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               <dc:title>Triquinoline‐ versus Fullerene‐Based Cycloparaphenylene Ionic Complexes: Comparison of Photoinduced Charge‐Shift Reactions</dc:title>
               <dc:creator>Stasyuk, Anton J.</dc:creator>
               <dc:creator>Stasyuk, Olga A.</dc:creator>
               <dc:creator>Solà i Puig, Miquel</dc:creator>
               <dc:creator>Voityuk, Alexander A.</dc:creator>
               <dc:subject>Química supramolecular</dc:subject>
               <dc:subject>Supramolecular chemistry</dc:subject>
               <dc:subject>Transferència de càrrega</dc:subject>
               <dc:subject>Charge transfer</dc:subject>
               <dc:subject>Ful·lerens</dc:subject>
               <dc:subject>Fullerenes</dc:subject>
               <dc:description>A triquinoline cationic moiety (TQ⋅H+) has recently been designed as a novel molecular unit for supramolecular chemistry. In addition to some useful features, TQ⋅H+ has strong electron‐acceptor properties, which renders the molecular cation a unique element in nanochemistry. TQ⋅H+ is found to form complexes with coronene (COR) and cycloparaphenylene (CPP). In this work, we report a computational study of photoinduced electron transfer in supramolecular complexes TQ⋅H+‐COR, TQ⋅H+⊂[12]CPP and (TQ⋅H+‐COR)⊂[12]CPP. The electron‐transfer rates are estimated by using the semi‐classical approach. The results are compared with the data previously obtained for a structurally similar inclusion complex Li+@C60⊂[10]CPP. In particular, we found a red solvatochromic shift for charge‐shift bands in the TQ⋅H+‐complexes unlike a blueshift showed by Li+@C60⊂[10]CPP. This distinction is explored in terms of electronic and structural features of the systems</dc:description>
               <dc:description>We are grateful for financial support from the Spanish MINECO (Network RED2018-102815-T, project CTQ2017‐85341‐P, and Juan de la Cierva formación contracts FJCI‐2016‐29448 to A.J.S. and FJCI‐2017‐32757 to O.A.S.), and the Catalan DIUE (2017SGR39, XRQTC, and ICREA Academia 2014 Award to M.S.).</dc:description>
               <dc:date>2024-06-18T13:55:40Z</dc:date>
               <dc:date>2024-06-18T13:55:40Z</dc:date>
               <dc:date>info:eu-repo/date/embargoEnd/2021-08-21</dc:date>
               <dc:date>2020-08-21</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:type>peer-reviewed</dc:type>
               <dc:identifier>http://hdl.handle.net/10256/18428</dc:identifier>
               <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202002179</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/issn/0947-6539</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1521-3765</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-85341-P/ES/AVANCES EN LA REACTIVIDAD DE FULLERENOS Y NANOTUBOS: ESTUDIOS TEORICO-EXPERIMENTALES DE CICLACIONES CATALIZADAS POR METALES DE TRANSICION/</dc:relation>
               <dc:rights>Tots els drets reservats</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Wiley</dc:publisher>
               <dc:source>© Chemistry: A European Journal, 2020, vol. 26, núm. 47, p.10896-10902</dc:source>
               <dc:source>Articles publicats (D-Q)</dc:source>
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