The synthesis of a new class of robust squaraine dyes, colloquially named 1,2-hemisquarimines (1,2-HSQiMs), through the microwave-assisted condensation of aniline derivatives with the 1,2-squaraine core is reported. In CH3CN, 1,2-HSQiMs show a broad absorption band with a high extinction coefficient and a maximum at around λ=530 nm, as well as an emission band centered at about λ=574 nm, that are pH dependent. Protonation of the imine nitrogen causes a redshift of both absorption and emission maxima, with a concomitant increase in the lifetime of the emitting excited state. Encapsulation of the chromophore into a cucurbit[7]uril host revealed fluorescence enhancement and increased photostability in water. The redox characteristics of 1,2-HSQiMs indicate that charge injection into TiO2 is possible; this opens up promising perspectives for their use as photosensitizers for solar energy conversion.

Christian C. De Filippo, Hao Tang, Luca Ravotto, Giacomo Bergamini, Patrizio Salice, Miriam Mba, et al. (2014). Synthesis and Electronic Properties of 1,2-Hemisquarimines and Their Encapsulation in a Cucurbit[7]uril Host. CHEMISTRY-A EUROPEAN JOURNAL, 20, 6412-6420 [10.1002/chem.201400039].

Synthesis and Electronic Properties of 1,2-Hemisquarimines and Their Encapsulation in a Cucurbit[7]uril Host

RAVOTTO, LUCA;BERGAMINI, GIACOMO;CERONI, PAOLA;
2014

Abstract

The synthesis of a new class of robust squaraine dyes, colloquially named 1,2-hemisquarimines (1,2-HSQiMs), through the microwave-assisted condensation of aniline derivatives with the 1,2-squaraine core is reported. In CH3CN, 1,2-HSQiMs show a broad absorption band with a high extinction coefficient and a maximum at around λ=530 nm, as well as an emission band centered at about λ=574 nm, that are pH dependent. Protonation of the imine nitrogen causes a redshift of both absorption and emission maxima, with a concomitant increase in the lifetime of the emitting excited state. Encapsulation of the chromophore into a cucurbit[7]uril host revealed fluorescence enhancement and increased photostability in water. The redox characteristics of 1,2-HSQiMs indicate that charge injection into TiO2 is possible; this opens up promising perspectives for their use as photosensitizers for solar energy conversion.
2014
Christian C. De Filippo, Hao Tang, Luca Ravotto, Giacomo Bergamini, Patrizio Salice, Miriam Mba, et al. (2014). Synthesis and Electronic Properties of 1,2-Hemisquarimines and Their Encapsulation in a Cucurbit[7]uril Host. CHEMISTRY-A EUROPEAN JOURNAL, 20, 6412-6420 [10.1002/chem.201400039].
Christian C. De Filippo;Hao Tang;Luca Ravotto;Giacomo Bergamini;Patrizio Salice;Miriam Mba;Paola Ceroni;Elena Galoppini;Michele Maggini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/376840
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