Lanthanide complexes with N-phosphorylated carboxamide as UV converters with excellent emission quantum yield and single-ion magnet behavior. Issue 29 (3rd July 2020)

• Record Type: Journal Article
• Authors: Pham, Yen H.; Trush, Viktor A.; Carneiro Neto, Albano N.; Korabik, Maria; Sokolnicki, Jerzy; Weselski, Marek; Malta, Oscar L.; Amirkhanov, V. M.; Gawryszewska, Paula
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 29(2020)
• Page Start: 9993
• Page End: 10009
• Publication Date: 2020-07-03
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d0tc01445a
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : Well-designed Ln compounds are UV converters with extremely high, triplet lifetime dependent emission QY, and show SIM behavior. Abstract : Lanthanide complexes with efficient antenna effect and multifunctional optical-magnetic activity are very appropriate for potential applications. Multidentate ligands efficiently sensitizing emission of different lanthanide ions are rare and complexes often suffer from bleaching. Presented here are photostable lanthanide complexes with single-magnet behavior as the first example in which, using the same sensitizer and the same excitation wavelength, extremely high overall emission quantum yields are achieved for various lanthanide ions ( Q LEu = Q LTb = 98%, Q LSm = 11%, Q LDy = 17%). This is confirmed through computational and experimental analyses. We rationalize the process of energy transfer from the ligand to Eu 3+, which was firstly understood in lanthanide compounds with N -phosphorylated carboxamides. The results revealed that in addition to the refractive index, the energy of the ligand triplet state and donor–acceptor distance, overall emission quantum yield is also a function of triplet state lifetime. It is demonstrated how proper design of the energetic and structural properties of the sensitizer and the introduction of excess Na ions into the structure of Ln complexes allow obtaining extremely efficient light converting molecular devices with single-ion magnet behavior.