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1
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34548730201
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Wang, Y.; Haze, O.; Dinnocenzo, J. P.; Farid, S.; Farid, R.; Gould, I. R. J. Org. Chem. 2007, 72. 6970.
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Wang, Y.1
Haze, O.2
Dinnocenzo, J.P.3
Farid, S.4
Farid, R.5
Gould, I.R.6
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3
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58149155163
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Because of the large energy gap between the ground configuration and both the LE and radical-ion pair configurations, the contribution from the ground configuration (C3, eq 1) to the exciplex state is usually negligible
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3, eq 1) to the exciplex state is usually negligible.
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8
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58149158411
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Shaik, S. S. In New Theoretical Concepts for Understanding Organic Reactions: Bertrán, J., Csizmadia. I. G.. Eds.; NATO ASI Series; Kluwer: Dordrecht, 1989; C267, p 165.
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(d) Shaik, S. S. In New Theoretical Concepts for Understanding Organic Reactions: Bertrán, J., Csizmadia. I. G.. Eds.; NATO ASI Series; Kluwer: Dordrecht, 1989; Vol. C267, p 165.
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9
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0033104833
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(e) Shaik, S.; Shurki, A. Angew. Chem., Int. Ed. 1999, 38, 586.
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Angew. Chem., Int. Ed
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, pp. 586
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Shaik, S.1
Shurki, A.2
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11
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58149176311
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Theoretical Chemistry Institute: University of Wisconsin, Madison
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Glendening, E. D.; Badenhoop, J, K.; Reed, A. E.; Carpenter, J. E.; Bohmann, J. A.; Morales, C. M.; Weinhold, F. NBO 5.O.; Theoretical Chemistry Institute: University of Wisconsin, Madison, 2001.
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(2001)
NBO 5.O
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Glendening, E.D.1
Badenhoop, J.K.2
Reed, A.E.3
Carpenter, J.E.4
Bohmann, J.A.5
Morales, C.M.6
Weinhold, F.7
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12
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0347568379
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For a literature summary regarding the assignment of the lowest ionic state of pyridine, see
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For a literature summary regarding the assignment of the lowest ionic state of pyridine, see: Tsubouchi, M.; Suzuki, T. J. Phys. Chem. A 2003, 107, 10897.
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(2003)
J. Phys. Chem. A
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Tsubouchi, M.1
Suzuki, T.2
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17
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49949125238
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(b) Favini, G.; Raimondi, M.; Gandolfo, C. Spectrochim. Acta 1968, 24A, 207.
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(1968)
C. Spectrochim. Acta
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, Issue.A
, pp. 207
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Favini, G.1
Raimondi, M.2
Gandolfo3
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18
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84870267943
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(c) Contreras, R. H.; Facelli, J. C.; de Kowalewski, D. G. Org. Magn. Reson. 1982, 20, 40.
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(1982)
Org. Magn. Reson
, vol.20
, pp. 40
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Contreras, R.H.1
Facelli, J.C.2
de Kowalewski, D.G.3
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19
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84986760731
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(d) Blonski, W. J. P.; Hruska, F. E.: Wildman, T. A. Org. Magn. Reson. 1984, 22, 505.
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Org. Magn. Reson
, vol.22
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Blonski, W.J.P.1
Hruska, F.E.2
Wildman, T.A.3
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20
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0002194131
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(e) Contreras. R. H.; Beikofsky, R. R.; de Kowalewski, D. G.; Orendt, A. M.; Facelli, J. C. J. Phys. Chem. 1993, 97, 91.
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J. Phys. Chem
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Contreras, R.H.1
Beikofsky, R.R.2
de Kowalewski, D.G.3
Orendt, A.M.4
Facelli, J.C.5
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21
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0035868865
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Schmidt. R.; Shafii. F.; Schweitzer, C.; Abdel-Shafi, A. A.; Wilkinson, F. J. Phys. Chem. A 2001, 105, 1811.
