Helicity control of an indolocarbazole foldamer by chiral organic anions

Jae Min Suk, Dan A. Kim, Kyu-Sung Jeong

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Chiral organic anions such as camphorsulfonates and cAMP give rise to the preferential formation of a one-handed helix of an indolocarbazole foldamer, thus inducing characteristic circular dichroic (CD) signals. Moreover, the on and off switching of the chiroptical signal can be operated by acid and base chemistry which efficiently controls the association and dissipation of the foldamer and cAMP.

Original languageEnglish
Pages (from-to)5018-5021
Number of pages4
JournalOrganic Letters
Volume14
Issue number19
DOIs
Publication statusPublished - 2012 Oct 5

Fingerprint

Anions
Association reactions
anions
Acids
helices
dissipation
chemistry
acids

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Suk, Jae Min ; Kim, Dan A. ; Jeong, Kyu-Sung. / Helicity control of an indolocarbazole foldamer by chiral organic anions. In: Organic Letters. 2012 ; Vol. 14, No. 19. pp. 5018-5021.
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Helicity control of an indolocarbazole foldamer by chiral organic anions. / Suk, Jae Min; Kim, Dan A.; Jeong, Kyu-Sung.

In: Organic Letters, Vol. 14, No. 19, 05.10.2012, p. 5018-5021.

Research output: Contribution to journalArticle

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