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34347251901
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For recent examples, see: a
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For recent examples, see: a) L. Sánchez, M. Sierra, N. Martín, A. J. Myles, T. J. Dale, J. Rebek, Jr., W. Seitz, D. M. Guldi, Angew. Chem. 2006, 118, 4753-4757;
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10
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37549064015
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c) F. D'Souza, R. Chitta, A. S. D. Sandanayaka, N. K. Subbaiyan, L. D'Souza, Y. Araki, O. Ito, J. Am. Chem. Soc. 2007, 129, 15865-15871;
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34250308316
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d) A. L. Schumacher, A. S. D. Sandanayaka, J. P. Hill, K. Ariga, P. A. Karr, Y. Araki, O. Ito, F. D'Souza, Chem. Eur. J. 2007, 13, 4628-4635.
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C. A. Hunter, K. R. Lawson, J. Perkins, C. J. Urch, J. Chem. Soc. Perkin Trans. 2 2001, 651-669.
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15
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33845716101
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a) Y. Yamamoto, T. Fukushima, Y. Suna, N. Ishii, A. Saeki, S. Seki, S. Tagawa, M. Taniguchi, T. Kawai, T. Aida, Science 2006, 314, 1761-1764;
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16
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38949139041
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b) J. L. Mynar, T. Yamamoto, A. Kosaka, T. Fukushima, N. Ishii, T. Aida, J. Am. Chem. Soc. 2008, 130, 1530-1531.
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a) C. Röger, Y. Miloslavina, D. Brunner, A. R. Holzwarth, F. Wuerthner, J. Am. Chem. Soc. 2008, 130, 5929-5939;
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19
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34249035443
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b) P. G. A. Janssen, J. Vandenbergh, J. L. J. Van Dongen, E. W. Meijer, A. P. H. J. Schenning, J. Am. Chem. Soc. 2007, 129, 6078-6079.
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23
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33744923427
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a) E. M. Pérez, L. Sánchez, G. Fernández, N. Martín, J. Am. Chem. Soc. 2006, 128, 7172-7173;
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J. Am. Chem. Soc
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Pérez, E.M.1
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24
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37249030790
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b) E. M. Pérez, M. Sierra, L. Sánchez, M. R. Torres, R. Viruela, P. M. Viruela, E. Ortí, N. Martín, Angew. Chem. 2007, 119, 1879-1883;
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34250835584
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Angew. Chem. Int. Ed. 2007, 46, 1847-1851;
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26
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46049098107
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c) G. Fernández, E. M. Pérez, L. Sánchez, N. Martín, Angew. Chem. 2008, 120, 1110-1113;
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38849152258
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39749089849
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d) G. Fernández, E. M. Pérez, L. Sánchez, N. Martín, J. Am. Chem. Soc. 2008, 130, 2410-2411;
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49449098659
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10674-10 683;
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e) G. Fernández, L. Sánchez, E. M. Pérez, N. Martín, J. Am. Chem. Soc. 2008, 130, 10674-10 683;
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52649149516
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f) E. M. Pérez, A. L. Capodilupo, G. Fernández, L. Sánchez, P. M. Viruela, R. Viruela, E. Ortí, M. Bietti, N. Martín, Chem. Commun. 2008, 4567-4569.
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Martín, N.9
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31
-
-
58249116610
-
-
60: 1669.991); see Figure S1 in the Supporting Information.
-
60: 1669.991); see Figure S1 in the Supporting Information.
-
-
-
-
33
-
-
12144288700
-
-
H. Nishikawa, S. Kojima, T. Kodama, I. Ikemoto, S. Suzuki, K. Kikuchi, M. Fujitsuka, H. Luo, Y. Araki, O. Ito, J. Phys. Chem. A 2004, 108, 1881-1890.
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Kikuchi, K.6
Fujitsuka, M.7
Luo, H.8
Araki, Y.9
Ito, O.10
-
34
-
-
58249102145
-
-
Rate constants of about 1012 s-1 for intracomplex deactivation were estimated by fluorescence quenching
-
-1 for intracomplex deactivation were estimated by fluorescence quenching.
