-
1
-
-
13644257674
-
-
T. Hasobe, H. Imahori, P. V. Kamat, T. K. Ahn, S. K. Kim, D. Kim, A. Fujimoto, T. Hirakawa and S. Fukuzumi, J. Am. Chem. Soc., 2005, 127, 1216;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1216
-
-
Hasobe, T.1
Imahori, H.2
Kamat, P.V.3
Ahn, T.K.4
Kim, S.K.5
Kim, D.6
Fujimoto, A.7
Hirakawa, T.8
Fukuzumi, S.9
-
2
-
-
11444269942
-
-
G. Bergamini, C. Saudan, P. Ceroni, M. Maestri, V. Balzani, M. Gorka, S.-K. Lee, J. van Heyst and F. Vögtle, J. Am. Chem. Soc., 2004, 126, 16466;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16466
-
-
Bergamini, G.1
Saudan, C.2
Ceroni, P.3
Maestri, M.4
Balzani, V.5
Gorka, M.6
Lee, S.-K.7
Van Heyst, J.8
Vögtle, F.9
-
3
-
-
7744241075
-
-
D. M. Guldi, I. Zilbermann, G. Anderson, N. A. Kotov, N. Tagmatarchis and M. Prato, J. Am. Chem. Soc., 2004, 126, 14340;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 14340
-
-
Guldi, D.M.1
Zilbermann, I.2
Anderson, G.3
Kotov, N.A.4
Tagmatarchis, N.5
Prato, M.6
-
4
-
-
4544284235
-
-
R. Konduri, N. R. de Tacconi, K. Rajeshwar and F. M. MacDonnell, J. Am Chem. Soc., 2004, 126, 11621;
-
(2004)
J. Am Chem. Soc.
, vol.126
, pp. 11621
-
-
Konduri, R.1
De Tacconi, N.R.2
Rajeshwar, K.3
MacDonnell, F.M.4
-
5
-
-
0035148647
-
-
D. Gust, T. A. Moore and A. L. Moore, Acc. Chem. Res., 2001, 34, 40;
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 40
-
-
Gust, D.1
Moore, T.A.2
Moore, A.L.3
-
6
-
-
0034128992
-
-
F. Fungo, A. Luis, L. A. Otero, L. Sereno, J. J. Silber and E. N. Durantini, J. Mater. Chem., 2000, 645;
-
(2000)
J. Mater. Chem.
, vol.645
-
-
Fungo, F.1
Luis, A.2
Otero, L.A.3
Sereno, L.4
Silber, J.J.5
Durantini, E.N.6
-
7
-
-
0030262702
-
-
C. Luo, C. Huang, L. Gan, D. Zhou, W. Xia, Q. Zhuang, Y. Zhao and Y. Huang, J. Phys. Chem., 1996, 100, 16685;
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 16685
-
-
Luo, C.1
Huang, C.2
Gan, L.3
Zhou, D.4
Xia, W.5
Zhuang, Q.6
Zhao, Y.7
Huang, Y.8
-
8
-
-
11744372773
-
-
D. Gust, T. A. Moore and A. L. Moore, Acc. Chem Res., 1993, 26, 198;
-
(1993)
Acc. Chem Res.
, vol.26
, pp. 198
-
-
Gust, D.1
Moore, T.A.2
Moore, A.L.3
-
9
-
-
0001236181
-
-
M. Nowakowska, V. P. Foyle and J. E. Guillet, J. Am. Chem. Soc., 1993, 115, 5975;
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5975
-
-
Nowakowska, M.1
Foyle, V.P.2
Guillet, J.E.3
-
12
-
-
0040257744
-
-
See, for example: V. Balzani, A. Juris, M. Venturi, S. Campagna and S. Serroni, Chem. Rev., 1996, 96, 759, and references therein
-
(1996)
Chem. Rev.
, vol.96
, pp. 759
-
-
Balzani, V.1
Juris, A.2
Venturi, M.3
Campagna, S.4
Serroni, S.5
-
13
-
-
0001518798
-
-
J.-P. Sauvage, J.-P. Collin, J.-C. Chambrori, S. Guillerez, V. Balzani, F. Barigelletti, L. De Cola and L. Flamigni, Chem. Rev., 1994, 94, 993, and references therein;
-
(1994)
Chem. Rev.
, vol.94
, pp. 993
-
-
Sauvage, J.-P.1
Collin, J.-P.2
Chambrori, J.-C.3
Guillerez, S.4
Balzani, V.5
Barigelletti, F.6
De Cola, L.7
Flamigni, L.8
-
15
-
-
0000611685
-
-
G. Denti, S. Serroni, S. Campagna, V. Ricevuto and V. Balzani, Coord. Chem. Rev., 1991, 111, 227;
-
(1991)
Coord. Chem. Rev.
, vol.111
, pp. 227
-
-
Denti, G.1
Serroni, S.2
Campagna, S.3
Ricevuto, V.4
Balzani, V.5
-
16
-
-
25944465119
-
-
F. Denti, S. Campagna, L. Sabatino, S. Lerroni, M. Ciano and V. Balzani, Inorg. Chem., 1990, 29, 4750.
-
(1990)
Inorg. Chem.
