1627-06-1Relevant articles and documents
Photoinduced electron transfer reactions of anthracene in CF3SO3H- CF3CO2H
Pagni, Richard M.,Mamantov, Gleb,Hondrogiannis, George,Unni, Aditya
, p. 486 - 487 (1999)
Photolysis of anthracene in a mixture consisting of 2% CF3SO3H in CF3CO2H (w/w), where anthracene is partially protonated, gives a mixture of oxidized, neutral and reduced monomeric and dimeric products, initiation of this chemistry being photoinduced electron transfer from anthracene to protonated anthracene.
Studies on photodimerization of 9-anthracenecarboxylic acid in its crystalline double salt with diamine
Ito, Yoshikatsu
, p. 247 - 253 (2007/10/03)
With the intention of obtaining uncommon head-to-head anthracene dimers, double salts of 9-anthracenecarboxylic acid (9-AC) with several diamines were photolyzed in the solid state. 9-AC underwent decarboxylation and reduction as well as dimerization. Although the head-to-tail dimer and an unsymmetrical dimer were obtained, the head-to-head one was not produced.
Photolysis of 2,3:5,6-Dibenzo-7,7,8,8-tetraisopropyl-7,8-disilabicycloocta-2,5-diene: Evidence for Cyclodimerization of a Disilene
Matsumoto, Hideyuki,Arai, Takeshi,Watanabe, Hamao,Nagai, Yoichiro
, p. 724 - 725 (2007/10/02)
Evidence for disilene dimerization was obtained by generating tetraisopropyldisilene from the title compound via the photochemical retrodiene process which produced the expected dimerization product, octaisopropylcyclotetrasilane (30percent), in addition to the H-abstraction product, 1,1,2,2-tetraisopropyldisilane (5percent).