A theoretical investigation of the two-photon absorption and fluorescent properties of coumarin-based derivatives for Pd2+ detection

Chun Zhang, Jing Fu Guo, Ai Min Ren*, Dan Wang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

Palladium is emitted due to automobile catalytic converters, and with rapid growth in the number of cars, palladium is thus a current threat to human health and the environment. Two-photon (TP) fluorescent probes are favorable and powerful molecular tools for palladium ion (Pd2+) detection due to localized excitation and reduced phototoxicity and photodamage. In the present study, a series of "turn-on" TP fluorescent dyes based on coumarin derivatives were designed for Pd2+ recognition. Our study revealed the origin of the peculiarly different fluorescence behaviors of the synthesized Pd2+ probe R1 and the product P′1 quantitatively and qualitatively from a theoretical perspective. Moreover, quantum-chemical calculations on electronic structures, one/two-photon absorption and fluorescence optical properties have first been carried out for these TP fluorescent chromophores using an ab initio approach. The calculated results demonstrate that chemical modifications of the coumarin core by the introduction of an electron-withdrawing group (-Cl or -CN) to its 4-position effectively increase the TP absorption cross-section per molecular weight more easily than extending the π-conjugated structure at the 3-position. In the present work, the product P′4, with a much smaller internal conversion rate (KIC = 1.28 × 106 s-1) than that of the Pd2+ probe R4 (KIC = 9.09 × 1011 s-1), possesses the largest TP absorption cross-section per molecular weight (3.91) and the longest fluorescence wavelength (590.3 nm) among all the studied molecules, which means it has better potential for Pd2+ detection. Consequently, we hope that this detailed study can provide guidance for the design and synthesis of new Pd2+ fluorescent probes.

Original languageEnglish
Pages (from-to)49505-49517
Number of pages13
JournalRSC Advances
Volume7
Issue number78
DOIs
Publication statusPublished - 2017
Externally publishedYes

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