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84890990991
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Shikata, K.1
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3543053117
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A. E. Shilov, A. K. Shilova, and E. F. Kvashina, Kinet. Ratal, 10, 1402 (1969);
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Shilov, A.E.1
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9
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37049132478
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A. E. Shilov, A. K. Shilova, E. F. Kvashina, and T. A. Vorontsova, Chem. Commun., 1590 (1971).
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Chem. Commun.
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Shilov, A.E.1
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10
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0007965407
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and literature cited therein
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E. E. van Tamelen, Accounts Chem. Res., 3, 361 (1970), and literature cited therein.
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Accounts Chem. Res.
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van Tamelen, E.E.1
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15
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4243714250
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3 was first obtained by treatment of TiCU with isobutene at 300° and 30–60 atm pressure
-
3 was first obtained by treatment of TiCU with isobutene at 300° and 30–60 atm pressure: H. Rohl, E. Lange, T. Gossel, and G. Roth, Angew. Chem., 74, 155 (1962).
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Rohl, H.1
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0002026266
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F. Calderazzo, J. J. Salzmann, and P. Mosimann, Inorg. Chim. Acta, 1, 65 (1967).
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Calderazzo, F.1
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0000017368
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James, B.D.1
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0011567195
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M. L. H. Green, J. A. McCleverty, L. Pratt, and G. Wilkinson, J. Chem. Soc., 4845 (1961).
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Green, M.L.H.1
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31
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0000148679
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2 toward tetrahydrofuran could explain some of the earlier observations concerning green and brown titanocene THF adducts: see
-
2 toward tetrahydrofuran could explain some of the earlier observations concerning green and brown titanocene THF adducts: see, A. K. Fischer and G. Wilkinson, J. Inorg. Nucl. Chem., 2, 149 (1956)
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Fischer, A.K.1
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1642519241
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and
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and G. A. Razuvaev, V. N. Latyaeva, L. I. Vyshinskaya, and G. A. Kilyakova, Z.H. Obshch. Khim., 36, 1491 (1966).
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Razuvaev, G.A.1
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36
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84932963395
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G. N. Nechiporenko, G. M. Tabrina, A. K. Shilova, and A. E. Shilov, Dokl. Akad. Nauk SSSR, 164, 1062 (1965).
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Nechiporenko, G.N.1
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85021468949
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Thesis, Rijksuniversiteit te Groningen
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H. A. Martin, Thesis, Rijksuniversiteit te Groningen, 1967.
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Martin, H.A.1
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and earlier references quoted there
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V. Gutmann and M. Michmayr, Monatsh. Chem., 99, 316 (1968), and earlier references quoted there.
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Dessy, R.E.1
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52
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37049133143
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This exchange between Ds and all the ring hydrogen positions has been observed before by
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This exchange between Ds and all the ring hydrogen positions has been observed before by H. A. Martin and R. O. de Jongh (Chem. Commun., 1366 (1969))
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(1969)
Chem. Commun.
, pp. 1366
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Martin, H.A.1
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53
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0007885481
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2 and the aromatic solvent, as has been observed with tantalocene and niobocene hydrides
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2 and the aromatic solvent, as has been observed with tantalocene and niobocene hydrides (E. K. Barefield, G. W. Parshall, and F. N. Tebbe, J. Amer. Chem. Soc., 92, 5235 (1970);
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Barefield, E.K.1
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Vol'pin, M.E.1
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85021471937
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2 and in the reduction of molecular nitrogen
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2 and in the reduction of molecular nitrogen.
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Schurig, V.1
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0000977192
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85021464425
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For a recent review see
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For a recent review see A. D. Allen, Advan. Chem. Ser., No. 100, 79 (1971).
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Allen, A.D.1
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0000314775
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The resulting bonding situation is then comparable to that of those alkyne complexes in which the acetylene ligand substitutes for two monodentate ligand groups, i.e., where the acetylene ligand is bound to a 14-electron species. In these complexes the red-shift of the C≡C stretching vibration is several times larger than in those alkyne complexes where the acetylene is coordinated to a species with 16 valence electrons
-
The resulting bonding situation is then comparable to that of those alkyne complexes in which the acetylene ligand substitutes for two monodentate ligand groups, i.e., where the acetylene ligand is bound to a 14-electron species. In these complexes the red-shift of the C≡C stretching vibration is several times larger than in those alkyne complexes where the acetylene is coordinated to a species with 16 valence electrons (E. O. Graves, C. J. L. Lock, and P. M. Maitlis, Can. J. Chem., 46, 3879 (1968)).
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Can. J. Chem.
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Graves, E.O.1
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85021469960
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A. J. Ashe III, personal communication.
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0000739225
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A. J. Bard and K. S. V. Santhanan in “Electroanalytical Chemistry,” Vol. 4, A. J. Bard, Ed., New York, N. Y., 1970, p 215.
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