| Literature DB >> 27463419 |
Lin Zhou1, Defang Xu2, Huaizhi Gao1, Chao Zhang1, Fangfang Ni1, Wenqi Zhao1, Dandan Cheng1, Xingliang Liu1, Aixia Han1.
Abstract
Novel β-furan-fused bis(difluoroboron)-1,2-bis((1H-pyrrol-2-yl)methylene)hydrazine (BOPHY) fluorescent dyes (F-BOPHY1-3) were prepared through an efficient process, and their structures were confirmed by (1)H NMR spectroscopy, (13)C NMR spectroscopy, MALDI-TOF HRMS, and element analysis. Their optical properties were then characterized by UV-vis absorption and photoluminescence (PL) spectroscopy. The UV-vis absorption and PL spectra of the dyes shifted to longer wavelengths relative to those of BOPHY because of the fusion of their furan rings, which extended π-conjugation of the molecules. All of the dyes exhibited large extinction coefficients (109700-12300 M(-1) cm(-1)), deep-red fluorescence emission (646-667 nm), moderate fluorescence quantum yields (0.30-0.45), as well as high chemical stability and photostability in solution. These advantageous properties show that these compounds are important to the design of efficient long-wavelength fluorescent dyes and are suitable for various applications in biotechnology and materials science.Entities:
Year: 2016 PMID: 27463419 DOI: 10.1021/acs.joc.6b01018
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354