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dc.contributor.authorConstantinides, Christos P.en
dc.contributor.authorIoannou, Theodosia A.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.creatorConstantinides, Christos P.en
dc.creatorIoannou, Theodosia A.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.description.abstractBenzo- and azino-fused bis(1,2,3-dithiazoles) were investigated computationally using density functional theory (DFT) in an attempt to relate structure to ground state multiplicity preference. Structural changes on the central arene by substitution with electron donating (EDG) and electron withdrawing groups (EWG) or replacement of the central arene by pyridino or pyrazino rings, were studied by optimizing the structures as singlet and triplet ground states. The aromaticity of each ring was probed using nucleus independent chemical shift (NICS) calculations. Molecular orbital analysis identified the substituent effects on the energy of the frontier orbitals. Calculations show that the ground state multiplicity can be effectively controlled with strategic substitutions. EWG directly attached on the negative cyanine of the central arene stabilize zwitterionic singlet states whereas EDG attached at the same position favor a triplet ground state. NICS calculations indicate that the central arenes sacrifice their aromaticity and become non-aromatic for molecules with zwitterionic ground states as an effective way to avoid their overall 4n π antiaromaticity. © 2013 Elsevier Ltd. All rights reserved.en
dc.titleManipulating the singlet-triplet energy gaps of arene-fused bis(1,2,3-dithiazoles): A computational studyen
dc.description.endingpage180 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied SciencesΤμήμα Χημείας / Department of Chemistry
dc.description.notes<p>Cited By :8</p>en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.contributor.orcidConstantinides, Christos P. [0000-0001-6364-1102]

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