Affiliation:
1. Department of Chemistry The University of Western Ontario 1151 Richmond St. N, London Ontario N6A 5B7 Canada
Abstract
Abstractπ‐Conjugated materials offer attractive traits including semiconductivity, low‐energy light absorption/photoluminescence, and solution processability that render them ubiquitous within the organic electronics field. Among many strategies for property tuning, the creation of asymmetric electronic structures through the installation of donor and acceptor substituents commonly results in low‐energy absorption/photoluminescence bands. Boron difluoride formazanate dyes are readily synthesized, can be asymmetrically substituted with donor and acceptor groups, and have unexpectedly low‐energy absorption/photoluminescence bands that extend into the near‐infrared. In this study, we prepared a series of donor‐acceptor substituted boron difluoride 3‐cyanoformazanate dyes and compared their properties to symmetric analogues. Our findings suggest that donor‐acceptor derivatives are highly delocalized with properties intermediate of their symmetric counterparts. Furthermore, the data obtained suggest that the N‐aryl substituents act as donors to the strongly accepting boron difluoride formazanate core, regardless of the functional groups appended to them. These properties were reproduced computationally, and while the frontier orbitals calculated for donor‐acceptor dyes were modestly asymmetric, there was no evidence of charge‐transfer character. This work provides significant insight into the unexpected properties of boron difluoride formazanates and reveals that their strongly accepting nature circumvents the predicted augmentation of electronic structure commonly observed for donor‐accepter substituted dyes.