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Synthesis and Fluorescent Property Study of Novel 1,8-Naphthalimide-Based Chemosensors.

ABSTRACT: A series of novel mono- and di-substituted N-n-butyl-1,8-naphthalimide derivatives were synthesized simultaneously via a three-step reaction. The single crystal structure of N-n-butyl-4-[N',N'-bis(2',4'-dichlorobenzoyl)ethylamino]-1,8-naphthalimide (3f) was determined. The UV-vis and fluorescence properties of compound 3f were investigated. The 3f showed highly selective and sensitive fluorescence changes response towards Pb2+. A titration of monomer with Pb2+ ion was performed. When Pb2+ ion concentration increased from 0 to 10 eq., the fluorescent intensity of 3f decreased from 199.97 to 48.21. The pH effect on 3f showed that it is stable in a wide range of pH. The results indicated that 3f might be a probe molecule for Pb2+.

SUBMITTER: Fu Y

PROVIDER: S-EPMC6017435 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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Synthesis and Fluorescent Property Study of Novel 1,8-Naphthalimide-Based Chemosensors.

Fu Ying Y Pang Xiao-Xiao XX Wang Zhi-Qiang ZQ Qu Hai-Tao HT Ye Fei F

Molecules (Basel, Switzerland) 20180210 2

A series of novel mono- and di-substituted N-n-butyl-1,8-naphthalimide derivatives were synthesized simultaneously via a three-step reaction. The single crystal structure of N-n-butyl-4-[N',N'-bis(2',4'-dichlorobenzoyl)ethylamino]-1,8-naphthalimide (3f) was determined. The UV-vis and fluorescence properties of compound 3f were investigated. The 3f showed highly selective and sensitive fluorescence changes response towards Pb2+. A titrat ...[more]

PMID: 29439399

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