Biscyclometalated platinum(II) complex bearing a persistent radical is reported. The complex possesses a doublet emission excited state (D2) with a short excited state lifetime at room temperature and a long excited triplet (T1
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Social Self‐Sorting of Ag4 and Au4 Alkynyl Complexes into Hetero–Tetranuclear Ag2Au2 Alkynyl Complexes: Ag4 Alkynyl Complex as a Highly Reactive Silver Species
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Ag4 and Au4 alkynyl complexes are formed by using the designed alkynyl ligand with a terphenyl framework. Interestingly, when the Ag4 and Au4 complexes are mixed in solution, a quantitative conversion to a social self-sorted product Ag2Au2 complex is observed. Detailed studies reveal that the Ag4 complex is more reactive than bare Ag ions or the Au4 complex.
The designed alkynyl ligand 1 with a terphenyl framework reacts with Ag or Au salts to produce soluble tetranuclear Ag4 and Au4 alkynyl complexes 2 and 3 in high yields. In contrast, when ligand 1 is simultaneously reacted with both Ag and Au salts, the only formed product is the hetero–tetranuclear Ag2Au2 alkynyl complex 4, rather than complexes 2 and 3. Interestingly, when Ag4 complex 2 is added to Au4 complex 3 at room temperature, Ag2Au2 complex 4 is formed immediately and in quantitative yield. In contrast, the addition of Ag salts to Au4 complex 3 results in incomplete or slow conversion. These findings suggest that Ag4 complex 2 is more reactive than simple Ag salts and Au4 complex 3 in the formation of Ag2Au2 complex 4. The high reactivity of Ag4 complex 2 is further explored through ligand exchange experiments and gel permeation chromatography analyses.
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