Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/132957
COMPARTIR / EXPORTAR:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE

Invitar a revisión por pares abierta
Título

Fullerene and corannulene derivatives acting as insulators of Cl- and BeH2

AutorMarín-Luna, Marta CSIC ORCID; Alkorta, Ibon CSIC ORCID ; Elguero, José CSIC ORCID; Mó, Otilia CSIC ORCID; Yáñez, Manuel
Fecha de publicación2016
EditorRoyal Society of Chemistry (UK)
CitaciónPhysical Chemistry Chemical Physics 18: 6059-6068 (2016)
ResumenThe capacity of corannulene and its benzo-derivatives CH (x = 20-60) as prototypes of non-planar π-aromatic systems which mimic the end of carbon nanotubes to act as insulators between BeH and Cl chemical entities has been explored by means of M06-2x/cc-pVDZ and M06-2x/6-311+G(d) calculations. For the sake of completeness, the set investigated includes also fullerene, C. All these aromatic derivatives lead to stable binary complexes either with BeH or halogen (Cl) anions. For BeH, however, only the complexes in which the interaction involves the convex face of the aromatic system are stable. No significant changes are observed when the binding energies (BEs) of the BeH complexes are compared to those involving planar aromatic compounds, but the ones involving Cl with the concave face of the aromatic moiety can be very large, because its curvature favors many contacts of the anion with the carbon atoms of the π-aromatic system. The formation of these binary complexes changes to a large extent the electrostatic potential on the free face of the aromatic system leading to a mutual reinforcement of both interactions, the beryllium bond and the interaction with Cl, when the ternary complexes are formed. As a result, the BEs for the triads are larger than the sum of the BEs of the corresponding binary complexes and the distances between the aromatic subunit and BeH or Cl become shorter in the triads than in the binary complexes. A MBIE analysis also indicates that the enhanced stability of ternary complexes arises mainly from the reinforcement of the beryllium bonds as well as from the three-body terms. An exploration of all the minima for BeH:CH:Cl shows that BeH binds preferentially to the peripheral aromatic rings than those in the more curved region.
Versión del editorhttp://dx.doi.org/10.1039/c5cp08046k
URIhttp://hdl.handle.net/10261/132957
DOI10.1039/c5cp08046k
Identificadoresdoi: 10.1039/c5cp08046k
issn: 1463-9076
e-issn: 1463-9084
Aparece en las colecciones: (IQM) Artículos




Ficheros en este ítem:
Fichero Descripción Tamaño Formato
accesoRestringido.pdf15,38 kBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo

CORE Recommender

SCOPUSTM   
Citations

4
checked on 16-mar-2024

WEB OF SCIENCETM
Citations

3
checked on 25-feb-2024

Page view(s)

231
checked on 19-mar-2024

Download(s)

117
checked on 19-mar-2024

Google ScholarTM

Check

Altmetric

Altmetric


NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.