Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors

Liuqing Yang, Lijian Zhong, Kazuhiro Yamato, Xiaheng Zhang, Wen Feng, Pengchi Deng, Lihua Yuan, Xiao C Zeng, Bing Gong

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

Aromatic oligoamide macrocycles consisting of six to ten meta-linked residues were prepared based on bimolecular coupling/cyclization of a pentameric diamine and oligomeric diacid chlorides, and adopt folded conformations enforced by intramolecular three-center H-bonds.

Original languageEnglish (US)
Pages (from-to)729-733
Number of pages5
JournalNew Journal of Chemistry
Volume33
Issue number4
DOIs
StatePublished - Apr 20 2009

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Diamines
Cyclization
Conformations
Chlorides

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Materials Chemistry

Cite this

Yang, L., Zhong, L., Yamato, K., Zhang, X., Feng, W., Deng, P., ... Gong, B. (2009). Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors. New Journal of Chemistry, 33(4), 729-733. https://doi.org/10.1039/b902495f

Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors. / Yang, Liuqing; Zhong, Lijian; Yamato, Kazuhiro; Zhang, Xiaheng; Feng, Wen; Deng, Pengchi; Yuan, Lihua; Zeng, Xiao C; Gong, Bing.

In: New Journal of Chemistry, Vol. 33, No. 4, 20.04.2009, p. 729-733.

Research output: Contribution to journalArticle

Yang, L, Zhong, L, Yamato, K, Zhang, X, Feng, W, Deng, P, Yuan, L, Zeng, XC & Gong, B 2009, 'Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors', New Journal of Chemistry, vol. 33, no. 4, pp. 729-733. https://doi.org/10.1039/b902495f
Yang, Liuqing ; Zhong, Lijian ; Yamato, Kazuhiro ; Zhang, Xiaheng ; Feng, Wen ; Deng, Pengchi ; Yuan, Lihua ; Zeng, Xiao C ; Gong, Bing. / Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors. In: New Journal of Chemistry. 2009 ; Vol. 33, No. 4. pp. 729-733.
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