End-capping of conjugated thiophene-benzene aromatic systems

Wex B.; Jradi F.M.; Patra D.; Kaafarani B.R.

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dc.contributor.author	Wex B.
dc.contributor.author	Jradi F.M.
dc.contributor.author	Patra D.
dc.contributor.author	Kaafarani B.R.
dc.contributor.editor
dc.date	2010
dc.date.accessioned	2017-10-03T15:45:22Z
dc.date.available	2017-10-03T15:45:22Z
dc.date.issued	2010
dc.identifier	10.1016/j.tet.2010.08.073
dc.identifier.isbn
dc.identifier.issn	00404020
dc.identifier.uri	http://hdl.handle.net/10938/12611
dc.description.abstract	The synthesis of end-capped thieno[3,2-f:4,5-f′]bis[1]benzothiophene was achieved from thiophene and 2,5-thiophenedicarboxaldehyde. Specifically, hexyl and dodecyl end-capping groups conferred reversible redox behavior as evidenced by cyclic voltammetry with oxidation potentials of 0.73 V versus Fc-Fc+ couple. An extensive spectrophotometric analysis is reported. © 2010 Elsevier Ltd. All rights reserved.
dc.format.extent
dc.format.extent	Pages: (8778-8784)
dc.language	English
dc.publisher	OXFORD
dc.relation.ispartof	Publication Name: Tetrahedron; Publication Year: 2010; Volume: 66; no. 45; Pages: (8778-8784);
dc.relation.ispartofseries
dc.relation.uri
dc.source	Scopus
dc.subject.other
dc.title	End-capping of conjugated thiophene-benzene aromatic systems
dc.type	Article
dc.contributor.affiliation	Wex, B., Department of Natural Sciences, Lebanese American University, PO Box 36, Byblos, Lebanon
dc.contributor.affiliation	Jradi, F.M., Department of Chemistry, American University of Beirut, Beirut 1107-2020, Lebanon
dc.contributor.affiliation	Patra, D., Department of Chemistry, American University of Beirut, Beirut 1107-2020, Lebanon
dc.contributor.affiliation	Kaafarani, B.R., Department of Chemistry, American University of Beirut, Beirut 1107-2020, Lebanon
dc.contributor.authorAddress	Wex, B.; Department of Natural Sciences, Lebanese American University, PO Box 36, Byblos, Lebanon; email: brigitte.wex@lau.edu.lb
dc.contributor.authorCorporate	University: American University of Beirut; Faculty: Faculty of Arts and Sciences; Department: Chemistry;
dc.contributor.authorDepartment	Chemistry
dc.contributor.authorDivision
dc.contributor.authorEmail	brigitte.wex@lau.edu.lb
dc.contributor.faculty	Faculty of Arts and Sciences
dc.contributor.authorInitials	Wex, B
dc.contributor.authorInitials	Jradi, FM
dc.contributor.authorInitials	Patra, D
dc.contributor.authorInitials	Kaafarani, BR
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress	Wex, B (reprint author), Lebanese Amer Univ, Dept Nat Sci, POB 36, Byblos, Lebanon.
dc.contributor.authorResearcherID
dc.contributor.authorUniversity	American University of Beirut
dc.description.cited	Barrash-Shiftan N, 1998, J PHYS ORG CHEM, V11, P743, DOI 10.1002-(SICI)1099-1395(1998100)11:10743::AID-POC393.0.CO;2-H; BAUERLE P, 1993, SYNTHESIS-STUTTGART, P1099, DOI 10.1055-s-1993-26009; Brusso JL, 2008, CHEM MATER, V20, P2484, DOI 10.1021-cm7030653; Coropceanu V, 2006, CHEM-EUR J, V12, P2073, DOI 10.1002-chem.200500879; Degheili JA, 2009, J PHYS CHEM A, V113, P1244, DOI 10.1021-jp8098363; Fichou D., 1999, HDB OLIGO POLYTHIOPH; Gao P, 2010, CHEM-EUR J, V16, P5119, DOI 10.1002-chem.200903562; Hains AW, 2010, ACS APPL MATER INTER, V2, P175, DOI 10.1021-am900634a; Helgesen M, 2010, MACROMOLECULES, V43, P1253, DOI 10.1021-ma9024812; Horowitz G, 2004, J