| Literature DB >> 28494580 |
Shinya Koga1, Shuhei Ueki1, Masaki Shimada1, Ryoma Ishii1, Yu Kurihara1, Yoshinori Yamanoi1, Junpei Yuasa2, Tsuyoshi Kawai2, Taka-Aki Uchida3, Munetaka Iwamura3, Koichi Nozaki3, Hiroshi Nishihara1.
Abstract
Asymmetric arylation of secondary silanes catalyzed by a Pd-chiral phosphoramidite complex was developed for application to low-molecular-weight circularly polarized luminescence (CPL) materials. The asymmetric arylation provided a convenient, efficient synthetic method for a variety of chiral tertiary silanes (2-21), which were key intermediates for preparing the quaternary silicon center. A stepwise, one-pot procedure was used to transform the appropriate aryl iodide to the quaternary silane (22) with good yield and enantioselectivity. Among compounds synthesized in this work, four optically pure tertiary silanes (18-21) were selected to investigate the relationship between the structure and optical properties. Optically pure (S,S)-21 displayed the highest CPL emission with a high fluorescence quantum yield (glum: +0.008, ΦF: 0.42). This simple molecular design provides new strategies for developing small organic CPL dyes.Entities:
Year: 2017 PMID: 28494580 DOI: 10.1021/acs.joc.7b00583
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354