-
8
-
-
34047152732
-
-
Yu Z., Zeng F., Sun X., Deng H., Dong J., Chen J., Wang H., and Pei C. J. Organomet. Chem. 692 (2007) 2306
-
(2007)
J. Organomet. Chem.
, vol.692
, pp. 2306
-
-
Yu, Z.1
Zeng, F.2
Sun, X.3
Deng, H.4
Dong, J.5
Chen, J.6
Wang, H.7
Pei, C.8
-
9
-
-
0033615288
-
-
Britovsek G.J.P., Bruce M., Gibson V.C., Kimberley B.S., Maddox P.J., Mastroiauni S., McTavish S.J., Redshaw C., Solan G.A., Strömberg S., White A.J.P., and Williams D.J. J. Am. Chem. Soc. 121 (1999) 8728
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 8728
-
-
Britovsek, G.J.P.1
Bruce, M.2
Gibson, V.C.3
Kimberley, B.S.4
Maddox, P.J.5
Mastroiauni, S.6
McTavish, S.J.7
Redshaw, C.8
Solan, G.A.9
Strömberg, S.10
White, A.J.P.11
Williams, D.J.12
-
12
-
-
17844361956
-
-
Jiang Y.-F., Xi C.-J., Liu Y.-Z., Niclós-Gutiérrez J., and Choquesillo-Lazarte D. Eur. J. Inorg. Chem. (2005) 1585
-
(2005)
Eur. J. Inorg. Chem.
, pp. 1585
-
-
Jiang, Y.-F.1
Xi, C.-J.2
Liu, Y.-Z.3
Niclós-Gutiérrez, J.4
Choquesillo-Lazarte, D.5
-
14
-
-
15344344412
-
-
Britovsek G.J.P., England J., Spitzmesser S.K., White A.J.P., and Williams D.J. Dalton Trans. (2005) 945
-
(2005)
Dalton Trans.
, pp. 945
-
-
Britovsek, G.J.P.1
England, J.2
Spitzmesser, S.K.3
White, A.J.P.4
Williams, D.J.5
-
23
-
-
0037067352
-
-
Chardon-Noblat S., Da Costa P., Deronzier A., Maniguet S., and Ziessel R. J. Electroanal. Chem. 529 (2002) 135
-
(2002)
J. Electroanal. Chem.
, vol.529
, pp. 135
-
-
Chardon-Noblat, S.1
Da Costa, P.2
Deronzier, A.3
Maniguet, S.4
Ziessel, R.5
-
25
-
-
30944467716
-
-
Mulhern D., Lan Y.-H., Brooker S., Gallagher J.F., Görls H., Rau S., and Vos J.G. Inorg. Chim. Acta 359 (2006) 736
-
(2006)
Inorg. Chim. Acta
, vol.359
, pp. 736
-
-
Mulhern, D.1
Lan, Y.-H.2
Brooker, S.3
Gallagher, J.F.4
Görls, H.5
Rau, S.6
Vos, J.G.7
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26
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69249245274
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note
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n (0.13 g, 0.59 mmol). The mixture was refluxed at 80 °C for 2.5 h. After cooling, a dark brown microcrystalline solid was collected, and washed with cooled absolute ethanol and then dried at air. Yield: 71%. Complex 2 was prepared by the similar procedure. Yield: 51%.
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27
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69249223325
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note
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+ 646.08 (100 %). Anal. Calc. for: C, 59.82; H, 6.50; N, 6.15. Found: C, 59.92; H, 6.78; N, 6.35%.
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28
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69249234607
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note
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2 (all data) = 0.1993.
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29
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0037416254
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Poyatos M., Mata J.A., Falomir E., Crabtree R.H., and Peris E. Organometallics 22 (2003) 1110
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(2003)
Organometallics
, vol.22
, pp. 1110
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Poyatos, M.1
Mata, J.A.2
Falomir, E.3
Crabtree, R.H.4
Peris, E.5
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30
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69249233500
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note
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iPrOH at 82 °C (ketone/catalyst/base = 500/1/24). The reaction was monitored by gas chromatography.
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