Journal
JOURNAL OF FLUORINE CHEMISTRY
Volume 220, Issue -, Pages 9-15Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2019.01.008
Keywords
BODIPY; Computational studies; Phosphoramidates; Fluorescent dyes
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Funding
- CNPq [404466/2016-8, PVE 401193/2014-4, PQ 305741/2017-9]
- FAPEMIG [PPM-00638-16]
- Capes-Humboldt research fellowship programme [88881.145517/2017-01]
- Sao Paulo Research Foundation (FAPESP) [2011/23342-9]
- CNPqPDS [110818/2016-4]
- Institute of Physics of University of Sao Paulo (Sao Carlos)
- FAPEMIG (Rede de Pesquisa e Inovacao para Bioengenharia de Nanossistemas) [RED-00282-16]
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New boro-dipyrromethene (BODIPY) fluorophores substituted with phosphoramidate groups have been synthesized using environmentally friendly methodologies, and their photophysical properties were evaluated experimentally and characterized in detail with respect to DFT and TD-DFT using B3LYP/6-31+G(d) level of theory. These fluorophores may be used as promising candidates for biological probes and optical materials.
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