<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li S</submitter><funding>National Natural Science Foundation of China</funding><pagination>5271-84</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4394475</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(3)</volume><pubmed_abstract>We carried out molecular orbital theory calculations for the homogeneous gas-phase formation of dibenzofuran from phenanthrene, fluorene, 9-methylfluorene and 9-fluorenone. Dibenzofuran will be formed if ∙OH adds to C8a, and the order of reactivity follows as 9-fluorenone > 9-methylfluorene > fluorene > phenanthrene. The oxidations initiated by ClO∙ are more favorable processes, considering that the standard reaction Gibbs energies are at least 21.63 kcal/mol lower than those of the equivalent reactions initiated by ∙OH. The adding of ∙OH and then O2 to phenanthrene is a more favorable route than adding ∙OH to C8a of phenanthrene, when considering the greater reaction extent. The reaction channel from fluorene and O2 to 9-fluorenone and H2O seems very important, not only because it contains only three elementary reactions, but because the standard reaction Gibbs energies are lower than -80.07 kcal/mol.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Mechanistic studies on the dibenzofuran formation from phenanthrene, fluorene and 9-fluorenone.</pubmed_title><pmcid>PMC4394475</pmcid><funding_grant_id>21337001</funding_grant_id><funding_grant_id>21177077</funding_grant_id><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanistic studies on the dibenzofuran formation from phenanthrene, fluorene and 9-fluorenone.</name><description>We carried out molecular orbital theory calculations for the homogeneous gas-phase formation of dibenzofuran from phenanthrene, fluorene, 9-methylfluorene and 9-fluorenone. Dibenzofuran will be formed if ∙OH adds to C8a, and the order of reactivity follows as 9-fluorenone > 9-methylfluorene > fluorene > phenanthrene. The oxidations initiated by ClO∙ are more favorable processes, considering that the standard reaction Gibbs energies are at least 21.63 kcal/mol lower than those of the equivalent reactions initiated by ∙OH. The adding of ∙OH and then O2 to phenanthrene is a more favorable route than adding ∙OH to C8a of phenanthrene, when considering the greater reaction extent. The reaction channel from fluorene and O2 to 9-fluorenone and H2O seems very important, not only because it contains only three elementary reactions, but because the standard reaction Gibbs energies are lower than -80.07 kcal/mol.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Mar</publication><modification>2024-11-05T17:48:25.616Z</modification><creation>2019-03-27T01:49:49Z</creation></dates><accession>S-EPMC4394475</accession><cross_references><pubmed>25756381</pubmed><doi>10.3390/ijms16035271</doi></cross_references></HashMap>