| Institution: | 1. Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic, Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, P. R. China;2. School of Materials Science & Engineering, Jiamusi University, Jiamusi, Heilongjiang, 154007 P. R. China;3. Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic, Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, P. R. China
Department of Chemistry, Queen's University, Kingston, Ontario, K7L 3N6 Canada |
| Abstract: | In order to examine competitive photoisomerization, a series of novel photochromic PtII molecules that contain both dithienylethene (DTE) and B(ppy)Mes2 units (ppy=2-phenylpyridine, Mes=mesityl) were successfully synthesized and fully structurally characterized. Their photochromic properties were examined by UV/Vis, emission and NMR spectroscopy. It was found that the DTE unit in all three compounds is the preferred photoisomerization site, exhibiting reversible photochromism with irradiation. The B(ppy)Mes2 unit does not undergo photoisomerization in these molecules, but likely enhances the photoisomerization quantum efficiency of the DTE moiety through the antenna effect. Extended irradiation with UV light leads to the rearrangement of the ring-closed isomers of DTE. TD-DFT computational studies indicate that the DTE photocyclization proceeds via a triplet pathway through an efficient energy transfer process. |