-
-
-
-
37
-
-
58249123344
-
-
-1.
-
-1.
-
-
-
-
38
-
-
0000402838
-
-
a) N. Martín, L. Sánchez, C. Seoane, E. Ortí, P. M. Viruela, R. Viruela, J. Org. Chem. 1998, 63, 1268-1279;
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Viruela, R.6
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39
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33645278648
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b) M. C. Díaz, B. M. Illescas, N. Martín, I. F. Perepichka, M. R. Bryce, E. Levillain, R. Viruela, E. Ortí, Chem. Eur. J. 2006, 12, 2709-2721;
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40
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2342433704
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c) M. C. Díaz, B. M. Illescas, N. Martín, R. Viruela, P. M. Viruela, E. Ortí, O. Brede, I. Zilbermann, D. M. Guldi, Chem. Eur. J. 2004, 10, 2067-2077.
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41
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32544436120
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M. Makha, A. Purich, C. L. Raston, A. N. Sobolev, Eur. J. Inorg. Chem. 2006, 507-517.
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Makha, M.1
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Sobolev, A.N.4
-
42
-
-
58249119525
-
-
Association binding energies are calculated as the difference between the total energy of the complex and the sum of the total energies of the receptor and C60
-
60.
-
-
-
-
43
-
-
34247148559
-
-
A Sygula, F. R. Fronczek, R. Sygula, P. W. Rabideau, M. M. Olmstead, J. Am. Chem. Soc. 2007, 129, 3842-3843.
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Olmstead, M.M.5
-
44
-
-
25144457993
-
-
a) T. Sato, T. Tsuneda, K. J. Hirao, Chem. Phys. 2005, 123, 104307;
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-
-
Sato, T.1
Tsuneda, T.2
Hirao, K.J.3
-
46
-
-
0037063502
-
-
c) M. O. Sinnokrot, E. F. Valeev, C. D. Sherrill, J. Am. Chem. Soc. 2002, 124, 10887-10893.
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-
-
Sinnokrot, M.O.1
Valeev, E.F.2
Sherrill, C.D.3
-
47
-
-
58249109417
-
-
Observed in chorobenzene at 429 nm, and calculated at 420 nm (f = 0.49). The LUMO for both MTW and PTW lies on the diester unit, and the lowest energy HOMO,HOMO-1→LUMO transitions have almost no intensity (f < 0.01).
-
Observed in chorobenzene at 429 nm, and calculated at 420 nm (f = 0.49). The LUMO for both MTW and PTW lies on the diester unit, and the lowest energy HOMO,HOMO-1→LUMO transitions have almost no intensity (f < 0.01).
-
-
-
-
48
-
-
58249102919
-
-
See the Supporting Information for a detailed description of the nature of the excited electronic states
-
See the Supporting Information for a detailed description of the nature of the excited electronic states.
-
-
-
-
50
-
-
58249102147
-
-
An additional band appears at 980 nm because of the singlet-singlet transition of free, uncomplexed C60
-
60.
-
-
-
-
51
-
-
17344392712
-
-
L. Sánchez, I. Pérez, N. Martín, D. M. Guldi, Chem. Eur. J. 2003, 9, 2457-2468.
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-
-
Sánchez, L.1
Pérez, I.2
Martín, N.3
Guldi, D.M.4
-
52
-
-
0037055108
-
-
See for example
-
See for example: T. J. Kesti, N. V. Tkachenko, V. Vehmanen, H. Yamada, H. Imahori, S. Fukuzumi, H. Lemmetyinen, J. Am. Chem. Soc. 2002, 124, 8067-8077.
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(2002)
J. Am. Chem. Soc
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, pp. 8067-8077
-
-
Kesti, T.J.1
Tkachenko, N.V.2
Vehmanen, V.3
Yamada, H.4
Imahori, H.5
Fukuzumi, S.6
Lemmetyinen, H.7
-
53
-
-
58249098468
-
-
•+ has lifetimes of 3.9 ps for PTW and 3.5 ps for MTW.
-
•+ has lifetimes of 3.9 ps for PTW and 3.5 ps for MTW.
-
-
-
|