<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(5)</volume><submitter>Zhang X</submitter><pubmed_abstract>Organic photocatalysis has been developed flourishingly to rely on bimolecular energy transfer (EnT) or oxidative/reductive electron transfer (ET), promoting a variety of synthetic transformations. However, there are rare examples to merge EnT and ET processes rationally within one chemical system, of which the mechanistic investigation still remains in its infancy. Herein, the first mechanistic illustration and kinetic assessments of the dynamically associated EnT and ET paths were conducted for realizing the C-H functionalization in a cascade photochemical transformation of isomerization and cyclization by using the dual-functional organic photocatalyst of riboflavin. An extended single-electron transfer model of transition-state-coupled dual-nonadiabatic crossings was explored to analyz</pubmed_abstract><journal>JACS Au</journal><pagination>1452-1463</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10206599</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Extended Single-Electron Transfer Model and Dynamically Associated Energy Transfer Event in a Dual-Functional Catalyst System.</pubmed_title><pmcid>PMC10206599</pmcid><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Fang WH</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wang J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Extended Single-Electron Transfer Model and Dynamically Associated Energy Transfer Event in a Dual-Functional Catalyst System.</name><description>Organic photocatalysis has been developed flourishingly to rely on bimolecular energy transfer (EnT) or oxidative/reductive electron transfer (ET), promoting a variety of synthetic transformations. However, there are rare examples to merge EnT and ET processes rationally within one chemical system, of which the mechanistic investigation still remains in its infancy. Herein, the first mechanistic illustration and kinetic assessments of the dynamically associated EnT and ET paths were conducted for realizing the C-H functionalization in a cascade photochemical transformation of isomerization and cyclization by using the dual-functional organic photocatalyst of riboflavin. An extended single-electron transfer model of transition-state-coupled dual-nonadiabatic crossings was explored to analyz</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-22T01:06:43.969Z</modification><creation>2025-04-05T19:51:17.601Z</creation></dates><accession>S-EPMC10206599</accession><cross_references><pubmed>37234115</pubmed><doi>10.1021/jacsau.3c00098</doi></cross_references></HashMap>