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0001645292
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Michelman, R. I.; Ball, G. E.; Bergman, R. G.; Andersen, R. A. Organometallics 1994, 13, 869-881.
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Michelman, R.I.1
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5
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0000821369
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Klein, D P.; Hayes, J. C.; Bergman, R. G. J. Am. Chem. Soc. 1988, 110, 3704.
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Klein, D.P.1
Hayes, J.C.2
Bergman, R.G.3
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6
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0000466399
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Glueck, D. S.; Winslow, L. J.; Bergman, R. G. Organometallics 1991, 10, 1462.
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Glueck, D.S.1
Winslow, L.J.2
Bergman, R.G.3
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7
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0001080640
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Rahim, M.; Bushweller, C. H.; Ahmed, K. J. Organametallics 1994, 13, 4952-4958.
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Rahim, M.1
Bushweller, C.H.2
Ahmed, K.J.3
-
8
-
-
0001687271
-
-
Imine hydrogenation catalyzed by rhodium and iridium complexes would be expected to occur through an amide complex. However, mechanistic data are scarce. A direct observation of imine insertion that produces an amide complex potentially similar to those in catalytic systems is the following: Fryzuk, M. D.; Piers, W. E. Organometallics 1990, 9, 986-98.
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Fryzuk, M.D.1
Piers, W.E.2
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9
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11344285868
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Dewey, M. A.; Knight, A.; Arif, A.; Gladysz, J. A. Chem. Ber. 1992, 125, 815-824.
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Dewey, M.A.1
Knight, A.2
Arif, A.3
Gladysz, J.A.4
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10
-
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0001280230
-
-
Sarneski, J. E.; McPhail, A. T.; Oran, K. D.; Reilley, C. N. J. Am. Chem. Soc. 1977, 99, 7376.
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Sarneski, J.E.1
McPhail, A.T.2
Oran, K.D.3
Reilley, C.N.4
-
12
-
-
15844380087
-
-
A few N-alkylarylamido complexes possess β-hydrogens: see refs 13-15
-
A few N-alkylarylamido complexes possess β-hydrogens: see refs 13-15.
-
-
-
-
13
-
-
0000629558
-
-
Matsunaga, P. T ; Hess, C. R.; Hillhouse, G. L. J. Am. Chem. Soc. 1994, 116, 3665-3666.
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Matsunaga, P.T.1
Hess, C.R.2
Hillhouse, G.L.3
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15
-
-
0000477046
-
-
Bryndza, H. A., Fultz, W. C.; Tam, W. Organometallics 1985, 4, 939.
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Bryndza, H.A.1
Fultz, W.C.2
Tam, W.3
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16
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37049098293
-
-
Bryan, E. G., Johnson, B. F. G., Lewis, J. J. Chem. Soc., Dalton Trans. 1977, 1328-1330.
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J. Chem. Soc., Dalton Trans.
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-
Bryan, E.G.1
Johnson, B.F.G.2
Lewis, J.3
-
17
-
-
15844391125
-
-
A few other examples have involved ammonia; see refs 18-20
-
A few other examples have involved ammonia; see refs 18-20.
-
-
-
-
18
-
-
0000161196
-
-
Casalnuovo, A. L.; Calabrese, J. C.; Milstein, D. Inorg. Chem. 1987, 26, 971-973.
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Casalnuovo, A.L.1
Calabrese, J.C.2
Milstein, D.3
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19
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33748234885
-
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Koelliker, R.; Milstein, D. Angew Chem., Int. Ed. Engl. 1991, 30, 707.
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Angew Chem., Int. Ed. Engl.
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, pp. 707
-
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Koelliker, R.1
Milstein, D.2
-
20
-
-
0000829320
-
-
Alcock, N. W ; Bergamini, P.; Kemp, T. J., Pringle, P. G.; Sostero, S.; Traverso, O. Inorg. Chem. 1991, 30, 1594.
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Alcock, N.W.1
Bergamini, P.2
Kemp, T.J.3
Pringle, P.G.4
Sostero, S.5
Traverso, O.6
-
22
-
-
0000235919
-
-
For a well-characterized example and related references, see: Ruiz, J.; Martinez, M. T.; Vicente, C.; Garcia, G.; Lopez, G.; Chaloner, P.; Hitchcock, P. B. Organometallics 1993, 12, 4321.
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Organometallics
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Ruiz, J.1
Martinez, M.T.2
Vicente, C.3
Garcia, G.4
Lopez, G.5
Chaloner, P.6
Hitchcock, P.B.7
-
23
-
-
0000650827
-
-
For a recent discussion of bond lengths and strengths, see: Ernst, R. D.; Freeman, J. W.; Stahl, L.; Wilson, D. R.; Arif, A. M.; Nuber, B.; Ziegler, M. L. J. Am. Chem. Soc. 1995, 117, 5075.
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Ernst, R.D.1
Freeman, J.W.2
Stahl, L.3
Wilson, D.R.4
Arif, A.M.5
Nuber, B.6
Ziegler, M.L.7
-
24
-
-
15844400713
-
-
The concentrations of water and amine were calculated on the basis of their known starting concentrations and the stoichiometry of the reaction depicted in eq 1
-
The concentrations of water and amine were calculated on the basis of their known starting concentrations and the stoichiometry of the reaction depicted in eq 1.
-
-
-
-
25
-
-
33845283243
-
-
The entropic contribution was shown to be small in the following case: Bryndza, H. E.; Fong, L. K.; Paciello, R. A.; Tam, W.; Bercaw, J. E. J. Am. Chem. Soc. 1987, 109, 1444.
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J. Am. Chem. Soc.
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-
-
Bryndza, H.E.1
Fong, L.K.2
Paciello, R.A.3
Tam, W.4
Bercaw, J.E.5
-
27
-
-
0000311245
-
-
Although the geometries of 1 and 4 are different, the bond dissociation energy as defined by the homolysis of the metal - hydroxo or - amido bond incorporates the rearrangements that are necessary to give the most stable geometry of the radical formed by such bond homolysis. For a relevant discussion, see ref 34 of Hartwig, J. F.; Andersen, R. A; Bergman. R. G. Organometallics 1991, 10, 1875. The O-H bond energy is a weighted average of those in the two isomers of 1.
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(1991)
Organometallics
, vol.10
, pp. 1875
-
-
Hartwig, J.F.1
Andersen, R.A.2
Bergman, R.G.3
-
28
-
-
15844379001
-
-
note
-
obs values were independent of the initial concentration of 1.
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