<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>102(29)</volume><submitter>Kobori Y</submitter><pubmed_abstract>Photoinduced primary charge-separation and charge-recombination are characterized by a combination of time-resolved optical and EPR measurements of a fullerene-porphyrin-linked triad that undergoes fast, stepwise charge-separation processes. The electronic coupling for the energy-wasting charge recombination is evaluated from the singlet-triplet electronic energy gap in the short-lived, primary charge-separated state. The electronic coupling is found to be smaller by approximately 40% than that for the primary charge-separation. This inhibition of the electronic interaction for the charge-recombination to excited triplet state largely results from a symmetry-broken electronic structure modulated by configuration interaction between 3(b1u,b3g) and 3(au, b3g) electronic states of the free-base porphyrin.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>10017-22</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1177418</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Primary charge-recombination in an artificial photosynthetic reaction center.</pubmed_title><pmcid>PMC1177418</pmcid><pubmed_authors>Yamauchi S</pubmed_authors><pubmed_authors>Akiyama K</pubmed_authors><pubmed_authors>Fukuzumi S</pubmed_authors><pubmed_authors>Kobori Y</pubmed_authors><pubmed_authors>Imahori H</pubmed_authors><pubmed_authors>Norris JR</pubmed_authors><pubmed_authors>Tero-Kubota S</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Primary charge-recombination in an artificial photosynthetic reaction center.</name><description>Photoinduced primary charge-separation and charge-recombination are characterized by a combination of time-resolved optical and EPR measurements of a fullerene-porphyrin-linked triad that undergoes fast, stepwise charge-separation processes. The electronic coupling for the energy-wasting charge recombination is evaluated from the singlet-triplet electronic energy gap in the short-lived, primary charge-separated state. The electronic coupling is found to be smaller by approximately 40% than that for the primary charge-separation. This inhibition of the electronic interaction for the charge-recombination to excited triplet state largely results from a symmetry-broken electronic structure modulated by configuration interaction between 3(b1u,b3g) and 3(au, b3g) electronic states of the free-base porphyrin.</description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Jul</publication><modification>2024-11-10T08:00:10.571Z</modification><creation>2019-03-27T01:09:08Z</creation></dates><accession>S-EPMC1177418</accession><cross_references><pubmed>16014413</pubmed><doi>10.1073/pnas.0504598102</doi></cross_references></HashMap>