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U. Stalmach, H. Kolshorn, I. Brehm, H. Meier, Liebigs Ann. 1996, 1449-1456.
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Stalmach, U.1
Kolshorn, H.2
Brehm, I.3
Meier, H.4
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77
-
-
14544291703
-
-
note
-
Compound 11b bearing one formyl group can be obtained as the major product from pentamer 10 by using DIBAL-H in a 1:1 stoichiometry.
-
-
-
-
78
-
-
0037018548
-
-
F. D'Souza, G. R. Deviprasad, M. E. Zandler, V.T. Hoang, A. Klykov, M. VanStipdonk, A. Perera, M. E. El-Khouly, M. Fujitsuka, O. Ito, J. Phys. Chem. A 2002, 106, 3243-3252.
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D'Souza, F.1
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Klykov, A.5
VanStipdonk, M.6
Perera, A.7
El-Khouly, M.E.8
Fujitsuka, M.9
Ito, O.10
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79
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0035913752
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D. M. Guldi, C. Luo, M. Prato, A. Troisi, F. Zerbetto, M. Scheloske, E. Dietel, W. Bauer, A. Hirsch, J. Am. Chem. Soc. 2001, 123, 9166-9167.
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Guldi, D.M.1
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Prato, M.3
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Zerbetto, F.5
Scheloske, M.6
Dietel, E.7
Bauer, W.8
Hirsch, A.9
-
81
-
-
14544272962
-
-
note
-
In line with such strong quenching, complementary fluorescence lifetime measurements did not yield any detectable signals for 12a and 12b in the 450-550 nm region that falls within the 100 ps detection limits. Note that the strong fluorescence of the oligomeric building blocks has lifetimes that are 1.2 and 0.8 ns for the trimer and pentamer, respectively.
-
-
-
-
82
-
-
14544267812
-
-
note
-
Both oligomeric building blocks have characteristic triplet-triplet absorptions (see previous section and Figure 5).
-
-
-
-
83
-
-
14544308050
-
-
note
-
60 fluorescence is stable.
-
-
-
-
84
-
-
0034696906
-
-
a) J. L. Segura, R. Gómez, N. Martín, C. Luo, D. M. Guldi, Chem. Commun. 2000, 701-702;
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Segura, J.L.1
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85
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-
0037154867
-
-
b) D. M. Guldi, C. Luo, A. Swartz, R. Gómez, J. L. Segura, N. Martín, C. Brabec, N. S. Sariciftci, J. Org. Chem. 2002, 67, 1141-1152.
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Guldi, D.M.1
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Martín, N.6
Brabec, C.7
Sariciftci, N.S.8
-
86
-
-
14544283765
-
-
note
-
60 precursor systems.
-
-
-
-
88
-
-
0000419295
-
-
b) R. A. Marcus, Angew. Chem. 1993, 105, 1161-1172; Angew. Chem. Int. Ed. Engl. 1993, 32, 1111-1121.
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Marcus, R.A.1
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89
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33748216903
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b) R. A. Marcus, Angew. Chem. 1993, 105, 1161-1172; Angew. Chem. Int. Ed. Engl. 1993, 32, 1111-1121.
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-
-
-
90
-
-
14544292622
-
-
note
-
The energies of the charge-separated state were calculated by simply adding the reduction and oxidation potentials. It is safe to assume that the Coulombic terms in the present donor-acceptor systems are negligible, especially in solvents with moderate or high polarity, because of the relatively large edge-to-edge distances.
-
-
-
-
91
-
-
0000394620
-
-
D. Gust, T. A. Moore, A. L. Moore, Res. Chem. Intermed. 1997, 23, 621-651.
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Gust, D.1
Moore, T.A.2
Moore, A.L.3
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92
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0034804017
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a) H. Imahori, D. M. Guldi, K. Tamaki, Y. Yoshida, C. Luo, Y. Sakata, S. Fukuzumi, J. Am. Chem. Soc. 2001, 123, 6617-6628;
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Imahori, H.1
Guldi, D.M.2
Tamaki, K.3
Yoshida, Y.4
Luo, C.5
Sakata, Y.6
Fukuzumi, S.7
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93
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-
0442311069
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b) D. M. Guldi, H. Imahori, K. Tamaki, Y. Kashiwagi, H. Yamada, Y. Sakata, S. Fukuzumi, J. Phys. Chem. A 2004, 108, 541-548.
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Guldi, D.M.1
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Yamada, H.5
Sakata, Y.6
Fukuzumi, S.7
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94
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0037187986
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a) H. Imahori, K. Tamaki, Y. Araki, T. Hasobe, O. Ito, A. Shimomura, S. Kundu, T. Okada, Y. Sakata, S. Fukuzumi, J. Phys. Chem. A 2002, 106, 2803-2814;
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Imahori, H.1
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Shimomura, A.6
Kundu, S.7
Okada, T.8
Sakata, Y.9
Fukuzumi, S.10
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95
-
-
0037042267
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b) H. Imahori, K. Tamaki, Y. Araki, Y. Sekiguchi, O. Ito, Y. Sakata, S. Fukuzumi, J. Am. Chem. Soc. 2002, 124, 5165-5174.
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Imahori, H.1
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Sakata, Y.6
Fukuzumi, S.7
-
96
-
-
14544267344
-
-
note
-
The temperature dependence prevents assignments regarding a superexchange or electron hopping mechanism. Considering the similar energetics we must also assume for 13b an interplay between both mechanisms, but with a smaller activation barrier.
-
-
-
-
97
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0037561572
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F. D'Souza, G. R. Deviprasad, M. E. Zandler, M. E. El-Khouly, M. Fujitsuka, O. Ito, J. Phys. Chem. A 2003, 107, 4801-4807.
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Fujitsuka, M.5
Ito, O.6
-
98
-
-
14544287018
-
-
note
-
These are even larger than those calculated for the dihedral angle between the two phenyl rings located at the two ends of the oligomer (28° for 13a and 34° for 13b).
-
-
-
-
99
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0025041156
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Polyenes: e) A. C. Benniston, V. Goulle, A. Harriman, J.-M. Lehn, B. Marczince, J. Phys. Chem. 1994, 98, 7798-7804;
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104
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0030714102
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0001488101
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