{"title":"Syntheses of Au(III) and Au(I) Complexes of 3,4,5,6-Tetraphenyl-2,2´-bipyridine","authors":"S. D. Perera","doi":"10.4038/ouslj.v18i1.7600","DOIUrl":null,"url":null,"abstract":"Treatment of the ligand 3,4,5,6-tetraphenyl-2,2´-bipyridine (LH) VIII with HAuCl4 in acetonitrile afforded the cyclometallated square-planar Au(III) complex [LAuCl]ClO4 (7) containing the anionic tridentate (N∧N∧C) ligand, via orthometallation. Treatment of (7) with 4-dimetylaminopyridine (DMAP) and AgClO4 in acetonitrile produced [LAu(DMAP)][ClO4]2 (8), showing the same coordination mode. Analogous complex [LAu(PPh3)][ClO4]2 (9)was prepared by using PPh3 instead of DMAP. Reaction of VIIIwith HAuCl4 at room temperature in aqueous acetonitrileresulted the non-cyclometallated Au(III) complex [(LH)AuCl2]Cl(10), in which VIII is a bidentate (N∧N) ligand. Treatment of VIIIwith the filtrate obtained by mixing [AuCl(PPh3)] and AgO2CCF3 in acetone resulted the non-cyclometallated Au(I) complex[(LH)Au(PPh3)]O2CCF3 (11) having bidentate (N∧N) ligand. Abovecomplexes were adequately characterized by a combination ofelemental analysis, IR, Mass and NMR spectroscopy. The X-raycrystal structures of (7) and (8) were determined.","PeriodicalId":105560,"journal":{"name":"Ousl Journal","volume":"25 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ousl Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4038/ouslj.v18i1.7600","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Treatment of the ligand 3,4,5,6-tetraphenyl-2,2´-bipyridine (LH) VIII with HAuCl4 in acetonitrile afforded the cyclometallated square-planar Au(III) complex [LAuCl]ClO4 (7) containing the anionic tridentate (N∧N∧C) ligand, via orthometallation. Treatment of (7) with 4-dimetylaminopyridine (DMAP) and AgClO4 in acetonitrile produced [LAu(DMAP)][ClO4]2 (8), showing the same coordination mode. Analogous complex [LAu(PPh3)][ClO4]2 (9)was prepared by using PPh3 instead of DMAP. Reaction of VIIIwith HAuCl4 at room temperature in aqueous acetonitrileresulted the non-cyclometallated Au(III) complex [(LH)AuCl2]Cl(10), in which VIII is a bidentate (N∧N) ligand. Treatment of VIIIwith the filtrate obtained by mixing [AuCl(PPh3)] and AgO2CCF3 in acetone resulted the non-cyclometallated Au(I) complex[(LH)Au(PPh3)]O2CCF3 (11) having bidentate (N∧N) ligand. Abovecomplexes were adequately characterized by a combination ofelemental analysis, IR, Mass and NMR spectroscopy. The X-raycrystal structures of (7) and (8) were determined.