Nag Mrinmoy, Jenks William S
Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.
J Org Chem. 2004 Nov 26;69(24):8177-82. doi: 10.1021/jo0490346.
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.
二苯并噻吩 - 5 - 氧化物(DBTO)在直接光解时能干净利落地生成二苯并噻吩(DBT),但其量子产率非常低。一种提出的机制涉及S - O键的断裂,该断裂与系间窜越步骤相耦合,从而通过单分子途径产生硫化物和O(³P)。为了验证这一假设,制备并光解了重原子取代的DBTO。碘代、溴代和氯代的DBTO脱氧的量子产率高于母体分子,其顺序与系间窜越相关的重原子效应一致。2 - 碘代二苯并噻吩也会发生光化学脱碘反应。磷光数据与重原子辅助的系间窜越一致。