期刊
CRYSTAL GROWTH & DESIGN
卷 15, 期 5, 页码 2235-2242出版社
AMER CHEMICAL SOC
DOI: 10.1021/cg501894u
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资金
- NSF CAREER program [CHE1355677]
- NSF IGERT program [DGE-0903685]
- NSF-EPSCoR [EPS-0554609]
- NSF-MRI grant [CHE-1229035]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1229035] Funding Source: National Science Foundation
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1355677] Funding Source: National Science Foundation
Previously, we reported that introducing perfluoroalkyl substituents onto aromatics promotes the formation of lamellar pi-pi stacked crystalline materials with short interplanar distances. In this report, we developed a new synthetic route that effectively prepares perfluoroalkylated N-containing aromatics by eliminating a side perfluoroalkylation reaction occurring on nonsubstituted C-sp2-H sites of the corresponding bromoaromatics without regioselectivity. This results in a significant improvement of the yield of target perfluoroalkylated aromatics and facilitates the purification and scale-up processes. X-ray single crystal structural analyses show that lamellar pi-pi stacked structures with tunable interplanar distances are achieved with fused N-containing aromatics with varying sizes of a-conjugation. Both crystal structures and theoretical calculations demonstrated that the interplanar distance can be fine-tuned with the size of a-conjugation, with larger a-conjugation favoring shorter interplanar distances while still maintaining a lamellar pi-pi stacked packing motif: Compared to our previous results, we find that simply changing the perfluoroalkyl substituent positions and patterns can change molecular topology to exclusively form lamellar pi-pi stacked packing motifs through prioritization of specific steric effects. Electrochemical results and absorption spectra confirm that the band gap is reduced due to increasing pi-conjugation, and the first reduction potential exhibits a significant positive shift due to both increasing pi-conjugation and perfluoroalkylation.
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