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See, for example: (a) Sánchez, G.; Momblona, F.; Sánchez, M.; Pérez, J.; López, G.; Casabó, J.; Molins, E.; Miravitlles, C. Eur. J. Inorg. Chem. 1998, 1199. (b) Sánchez, G.; Momblona, F.; Garcia, G.; López, G.; Pinilla, E.; Monge, A. J. Chem. Soc., Dalton Trans. 1994, 2271. Wei, C. H.; Dahl, L. F. Inorg. Chem. 1970, 9, 1878. Gibson, D.; Lippard, S. J. Inorg. Chem. 1986, 25, 219. (e) Henkel, G.; Kriege, M.; Matsumoto, K. J. Chem. Soc., Dalton Trans. 1988, 657. See, for example: (a) Song, L.-C.; Dong, Y.-B.; Hu, Q.-M.; Li, Y.-K.; Sun, J. Polyhedron 1998, 17, 1579. (b) Teo, B. K.; Bakirtzis, V.; Snyder-Robinson, P. A. J. Am. Chem. Soc. 1983, 105, 6330. North, T. E.; Thoden, J. B.; Spencer, B.; Dahl, L. F. Organometallics 1993, 12, 1299. Braunstein, P.; Sappa, E.; Tiripicchio, A.; Tiripicchio Camellini, M. Inorg. Chim. Acta 1980,45, L191. (e) Cecconi, F.; Ghilardi, C. A.; Midollini, S.; Orlandini, A.; Vacca, A.; Ramirez, J. A. J. Chem. Soc., Dalton Trans. 1990, 773.
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See, for example: (a) Sánchez, G.; Momblona, F.; Sánchez, M.; Pérez, J.; López, G.; Casabó, J.; Molins, E.; Miravitlles, C. Eur. J. Inorg. Chem. 1998, 1199. (b) Sánchez, G.; Momblona, F.; Garcia, G.; López, G.; Pinilla, E.; Monge, A. J. Chem. Soc., Dalton Trans. 1994, 2271. Wei, C. H.; Dahl, L. F. Inorg. Chem. 1970, 9, 1878. Gibson, D.; Lippard, S. J. Inorg. Chem. 1986, 25, 219. (e) Henkel, G.; Kriege, M.; Matsumoto, K. J. Chem. Soc., Dalton Trans. 1988, 657. See, for example: (a) Song, L.-C.; Dong, Y.-B.; Hu, Q.-M.; Li, Y.-K.; Sun, J. Polyhedron 1998, 17, 1579. (b) Teo, B. K.; Bakirtzis, V.; Snyder-Robinson, P. A. J. Am. Chem. Soc. 1983, 105, 6330. (c) North, T. E.; Thoden, J. B.; Spencer, B.; Dahl, L. F. Organometallics 1993, 12, 1299. Braunstein, P.; Sappa, E.; Tiripicchio, A.; Tiripicchio Camellini, M. Inorg. Chim. Acta 1980,45, L191. (e) Cecconi, F.; Ghilardi, C. A.; Midollini, S.; Orlandini, A.; Vacca, A.; Ramirez, J. A. J. Chem. Soc., Dalton Trans. 1990, 773.
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44
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2442760441
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note
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8): δ 80.37 (d, J = 30.5 Hz), 70.61 (d, J = 30.5 Hz).
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45
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2442725455
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Alternatively, A could react with 1b to generate 2b, although this pathway is more complicated than a simple dimerization of transient A as loss of a second molecule of benzene by a different mechanism must be involved
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Alternatively, A could react with 1b to generate 2b, although this pathway is more complicated than a simple dimerization of transient A as loss of a second molecule of benzene by a different mechanism must be involved.
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46
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84981759690
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Huisgen, R.; Seidl, H.: Brtining, I. Chem. Ber. 1969, 102, 1102.
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Huisgen, R.1
Seidl, H.2
Brtining, I.3
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48
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2442768768
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In control experiments, the sulfido dimers 2 do not react with 4 or 6 at room temperature to yield any observable products by NMR spectroscopy
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In control experiments, the sulfido dimers 2 do not react with 4 or 6 at room temperature to yield any observable products by NMR spectroscopy.
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