Elena Zaborova

Influence of the electron donor groups on the optical and electrochemical properties of borondifluoride complexes of curcuminoid derivatives: a joint theoretical and experimental study

Molecules displaying a p-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. Compounds 1–15 differ by the nature of the terminal D groups. We have also studied unsymmetrical compounds 16–23 that contain two different terminal donor groups, as well as compounds 24–32 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 s and s + 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 s) 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 s), 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.

Synthesis, electrochemical and photophysical studies of the borondifluoride complex of a meta-linked biscurcuminoid

The synthesis of the borondifluoride complex of a biscurcuminoid system is described, and its electrochemical and photophysical properties are compared to those of a series of monochromophoric models. The data show that the meta-linked biscurcuminoid exhibits enhanced optical properties in solution, such as high optical brightnesses obtained at one- and two-photon excitation (B1 = 87 000 M−1 cm−1 and B2 = 313 GM, respectively). UV/visible absorption of solid-state particles formed in water solution revealed that the four investigated dyes are strongly aggregated and fluorescence spectroscopy showed that they are emissive in the NIR with fluorescence quantum yields spanning from 1.5 to 12.5%. In the case of the meta-linked biscurcuminoid, a high brightness is obtained using one- and two-photon excitation (B1 = 6952 M−1 cm−1 and B2 = 70 GM, respectively). Such red-shifted emission combined with a yet significant brightness in the solid-state is believed to arise from the choice of the meta-linkage which limits strong intermolecular packing.