芳香族ニトロ化合物の光還元 : 励起状態の性質と反応性
スポンサーリンク
概要
- 論文の詳細を見る
Photochemical reduction of nitroaromatic species has been critically reviewed. The photoreaction mechanism of nitroaromatic compounds has been less understood in comparison with that of aromatic carbonyl compounds, because the properties of nitroaromatic excited states are still ambiguously described. At least three different lower electronically excited states are involved in the longest wavelength absorption band. These are L<SUB>a</SUB> (long-axis polarization), L<SUB>b</SUB> (short-axis polarization), and nπ<SUP>*</SUP> states. The relative location of these three states is dependent upon the nature of substituents and solvents, and therefore the characterization of lower excited states of nitrobenzene derivatives are rather difficult.<BR>Since complications due to the secondary process of primary photoproducts are inevitable, an intermolecular photoreduction for nitroaromatic species is practically of minor importance. On the other hand, some intramolecular photoredox reactions involving ο-nitrobenzyl moiety have been used for photosensitive protection of a certain functional group and photoresists.
- 社団法人 有機合成化学協会の論文
著者
関連論文
- 芳香族ニトロ化合物の光還元 : 励起状態の性質と反応性
- 光化学反応における磁場効果 : ラジカル対とビラジカルを中間体とする光反応を中心にして
- 分光学的データからみた置換基効果 : 物理的性質と化学反応性
- 芳香族光置換反応の配向性と反応機構