4.4 Article

Synthesis of organogelling, fluoride ion-responsive, cholesteryl-based benzoxazole containing intra- and intermolecular hydrogen-bonding sites

Journal

TETRAHEDRON LETTERS
Volume 51, Issue 42, Pages 5596-5600

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.08.053

Keywords

Organogel; Cholesteryl group; Fluoride anion; Recognition

Funding

  1. National Research Foundation (NRF)
  2. Korea government (MEST) [R01-2007-000-10740-0, 2009-008146]
  3. National Research Foundation of Korea [R01-2007-000-10740-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A cholesteryl-based 2-(2'-hydroxyphenyl)benzoxazole (HPB) derivative 3 linked with an amide bond was prepared through an efficient synthetic pathway. The HPB, amide, and cholesteryl groups play important roles in constructing the supramolecular gel structure. UV-vis and fluorescence spectroscopy also showed that HPB and amide groups, which provide intra- and intermolecular hydrogen bonding, respectively, also contribute the recognition of fluoride anions. (C) 2010 Elsevier Ltd. All rights reserved.

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