Picolyl armed C-1,2 alternate tetrahomodioxacalix[4]arene tetraamides

  • K. No*
  • , Jeong H. Lee
  • , Seung H. Yang
  • , Kwan H. Noh
  • , Sung K. Kim
  • , J. Seo
  • , Shim S. Lee
  • , Jong S. Kim
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

A series of benzyl, 2-picolyl, 3-picolyl armed tetrahomodioxacalix[4]arene tetraamides with four p-phenyl groups on the upper rim were synthesized. They were found to be in the C-1,2-alternate conformation by 1H, 13C NMR, and X-ray crystal structure. The nitrogen atom of the 2-picolyl group played an important role in the metal ion complexation.

Original languageEnglish
Pages (from-to)167-171
Number of pages5
JournalJournal of Inclusion Phenomena
Volume47
Issue number3-4
DOIs
Publication statusPublished - 2003 Dec
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by Korea Research Foundation Grant (KRF-2002-015-CP0226). We also gratefully thank KBSI in Daejon for the instrumentation support (1H and 13C NMR).

Keywords

  • Calixarene
  • Complexation
  • Homooxacalixarene
  • X-ray crystal structure

ASJC Scopus subject areas

  • Food Science
  • General Chemistry
  • Condensed Matter Physics

Fingerprint

Dive into the research topics of 'Picolyl armed C-1,2 alternate tetrahomodioxacalix[4]arene tetraamides'. Together they form a unique fingerprint.

Cite this