Fusion and planarization of bisBODIPY: a new family of photostable near infrared dyes
Chemical Communications2015Vol. 51(94), pp. 16852–16855
Citations Over TimeTop 10% of 2015 papers
Changjiang Yu, Lijuan Jiao, Tingting Li, Qinghua Wu, Wei Miao, Jun Wang, Yun Wei, Xiaolong Mu, Erhong Hao
Abstract
We have synthesized a new family of directly-fused bisBODIPY BBP 1 through a key FeCl3-mediated intramolecular oxidative cyclodehydrogenation reaction and its derivatives 2 and 3 from the Knoevenagel reaction. These dyes display effective expansion of π-conjugation over the two BODIPYs due to their locked coplanar conformation, showing intriguing electrochemical and spectroscopic properties, such as intensive absorption/emission bands ranging from 676 to 877 nm and high photostability.
Related Papers
- → Characterization of Z-DNA by Infrared Spectroscopy(2023)4 cited
- → The study of some normal and abnormal montmorillonites by thermal analysis and infrared spectroscopy(1987)8 cited
- → Chapter 3 Theory of infrared spectroscopy(2001)4 cited
- → The infrared spectrum of gaseous Sb4O6(1993)9 cited
- → Molecular Orientation Analysis in Organic Thin Films by Infrared Spectroscopy(2007)2 cited