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pubmed-article:15369329pubmed:dateCreated2004-9-16lld:pubmed
pubmed-article:15369329pubmed:abstractTextTo investigate the role of hydrogen-bonding on colorimetric transition of polydiacetylene supramolecules, novel diacetylene derivatives allowing various hydrogen-bonding states were synthesized by coupling carboxy-substituted (ortho-, meta-, and para-) anilide groups with a typical single-chain diacetylene lipid. One with a terminal carboxyl group at the meta position provided the resulting supramolecular Langmuir-Schaefer films with enhanced hydrogen-bonding, and hence resulted in unprecedented colorimetric reversibility under both thermal and pH stimuli.lld:pubmed
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pubmed-article:15369329pubmed:authorpubmed-author:KimJong-ManJMlld:pubmed
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pubmed-article:15369329pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:15369329pubmed:articleTitleColorimetric reversibility of polydiacetylene supramolecules having enhanced hydrogen-bonding under thermal and pH stimuli.lld:pubmed
pubmed-article:15369329pubmed:affiliationDepartment of Chemical & Biological Engineering, Korea University, Seoul 136-701, Korea. ahn@korea.ac.krlld:pubmed
pubmed-article:15369329pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15369329pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed