| Literature DB >> 31419366 |
Adyn Melenbacher1, Jasveer S Dhindsa1,2, Joe B Gilroy1,2, Martin J Stillman1.
Abstract
Boron difluoride (BF2 ) formazanate dyes are contenders for molecular species that exhibit a large Stokes shift and bright red emission. Excitation of 3-cyanoformazanate complexes with 10 μs wide pulses of specific wavelengths resulted in strong luminescence at 663 nm at both room temperature in solution and at 77 K in a frozen solution. Analysis of the short-lived excitation spectrum from this luminescence shows that it arises from a vibronic manifold of a higher-lying excited state. This dark state relaxes to the emitting state over 10 μs. TD-DFT calculations of the two lowest-energy excited states show that the relaxed geometries are planar for S1 but highly distorted in S2 . The specific time- and wavelength-dependence of the excitation profile provides a unique optical encryption capability through the comparison of emission intensities between adjacent vibronic bands only accessible in the 0-12 μs time domain.Entities:
Keywords: BODIPY; boron difluoride dyes; fluorescence spectroscopy; optical encryption; vibronic structure
Year: 2019 PMID: 31419366 DOI: 10.1002/anie.201908999
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336