Influence of the electron donor groups on the optical and electrochemical properties of borondifluoride complexes of curcuminoid derivatives: a joint theoretical and experimental study. Issue 17 (6th February 2017)

• Record Type: Journal Article
• Authors: Canard, Gabriel; Ponce-Vargas, Miguel; Jacquemin, Denis; Le Guennic, Boris; Felouat, Abdellah; Rivoal, Morgane; Zaborova, Elena; D'Aléo, Anthony; Fages, Frédéric
• Is Part Of: RSC advances. Volume 7:Issue 17(2017)
• Page Start: 10132
• Page End: 10142
• Publication Date: 2017-02-06
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra25436e
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The optical and electrochemical properties of borondifluoride complexes of curcuminoids differently substituted with lateral aromatic and/or meso groups were systematically investigated. Abstract : Molecules displaying a π-conjugated D–A–D structure, in which D and A are electron donor and acceptor groups, respectively, represent an important class of dyes. In this work, we present a series of borondifluoride complexes of curcuminoid derivatives in which the central dioxaborine ring acts as a strong electron acceptor unit. Compounds1–15 differ by the nature of the terminal D groups. We have also studied unsymmetrical compounds16–23 that contain two different terminal donor groups, as well as compounds24–32 in which an electron acceptor or donor unit has been introduced at the meso position of the dioxaborine ring. We describe the synthesis of the dyes that have not yet been reported in the literature, and report the electrochemical, absorption and fluorescence properties of all the compounds in dichloromethane. To gain insights into the electronic structures and optical properties, we performed DFT/TD-DFT calculations for a panel of representative compounds. We established correlations between the reduction potential and the Hammett σ and σ + constants, as well as between the redox gap and the emission wavelength. The electron donor character of one terminal D unit strongly influences (88 mV per unit of σ ) the reduction potential due to the strong resonance interaction along the curcuminoid backbone. The correlation points to the smaller effect of the meso substituent (50 mV per unit of σ ), which we relate to the twisted ground-state geometry of the meso aryl substituent. The correlation models established in this study may be useful to anticipate the optical and electrochemical properties of borondifluoride complexes of curcuminoids with good reliability.