J
Jacques Vicens
Researcher at International Pentecostal Holiness Church
Publications - 125
Citations - 2137
Jacques Vicens is an academic researcher from International Pentecostal Holiness Church. The author has contributed to research in topics: Calixarene & Crystal structure. The author has an hindex of 23, co-authored 125 publications receiving 2077 citations. Previous affiliations of Jacques Vicens include University of East Anglia & University of Strasbourg.
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Journal ArticleDOI
A Pyrenyl-Appended Triazole-Based Calix[4]arene as a Fluorescent Sensor for Cd2+ and Zn2+
Sun Young Park,Jung Hee Yoon,Chang Seop Hong,Rachid Souane,Jong Seung Kim,Susan E. Matthews,Jacques Vicens +6 more
TL;DR: The synthesis and evaluation of a novel calix[4]arene-based fluorescent chemosensor 8 for the detection of Cd(2+) and Zn(2+) and the fluorescent spectra changes observed upon addition of various metal ions show that 8 is highly selective for Cd (2+)
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A new fluorescent chemosensor for F− based on inhibition of excited-state intramolecular proton transfer
TL;DR: In this article, a new fluorescent chemosensor 1 with two amidoanthraquinone groups (1-AAQs) at the lower rim of ptert-butylcalix[4]arene has been synthesized.
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Bis(crown ether) and Azobenzocrown Derivatives of Calix[4]arene. A Review of Structural Information from Crystallographic and Modelling Studies
TL;DR: The association within one molecule of calix[4]arene and crown ether moieties leads to ligands with new complexing properties as mentioned in this paper, and some of its derivatives have been shown to be highly selective extractants for caesium ions.
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Cation binding properties of a novel 1,3-alternate calix[4]biscrown. Formation of 1:1 and 1:2 complexes and unique cation tunneling across a calix[4]arene cavity
TL;DR: In this article, a 1,3-alternate calix[4]biscrown was synthesized by the reaction of tetraethyleneglycol ditosylate in the presence of K 2 CO 3.
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Fluoride sensing with a PCT-based calix[4]arene
TL;DR: In this paper, a novel calixarene-based anion sensor with two coumarin units attached via amido functions acting also as binding sites is presented, which causes selectively red-shift in UV-vis absorption and in fluorescence emission due to H-bonding followed by deprotonation of NHamide groups.