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Metallic State of a Mixed-Sequence Oligomer Salt That Models Doped PEDOT Family

低聚物 化学 三聚体 四聚体 佩多:嘘 结晶学 兴奋剂 导电聚合物 二聚体 聚合物 高分子化学 材料科学 有机化学 光电子学
作者
Kota Onozuka,Tomoko Fujino,Ryohei Kameyama,Shun Dekura,Kazuyoshi Yoshimi,Toshikazu Nakamura,Tatsuya Miyamoto,T Yamakawa,Hiroshi Okamoto,Hiroyasu Sato,Taisuke Ozaki,Hatsumi Mori
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:145 (28): 15152-15161 被引量:13
标识
DOI:10.1021/jacs.3c01522
摘要

Modern organic conductors are typically low-molecular-weight or polymer-based materials. Low-molecular-weight materials can be characterized using crystallographic information, allowing structure-conductivity relationships to be established and conduction mechanisms to be understood. However, controlling their conductive properties through molecular structural modulation is often challenging because of their relatively narrow conjugate areas. In contrast, polymer-based materials have highly π-conjugated structures with wide molecular-weight distributions, and their structural inhomogeneity makes characterizing their structures difficult. Thus, we focused on the less-explored intermediate, i.e., single-molecular-weight oligomers that model doped poly(3,4-ethylenedioxythiophene) (PEDOT). The dimer and trimer models provided clear structures; however, the short oligomers led to much lower conductivities (<10-3 S cm-1) than that of doped PEDOT. Herein, we elongated the oligomer to a tetramer through geometrical tuning based on a mixed sequence. The "P-S-S-P" sequence (S: 3,4-ethylenedithiothiophene; P: 3,4-(2',2'-dimethypropylenedioxy)thiophene) with twisted S-S enhanced the solubility and chemical stability. The subsequent oxidation process planarized the oligomer and expanded the conjugate area. Interestingly, the sequence involving sterically bulky outer P units allowed the doped oligomer to form a pitched π-stack in the single-crystal form. This enabled the inclusion of excess counter anions, which modulated the band filling. The combined effects of conjugate area expansion and band-filling modulation significantly increased the room-temperature conductivity to 36 S cm-1. This is the highest value reported for a single-crystalline oligomer conductor. Furthermore, a metallic state was observed above room temperature in a single-crystalline oligoEDOT for the first time. This unique mixed-sequence strategy for oligomer-based conductors enabled the precise control of conductive properties.
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