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Verfasst von:Horn, Shawn [VerfasserIn]   i
 Plasser, Felix [VerfasserIn]   i
 Müller, Thomas [VerfasserIn]   i
 Libisch, Florian [VerfasserIn]   i
 Burgdörfer, Joachim [VerfasserIn]   i
 Lischka, Hans [VerfasserIn]   i
Titel:A comparison of singlet and triplet states for one- and two-dimensional graphene nanoribbons using multireference theory
Verf.angabe:Shawn Horn, Felix Plasser, Thomas Müller, Florian Libisch, Joachim Burgdörfer, Hans Lischka
E-Jahr:2014
Jahr:15 June 2014
Fussnoten:Gesehen am 10.08.2020
Titel Quelle:Enthalten in: Theoretical chemistry accounts
Ort Quelle:Berlin : Springer, 1962
Jahr Quelle:2014
Band/Heft Quelle:133(2014,8) Artikel-Nummer 1511, 9 Seiten
ISSN Quelle:1432-2234
Abstract:This study examines the radical nature and spin symmetry of the ground state of the quasi-linear acene and two-dimensional periacene series. For this purpose, high-level ab initio calculations have been performed using the multireference averaged quadratic coupled cluster theory and the COLUMBUS program package. A reference space consisting of restricted and complete active spaces is taken for the π-conjugated space, correlating 16 electrons with 16 orbitals with the most pronounced open-shell character for the acenes and a complete active-space reference approach with eight electrons in eight orbitals for the periacenes. This reference space is used to construct the total configuration space by means of single and double excitations. By comparison with more extended calculations, it is shown that a focus on the π space with a 6-31G basis set is sufficient to describe the major features of the electronic character of these compounds. The present findings suggest that the ground state is a singlet for the smaller members of these series, but that for the larger ones, singlet and triplet states are quasi-degenerate. Both the acenes and periacenes exhibit significant polyradical character beyond the traditional diradical.
DOI:doi:10.1007/s00214-014-1511-8
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1007/s00214-014-1511-8
 DOI: https://doi.org/10.1007/s00214-014-1511-8
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1726709957
Verknüpfungen:→ Zeitschrift

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