, vol.29
, pp. 4750
-
-
Denti, F.1
Campagna, S.2
Sabatino, L.3
Lerroni, S.4
Ciano, M.5
Balzani, V.6
-
17
-
-
0001762202
-
-
Stoichiometric reaction: V. W. Yam, V. W. Lee and K.-K. Cheung, Organometallics, 1997, 16, 2833;
-
(1997)
Organometallics
, vol.16
, pp. 2833
-
-
Yam, V.W.1
Lee, V.W.2
Cheung, K.-K.3
-
18
-
-
0035903722
-
-
catalytic olefin isomerization: M. Osawa, M. Hoshino and Y. Wakatsuki, Angew. Chem., Int. Ed, 2001, 40, 3472
-
(2001)
Angew. Chem., Int. Ed
, vol.40
, pp. 3472
-
-
Osawa, M.1
Hoshino, M.2
Wakatsuki, Y.3
-
19
-
-
28044474098
-
-
note
-
2. Details of the synthetic procedure and spectroscopic data are given as ESI.
-
-
-
-
20
-
-
28044438712
-
-
note
-
4) CCDC 275767. See http:// dx.doi.org/10.1039/b508013d for crystallographic data in CIF or other electronic format.
-
-
-
-
21
-
-
0001800880
-
-
P. K. Byers, A. J. Canty, B. W. Skelton and A. H. White, J. Organomet. Chem., 1987, 336, C55;
-
(1987)
J. Organomet. Chem.
, vol.336
-
-
Byers, P.K.1
Canty, A.J.2
Skelton, B.W.3
White, A.H.4
-
22
-
-
0000403322
-
-
P. K. Byers, A. J. Canty, B. W. Skelton and A. H. White, J. Organomet. Chem., 1990, 393, 299;
-
(1990)
J. Organomet. Chem.
, vol.393
, pp. 299
-
-
Byers, P.K.1
Canty, A.J.2
Skelton, B.W.3
White, A.H.4
-
23
-
-
0001595922
-
-
B. A. Markies, A. J. Canty, W. de Graaf, J. Boersma, M. D. Janssen, M. P. Hogerheide, W. J. J. Smeets, A. L. Spek and G. van Koten, J. Organomet. Chem., 1994, 482, 191;
-
(1994)
J. Organomet. Chem.
, vol.482
, pp. 191
-
-
Markies, B.A.1
Canty, A.J.2
De Graaf, W.3
Boersma, J.4
Janssen, M.D.5
Hogerheide, M.P.6
Smeets, W.J.J.7
Spek, A.L.8
Van Koten, G.9
-
24
-
-
0000865739
-
-
A. Bayler, A. J. Canty, P. G. Edwards, B. W. Skelton and A. H. White, J. Chem. Soc., Dalton Trans., 2000, 3325.
-
(2000)
J. Chem. Soc., Dalton Trans.
, pp. 3325
-
-
Bayler, A.1
Canty, A.J.2
Edwards, P.G.3
Skelton, B.W.4
White, A.H.5
-
25
-
-
28044434644
-
-
note
-
3- dimethyldihydromuconate). When the formation rate of the dimers were compared under the same reaction condition, that of styrene, 1-hexene and methyl acrylate was much smaller than that of α-methylstyrene (α-methylstyrene > 1-hexene, methyl acrylate > styrene).
-
-
-
-
26
-
-
28044461268
-
-
note
-
1H NMR and/or GC after appropriate time intervals.
-
-
-
-
27
-
-
28044443671
-
-
note
-
30).
-
-
-
-
28
-
-
33845282898
-
Dimerization of methyl methacrylate catalyzed by alkylcobaloxime
-
Dimerization of methyl methacrylate catalyzed by alkylcobaloxime: M. Kijima, K. Miyamori and T. Sato, J. Org. Chem., 1987, 52, 706;
-
(1987)
J. Org. Chem.
, vol.52
, pp. 706
-
-
Kijima, M.1
Miyamori, K.2
Sato, T.3
-
29
-
-
0037425133
-
-
3 as an acid co-catalyst: T. Tsuchimoto, S. Kamiyama, R. Negoro, E. Shirakawa and Y. Kawakami, Chem. Commun., 2003, 852;
-
(2003)
Chem. Commun.
, pp. 852
-
-
Tsuchimoto, T.1
Kamiyama, S.2
Negoro, R.3
Shirakawa, E.4
Kawakami, Y.5
-
30
-
-
5244339600
-
-
dimerization of α-methylstyrene by Pd catalyst giving 1,3,3-trimethyl-1-phenylindan as a product: Z. Jiang and A. Sen, Organometallics, 1993, 12, 1406.
-
(1993)
Organometallics
, vol.12
, pp. 1406
-
-
Jiang, Z.1
Sen, A.2
-
31
-
-
28044436517
-
-
note
-
3), 5.91 (qq, J = 6.84, 1.38 Hz, 1H, =C(Me)H). Ph protons were not fully characterized because they overlap with other aromatic protons. m/z (GCMS) 132 (M, 59%), 117 (M - 5, 100). 6 was characterized according to the reported spectroscopic data in the following references:
-
-
-
-
32
-
-
0000848348
-
-
E. Vedejs, J. Cabaj and M. J. Peterson, J. Org. Chem., 1993, 58, 6509;
-
(1993)
J. Org. Chem.
, vol.58
, pp. 6509
-
-
Vedejs, E.1
Cabaj, J.2
Peterson, M.J.3
-
33
-
-
0037271149
-
-
P. Fristrup, D. Tanner and P.-O. Norrby, Chirality, 2003, 15, 360.
-
(2003)
Chirality
, vol.15
, pp. 360
-
-
Fristrup, P.1
Tanner, D.2
Norrby, P.-O.3
-
34
-
-
28044472029
-
-
note
-
106Pd}.
-
-
-
-
35
-
-
28044469535
-
-
note
-
13C NMR, and ESI-MS spectral data are given as Electronic supplementary information.
-
-
-
-
36
-
-
28044462932
-
-
note
-
Although the formation of C was observed under the dark condition, the dimer 4 did not form over a prolonged reaction time.
-
-
-
-
37
-
-
28044444885
-
-
note
-
When the formation rate of C from A was compared between the irradiated and dark conditions, the rate under irradiation was nearly as twice as fast compared to that under the dark condition.
-
-
-
|