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dc.contributor.authorSerwinski, P. R.en
dc.contributor.authorWalton, R.en
dc.contributor.authorSanborn, J. A.en
dc.contributor.authorLahti, P. M.en
dc.contributor.authorEnyo, T.en
dc.contributor.authorMiura, D.en
dc.contributor.authorTomioka, H.en
dc.contributor.authorNicolaïdes, Andrew N.en
dc.creatorSerwinski, P. R.en
dc.creatorWalton, R.en
dc.creatorSanborn, J. A.en
dc.creatorLahti, P. M.en
dc.creatorEnyo, T.en
dc.creatorMiura, D.en
dc.creatorTomioka, H.en
dc.creatorNicolaïdes, Andrew N.en
dc.date.accessioned2019-11-21T06:22:45Z
dc.date.available2019-11-21T06:22:45Z
dc.date.issued2001
dc.identifier.issn1523-7060
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56116
dc.description.abstract(Matrix Presented) UV-vis, FTIR, and ESR spectroscopic studies were carried out on samples of 1,4- and 1,5-naphthalenediazide that were photolyzed at cryogenic temperatures in argon and frozen solvent matrices. Mononitrenes and diiminediyl systems are produced. Spectral and computational results are consistent with quinonoidal singlet ground-state structures for the diiminediyls, rather than aromatic dinitrene structures.en
dc.sourceOrganic lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0442327200&doi=10.1021%2fol0068288&partnerID=40&md5=74ab586396d75bb5085dcd920e5bbb10
dc.titleConnectivity Effects in Isomeric Naphthalenedinitrenesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ol0068288
dc.description.volume3
dc.description.issue3
dc.description.startingpage357
dc.description.endingpage360
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 :4</p>en
dc.source.abbreviationOrg.Lett.en


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