Crystal engineering of heterocyclic arylene(ethynylene) oligomers through programmed aromatic stacking. Issue 31 (11th July 2022)

• Record Type: Journal Article
• Authors: Mullin, William J.; Müller, Peter; Schaefer, Anthony J.; Guzman, Elisa; Wheeler, Steven E.; Thomas III, Samuel W.
• Is Part Of: Journal of materials chemistry. Volume 10:Issue 31(2022)
• Page Start: 11199
• Page End: 11210
• Publication Date: 2022-07-11
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d2tc01292h
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : Electron-rich heteroarenes stack with perfluoroarene side chains and twist arylene-ethynylene conjugated oligomers, while electron deficient heterocycles do not. These trends correlate with X-ray structures, optical spectra, and computations. Abstract : Conjugated oligomers and polymers consisting of aromatic heterocycles are examples of next-generation organic electronic materials. However, control and optimization of the self-assembly of these materials in the solid-state, which is a crucial parameter for high efficiency performance, remains an unsolved challenge in materials development. In this work, we provide valuable insight into aromatic stacking interactions between fluorinated arene rings (ArF) and heterocycles with different electronic character (Het), and elaborate on the prospect of using these interactions to control the solid-state configurations of three-ring phenyleneethynylene oligomers (PEs). Oligomers possessing heterocycles typically thought of as electron-rich (ER) show blue-shifted optical spectra in the solid-state, while those incorporating heterocycles typically thought of us electron deficient (ED) show red-shifted solid-state optical spectra. Crystal structures show ArF-Het stacking interactions between the fluorinated side-chains and ER units, which twist the backbone out of planarity and prevent chromophore aggregation. The interactions are absent in ED oligomers, highlighting cofacial incompatibility between ArF rings and ED units. A combination of TD-DFT computations and novel heterocycle descriptors reinforce our assignment of the oligomers as ED or ER, while exhaustive conformer analysis shows ArF-Het stacking interactions are a significant contributor to compound stability. Overall, this work describes the importance of heterocycle electronics in conformational control in the solid state, understanding of which can be a valuable asset in the development of novel optoelectronic materials.