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Synthesis and evaluation of a novel pyrenyl-appended triazole-based thiacalix[4]arene as a fluorescent sensor for Ag+ ion

Ni, Xin Long; Zeng, Xi; Redshaw, Carl; Yamato, Takehiko

Authors

Xin Long Ni

Xi Zeng

Profile image of Carl Redshaw

Professor Carl Redshaw C.Redshaw@hull.ac.uk
Professor of Inorganic Materials Chemistry and REF Lead for Chemistry

Takehiko Yamato



Abstract

New fluorescent chemosensors 1,3-alternate-1 and 2 with pyrenyl-appended triazole-based on thiacalix[4]arene were synthesized. The fluorescence spectra changes suggested that chemosensors 1 and 2 are highly selective for Ag + over other metal ions by enhancing the monomer emission of pyrene in neutral solution. However, other heavy metal ions, such as Cu2+, and Hg2+ quench both the monomer and excimer emission of pyrene acutely. The 1H NMR results indicated that Ag+ can be selectively recognized by the triazole moieties on the receptors 1 and 2 together with the ionophoricity cavity formed by the two inverted benzene rings and sulfur atoms of the thiacalix[4]arene. © 2011 Elsevier Ltd. All rights reserved.

Citation

Ni, X. L., Zeng, X., Redshaw, C., & Yamato, T. (2011). Synthesis and evaluation of a novel pyrenyl-appended triazole-based thiacalix[4]arene as a fluorescent sensor for Ag+ ion. Tetrahedron, 67(18), 3248-3253. https://doi.org/10.1016/j.tet.2011.03.008

Journal Article Type Article
Acceptance Date Mar 2, 2011
Online Publication Date Mar 9, 2011
Publication Date May 6, 2011
Deposit Date Jun 8, 2022
Journal Tetrahedron
Print ISSN 0040-4020
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 67
Issue 18
Pages 3248-3253
DOI https://doi.org/10.1016/j.tet.2011.03.008
Public URL https://hull-repository.worktribe.com/output/3622442