Zhao Mengna, Yuan Zhibin, Zhou Yifeng
College of Life Science, China Jiliang University, Hangzhou 310018, Zhejiang, China.
Org Lett. 2024 Oct 18;26(41):8837-8841. doi: 10.1021/acs.orglett.4c03270. Epub 2024 Oct 9.
1-Azaazulene was adopted as a new ligand moiety for boron difluoride (BF) complexes, resulting in large red shifts of the absorption bands up to 103 nm compared to their isomeric quinoline-based complexes. Such change was attributed to the nonalternant nature of 1-azaazulene, as the complexes maintained the intrinsic 10π-peripheral electronic structure. exhibited the most red-shifted absorption among reported BF complexes containing a phenolic backbone, and the absorption edge of reached the red region.
1-氮杂薁被用作二氟化硼(BF)配合物的新型配体部分,与它们的基于喹啉的异构配合物相比,吸收带产生了高达103 nm的大红移。这种变化归因于1-氮杂薁的非交替性质,因为这些配合物保持了固有的10π周边电子结构。在报道的含有酚醛主链的BF配合物中表现出最大的红移吸收,并且的吸收边缘达到了红色区域。