Photochemistry and photophysics of halogen-substituted dibenzothiophene oxides. 2004

Mrinmoy Nag, and William S Jenks
Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.

Dibenzothiophene-5-oxide (DBTO) cleanly produces dibenzothiophene (DBT) on direct photolysis, but with very low quantum yield. A proposed mechanism involves scission of the S-O bond which is coupled to an intersystem crossing step, thus producing the sulfide and O((3)P) via a unimolecular pathway. To test this hypothesis, heavy atom substituted DBTOs were prepared and photolyzed. Iodo-, bromo-, and chloro-substituted DBTOs show higher quantum yields for deoxygenation than does the parent molecule, in the order consistent with an intersystem crossing-related heavy atom effect. 2-Iododibenzothiophene also undergoes photochemical deiodination. Phosphorescence data are consistent with heavy-atom assisted intersystem crossing.

UI MeSH Term Description Entries
D010777 Photochemistry A branch of physical chemistry which studies chemical reactions, isomerization and physical behavior that may occur under the influence of visible and/or ultraviolet light. Photochemistries
D010782 Photolysis Chemical bond cleavage reactions resulting from absorption of radiant energy. Photodegradation
D006219 Halogens A family of nonmetallic, generally electronegative, elements that form group 17 (formerly group VIIa) of the periodic table. Halogen,Group 17 Elements,Elements, Group 17
D013876 Thiophenes A monocyclic heteroarene furan in which the oxygen atom is replaced by a sulfur. Thiophene
D014466 Ultraviolet Rays That portion of the electromagnetic spectrum immediately below the visible range and extending into the x-ray frequencies. The longer wavelengths (near-UV or biotic or vital rays) are necessary for the endogenous synthesis of vitamin D and are also called antirachitic rays; the shorter, ionizing wavelengths (far-UV or abiotic or extravital rays) are viricidal, bactericidal, mutagenic, and carcinogenic and are used as disinfectants. Actinic Rays,Black Light, Ultraviolet,UV Light,UV Radiation,Ultra-Violet Rays,Ultraviolet Light,Ultraviolet Radiation,Actinic Ray,Light, UV,Light, Ultraviolet,Radiation, UV,Radiation, Ultraviolet,Ray, Actinic,Ray, Ultra-Violet,Ray, Ultraviolet,Ultra Violet Rays,Ultra-Violet Ray,Ultraviolet Black Light,Ultraviolet Black Lights,Ultraviolet Radiations,Ultraviolet Ray
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular

Related Publications

Mrinmoy Nag, and William S Jenks
April 2000, The Journal of organic chemistry,
Mrinmoy Nag, and William S Jenks
July 2003, Chemical Society reviews,
Mrinmoy Nag, and William S Jenks
May 1977, Photochemistry and photobiology,
Mrinmoy Nag, and William S Jenks
February 2003, Photochemistry and photobiology,
Mrinmoy Nag, and William S Jenks
March 2010, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology,
Mrinmoy Nag, and William S Jenks
May 2009, The journal of physical chemistry. A,
Mrinmoy Nag, and William S Jenks
November 2021, Photochemistry and photobiology,
Mrinmoy Nag, and William S Jenks
October 2008, The journal of physical chemistry. A,
Mrinmoy Nag, and William S Jenks
January 2006, Photochemistry and photobiology,
Mrinmoy Nag, and William S Jenks
July 2008, The Journal of organic chemistry,
Copied contents to your clipboard!