| Literature DB >> 33830589 |
Guanzhao Wu1,2, Yangxue Liu1, Hossein Rouh1, Liulei Ma1, Yao Tang1, Sai Zhang1, Peng Zhou2, Jia-Ying Wang2, Shengzhou Jin2, Daniel Unruh1, Kazimierz Surowiec1, Yanzhang Ma3, Guigen Li1,2.
Abstract
The first asymmetric catalytic approach to multilayer 3D chirality has been achieved by using Suzuki-Miyaura cross-couplings. New chiral catalysts were designed and screened under various catalytic systems that proved chiral amide-phosphines to be more efficient ligands than other candidates. The multilayer 3D framework was unambiguously determined by X-ray structural analysis showing a parallel pattern of three layers consisting of top, middle and bottom aromatic rings. The X-ray structure of a catalyst complex, dichloride complex of Pd-phosphine amide, was obtained revealing an interesting asymmetric environment nearby the Pd metal center. Three rings of multilayer 3D products can be readily changed by varying aromatic ring-anchored starting materials. The resulting multilayer products displayed strong luminescence under UV irradiation and strong aggregation-induced emission (AIE). In the future, this work would benefit not only the field of asymmetric synthesis but also materials science, in particular polarized organic electronics, optoelectronics and photovoltaics.Entities:
Keywords: Suzuki-Miyaura cross-coupling; aggregation-induced emission; chirality; multilayer organic frameworks
Year: 2021 PMID: 33830589 DOI: 10.1002/chem.202100700
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236