The concentration dependence of spectral-luminescence properties of solutions boron difluoride dibenzoylmethanate (DBMBF2) in benzene and chloroform has been studied through stationary and time-resolved emission spectroscopy methods. The formation of J-aggregates in the solution of DBMBF2 in chloroform has been revealed and a crystalline adduct of DBMBF2 with benzene has been obtained. A bright blue adduct luminescence is due only to the luminescence of J-aggregates, unlike the crystals of DBMBF2, for which the luminescence of excimers and J-aggregates has been observed. The quantum chemistry simulation of geometric and electronic structure of the DBMBF2 С6Н6 solvate has been performed, and the absorption spectra of DBMBF2 and it is adduct have been calculated.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.saa.2013.10.016 | DOI Listing |
J Am Chem Soc
December 2024
Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, People's Republic of China.
Narrowband fluorescent emitters are receiving significant attention due to the great potential for creating ultrahigh-definition organic light-emitting diode displays (UHD-OLED). Unveiling innovative mechanisms to design new high-performance narrowband fluorescent emitters is a concerted endeavor in both academic and industrial circles. Theoretical calculations reveal that the centrosymmetric dianilido-bipyridine boron difluoride framework (-DAPBF) exhibits significantly reduced structural relaxation compared to previously reported asymmetric structures with monofluoroboron cores, creating new opportunities for the development of narrowband fluorescent emitters.
View Article and Find Full Text PDFSensors (Basel)
November 2024
College of Chemistry and Chemical Engineering, Xinjiang Agricultural University, Urumqi 830002, China.
BF, volatile amines (VOAs), and biogenic amines (BAs) are the key indicators in chemical reaction catalysis and food quality monitoring. In this study, we present two types of fluorescent sensors, a hydrazone ligand (HL)-based fluorescent sensor for BF detection and a novel sensor array using six boron difluoride (BF) hydrazone complexes (BFHs) for monitoring VOAs and BAs. Spectral research indicates that the interaction mechanism between the HLs and BF is based on intramolecular charge transfer (ICT).
View Article and Find Full Text PDFMacromol Rapid Commun
October 2024
Department of Chemistry, The University of Western Ontario, 1151 Richmond St. N., London, ON, N6A 5B7, Canada.
ACS Appl Mater Interfaces
November 2024
Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
Two donor-acceptor dyes with an -phenylene-linked carbazole electron donor and a benzothiazole-fused boron heterocyclic acceptor were designed, synthesized, and spectroscopically investigated. Due to the steric effects of boron heterocyclic units, the dyes demonstrate different conformations in the crystalline state. The presence of numerous hydrogen-bonding intermolecular interactions and the very weak π-π stacking in the molecular packing results in intense solid-state emission with photoluminescence quantum yields of 40 and 18% for crystals and 50 and 42% for host-based light-emitting layers.
View Article and Find Full Text PDFACS Nano
October 2024
Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, Division of Life Science, State Key Laboratory of Molecular Neuroscience, and Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, P. R. China.
Electron acceptor possessing strong electron-withdrawing ability and exceptional stability is crucial for developing donor-acceptor-donor (D-A-D) structured aggregation-induced emission luminogens (AIEgens) with second near-infrared (NIR-II) emission. Although 6,7-diphenyl-[1,2,5] thiadiazolo [3,4-] quinoxaline (PTQ) and benzobisthiadiazole (BBT) are widely employed as NIR-II building blocks, they still suffer from limited electron-withdrawing capacity or inadequate chemo-stability under alkaline conditions. Herein, a boron difluoride formazanate (BFF) acceptor is utilized to construct NIR-II AIEgen, which exhibits a better overall performance in terms of NIR-II emission and chemo-stability compared to the PTQ- and BBT-derived fluorophores.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!