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(c) Jia, G.; Lough, A. J.; Morris, R. H. Organometallics 1992, 11, 161-171.
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6
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0041732421
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33751542454
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8
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33846155543
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Belkova, N.V.7
Dub, P.A.8
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9
-
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0001309645
-
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Jia, G.; Ng, W. S.; Yao, J.; Lau, Ch.-P.; Chen, Y. Organometallics 1996, 15, 5039-5045.
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10
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33646504099
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Perkins, G. J.; Bruce, M. I.; Skelton, B. W.; White, A. H. Inorg. Chim. Acta 2006, 359, 2644-2649.
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-
11
-
-
47949099718
-
-
4 reduction by concentrated HCl, which is usually done in the presence of Fe(II) [ Dwyer, F. P.; Hogarth, J. W. Inorg. Synth. 1957, 5, 206. ],
-
4 reduction by concentrated HCl, which is usually done in the presence of Fe(II) [ Dwyer, F. P.; Hogarth, J. W. Inorg. Synth. 1957, 5, 206. ],
-
-
-
-
13
-
-
31544447161
-
-
Turner, A. G.; Clifford, A. F.; Ramachandra; Rao, C. N. Anal. Chem. 1958, 30, 1708-1709.
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, pp. 1708-1709
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-
Turner, A.G.1
Clifford, A.F.2
Ramachandra3
Rao, C.N.4
-
14
-
-
47949084871
-
-
See Supplementary Information for details
-
See Supplementary Information for details.
-
-
-
-
15
-
-
0001836333
-
-
Liles, D. C.; Shaver, A.; Singleton, E.; Wiege, M. B. J. Organomet. Chem. 1985, 288, C33-C36.
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Liles, D.C.1
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Wiege, M.B.4
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18
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34248529991
-
-
Gross, C. L.; Brumaghim, J. L.; Girolami, G. S. Organometallics 2007, 26, 2258-2265.
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Gross, C.L.1
Brumaghim, J.L.2
Girolami, G.S.3
-
19
-
-
47949085667
-
-
-1).
-
-1).
-
-
-
-
20
-
-
47949106695
-
-
-1 at T = 300 K.
-
-1 at T = 300 K.
-
-
-
-
21
-
-
0001740569
-
-
Serron, S. A.; Luo, L.; Li, C.; Cucullu; M, E.; Stevens, E. D.; Nolan, S. P. Organometallics 1995, 14, 5290-5297.
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Serron, S. A.; Luo, L.; Li, C.; Cucullu; M, E.; Stevens, E. D.; Nolan, S. P. Organometallics 1995, 14, 5290-5297.
-
-
-
-
23
-
-
47949095419
-
-
The Cp* ligand is found disordered with two different orientations with 0.58 and 0.42 occupancies; the position of the hydride ligand was refined in isotropic approximation in a riding model. See the Supporting Information for further details.
-
The Cp* ligand is found disordered with two different orientations with 0.58 and 0.42 occupancies; the position of the hydride ligand was refined in isotropic approximation in a riding model. See the Supporting Information for further details.
-
-
-
-
24
-
-
19744370551
-
-
Guan, H.; Iimura, M.; Magee, M. P.; Norton, J. R.; Zhu, G. J. Am. Chem. Soc. 2005, 127, 7805-7814.
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Guan, H.1
Iimura, M.2
Magee, M.P.3
Norton, J.R.4
Zhu, G.5
-
25
-
-
47949109393
-
-
With normalization of the C-H length to the ideal value of 1.08 Å. This r(HH) value is certainly overestimated since M-H bond lengths are usually underestimated in X-ray
-
With normalization of the C-H length to the ideal value of 1.08 Å. This r(HH) value is certainly overestimated since M-H bond lengths are usually underestimated in X-ray.
-
-
-
-
27
-
-
47949096281
-
-
+.
-
+.
-
-
-
-
28
-
-
12044250626
-
-
(a) Desrosiers, P. J.; Cai, L.; Lin, Z.; Richards, R.; Halpern, J. J. Am. Chem. Soc. 1991, 113, 4173-4184.
