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Author: search.filters.author.Chang, Kai-ChiSubject: search.filters.subject.fluorescence

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    Anthryl-1,2,4-oxadiazole-Substituted Calix[4]arenes as Highly Selective Fluorescent Chemodosimeters for Fe3+
    (2015-04-01)
    Chen, Ying-Jung
    ;
    Yang, Shun-Chieh
    ;
    Tsai, Chia-Chen
    ;
    Chang, Kai-Chi
    ;
    Chuang, Wen-Han
    Fluorescent chemosensors 1 and 2, with 1,2,4-oxadiazoles as the binding ligands and anthracene as the fluorophore, were synthesized through sequential 1,3-dipolar cycloaddition reactions of 25,27-dioxyacetonitrilecalix[4]arenes 8 and 11. The fluorescence of 1 was severely quenched by both Fe3+ and Cu2+, whereas that of 2 was selectively quenched only by Fe3+. Control compound 4 was also selectively quenched by Fe3+, which implied the importance of anthryl-1,2,4-oxadiazole core; furthermore, it was shown to give various oxidation products such as oxanthrone 13, anthraquinone 14, and imidazolyl oxanthrone 15. In addition to product separation and identification, the fluorescent quenching mechanism of these 9-anthryl-1,2,4-oxadiazolyl derivatives by Fe3+ is also discussed. Furthermore, it should be noted that the oxadiazole-substituted anthracene 4 and calix[4]arene 2 are Fe3+-selective fluorescent chemodosimeters without the interference by Cu2+.
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    Cooperative Recognition of a Copper Cation and Anion by a Calix[4]arene Substituted at the Lower Rim by a beta-Amino-alpha,beta-Unsaturated Ketone
    (2009)
    Senthilvelan, Annamalai
    ;
    ho, I. -Ting
    ;
    Chang, Kai-Chi
    ;
    Lee, Gene-Hsiang
    ;
    Liu, Yi-Hung
    We report herein a new ditopic calix[4]arene receptor 25,27-bis{[4-amino-4-(1-naphthyl)-2-oxo-3-butenyl]oxy}-26,28-dihydroxycalix[4]arene (2) for the simultaneous complexation of anionic and cationic species. The host molecule 25,27-bis{[3-(1-naphthyl)-5-isoxazolyl]methoxy}-26,28-dihydroxycalix[4]arene (1) was synthesised first and was followed by a [Mo(CO)(6)]mediated ring-opening reaction to give the target receptor 2. The binding properties of ligands 1 and 2 towards metal ions in CH(3)CN were investigated by UV/Vis and fluorescence spectroscopies. The results showed that both ligands I and 2 were highly selective for Cu(II) ions. Upon titration with Cu(II), the fluorescence of I was severely quenched, whereas 2 showed strong fluorescence enhancement because the metal ions help to lock the conformation of the fluorophores. During the complexation of 2 with Cu(II), the Cu(II) was reduced to Cu(I) by the free phenolic OH of 2, whereas the phenol was oxidised by Cu(II), after which it assisted in the trapping of Cu(I). Ditopic behaviour was observed for the complex 2 center dot Cu(I), which showed further enhancement of its fluorescence intensity upon complexation with anions such as acetate or fluoride.