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0001663042
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24
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0000518146
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84989699766
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29
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0000137131
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0343565597
-
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Aveline, B.M.1
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-
32
-
-
10344247364
-
-
2O and OH is scavenged by reaction with t-BuOH. In the presence of 2,4-HD (∼300 μM), the species absorbing at 370 and 460 nm are quenched
-
2O and OH is scavenged by reaction with t-BuOH. In the presence of 2,4-HD (∼300 μM), the species absorbing at 370 and 460 nm are quenched.
-
-
-
-
33
-
-
10344264151
-
-
exc = 308 or 355 nm
-
exc = 308 or 355 nm.
-
-
-
-
34
-
-
0013599027
-
-
Bohne, C.; Boch, R.; Scaiano, J. C. J. Org. Chem. 1990, 55, 5414-5418.
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Bohne, C.1
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-
36
-
-
0013574263
-
-
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-
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Alam, M.M.1
Watanabe, A.2
Ito, O.3
-
37
-
-
0002367212
-
-
Ellison, D. H.; Salmon, G. A.; Wilkinson, F. Proc. R. Soc. London, Ser. A 1972, 328, 23-36.
-
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, pp. 23-36
-
-
Ellison, D.H.1
Salmon, G.A.2
Wilkinson, F.3
-
38
-
-
10344230138
-
-
See Figure 3 in ref 17
-
See Figure 3 in ref 17.
-
-
-
-
39
-
-
10344251705
-
-
The lack of energy transfer to merocyanine 540 was used to verify that N-HPT in buffer at pH = 7 does not undergo intersystem crossing, leading to triplet state formation
-
The lack of energy transfer to merocyanine 540 was used to verify that N-HPT in buffer at pH = 7 does not undergo intersystem crossing, leading to triplet state formation.
-
-
-
-
40
-
-
0002764039
-
-
Lambert, C.; Sarna, T.; Truscott, T. G. J. Chem. Soc., Faraday Trans. 1990, 86, 3879-3882.
-
(1990)
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-
-
Lambert, C.1
Sarna, T.2
Truscott, T.G.3
-
41
-
-
10344254013
-
-
note
-
(SCN)2•- was calculated as the differential between the two initial slopes of energy dependence plots obtained.
-
-
-
-
42
-
-
10344255326
-
-
-, OH, and N-HPT yield intermediates which absorb around 345 and 420 nm, respectively, and subsequently lead to the formation of other transient absorptions complicating the identification of the reaction products
-
-, OH, and N-HPT yield intermediates which absorb around 345 and 420 nm, respectively, and subsequently lead to the formation of other transient absorptions complicating the identification of the reaction products.
-
-
-
-
43
-
-
10344231146
-
-
•), which are originally first-order, become increasingly second-order in character as the radical-radical reaction processes become more probable
-
•), which are originally first-order, become increasingly second-order in character as the radical-radical reaction processes become more probable.
-
-
-
-
45
-
-
0001430211
-
-
Bhattacharyya, K.; Ramamurthy, V.; Das, P. K. J. Phys. Chem. 1987, 91, 5626-5631.
-
(1987)
J. Phys. Chem.
, vol.91
, pp. 5626-5631
-
-
Bhattacharyya, K.1
Ramamurthy, V.2
Das, P.K.3
-
46
-
-
0028528701
-
-
Redmond, R. W.; Srichai, M. B.; Bilitz, J. M.; Schlomer, D. D.; Krieg, M. Photochem. Photobiol. 1994, 60, 348-355.
-
(1994)
Photochem. Photobiol.
, vol.60
, pp. 348-355
-
-
Redmond, R.W.1
Srichai, M.B.2
Bilitz, J.M.3
Schlomer, D.D.4
Krieg, M.5
-
47
-
-
10344251186
-
-
When merocyanine 540 alone was excited under the same conditions, the intensity of the 660 nm band was about 5% of that recorded in the presence of N-HPT
-
When merocyanine 540 alone was excited under the same conditions, the intensity of the 660 nm band was about 5% of that recorded in the presence of N-HPT.
