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The Class I compounds are more soluble in the nonpolar solvents than the Class II compounds, while the Class II compounds are more soluble than Class I in polar solvents.
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0011388351
-
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note
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X(0,0) bleaching and stimulated emission.
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34
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0011488920
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note
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Over the probe wavelengths (700-800 nm), the time constant varied from 2 to 8 ps, with an average value of 5 ps.
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35
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0034228577
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-
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0011433522
-
-
note
-
2u orbital-energy spacing but not the ordering. The ordering of the two orbitals is normally derived from EPR experiments on the oxidized compounds. For simplicity, it is assumed that this ordering is preserved in the neutral complexes, although this is not necessarily the case.
-
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-
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41
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33845278875
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44
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0011387220
-
-
note
-
2u lying above the alu orbital (see ref 2c).
-
-
-
-
45
-
-
0011434469
-
-
note
-
f and τ were substituted into eq 1. However, minute impurities can influence the fluorescence yields, given the very weak emission characteristic of the nonplanar porphyrins.
-
-
-
-
46
-
-
0011387870
-
-
note
-
X(0,0) intensity in the calculation.
-
-
-
-
47
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-
0011389169
-
-
note
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-1 (see ref 10).
-
-
-
-
48
-
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0011431435
-
-
note
-
2TPP standard as in part c.
-
-
-
-
49
-
-
0011482013
-
-
note
-
2TPP standard as in part c; a source of error here is associated with the extinction coefficients, which can span a range of values for a given compound.
-
-
-
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51
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53
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0011388047
-
-
note
-
(b) For the highly fluorinated nonplanar porphyrins, one effect of these enhanced interactions with polar solvents may be stabilization of charge-transfer excited-state configurations involving the macrocycle and fluorinated aryl rings. Mixing of the charge-transfer and (π,π*) configurations may provide a contribution to the enhanced nonradiative decay, in addition to the dominant effects associated with nonplanarity (conformational changes, multiple accessible configurations, enhanced Franck-Condon factors) discussed in the text.
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55
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