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For some prior examples of 16-electron Pd alkene complexes see: (a) Hodgson, M.; Parker, D.; Taylor, R. J.; Ferguson, G. J. Chem. Soc., Chem. Commun. 1987, 1309. (b) Benn, R.; Betz, P.; Goddard, R.; Jolly, P. W.; Kokel, N.; Kruger, C.; Topalovic, I. Z. Naturforsch. B 1991, 46, 1395. (c) Herrmann, W. A.; Thiel, W. R.; Brossmer, C.; Ofele, K.; Priermeier, T.; Scherer, W. J. Organomet. Chem. 1993, 461, 51. (d) Fawcett, J.; Kemmitt, R.; Russell, D. R.; Serindag, O. J. Organomet. Chem. 1995, 486, 171. (e) Goddard, R.; Hopp, G.; Jolly, P. W.; Kruger, C.; Mynott, R.; Wirtz, C. J. Organomet. Chem. 1995, 486, 163.
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24
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For some prior examples of 16-electron Pd alkene complexes see: (a) Hodgson, M.; Parker, D.; Taylor, R. J.; Ferguson, G. J. Chem. Soc., Chem. Commun. 1987, 1309. (b) Benn, R.; Betz, P.; Goddard, R.; Jolly, P. W.; Kokel, N.; Kruger, C.; Topalovic, I. Z. Naturforsch. B 1991, 46, 1395. (c) Herrmann, W. A.; Thiel, W. R.; Brossmer, C.; Ofele, K.; Priermeier, T.; Scherer, W. J. Organomet. Chem. 1993, 461, 51. (d) Fawcett, J.; Kemmitt, R.; Russell, D. R.; Serindag, O. J. Organomet. Chem. 1995, 486, 171. (e) Goddard, R.; Hopp, G.; Jolly, P. W.; Kruger, C.; Mynott, R.; Wirtz, C. J. Organomet. Chem. 1995, 486, 163.
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0006583739
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For some prior examples of 16-electron Pd alkene complexes see: (a) Hodgson, M.; Parker, D.; Taylor, R. J.; Ferguson, G. J. Chem. Soc., Chem. Commun. 1987, 1309. (b) Benn, R.; Betz, P.; Goddard, R.; Jolly, P. W.; Kokel, N.; Kruger, C.; Topalovic, I. Z. Naturforsch. B 1991, 46, 1395. (c) Herrmann, W. A.; Thiel, W. R.; Brossmer, C.; Ofele, K.; Priermeier, T.; Scherer, W. J. Organomet. Chem. 1993, 461, 51. (d) Fawcett, J.; Kemmitt, R.; Russell, D. R.; Serindag, O. J. Organomet. Chem. 1995, 486, 171. (e) Goddard, R.; Hopp, G.; Jolly, P. W.; Kruger, C.; Mynott, R.; Wirtz, C. J. Organomet. Chem. 1995, 486, 163.
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26
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85088279349
-
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note
-
1H NMR spectroscopy at 500 MHz. The disappearance of the signals corresponding to complex 3 was monitored, and these were integrated against the emergence of new peaks corresponding to methyl cinnamate and methyl acrylate.
-
-
-
-
27
-
-
85088279213
-
-
note
-
4NCl, respectively.
-
-
-
-
28
-
-
3743071124
-
-
note
-
13). The equilibrium is thus considerably in favor of (dppf)Pd(MeA), and the complex is not very labile, in accord with NMR observations (ref 10).
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30
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3743072223
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note
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2PdX anion (Pa = dppf) under comparable conditions.
-
-
-
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32
-
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3743102257
-
-
note
-
The rate of decomposition was less than that of the oxidative addition; nevertheless the cation and the aryl derivative were added to the (dppf)Pd(MeA) solution as a premixed solution.
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33
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