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Correlating Redox and Photophysical Properties of Donor-Acceptor (aza)BODIPY-Based Dyads and Triads with Their Electronic Structures Toward a Rational Design of New Light-Harvesting Material

Monday, 14 May 2018: 11:20
Room 204 (Washington State Convention Center)
V. V. Nemykin (University of Manitoba), Y. V. Zatsikha (Univesity of Manitoba), Y. P. Kovtun (Institute of Organic Chemistry), and D. A. Blank (University of Minnesota)
Redox and photophysical properties of a large number of the BODIPY-, aza-BODIPY-, and BOPHY-based donor-acceptor dyads and triads (with representative examples given in Figure 1) have been investigated by the variety of steady-state and time-resolved spectroscopic methods. An influence of the catechol bridge between organic chromophore and the nanocarbon-based acceptor was studied in details and correlated with the electronic structures of new compounds investigated by the Density Functional Theory (DFT) and Time-Dependent DFT (TD-DFT) methods. It was found that catechol bridge is quite efficient electron-donor, which hinders the photo-induced electron-transfer processes in dyads and triads.

Fig. 1. Representative examples of BODIPY-, aza-BODIPY-, and BOPHY-based dyads and triads.