Leng Mingwan, Alturaifi Turki M, Pearce Josiah, Lin Hengyu, Yu Guanghua, Al-Hashimi Mohammed, Zhou Hong-Cai, Liu Peng, Fang Lei
Department of Chemistry, Texas A&M University, 3255 TAMU, College Station, TX 77843-3255, USA.
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.
Angew Chem Int Ed Engl. 2024 Dec 2;63(49):e202409149. doi: 10.1002/anie.202409149. Epub 2024 Oct 29.
A novel resonance-assisted self-doping mechanism has been demonstrated in ladder-type oligoaniline-derived organic conductors. The new class of compounds has a unique structure incorporating acidic phenolic hydroxyl groups into the ladder-type cyclohexadiene-1,4-diimine core, enabling efficient resonance-assisted proton transfer and electronic doping without the need for external dopants. Mechanistic and computational studies confirm the open-shell, zwitterionic nature of the self-doped state and the significant role played by the dielectric environment. This new self-doping mechanism allows for higher stability and durability in the material's electronic performance. The self-doped form retains durability under harsh conditions and maintains its properties over extended periods of time.
一种新型的共振辅助自掺杂机制已在梯型低聚苯胺衍生的有机导体中得到证实。这类新型化合物具有独特的结构,即将酸性酚羟基引入梯型环己二烯-1,4-二亚胺核心,从而实现高效的共振辅助质子转移和电子掺杂,而无需外部掺杂剂。机理和计算研究证实了自掺杂态的开壳两性离子性质以及介电环境所起的重要作用。这种新的自掺杂机制使材料的电子性能具有更高的稳定性和耐久性。自掺杂形式在苛刻条件下仍保持耐久性,并能在较长时间内维持其性能。