Allocation of Ambipolar Charges on an Organic Diradical with a Vinylene-Phenylenediyne Bridge

التفاصيل البيبلوغرافية
العنوان: Allocation of Ambipolar Charges on an Organic Diradical with a Vinylene-Phenylenediyne Bridge
المؤلفون: Joaquín Calbo, Jaume Veciana, Paula Mayorga-Burrezo, Francesc Bejarano, Núria Crivillers, Vega Lloveras, J. Alejandro de Sousa, Xiaotao Zhao, Concepció Rovira, Martin R. Bryce, Enrique Ortí
المساهمون: Ministerio de Ciencia e Innovación (España), European Commission, Generalitat de Catalunya, Generalitat Valenciana, Centro de Investigación Biomédica en Red Bioingeniería, Biomateriales y Nanomedicina (España), Instituto de Salud Carlos III
المصدر: Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
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The journal of physical chemistry letters, 2021, Vol.12(26), pp.6159-6164 [Peer Reviewed Journal]
سنة النشر: 2021
مصطلحات موضوعية: endocrine system, 010405 organic chemistry, Radical anion, 010402 general chemistry, 01 natural sciences, 3. Good health, 0104 chemical sciences, Political science, Oxidation, General Materials Science, Stilbene analogue, Physical and Theoretical Chemistry, PTM radical, Mixed-valence species, Humanities, Dimerization, Oligoyne
الوصف: Two redox and magnetically active perchlorotriphenylmethyl (• PTM) radical units have been connected as end-capping groups to a bis(phenylene)diyne chain through vinylene linkers. Negative and positive charged species have been generated, and the influence of the bridge on their stabilization is discussed. Partial reduction of the electron-withdrawing • PTM radicals results in a class-II mixed-valence system with the negative charge located on the terminal PTM units, proving the efficiency of the conjugated chain for the electron transport between the two terminal sites. Counterintuitively, the oxidation process does not occur along the electron-rich bridge but on the vinylene units. The • PTM radicals play a key role in the stabilization of the cationic species, promoting the generation of quinoidal ring segments.
This work was supported by the MICINN of Spain (Projects CTQ2016-80030-R, PGC2018-099568-B-I00 (EU Feder Funds), PID2019-111682RB-I00, Severo Ochoa FUNFUTURE CEX2019-000917-S, and María de Maeztu CEX2019- 000919-M), the Generalitat de Catalunya (2017-SGR-918), the Generalitat Valenciana (PROMETEO/2020/077), and the Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Development Fund. P.M.- B. gratefully thanks financial support from the Juan de la Cierva-Formación 2015 programme (FJCI-2015-23577) supported by MICINN. F.B. thanks the MECD for a predoctoral FPU fellowship. J.C. acknowledges the Generalitat Valenciana (APOSTD/2017/081). J.A.d.S. is enrolled in the Materials Science doctoral program of the UAB. J.A.d.S. thanks the MINECO for the FPI-SO fellowship. The authors acknowledge A. Bernabé from ICMAB for the MALDI-ToF measurements and Dr. Mireia Díaz and Dr. Marta Vilaseca, from the IRB Barcelona Mass Spectrometry and Proteomics Core Facility (unity member of ProteoRed, PRB3-ISCIII, supported by Grant PRB3 (IPT17/0019-ISCIII-SGEFI/ERDF), for the ES+ ToF MS experiments. The work in Durham was supported by the EC FP7 ITN project MOLESCO (606728).
وصف الملف: application/pdf
تدمد: 1948-7185
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a51a3cd32fe162dac423cb53af4308eb
https://pubmed.ncbi.nlm.nih.gov/34184906
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....a51a3cd32fe162dac423cb53af4308eb
قاعدة البيانات: OpenAIRE