Abstract
It was shown that in the series of complexes Tp2LnL (Ln = Eu, Tb; Tp– = tris(pyrazolyl)borate anion; L– = 3-arylacetylacetonate) the energy of the triplet state of L– decreases with elongation of the conjugation chain of the aromatic substituent, resulting in change of the nature of emission from metal-centered to ligand-centered. It was found, that the introduction of two antenna ligands of different nature leads to increase of the luminescence quantum yield (to 74%) in the case of the Tb3+ compounds, probably, due to optimization of energy transfer. In the Eu3+ compounds it leads to emission quenching, likely, as a result of increased efficiency of energy transfer and non-radiative deactivation of the excited states.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
