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Bispalladium(II) Complexes of di-p-Pyrirubyrin Derivatives as Promising Near-Infrared Photoacoustic Dyes.
Hurej, Karolina; Oszczeda, Weronika; Opas, Ewelina; Zelewski, Szymon J; Pawlicki, Milosz; Bialek, Michal J; Orzel, Lukasz; Latos-Grazynski, Lechoslaw.
Afiliação
  • Hurej K; Department of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50383, Wroclaw, Poland.
  • Oszczeda W; Department of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50383, Wroclaw, Poland.
  • Opas E; Department of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50383, Wroclaw, Poland.
  • Zelewski SJ; Department of Semiconductor Materials Engineering, Faculty of Fundamental Problems of Technology, Wroclaw University of Science and Technology, Wyb. Wyspianskiego 27, 50370, Wroclaw, Poland.
  • Pawlicki M; Department of Physics, Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge, CB3 0HE, UK.
  • Bialek MJ; Department of Chemistry, Jagiellonian University, Gronostajowa 2, 30358, Kraków, Poland.
  • Orzel L; Department of Chemistry, University of Wroclaw, F. Joliot-Curie 14, 50383, Wroclaw, Poland.
  • Latos-Grazynski L; Department of Chemistry, Jagiellonian University, Gronostajowa 2, 30358, Kraków, Poland.
Angew Chem Int Ed Engl ; 62(28): e202303394, 2023 Jul 10.
Article em En | MEDLINE | ID: mdl-37178418
ABSTRACT
The insertion of palladium(II) into di-p-pyrirubyrin results in mutually convertible bimetallic complexes. Post-synthetic functionalization of one of them yielded bispalladium(II) dioxo-di-p-pyrirubyrin and, after demetallation, dioxo-di-p-pyrirubyrin, introducing for the first time the α,ß'-pyridin-2-one unit into the macrocyclic frame. Bispalladium(II) di-p-pyrirubyrin 6, bispalladium(II) dioxo-di-p-pyrirubyrin 9, and dioxo-di-p-pyrirubyrin 10 absorb and emit light around 1000 nm and are characterized by high photostability. Thus, they are promising candidates for near-infrared photoacoustic dyes, ideally targeting (9) the wavelength of Yb-based fiber lasers. The incorporation of an α,ß'-pyridine moiety into expanded porphyrins opens a highly interesting area of research due to the attractive optical and coordination properties of the resulting molecules.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia
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