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(2001)
J. Phys. Chem. A
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Schmidt, R.1
Shafii, F.2
Schweitzer, C.3
Abdel-Shafi, A.A.4
Wilkinson, F.5
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22
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7444264096
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The reduction potential of 4-CNPy was determined vs 1-cyanonaphthalene by redox equilibration by using a method analogous to that previously described: Guirado, G.; Fleming, C. N.; Lingenfelter, T. G.; Williams, M. L.; Zuilhof, H.; Dinnocenzo, J. P. J. Am. Chem. Soc. 2004, 126, 14086.
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The reduction potential of 4-CNPy was determined vs 1-cyanonaphthalene by redox equilibration by using a method analogous to that previously described: Guirado, G.; Fleming, C. N.; Lingenfelter, T. G.; Williams, M. L.; Zuilhof, H.; Dinnocenzo, J. P. J. Am. Chem. Soc. 2004, 126, 14086.
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23
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58149155170
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The reduction potential of 3-CNPy was determined from the value for 4-CNPy and the difference in eletrochemical reduction potentials reported previously: Loutfv, R. O.: Loutfv, R. O. Can. J. Chem. 1973, 51, 1169
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(b) The reduction potential of 3-CNPy was determined from the value for 4-CNPy and the difference in eletrochemical reduction potentials reported previously: Loutfv, R. O.: Loutfv, R. O. Can. J. Chem. 1973, 51, 1169)
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24
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58149156900
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Based on the reported difference in oxidation between DCA and 9, 10-diphenylanthracene (DPA) of 0.57 V
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Based on the reported difference in oxidation between DCA and 9, 10-diphenylanthracene (DPA) of 0.57 V
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25
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2442607765
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Clegg, A. D.; Rees, N. V.; Klymenko, O. V.; Coles, B. A; Compton. R. G. J. Am. Chem. Soc. 2004, 126, 6185 and the oxidation potential reported for DPA of 1.18 V vs SCE in acetonitrile
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(a) Clegg, A. D.; Rees, N. V.; Klymenko, O. V.; Coles, B. A; Compton. R. G. J. Am. Chem. Soc. 2004, 126, 6185 and the oxidation potential reported for DPA of 1.18 V vs SCE in acetonitrile
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27
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0141654815
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The difference in oxidation potential for PS and PMeOS can be roughly approximated by the difference in the oxidation potentials of toluene and 4-methylanisole, which are 2.33 and 1.53 V vs SCE, respectively ref 1 and. Suzuki, T, Fujii, H, Yamashita, Y, Kabuto, C, Tanaka, S, Harasawa, M, Mukai, T, Mivashi, T. J. Am. Chem. Soc. 1992, 114. 3034
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The difference in oxidation potential for PS and PMeOS can be roughly approximated by the difference in the oxidation potentials of toluene and 4-methylanisole, which are 2.33 and 1.53 V vs SCE, respectively (ref 1 and. Suzuki, T.; Fujii, H.: Yamashita, Y.; Kabuto, C.; Tanaka, S.; Harasawa, M.: Mukai, T.; Mivashi, T. J. Am. Chem. Soc. 1992, 114. 3034)
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28
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0026419841
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Farid, S.; Daly, R. C.; Moody, R. E.; Huang, W.-Y.; Reiser, A. Macromolecules 1991, 24, 4041.
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(1991)
Macromolecules
, vol.24
, pp. 4041
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Farid, S.1
Daly, R.C.2
Moody, R.E.3
Huang, W.-Y.4
Reiser, A.5
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29
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58149151719
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Adapted with permission from ref 1. Copyright 2007 American Chemical Society.
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Adapted with permission from ref 1. Copyright 2007 American Chemical Society.
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30
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0000136805
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(a) Gould, I. R.; Young, R. H.; Mueller. L. J.; Farid, S. J. Am. Chem. Soc. 1994, 116, 8176.
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(1994)
J. Am. Chem. Soc
, vol.116
, pp. 8176
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Gould, I.R.1
Young, R.H.2
Mueller, L.J.3
Farid, S.4
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34
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58149158406
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D = 3 Å.
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D = 3 Å.
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36
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58149146092
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A+D = 6 Å.
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A+D = 6 Å.
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