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Abstract:
The reaction of ferrocenecarboxaldehyde with (2-aminoethoxy)diphenylborane led to the formation of ferrocenyl-substituted boronate receptor 1, which was characterized by IR, MS, HRMS, 11B, 1H and 13C NMR spectra. The signaling process was confirmed by UV-vis, electrochemistry measurements as well as 1H and 19F NMR spectroscopy. The receptor 1 exhibited high selectivity for F- in CH3CN solution over all the other anions in the DPVs (differential pulse voltammetry). 1H NMR titrations indicated that F- ion induced tautomerism of E- and Z-isomer transformations of the receptor 1 and there were three kinds of protons showing obvious highfield shifts for receptor 1 in DMSO-d6. UV-vis titrations demonstrated that the receptor 1 could bind F- ion forming 1:1 stoichiometric complexes and show high selectivity and sensitivity towards F- ion. © 2015 Elsevier B.V. All rights reserved.
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ISSN: 0022-328X
Year: 2015
Volume: 788
Page: 17-26
Language: English
2 . 3 3 6
JCR@2015
2 . 1 0 0
JCR@2023
ESI HC Threshold:265
JCR Journal Grade:2
CAS Journal Grade:3
Cited Count:
WoS CC Cited Count: 0
SCOPUS Cited Count: 14
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 4
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