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The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles.
Krzeszewski, Maciej; Swider, Pawel; Dobrzycki, Lukasz; Cyranski, Michal K; Danikiewicz, Witold; Gryko, Daniel T.
Affiliation
  • Krzeszewski M; Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland. dtgryko@icho.edu.pl witold.danikiewicz@icho.edu.pl.
  • Swider P; Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland. dtgryko@icho.edu.pl witold.danikiewicz@icho.edu.pl.
  • Dobrzycki L; Warsaw University, Chemistry Department, Pasteura 1, 01-224 Warsaw, Poland. chamis@chem.uw.edu.pl.
  • Cyranski MK; Warsaw University, Chemistry Department, Pasteura 1, 01-224 Warsaw, Poland. chamis@chem.uw.edu.pl.
  • Danikiewicz W; Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland. dtgryko@icho.edu.pl witold.danikiewicz@icho.edu.pl.
  • Gryko DT; Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland. dtgryko@icho.edu.pl witold.danikiewicz@icho.edu.pl.
Chem Commun (Camb) ; 52(77): 11539-11542, 2016 Sep 20.
Article in En | MEDLINE | ID: mdl-27709209
The presence of steric hindrance triggers different reaction pathways in the intramolecular oxidative aromatic coupling of tetraaryl-pyrrolo[3,2-b]pyrroles and leads to the formation of a fluorene moiety and a new cationic π-system linked together by a spiro carbon atom. Computational studies elegantly rationalized these results. These previously unknown functional dyes emit red light with reasonable efficiency.
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Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2016 Document type: Article Country of publication: United kingdom
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Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2016 Document type: Article Country of publication: United kingdom