Synthesis and characterization of quinoidal diketopyrrolopyrrole derivatives with exceptionally high electron affinities

dc.citation.epage16097en_US
dc.citation.issueNumber30en_US
dc.citation.spage16088en_US
dc.citation.volumeNumber121en_US
dc.contributor.authorRay, S.en_US
dc.contributor.authorSharma, S.en_US
dc.contributor.authorSalzner, U.en_US
dc.contributor.authorPatil, S.en_US
dc.date.accessioned2018-04-12T11:09:03Z
dc.date.available2018-04-12T11:09:03Z
dc.date.issued2017en_US
dc.departmentDepartment of Chemistryen_US
dc.description.abstractOpen-shell singlet biradicaloids are short-lived intermediates, but they exhibit fascinating properties for spin-based devices. Therefore, understanding the nature of their electronic structure and stability is critical for harnessing them in optoelectronic or spintronic devices. Toward this goal, we have synthesized a series of diketopyrrolopyrrole-based quinoidal molecules to investigate the contribution and relative importance of the biradical form on the ground-state electronic structure and distribution of spin density. Possibility of crossover from a closed-shell to an open-shell structure with increase in the C=C/C-C conjugation length was investigated. The ground-state properties were systematically investigated by nuclear magnetic resonance (NMR) spectroscopy, single-crystal X-ray diffraction, and electrochemical studies. Furthermore, n-doping has been carried out in solution at ambient conditions to understand the nature of doped species and demonstrate air stability. Doped species were probed by UV-visible and electron spin resonance (ESR) spectroscopy to unambiguously establish the generation of anionic species in solution. Experimental results are complemented by theoretical calculations to provide insight into the trend toward biradicaloid spin states with increasing conjugation length.en_US
dc.description.provenanceMade available in DSpace on 2018-04-12T11:09:03Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 179475 bytes, checksum: ea0bedeb05ac9ccfb983c327e155f0c2 (MD5) Previous issue date: 2017en
dc.identifier.doi10.1021/acs.jpcc.7b04085en_US
dc.identifier.eissn1932-7455
dc.identifier.issn1932-7447
dc.identifier.urihttp://hdl.handle.net/11693/37296
dc.language.isoEnglishen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acs.jpcc.7b04085en_US
dc.source.titleJournal of Physical Chemistry Cen_US
dc.titleSynthesis and characterization of quinoidal diketopyrrolopyrrole derivatives with exceptionally high electron affinitiesen_US
dc.typeArticleen_US

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