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AuthorHrobarik, P.
AuthorHrobarikova, V.
AuthorSemak, V.
AuthorKasak, P.
AuthorRakovsky, E.
AuthorPolyzos, I.
AuthorFakis, M.
AuthorPersephonis, P.
Available date2016-01-14T13:24:26Z
Publication Date2014-12
Publication NameOrganic Letters
CitationPeter Hrobarik, Veronika Hrobarikova, Vladislav Semak, Peter Kasak?, Erik Rakovsky, Ioannis Polyzos, Mihalis Fakis, and Peter Persephonis, "Quadrupolar Benzobisthiazole-Cored Arylamines as Highly Efficient Two-Photon Absorbing Fluorophores", Organic Letters, 2014, 16 (24), pp 6358�6361
ISSN1523-7060
URIhttp://dx.doi.org/10.1021/ol503137p
URIhttp://hdl.handle.net/10576/4080
AbstractA computer-aided design of novel D-?-A-?-D styrylamines containing five isomeric benzobisthiazole moieties as the electron-accepting core has revealed the linear centrosymmetric benzo[1,2-d:4,5-d?]bisthiazole as the most promising building block for engineering chromophores displaying high two-photon absorption (TPA) in the near-IR region, as also confirmed experimentally. The ease of synthesis of quadrupolar derivatives thereof, combined with extraordinarly high TPA action cross sections (?TPA?f > 1500 GM), makes these heteroaromatic systems particularly attractive as diagnostic agents in 3D fluorescence imaging.
SponsorAlexander von Humboldt foundation for a research fellowship
Languageen
PublisherAmerican Chemical Society
Subject3D fluorescence
Subjectisomeric benzobisthiazole
SubjectIR region
SubjectQuadrupolar
TitleQuadrupolar benzobisthiazole-cored arylamines as highly efficient two-photon absorbing fluorophores
TypeArticle
Pagination6358-6361
Issue Number24
Volume Number16


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