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Icli, S; Icil, H; Whitten, DG; Sayil, C; Dityapak, I
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/103791</identifier> <creators> <creator> <creatorName>Icli, S</creatorName> <givenName>S</givenName> <familyName>Icli</familyName> </creator> <creator> <creatorName>Icil, H</creatorName> <givenName>H</givenName> <familyName>Icil</familyName> </creator> <creator> <creatorName>Whitten, DG</creatorName> <givenName>DG</givenName> <familyName>Whitten</familyName> </creator> <creator> <creatorName>Sayil, C</creatorName> <givenName>C</givenName> <familyName>Sayil</familyName> </creator> <creator> <creatorName>Dityapak, I</creatorName> <givenName>I</givenName> <familyName>Dityapak</familyName> </creator> </creators> <titles> <title>Fluorescence Quenching Between Strong Pi-Electron Donor-Acceptors Of Carbazolocarbazole And Tetranitrofluorenone Leading To Electron Transfer</title> </titles> <publisher>Aperta</publisher> <publicationYear>1997</publicationYear> <dates> <date dateType="Issued">1997-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/103791</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.103790</relatedIdentifier> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.81043/aperta.103791</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract">Singlet energies and fluorescence quantum yields of synthesized dihydrocarbazolocarbazole, 1, dimethylcarbazolocarbazole, 2, dibenzylcarbazolocarbazole, 3, were measured to be between 76.5-74.3 kcal/mol and 0.07-0.02 respectively. A Stern-Volmer plot of fluorescence quenching of dihydrocarbazolocarbazole, 1, with 2,4,5,7-tetranitrofluorenone, 4, has given a rate constant of quenching of k(q) = 7.4 x 10(12) M(-1)s(-1). The free energies of the exothermic electron transfer reaction are calculated to be -33.6 kcal/mol for dihydrocarbazolocarbazole, 1, and -26.8 kcal/mol for dimethylcarbazolocarbazole, 2. High values for the rate of fluorescence quenching and the free energies are the evidence for an electron transfer process between these strong pi-electron donor-acceptor complexed molecules.</description> </descriptions> </resource>
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