Highly selective luminescent sensing of Cu2+ in aqueous solution based on a Eu(III)-centered periodic mesoporous organosilicas hybrid
Using Pluronic P123 surfactant as template, a periodic mesoporous organosilica (PMO) functionalized with 4′-(4-carboxy-methyleneoxy phenyl)-2,2′:6′,2″-terpyridine (L-COOH) was successfully prepared via co-condensation using 1,2-bis(triethoxysilyl)ethane (BTESE) and the modified L-COOH (L-COOH-NH2)....
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Published in | Materials & design Vol. 172; p. 107712 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
15.06.2019
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Using Pluronic P123 surfactant as template, a periodic mesoporous organosilica (PMO) functionalized with 4′-(4-carboxy-methyleneoxy phenyl)-2,2′:6′,2″-terpyridine (L-COOH) was successfully prepared via co-condensation using 1,2-bis(triethoxysilyl)ethane (BTESE) and the modified L-COOH (L-COOH-NH2). This terpyridine moiety forms interesting chelates to europium ions and enhances the luminescence of Eu3+ ions. Thus, a novel luminescent hybrid material was developed via linking Eu3+ complex Eu(NTA)3(H2O)2 to L-COOH-functionalized PMO material (L-COOH-PMO) using ligand exchange reactions. Investigation of photoluminescent properties shows that the prepared mesoporous hybrid Eu(NTA)3L-COOH-PMO exhibited red emission, long lifetime and high absolute quantum efficiency Φ in solid-state and aqueous solution. More interestingly, it demonstrates greatly sensitive and selective detection of Cu2+ ions in aqueous medium among test ions. The sensing mechanism was also discussed in this report.
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•A terpyridine based europium centered periodic mesoporous hybrid has been synthesized.•The hybrid retained the well-ordered mesoporous structures and showed good thermal stability.•The hybrid possesses excellent luminescent property both in solid-state and aqueous solution.•The hybrid exhibited highly sensitive and selective sensing of Cu2+ ions in aqueous solution. |
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ISSN: | 0264-1275 1873-4197 |
DOI: | 10.1016/j.matdes.2019.107712 |