Phenoxazine based units--synthesis, photophysics and electrochemistry.
Identifieur interne : 001F45 ( PubMed/Corpus ); précédent : 001F44; suivant : 001F46Phenoxazine based units--synthesis, photophysics and electrochemistry.
Auteurs : Anna Nowakowska-Oleksy ; Jadwiga Sołoducho ; Joanna CabajSource :
- Journal of fluorescence [ 1573-4994 ] ; 2011.
Abstract
A few new phenoxazine-based conjugated monomers were synthesized, characterized, and successfully used as semiconducting materials. The phenoxazine-based oligomers have low ionization potentials or high-lying HOMO levels (~4.7 eV), which were estimated from cyclic voltammetry. Conjugated oligomers offer good film-forming, mechanical and optical properties connected with their wide application. These results demonstrate that phenoxazine-based conjugated mers are a promising type of semiconducting and luminescent structures able to be used as thin films in organic electronics.
DOI: 10.1007/s10895-010-0701-6
PubMed: 20625802
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The phenoxazine-based oligomers have low ionization potentials or high-lying HOMO levels (~4.7 eV), which were estimated from cyclic voltammetry. Conjugated oligomers offer good film-forming, mechanical and optical properties connected with their wide application. These results demonstrate that phenoxazine-based conjugated mers are a promising type of semiconducting and luminescent structures able to be used as thin films in organic electronics.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">20625802</PMID><DateCompleted><Year>2011</Year><Month>05</Month><Day>10</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1573-4994</ISSN><JournalIssue CitedMedium="Internet"><Volume>21</Volume><Issue>1</Issue><PubDate><Year>2011</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Journal of fluorescence</Title><ISOAbbreviation>J Fluoresc</ISOAbbreviation></Journal><ArticleTitle>Phenoxazine based units--synthesis, photophysics and electrochemistry.</ArticleTitle><Pagination><MedlinePgn>169-78</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s10895-010-0701-6</ELocationID><Abstract><AbstractText>A few new phenoxazine-based conjugated monomers were synthesized, characterized, and successfully used as semiconducting materials. The phenoxazine-based oligomers have low ionization potentials or high-lying HOMO levels (~4.7 eV), which were estimated from cyclic voltammetry. Conjugated oligomers offer good film-forming, mechanical and optical properties connected with their wide application. These results demonstrate that phenoxazine-based conjugated mers are a promising type of semiconducting and luminescent structures able to be used as thin films in organic electronics.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Nowakowska-Oleksy</LastName><ForeName>Anna</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Faculty of Chemistry, Wrocław University of Technology, Wrocław, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sołoducho</LastName><ForeName>Jadwiga</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Cabaj</LastName><ForeName>Joanna</ForeName><Initials>J</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2010</Year><Month>07</Month><Day>13</Day></ArticleDate></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>J Fluoresc</MedlineTA><NlmUniqueID>9201341</NlmUniqueID><ISSNLinking>1053-0509</ISSNLinking></MedlineJournalInfo></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2010</Year><Month>04</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2010</Year><Month>06</Month><Day>22</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2010</Year><Month>7</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2010</Year><Month>7</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2010</Year><Month>7</Month><Day>14</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">20625802</ArticleId><ArticleId IdType="doi">10.1007/s10895-010-0701-6</ArticleId><ArticleId IdType="pmc">PMC3032184</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>J Org Chem. 2005 Jul 22;70(15):5987-96</Citation><ArticleIdList><ArticleId IdType="pubmed">16018695</ArticleId></ArticleIdList></Reference><Reference><Citation>J Phys Chem A. 2006 Dec 28;110(51):13989-94</Citation><ArticleIdList><ArticleId IdType="pubmed">17181360</ArticleId></ArticleIdList></Reference><Reference><Citation>Chem Rev. 2006 Jul;106(7):2651-710</Citation><ArticleIdList><ArticleId IdType="pubmed">16836296</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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