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dc.contributor.authorWudl, F.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.contributor.authorWeitz, A.en
dc.contributor.authorMa, B.en
dc.contributor.authorStrassner, T.en
dc.contributor.authorHouk, K. N.en
dc.contributor.authorKhan, S. I.en
dc.creatorWudl, F.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.creatorWeitz, A.en
dc.creatorMa, B.en
dc.creatorStrassner, T.en
dc.creatorHouk, K. N.en
dc.creatorKhan, S. I.en
dc.date.accessioned2019-11-21T06:23:33Z
dc.date.available2019-11-21T06:23:33Z
dc.date.issued1999
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56290
dc.description.abstractThe evolution of heterocycles from hexaazaanthracene to tetraazapentacenes led to the discovery that syn aza-substituted polyazaacenes possess unusual zwitterionic structures. One of these, 5,7-diphenyl-5H,12H-quinoxalino[2,3-b]phenazine 4, first claimed in 1898 was fully characterized, including an X-ray crystal structure. These heteroacenes have a low calculated singlet-triplet gap and have unusual photophysical properties. ©1999 IUPAC.en
dc.sourcePure and Applied Chemistryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0002472794&partnerID=40&md5=0e32e228e3344f0c1dbebad2d9702bc7
dc.titlePolyazaacenes: New tricks for old dogsen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume71
dc.description.issue2
dc.description.startingpage295
dc.description.endingpage302
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :52</p>en
dc.source.abbreviationPure Appl.Chem.en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-4652-7567


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