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dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.contributor.authorChen, Y. Z.en
dc.contributor.authorCao, Yun Zhenen
dc.contributor.authorBest, T. P.en
dc.contributor.authorItkis, M. E.en
dc.contributor.authorBeer, L.en
dc.contributor.authorOakley, R. T.en
dc.contributor.authorCordes, A. W.en
dc.contributor.authorBrock, C. P.en
dc.contributor.authorHaddon, R. C.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.creatorChen, Y. Z.en
dc.creatorCao, Yun Zhenen
dc.creatorBest, T. P.en
dc.creatorItkis, M. E.en
dc.creatorBeer, L.en
dc.creatorOakley, R. T.en
dc.creatorCordes, A. W.en
dc.creatorBrock, C. P.en
dc.creatorHaddon, R. C.en
dc.date.accessioned2019-11-21T06:20:31Z
dc.date.available2019-11-21T06:20:31Z
dc.date.issued2001
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55720
dc.description.abstractWe report the preparation and solid-state characterization of the perchlorophenalenyl radical (1). The radical is initially obtained as a yellow-green solid by reduction of the perchlorophenalenium salt (12+). This solid sublimes in a sealed tube to give black shiny hexagonal crystals of the perchlorophenalenyl radical (1). The I structure consists of 1-dimensional stacks of the monomeric radical. The peri-chlorine atoms force the phenalenyl system to be strongly nonplanar leading to a large separation between adjacent molecules within the stacks (3.78 Å), and the molecules adopt two distinct stacking motifs (quasisuperimposed and rotated by 60° with respect to neighbors). Because of the packing frustration in the lattice and the large intermolecular spacing, the solid shows Curie paramagnetism in the temperature range 100-400 K, before antiferromagnetic coupling sets in at low temperatures. Due to the narrow bandwidth that results from the isolation of the individual molecules, the solid is a Mott-Hubbard insulator, with a room-temperature conductivity of ρRT = 10-10 S/cm.en
dc.sourceJournal of the American Chemical Societyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0034789097&doi=10.1021%2fja0018015&partnerID=40&md5=4d875653cd695a8979c27682219bff8e
dc.subjectarticleen
dc.subjectunclassified drugen
dc.subjectdimerizationen
dc.subjectAntiferromagnetismen
dc.subjectParamagnetismen
dc.subjectcrystal structureen
dc.subjectchemical structureen
dc.subjectferromagnetic materialen
dc.subjectCrystalsen
dc.subjectChlorineen
dc.subjecttemperatureen
dc.subjectreaction analysisen
dc.subjectLattice constantsen
dc.subjectSodium chlorideen
dc.subjectmonomeren
dc.subjectOrganic compoundsen
dc.subjectaromatic compounden
dc.subjectradicalen
dc.subjectreductionen
dc.subjectchlorine derivativeen
dc.subjectpercholorophenalenyl radicalen
dc.subjectSolid state characterizationen
dc.titlePerchlorophenalenyl radicalen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ja0018015
dc.description.volume123
dc.description.issue17
dc.description.startingpage3864
dc.description.endingpage3871
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 :99</p>en
dc.source.abbreviationJ.Am.Chem.Soc.en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-4652-7567


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