Reversible formation and cleavage of Pt→Ag dative bonds in a pre-organized cavity of a luminescent heteropolynuclear platinum(ii ) complex
| Autor: | Misa Ueda, Shinnosuke Horiuchi, Keisuke Umakoshi, Eri Sakuda, Yasuhiro Arikawa, Yoshihide Nakao |
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| Rok vydání: | 2017 |
| Předmět: |
010405 organic chemistry
Chemistry Ligand Inorganic chemistry Metals and Alloys chemistry.chemical_element General Chemistry 010402 general chemistry Cleavage (embryo) 01 natural sciences Chloride Catalysis 0104 chemical sciences Surfaces Coatings and Films Electronic Optical and Magnetic Materials Ion Crystallography Atom Materials Chemistry Ceramics and Composites medicine Chelation Luminescence Platinum medicine.drug |
| Zdroj: | Chemical Communications. 53:6405-6408 |
| ISSN: | 1364-548X 1359-7345 |
| DOI: | 10.1039/c7cc03447d |
| Popis: | A U-shaped Pt2Ag2 complex [Pt2Ag2(ppy)2(Ph2pz)4] with a pre-organized cavity (ppy = 2-phenylpridinate and Ph2pz = 3,5-diphenylpyrazolate) and related complexes have been prepared. The Pt2Ag2 complexes react with Ag(I) ions to give the corresponding Pt2Ag3 complexes containing Pt→Ag dative bonds. It became obvious that the existence of the C(ipso) atom in the chelate ligand is important as the driving force for forming Pt→Ag dative bonds. However, once the Pt2Ag3 complex is formed, the trapped Ag(I) ion is mainly stabilized by the Pt→Ag dative bonds, which are stronger than the Ag?C(ipso) bond. The trapped Ag(I) ion can be abstracted from the cavity selectively by adding an equivalent amount of chloride ion into the solution of Pt2Ag3 complexes to reproduce the original Pt2Ag2 complexes. Related illustration appears in this issue's inside back cover. The URL is as follows: http://dx.doi.org/10.1039/C7CC90232H Chemical Communications, 53(48), pp.6405-6408; 2017 |
| Databáze: | OpenAIRE |
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