Mechanism of the chemiluminescence of lucigenin. II. The charge-transfer structure of lucigenin and reduction of 10,10'-dimethyl-9,9'-biacridinium dication by electron transfer from nucleophiles.
スポンサーリンク
概要
- 論文の詳細を見る
Lucigenin (10,10′-dimethyl-9,9′-biacridinium dinitrate, DBA<SUP>2+</SUP>2NO<SUB>3</SUB><SUP>−</SUP>) was found to be a CT complex between DBA<SUP>2+</SUP> and NO<SUB>3</SUB><SUP>−</SUP>. In the reaction of lucigenin with several nucleophiles in the absence of molecular oxygen or oxidizing agents the following four types of products were obtained, depending upon the relative power of the nucleophiles to donate electrons to DBA<SUP>2+</SUP>: (1) salts of DBA<SUP>2+</SUP> (DBA<SUP>2+</SUP>2X<SUP>−</SUP>) which are the CT complex between DBA<SUP>2+</SUP> and the nucleophiles, such as Cl<SUP>−</SUP>, Br<SUP>−</SUP>, SCN<SUP>−</SUP>, and I<SUP>−</SUP>, (2) the cation radical DBA<SUP>\underset.+</SUP> produced by one-electron transfer from nucleophiles, such as C<SUB>6</SUB>H<SUB>5</SUB>COCH<SUB>2</SUB><SUP>−</SUP> and CH<SUB>3</SUB>COCH<SUB>2</SUB><SUP>−</SUP>, to DBA<SUP>2+</SUP>, (3) the biradical DBA<SUP>\underset.2</SUP> produced by two-electron transfer from nucleophiles such as OH<SUP>−</SUP>, CN<SUP>−</SUP>, CCl<SUB>3</SUB><SUP>−</SUP>, and C<SUB>6</SUB>H<SUB>5</SUB>S<SUP>−</SUP> and (4) 10,10′-dimethyl-9,9′-bi(dihydroacridinylidene) produced from DBA<SUP>\underset.2</SUP>. Only the nucleophiles of (3), which produced DBA<SUP>\underset.2</SUP> brought about the luminescence of lucigenin in the presence of oxygen, and DBA<SUP>\underset.2</SUP> also showed luminescence in organic solvents in the presence of oxygen. From these findings it was concluded that the first process of the chemiluminescent reaction of lucigenin was the electron transfer reduction of DBA<SUP>2+</SUP> by the nucleophiles to form the biradical DBA<SUP>\underset.2</SUP>.
- 公益社団法人 日本化学会の論文
著者
-
Maeda Koko
Department Of Chemistry Faculty Of Science Ochanomizu University
-
Tokuyama Mizue
Department of Chemistry, Faculty of Science, Ochanomizu University
-
Kashiwabara Toshi
Department of Chemistry, Faculty of Science, Ochanomizu University
関連論文
- Radical Dissociation of 2,2'-Bis(2-aryl-3-benzothiophenonyl)s by Mechanical Energy
- Photochemistry of Amino-Linked Bichromophoric Anthracenes. Efficient Cyclomerization of 9-(1-Naphthylmethylaminomethyl)anthracene and Adiabatic Cycloreversion of the Cyclomer
- Crystal Structure and Stereoselective Solid-State Photodimerization of 1-(9-Anthryl)alkyl Acetates
- A New Phenomenon of Storage Light Energy by Solution of Photo-chromatic 1, 1′-Bi(2, 4, 5-triphenylimidazyl) at Low Temperatures
- Optical and ESR Studies on Triphenylimidazolyl Radicals Produced by Photolysis and Radiolysis at Low Temperature
- The Formation of Triaryl-s-triazine in the Chemiluminescence Reaction of Triarylimidazole and in the Photo-oxygenation of Triarylimidazole in the Presence of Ammonia
- The Photochromism, Thermochromism, and Piezochromism of Dimers of Tetraphenylpyrryl
- The crystal and molecular structures of 2,4,4,6-tetraphenyl-1,4-dihydropyridine and 4-benzyl-1-methyl-2,4,6-triphenyl-1,4-dihydropyridine.
- The Formation of Substituted Quinazolines from Substituted Indoles by the Sensitized Photo-oxygenation in the Presence of Ammonium Acetate
- The Mechanism of Photochromism, Thermochromism and Piezochromism of Dimers of Triarylimidazolyl
- Mechanism of the chemiluminescence of lucigenin. II. The charge-transfer structure of lucigenin and reduction of 10,10'-dimethyl-9,9'-biacridinium dication by electron transfer from nucleophiles.
- The crystal and molecular structures of 2,2,4,6-tetraphenyldihydro-1,3,5-triazine aceton solvate and 2-propanol solvate.
- Crystal structure and photochemical behavior of 2,2,4,6-tetraphenyldihydro-1,3,5-triazine and its inclusion compounds.
- On Liquefaction Caused by the Trituration of Pairs of Solid Compounds. II