Synthesis and acid-responsive electron-Transfer disproportionation of non- and tetramesityl-substituted 1,1',9,9'-bicarbazole

Palash Pandit, Toshikazu Nakamura, Shuhei Higashibayashi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Non-substituted 1,1',9,9'-bicarbazole and 3,3',6,6'-Tetramesityl- 1,1',9,9'-bicarbazole were synthesized through dimerization of carbazole derivatives and oxidative NN bond formation reaction. Non-substituted 1,1',9,9'-bicarbazole formed a stacking packing structure in crystal. Both bicarbazoles were found to undergo acid-responsive electron-Transfer disproportionation. The radical cation generated from the non-substituted 1,1',9,9'- bicarbazole was stable in solution under air at room temperature, even without protecting bulky substituents.

Original languageEnglish
Pages (from-to)1336-1338
Number of pages3
JournalChemistry Letters
Volume44
Issue number10
DOIs
Publication statusPublished - 2015
Externally publishedYes

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Dimerization
Cations
Derivatives
Crystals
Acids
Electrons
Air
Temperature
carbazole

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Synthesis and acid-responsive electron-Transfer disproportionation of non- and tetramesityl-substituted 1,1',9,9'-bicarbazole. / Pandit, Palash; Nakamura, Toshikazu; Higashibayashi, Shuhei.

In: Chemistry Letters, Vol. 44, No. 10, 2015, p. 1336-1338.

Research output: Contribution to journalArticle

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