亚辛
材料科学
电子迁移率
戒指(化学)
单晶
晶体管
结晶学
光电子学
化学
分子
电压
有机化学
量子力学
物理
作者
Chenglong Li,Yanan Sun,Ning Xue,Yongkang Guo,Ruijun Jiang,Yuanhui Wang,Yujian Liu,Lang Jiang,Xuguang Liu,Zhaohui Wang,Wei Jiang
标识
DOI:10.1002/anie.202423002
摘要
The in-depth research on the charge transport properties of BN-embedded polycyclic aromatic hydrocarbons (BN-PAHs) still lags far behind studies of their emitting properties. Herein, we report the successfully synthesis of novel ladder-type BN-PAHs (BCNL1 and BCNL2) featuring a highly ordered BC3N2 acene unit, achieved via a nitrogen-directed tandem C-H borylation. Single-crystal X-ray diffraction analysis unambiguously revealed their unique and compact herringbone packing structures. Micro-sized single-crystalline organic field-effect transistors (OFETs) demonstrated that an enhanced charge transport capability, with BCNL2 achieving a hole mobility of up to 0.62 cm2 V-1 s-1-three orders of magnitude higher than that of BCNL1 (μhmax = 6 × 10-4 cm2 V-1 s-1), ranking among the highest values for BN-PAHs-based OFETs. Detailed calculations attribute this significant enhancement in the hole mobility to the marked reduction in reorganization energy (λ) of BCNL2, resulting from the five-membered pyrrole ring annulation and molecular skeleton elongation. This work provides insight into molecular design principles for potential BN-PAHs in optoelectronic applications.
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