MATER RES, V19, P1946, DOI 10.1557-JMR.2004.0266; Kagan C. R., 2003, THIN FILM TRANSISTOR; KALYANASUNDARAM K, 1977, J AM CHEM SOC, V99, P2039, DOI 10.1021-ja00449a004; Lakowicz J. R., 1999, PRINCIPLES FLUORESCE; LIPPERT E, 1957, Z ELEKTROCHEM, V61, P962; MATAGA N, 1956, B CHEM SOC JPN, V29, P465, DOI 10.1246-bcsj.29.465; Miyazaki E, 2009, J MATER CHEM, V19, P5913, DOI 10.1039-b910824f; MIYAZAKI E, 2008, Patent No. 2008108442; Moustafa RM, 2009, J PHYS CHEM A, V113, P1235, DOI 10.1021-jp809830x; Parker C.A., 1968, PHOTOLUMINESCENCE SO; Reichardt C., 1988, SOLVENTS SOLVENT EFF; REICHARDT C, 1994, CHEM REV, V94, P2319, DOI 10.1021-cr00032a005; SARAF SD, 1974, J MATH SCI, V1, P75; Shinamura S, 2010, J ORG CHEM, V75, P1228, DOI 10.1021-jo902545a; Shyamala T, 2006, CHEM PHYS, V330, P469, DOI 10.1016-j.chemphys.2006.09.018; Singh TB, 2006, ANNU REV MATER RES, V36, P199, DOI 10.1146-annurev.matsci.36.022805.094757; Subuddhi U, 2006, PHOTOCH PHOTOBIO SCI, V5, P459, DOI 10.1039-b600009f; Wex B, 2006, J MATER CHEM, V16, P1121, DOI 10.1039-b512191d; Wex B, 2006, J PHYS CHEM A, V110, P13754, DOI 10.1021-jp065548s; Wex B, 2005, J ORG CHEM, V70, P4502, DOI 10.1021-jo048010w; Wex B, 2004, J ORG CHEM, V69, P2197, DOI 10.1021-jo035769j; Xia CJ, 2002, ORG LETT, V4, P2067, DOI 10.1021-ol025943a
dc.description.citedCount
dc.description.citedTotWOSCount	0
dc.description.citedWOSCount	0
dc.format.extentCount	7
dc.identifier.articleNo
dc.identifier.coden	TETRA
dc.identifier.pubmedID
dc.identifier.scopusID	77957980899
dc.identifier.url
dc.publisher.address	THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
dc.relation.ispartofConference
dc.relation.ispartofConferenceCode
dc.relation.ispartofConferenceDate
dc.relation.ispartofConferenceHosting
dc.relation.ispartofConferenceLoc
dc.relation.ispartofConferenceSponsor
dc.relation.ispartofConferenceTitle
dc.relation.ispartofFundingAgency
dc.relation.ispartOfISOAbbr	Tetrahedron
dc.relation.ispartOfIssue	45
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle	Tetrahedron
dc.relation.ispartofPubTitleAbbr	Tetrahedron
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume	66
dc.source.ID	WOS:000283696400028
dc.type.publication	Journal
dc.subject.otherAuthKeyword	End-capping
dc.subject.otherAuthKeyword	Reversible redox behavior
dc.subject.otherAuthKeyword	Thieno[3,2-f:4,5-f′]bis[1]benzothiophene
dc.subject.otherChemCAS	benzene, 71-43-2
dc.subject.otherChemCAS	thiophene, 110-02-1
dc.subject.otherIndex	aromatic compound
dc.subject.otherIndex	benzene
dc.subject.otherIndex	thieno[3,2 f-4,5 f']bis[1]benzothiophene
dc.subject.otherIndex	thiophene
dc.subject.otherIndex	unclassified drug
dc.subject.otherIndex	article
dc.subject.otherIndex	conjugation
dc.subject.otherIndex	cyclic potentiometry
dc.subject.otherIndex	oxidation
dc.subject.otherIndex	priority journal
dc.subject.otherIndex	spectrophotometry
dc.subject.otherIndex	synthesis
dc.subject.otherKeywordPlus	PHOTOPHYSICAL PROPERTIES
dc.subject.otherKeywordPlus	ORGANIC SEMICONDUCTORS
dc.subject.otherKeywordPlus	HOMOGENEOUS MEDIA
dc.subject.otherKeywordPlus	EXTENDED CHAINS
dc.subject.otherKeywordPlus	PYRENE
dc.subject.otherKeywordPlus	FLUORESCENCE
dc.subject.otherKeywordPlus	MOLECULES
dc.subject.otherKeywordPlus	PERFORMANCE
dc.subject.otherKeywordPlus	BEHAVIOR
dc.subject.otherKeywordPlus	ISOMERS
dc.subject.otherWOS	Chemistry, Organic

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