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Desrosiers, P.J.1
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Lin, Z.3
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29
-
-
0035796188
-
-
(b) Bayse, C. A.; Luck, R. L.; Schelter, E. J. Inorg. Chem. 2001, 40, 3463-3467.
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-
-
Bayse, C.A.1
Luck, R.L.2
Schelter, E.J.3
-
30
-
-
47949118025
-
-
The addition of the extra proton could be explained by the exchange of o-CH of the phenyl ring of the dppe ligand and the osmium-bound deuterium via an electrophilic substitution on the arene ring the cationic dihydride serves as acid
-
The addition of the extra proton could be explained by the exchange of o-CH of the phenyl ring of the dppe ligand and the osmium-bound deuterium via an electrophilic substitution on the arene ring (the cationic dihydride serves as acid).
-
-
-
-
32
-
-
47949114240
-
-
-1.
-
-1.
-
-
-
-
34
-
-
0001562626
-
-
(b) Esteruelas, N.; Gomez, A. V.; Lopez, A. M.; Oro, L. A. Organometallics 1996, 15, 878-881.
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Esteruelas, N.1
Gomez, A.V.2
Lopez, A.M.3
Oro, L.A.4
-
37
-
-
47949091277
-
-
+ appearance, respectively.
-
+ appearance, respectively.
-
-
-
-
38
-
-
34248371261
-
-
Egbert, J. D.; Bullock, R. M.; Heinekey, D. M. Organometallics 2007, 26, 2291-2295.
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, pp. 2291-2295
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-
Egbert, J.D.1
Bullock, R.M.2
Heinekey, D.M.3
-
39
-
-
19944432322
-
-
Belkova, N. V.; Collange, E.; Dub, P.; Epstein, L. M.; Lemenovskii, D. A.; Lledós, A.; Maresca, O.; Maseras, F.; Poli, R.; Revin, P. O.; Shubina, E. S.; Vorontsov, E. V. Chem. -Eur. J. 2005, 11, 873-888.
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Collange, E.2
Dub, P.3
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Lledós, A.6
Maresca, O.7
Maseras, F.8
Poli, R.9
Revin, P.O.10
Shubina, E.S.11
Vorontsov, E.V.12
-
41
-
-
33745177794
-
-
Belkova, N. V.; Revin, P. O.; Besora, M.; Baya, M.; Epstein, L. M.; Lledós, A.; Poli, R.; Shubina, E. S.; Vorontsov, E. V. Eur. J. Inorg. Chem. 2006, 2192-2209.
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Belkova, N.V.1
Revin, P.O.2
Besora, M.3
Baya, M.4
Epstein, L.M.5
Lledós, A.6
Poli, R.7
Shubina, E.S.8
Vorontsov, E.V.9
-
42
-
-
3543064648
-
-
(a) Andrieu, J.; Belkova, N. V.; Besora, M.; Collange, E.; Epstein, L. M.; Lledós, A.; Poli, R.; Revin, P. O.; Shubina, E. S.; Vorontsov, E. V. Russ. Chem. Bull. 2003, 52, 2679-2682.
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Andrieu, J.1
Belkova, N.V.2
Besora, M.3
Collange, E.4
Epstein, L.M.5
Lledós, A.6
Poli, R.7
Revin, P.O.8
Shubina, E.S.9
Vorontsov, E.V.10
-
43
-
-
47949108827
-
-
Manuscript in preparation
-
(b) Belkova, N. V.; Besora, M.; Baya, M.; Dub, P. A.; Epstein, L. M.; Lledós, A.; Poli, R.; Revin, P. O.; Shubina, E. S. Manuscript in preparation.
-
-
-
Belkova, N.V.1
Besora, M.2
Baya, M.3
Dub, P.A.4
Epstein, L.M.5
Lledós, A.6
Poli, R.7
Revin, P.O.8
Shubina, E.S.9
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