139586-47-3Relevant academic research and scientific papers
Mechanism for photodecomposition of 4,8,10-trithiadibenzo[cd,ij]azulene 8-oxides
Fujii, Takayoshi,Kusanagi, Hiroki,Furukawa, Naomichi
, p. 655 - 656 (1996)
4,8,10-Trithiadibenzo[cd,ij]azulene 8-oxides were prepared and their photolysis provided a convenient procedure to yield the corresponding aldehydes and ketones together with 4,8,9-trithiacyclopenta[def]phenanthrene.
Photochemical studies on the through-space S···S interaction of 2- phenylnaphtho[1,8-de][1,3]dithiin 1-oxide, 5-phenyl[1]benzothieno[4,3,2- def][1,3]benzodithiepin 4-oxide, and 2-phenyldibenzo[d,f][1,3]dithiepin 1- oxide
Fujii, Takayoshi,Kusanagi, Hiroki,Takahashi, Ohgi,Horn, Ernst,Furukawa, Naomichi
, p. 5027 - 5046 (2007/10/03)
2-Phenylnaphtho[1,8-de][1,3]dithiin 1-oxide (4a), 5- phenyl[1]benzothieno[4,3,2-def][1,3]benzodithiepin 4-oxide (4b), and 2- phenyldibenzo[d,f][1,3]dithiepin 1-oxide (4c) underwent facile consecutive photochemical reactions to give the corresponding disulfide, naphtho[1,8- cd][1,2]dithiole (1a), [1]benzothieno[4,3,2-cde][1,2]benzodithiin (1b), and dibenzo[c,e][1,2]dithiin (1c) and benzaldehyde (7), respectively, via the sulfur-sulfur (S···S) interaction. The proposed mechanism for these photochemical reactions is based on the quantum yields measurements, photo- intensity effects, and sensitizer effects. Ab initio calculations were also carried out for a model compound of the primary photoproduct, which showed that the S···S distance becomes shorter and the S-O distance becomes longer upon the excitation to the S1 state.
