Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/116366
Title: Molecular logic with ferrocene-rylene conjugates : a comparison of naphthalenediimide, naphthalimide and perylenediimide Pourbaix sensor designs
Authors: Grech, Joseph
Spiteri, Jake C.
Scerri, Glenn J.
Magri, David C.
Keywords: Photoionization
Charge exchange
Ferrocene
Chemistry
Issue Date: 2023
Publisher: Elsevier BV
Citation: Grech, J., Spiteri, J. C., Scerri, G. J., & Magri, D. C. (2023). Molecular logic with ferrocene-rylene conjugates: A comparison of naphthalenediimide, naphthalimide and perylenediimide Pourbaix sensor designs. Inorganica Chimica Acta, 544, 121176.
Abstract: Four molecules designed as Pourbaix sensors with rylene dyes (naphthalenediimide, 4-amino-1,8-naphthalimide, perylenediimide) are compared. Each molecule is constructed modularly according to an electron-donor–spacer–fluorophore–spacer–receptor format based on photoinduced electron transfer (PET). The modules consist of ferrocene as the electron donor, a tertiary alkyl amine as the proton receptor, and a rylene dye as the fluorophore connected by a methylene and ethylene spacer, respectively. The proton and oxidant-induced fluorescent spectral changes of the 4-amino-1,8-naphthalimide models include internal charge transfer (ICT) character. Two of the discussed logic gates switch on emitting fluorescence in the presence of acid (H+) and oxidant (Fe3+) according to two-input AND logic, while two of the logic gates remain off according to two-input PASS 0 logic.
URI: https://www.um.edu.mt/library/oar/handle/123456789/116366
Appears in Collections:Scholarly Works - FacSciChe



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