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-1. No photoproduct having absorption around this frequency was observed in the present study.
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46
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84855928233
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-1 was observed in the reaction of oxygen atoms with benzene at 280 nm, in the study of Parker and Davis (Ref.). In that study, the carrier of this doublet band remained unassigned.
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5OH isomers do not yield cyclopentadiene upon decomposition, as deduced from the experiments using irradiations at shorter wavelengths of UV light (see below).
-
5OH isomers do not yield cyclopentadiene upon decomposition, as deduced from the experiments using irradiations at shorter wavelengths of UV light (see below).
-
-
-
-
59
-
-
84855975873
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-
-1 due to the antisymmetric C=C=C stretching vibration.
-
-1 due to the antisymmetric C=C=C stretching vibration.
-
-
-
-
60
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-
84855945479
-
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-1 due to the antisymmetric CH stretching vibration.
-
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-
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61
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84855945478
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In particular, cyclopentadiene does not look to be among the products generated from 2,5-cyclohexadienone (5). Decrease of population of (5), induced by irradiation at 245 nm, was not accompanied by any increase of IR bands ascribed to cyclopentadiene.
-
In particular, cyclopentadiene does not look to be among the products generated from 2,5-cyclohexadienone (5). Decrease of population of (5), induced by irradiation at 245 nm, was not accompanied by any increase of IR bands ascribed to cyclopentadiene.
-
-
-
-
63
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84855955351
-
-
-1 below the OD stretching frequency of HCCOD.
-
-1 below the OD stretching frequency of HCCOD.
-
-
-
-
64
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-
84855928236
-
-
5-analogs of (2, 5, 7, 8) and their proposed assignments (Table S3). The original experimental spectra related to Figures are available in numeric format (.SPA files for OMNIC software).
-
5-analogs of (2, 5, 7, 8) and their proposed assignments (Table S3). The original experimental spectra related to Figures are available in numeric format (.SPA files for OMNIC software).
-
-
-
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