Xin Long Ni
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
Xi Zeng
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 |
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