The new lanthanide-dicyanoaurate coordination polymers [BuN][Ln(NO)Au(CN)] (Ln = Sm, Dy) and Sm[Au(CN)]·3HO were prepared and structurally characterized and their luminescence spectra described. The emissions of solid-solutions of [BuN][Ln(NO)Au(CN)] (Ln = Ce, Sm, Eu, Tb, and Dy) were explored with an emphasis on their capacity for luminescent color tuning and white-light emission via the selection of composition, excitation wavelength, and temperature. Specifically, the binary solid-solutions [BuN][CeDy(NO)Au(CN)] and [BuN][SmTb(NO)Au(CN)], and the ternary solid-solutions [BuN][CeSmTb(NO)Au(CN)] and [BuN][CeEuTb(NO)Au(CN)], were prepared and examined in terms of suitability for color-tuning capacity. These results showcase that the emission from the [BuN][Ln(NO)Au(CN)] framework has the capacity to be tuned to extremes corresponding to deep reds (CIE coordinates 0.65, 0.35), greens (0.28, 0.63), and deep blue/violet (0.16, 0.06) as well as white (0.31, 0.33). Conversely, the emission of the Sm[Au(CN)]·3HO framework, when doped with the green phosphor Tb(III), changes only slightly because of the predominantly Au(I)-based emission and Sm(III) → Au(I) energy transfer.
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http://dx.doi.org/10.1021/acs.inorgchem.7b00735 | DOI Listing |
Inorg Chem
July 2017
Department of Chemistry, Simon Fraser University , 8888 University Drive, Burnaby, British Columbia V5A 1S6, Canada.
The new lanthanide-dicyanoaurate coordination polymers [BuN][Ln(NO)Au(CN)] (Ln = Sm, Dy) and Sm[Au(CN)]·3HO were prepared and structurally characterized and their luminescence spectra described. The emissions of solid-solutions of [BuN][Ln(NO)Au(CN)] (Ln = Ce, Sm, Eu, Tb, and Dy) were explored with an emphasis on their capacity for luminescent color tuning and white-light emission via the selection of composition, excitation wavelength, and temperature. Specifically, the binary solid-solutions [BuN][CeDy(NO)Au(CN)] and [BuN][SmTb(NO)Au(CN)], and the ternary solid-solutions [BuN][CeSmTb(NO)Au(CN)] and [BuN][CeEuTb(NO)Au(CN)], were prepared and examined in terms of suitability for color-tuning capacity.
View Article and Find Full Text PDFInorg Chem
July 2014
Department of Chemistry, University of Maine, Orono, Maine 04469, United States.
This investigation is focused on comparing photophysical properties between two series of lanthanide-dicyanoaurate coordination polymers that contain and lack aurophilic interactions, respectively. Luminescence and crystallographic studies have been carried out on five different coordination polymer chain frameworks: the non-aurophilic [(n)Bu4N]2[LnxGd1-x(NO3)4Au(CN)2] (Ln = Eu, Tb; x = 0.01, 0.
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