in Russian).
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Berenblyum, A.S.1
Aseeva, A.P.2
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Petrovsky, V.V.4
Moiseev, I.I.5
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26
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(a) Bianchini, C., Meli, A.; Peruzzini, M.; Vizza, F.; Zanobini, F.; Frediani, P. Organometallics 1989, 8, 2080.
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See, for exampl: (a) van Laren, M. W.; Duin, M. A.; Klerk, C.; Naglia, M.; Rogolino, D.; Pelagatti, P.; Bacchi, A.; Pelizzi, C.; Elsevier, C. J. Organometallics 2002, 21, 1546.
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Elsevier, C.J.9
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30
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(a) Pelagatti, P.; Venturini, A.; Leporati, A.; Carcelli, M.; Costa, M.; Bacchi, A.; Pelizzi, G.; Pelizzi, C. J. Chem. Soc., Dalton Trans. 1998, 2715.
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Pelagatti, P.1
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Elsevier, C.J.2
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33
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1642499753
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note
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6 at 20 °C) performed at the University of Lausanne, also did reveal any intermediates.
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34
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1642581139
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note
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(a) The mercury test18b was not suitable in this case, since the title cluster reacts rapidly with Hg. In fact, reactivity between a Pd species and Hg has been observed before.18c
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35
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0020169566
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(b) Fusi, A.; Ugo, R.; Psaro, R.; Braunstein, P.; Dehand, J. J. Mol. Catal. 1982, 16, 217.
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Fusi, A.1
Ugo, R.2
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Dehand, J.5
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36
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0001240579
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(c) Harvey, P. D.; Aye, K. T.; Hierso, K.; Isabel, E.; Lognot, I.; Mugnier, Y.; Rochon, F. D. Inorg. Chem. 1994, 33, 5981.
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Harvey, P.D.1
Aye, K.T.2
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Isabel, E.4
Lognot, I.5
Mugnier, Y.6
Rochon, F.D.7
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37
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0005218809
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9 dimeric species axially functionalized by good coordinating solvent molecules have already been reported in the past. See, for examples: (a) Maekawa, M.; Munakata, M.; Kudora-Sowa, T.; Suenaga, Y. Polyhedron 1998, 17, 3657.
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Polyhedron
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Maekawa, M.1
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Suenaga, Y.4
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38
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0001679032
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(b) Maekawa, M.; Munakata, M.; Kuroda-Sowa, T.; Suenaga, Y. Inorg. Chim. Acta 1998, 281, 116.
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Maekawa, M.1
Munakata, M.2
Kuroda-Sowa, T.3
Suenaga, Y.4
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39
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0345003699
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(c) Hill, R. H.; De Mayo, P.; Puddephatt, R. J. Inorg. Chem. 1982, 21, 3642.
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Hill, R.H.1
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40
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0002544916
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Addition of alkynes onto Pd-Pd bonds is well documented. See, for examples: (a) Davies, J. A.; Pinkerton, A. A.; Syed, R.; Vilmer, M. J. Chem. Soc., Chem. Commun. 1988, 47.
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0000449555
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(b) Davies, J. A.; Kirschbaum, K.; Kluwe, C. Organometallics 1994, 13, 3664.
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49249148007
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(e) Balch, A. L.; Lee, C.-L.; Lindsay, C. H.; Olmstead, M. M. J. Organomet. Chem. 1979, 177, C22.
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(f) Lee, C.-L.; Hunt, C. T.; Balch, A. L. Inorg. Chem. 1981, 20, 2498.
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Lee, C.-L.1
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48
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1642540620
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note
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1H NMR or the appearance of other peaks in the GC/MS.
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50
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0001467798
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+,23d.e suggests that such a formulation is reasonable. (a) Grushin, V. V. Chem. Rev. 1996, 96, 2011.
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Grushin, V.V.1
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0345425081
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(b) Stockland, R. A., Jr.; Anderson, G. K.; Rath, N. P. J. Am. Chem. Soc. 1999, 121, 7945.
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Stockland Jr., R.A.1
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(c) Stockland, R. A., Jr.; Anderson, G. K.; Rath, N. P. Inorg. Chim. Acta 2000, 300, 395.
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Stockland Jr., R.A.1
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3543065535
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(d) Brown, M. P.; Puddephatt, R. J.; Rashidi, M.; Seddon, K. R. Inorg. Chim. Acta 1977, 23, L33.
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Brown, M.P.1
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(e) Brown, M. P.; Puddephatt, R. J.; Rashidi, M.; Seddon, K. R. J. Chem. Soc., Dalton Trans. 1978, 516.
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55
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1642458765
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note
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2. The alkyne substrate acted as a spectator and 2 was never observed.
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56
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1642540619
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note
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2) were inserted with the cluster was performed to demonstrate that the alkyne substrate is preferentially hydrogenated over the alkene. The alkyne substrate is hydrogenated first, resulting in an increase of the total [cis-alkene]. Then, [cis-alkene] starts decreasing after 20 min.
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57
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1642540618
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note
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4), has been reported in the literature.
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58
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0001167977
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(c) Espinet, P.; Fornies, J.; Fortunato, C.; Hidalgo, G.; Martinez, F.; Thomas, M.; Welch, A. J. J. Organomet. Chem. 1986, 317, 105.
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Espinet, P.1
Fornies, J.2
Fortunato, C.3
Hidalgo, G.4
Martinez, F.5
Thomas, M.6
Welch, A.J.7
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59
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0040464218
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Brown, M. P.; Fisher, J. R.; Hill, R. H.; Puddephatt, R. J.; Seddon, K. R. Inorg. Chem. 1981, 20, 3516.
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Brown, M.P.1
Fisher, J.R.2
Hill, R.H.3
Puddephatt, R.J.4
Seddon, K.R.5
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60
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0004076526
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Cotton, F. A.; Wilkinson, G.; Gaus, P. Basic Inorganic Chemistry, 3rd ed.; Wiley: Toronto, 1987; p 208.
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Cotton, F.A.1
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2 species is precedented.
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(b) Balch, A. L.; Hunt, C. T.; Lee, C.-L.; Olmstead, M. M.; Farr, J. P. J. Am. Chem. Soc. 1981, 103, 3764.
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Balch, A.L.1
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Lee, C.-L.3
Olmstead, M.M.4
Farr, J.P.5
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63
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(c) Uson, R.; Fornies, J.; Espinet, P.; Martinez, F.; Fortuno, C.; Menjon, B. J. Organomet. Chem. 1983, 256, 365.
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Menjon, B.6
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Chin, C.C.H.1
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Hor, T.S.A.6
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65
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(a) Another example where the hydrogenation is stopped at the alkene using Py as the solvent exists: Kerr, J. M.; Suckling, C. J.; Bamfield, P. J. Chem. Soc., Perkin Trans. 1 1990, 4, 887.
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Kerr, J.M.1
Suckling, C.J.2
Bamfield, P.3
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66
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1642581138
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note
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3. As alkynes are more reactive than alkenes based on this work, it is possible that hydrogenation reactions for both alkynes and alkenes are slowed to the point that the hydrogenation of alkenes are too slow to be observed in the conditions used.
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