-
2
-
-
33645456932
-
-
B. Cornils and W. A. Herrmann, Wiley-VCH, Weinheim
-
Aqueous-Phase Organometallic Catalysis, ed. B. Cornils and W. A. Herrmann, Wiley-VCH, Weinheim, 2004.
-
(2004)
Aqueous-Phase Organometallic Catalysis
-
-
-
4
-
-
84891498804
-
-
B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou and D. Vogt, Wiley-VCH, Weinheim
-
Multiphase Homogeneous Catalysis, ed. B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou and D. Vogt, Wiley-VCH, Weinheim, 2005.
-
(2005)
Multiphase Homogeneous Catalysis
-
-
-
10
-
-
53349165810
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-
K. Yamamoto, Nova Science Publishers, New York
-
V. Cadierno and P. Crochet, in Advances in Organometallic Chemistry Research, ed. K. Yamamoto, Nova Science Publishers, New York, 2007, pp. 37–65.
-
(2007)
Advances in Organometallic Chemistry Research
, pp. 37-65
-
-
Cadierno, V.1
Crochet, P.2
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12
-
-
84906435235
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-
R. H. Crabtree and D. M. P. Mingos, Elsevier, Oxford
-
J. Gimeno, V. Cadierno and P. Crochet, in Comprehensive Organometallic Chemistry III, ed. R. H. Crabtree and D. M. P. Mingos, Elsevier, Oxford, 2006, vol. 6, pp. 465.
-
(2006)
Comprehensive Organometallic Chemistry III
, vol.6
, pp. 465
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Gimeno, J.1
Cadierno, V.2
Crochet, P.3
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28
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37049118608
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Preparation and characterization of the new compound 3c are described in the ESI. Complexes 3a–b and 3d–e were synthesized following the procedures previously reportedin ref. 11 and in
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Preparation and characterization of the new compound 3c are described in the ESI. Complexes 3a–b and 3d–e were synthesized following the procedures previously reportedin ref. 11 and in: M. A. Bennett A. K. Smith J. Chem. Soc., Dalton Trans. 1974 233.
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(1974)
J. Chem. Soc., Dalton Trans.
, pp. 233
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Bennett, M.A.1
Smith, A.K.2
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31
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9144265784
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For similar hydrolysis processes see for example
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For similar hydrolysis processes see for example: P. Csabai F. Joó Organometallics 2004 23 5640.
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(2004)
Organometallics
, vol.23
, pp. 5640
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Csabai, P.1
Joó, F.2
-
33
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20444400159
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C. Scolaro A. Bergamo L. Brescacin R. Delfino M. Cocchietto G. Laurenczy T. J. Geldbach G. Sava P. J. Dyson J. Med. Chem. 2005 48 4161.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4161
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Scolaro, C.1
Bergamo, A.2
Brescacin, L.3
Delfino, R.4
Cocchietto, M.5
Laurenczy, G.6
Geldbach, T.J.7
Sava, G.8
Dyson, P.J.9
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34
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85032769237
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3)] (details of X-ray diffraction study given in the ESI)
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3)] (details of X-ray diffraction study given in the ESI).
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38
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0001507732
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Redox potentials of some p-cymene and benzene ruthenium(II) complexes have been already reported but under different experimental conditions
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Redox potentials of some p-cymene and benzene ruthenium(II) complexes have been already reported but under different experimental conditions: D. Devanne P. H. Dixneuf J. Organomet. Chem. 1990 390 371.
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(1990)
J. Organomet. Chem.
, vol.390
, pp. 371
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Devanne, D.1
Dixneuf, P.H.2
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42
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85032767700
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Formal oxidation potentials (in V): 2a, 0.82; 2b, 0.77; 2c, 0.70; 2d, 0.86; 2e, 0.71; 3a, 0.71; 3b, 0.66; 3c, 0.61; 3d, 0.76; 3e, 0.60; 4a, 0.85; 4b, 0.83; 4c, 0.74; 4e, 0.81
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Formal oxidation potentials (in V): 2a, 0.82; 2b, 0.77; 2c, 0.70; 2d, 0.86; 2e, 0.71; 3a, 0.71; 3b, 0.66; 3c, 0.61; 3d, 0.76; 3e, 0.60; 4a, 0.85; 4b, 0.83; 4c, 0.74; 4e, 0.81.
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58
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85032771848
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3: 107, 123, 128, 130 and 145°, respectively
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3: 107, 123, 128, 130 and 145°, respectively.
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61
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85032766633
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Coordination of the C═C bond on the metal during the catalytic cycle is usually proposed for these processes. See, for example, ref. 24 and 26b
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Coordination of the C═C bond on the metal during the catalytic cycle is usually proposed for these processes. See, for example, ref. 24 and 26b.
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