Publication:
Enabling Racemization of Axially Chiral Subphthalocyanine-Tetracyanobutadiene-Aniline Enantiomers by Triplet State Photogeneration

dc.contributor.affiliation"Departamento de Química Orgánica, Universidad Autónoma de Madrid, Campus de Cantoblanco, Madrid, 28049, Spain"," IMDEA-Nanociencia, c/Faraday 9, Campus de Cantoblanco, Madrid, 28049, Spain"," Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, Madrid, 28049, Spain"," Scuola Normale Superiore, Piazza dei Cavalieri 7, Pisa, 56126, Italy"," Istituto Nazionale di Fisica Nucleare, Largo Pontecorvo 3, Pisa, 56100, Italy"en
dc.contributor.affiliation000000041762408X
dc.contributor.authorLavarda G.
dc.contributor.authorBhattacharjee N.
dc.contributor.authorBrancato G.
dc.contributor.authorTorres, Tomás
dc.contributor.authorBottari, Giovanni
dc.date.accessioned2020-12-04T11:40:16Z
dc.date.available2020-12-04T11:40:16Z
dc.date.issued2020
dc.identifier.doi10.1002/anie.202010133
dc.identifier.urihttp://hdl.handle.net/20.500.12614/724
dc.journal.titleAngewandte Chemie - International Edition
dc.language.isoen
dc.page.initial21224
dc.relation.projectIDTEMPFinancial support from Spanish MICINN (CTQ2017?85393?P), Scuola Normale Superiore research program and the computing time at the CINECA and Avogadro HPC centers is acknowledged. IMDEA Nanociencia acknowledges support from the “Severo Ochoa” Programme for Centres of Excellence in R&D (MINECO, Grant SEV2016?0686).
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleEnabling Racemization of Axially Chiral Subphthalocyanine-Tetracyanobutadiene-Aniline Enantiomers by Triplet State Photogeneration
dc.typeresearch article
dc.volume.number59
dspace.entity.typePublication
relation.isAuthorOfPublication64ff123a-bd77-4339-b4af-a8a86d733054
relation.isAuthorOfPublicationafbbdf20-ff63-4c01-8cb4-699b552f3b2c
relation.isAuthorOfPublication.latestForDiscovery64ff123a-bd77-4339-b4af-a8a86d733054

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