Two new anthracene derivatives were synthesized as emitter for low power triplet-triplet annihilation upconversion. Compared with anthracene, the emitter exhibits high quantum yields up to 85%. Pd (II) tetraphenylporphyrin which was selected as the sensitizer with the existence of BBA in DMF, We find a pretty high efficiency (Φuc=21.9%) of the upconversion fluorescence at 532nm with a low excitation power density of 0.5w/cm2.With the comparison of Anthracene, BBA and BTPA systems, quantum yield of the emitter is very important to the improving of the efficiency of upconversion.
Exploring the structure-property relationships is a fundamental but significant work for the design of new molecular. Rationaly designing of electrochromic materials that can switch rapidly and durably requires sophisticated understanding of the correlations between molecular structure and the performance. This work presents four electro-polymerizable metallosupramolecular coordinations self-assembled from triphenylamine-based terpyridine ligands and metal ions (Fe2+, Ru2+). The polymerized metal complexes can exhibit reversible change of the metal-to-ligand charge transfer (MLCT) absorption intensity. Along with the increase of voltage, the intensity of MLCT absorption peaks gradually reduced to disappear. Structure/performance correlations in electrochromic performance, especially the influence of different ligands and metal ions upon the coloration efficiency have been discussed.
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