-
-
-
-
48
-
-
10344260387
-
-
note
-
• at this wavelength.
-
-
-
-
49
-
-
10344252996
-
-
-1 was used for the molar absorption coefficient of the ground-state
-
-1 was used for the molar absorption coefficient of the ground-state.
-
-
-
-
52
-
-
10344232188
-
-
note
-
-1.
-
-
-
-
53
-
-
10344259850
-
-
•
-
•.
-
-
-
-
54
-
-
10344233385
-
-
The identification of this compound is facile since it is the only photoproduct of N-HPT to present an absorption at long wavelength (≥350 nm)
-
The identification of this compound is facile since it is the only photoproduct of N-HPT to present an absorption at long wavelength (≥350 nm).
-
-
-
-
55
-
-
10344241680
-
-
• and the triplet state (vide infra)
-
• and the triplet state (vide infra).
-
-
-
-
56
-
-
10344265714
-
-
3(N-HPT)*
-
3(N-HPT)*.
-
-
-
-
57
-
-
10344238807
-
-
This method could not be used to determine the quantum yield of intersystem crossing of N-HPT in aqueous buffer at pH = 2 as the solubility of M540 in that solvent was found to be too low
-
This method could not be used to determine the quantum yield of intersystem crossing of N-HPT in aqueous buffer at pH = 2 as the solubility of M540 in that solvent was found to be too low.
-
-
-
-
58
-
-
10344233901
-
-
In that case, 2-hydroxybenzophenone, a photoinert reagent, was added to the solution to mimic the filter effect due to N-HPT in the second experiment
-
In that case, 2-hydroxybenzophenone, a photoinert reagent, was added to the solution to mimic the filter effect due to N-HPT in the second experiment.
-
-
-
-
59
-
-
10344267163
-
-
Tfrom eq 3
-
Tfrom eq 3.
-
-
-
-
60
-
-
10344225850
-
-
-1) with β-carotene
-
-1) with β-carotene.
-
-
-
-
61
-
-
10344264150
-
-
• and prevent the formation of the secondary species which is otherwise visible at that wavelength
-
• and prevent the formation of the secondary species which is otherwise visible at that wavelength.
-
-
-
-
62
-
-
0038334983
-
-
Elliot, A. J.; McEachern, R. J.; Armstrong, D. A. J. Phys. Chem. 1981, 85, 68-75.
-
(1981)
J. Phys. Chem.
, vol.85
, pp. 68-75
-
-
Elliot, A.J.1
McEachern, R.J.2
Armstrong, D.A.3
-
63
-
-
10344230137
-
-
• with their precursor
-
• with their precursor.
-
-
-
-
64
-
-
37049075785
-
-
Sako, M.; Nagai, K.; Maki, Y. J. Chem. Soc., Chem. Commun. 1993, 9, 750-751.
-
(1993)
J. Chem. Soc., Chem. Commun.
, vol.9
, pp. 750-751
-
-
Sako, M.1
Nagai, K.2
Maki, Y.3
-
66
-
-
0001712678
-
-
Feitelson, J.; Hayon, E.; Treinin, A. J. Am. Chem. Soc. 1973, 95, 1025-1029.
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 1025-1029
-
-
Feitelson, J.1
Hayon, E.2
Treinin, A.3
-
68
-
-
10344229652
-
-
This concentration can be determined to be ∼3 μM, based on the published molar ratio of 54 between the thione and the thiol forms
-
This concentration can be determined to be ∼3 μM, based on the published molar ratio of 54 between the thione and the thiol forms.
-
-
-
-
69
-
-
10344226354
-
-
T ≈ 0.05), the detection of the IR emission of singlet oxygen was not attempted
-
T ≈ 0.05), the detection of the IR emission of singlet oxygen was not attempted.
-
-
-
|