{"title":"Gold(I) {2}‐Metallacoronates derived from a Catechol‐scaffolding Aroylbis(N,N‐diethylthiourea): Syntheses and Structures","authors":"Chien Thang Pham, Hung Huy Nguyen, Ulrich Abram, Thu Thuy Pham","doi":"10.1002/zaac.202400012","DOIUrl":null,"url":null,"abstract":"One‐pot reactions of a catechol‐scaffolding aroylbis(N,N‐diethylthiourea) H2Lcat and mixtures of lanthanide nitrates Ln(NO3)3 (Ln3+ = La3+, Nd3+ or Yb3+) or indium(III) chloride InCl3 and [Au(tht)Cl] in methanol in the presence of the supporting base Et3N result in gold(I) {2}‐metallacoronates. Depending on radii of the trivalent metal ions, the corresponding complexes are separated either in the neutral form with the composition {(NO3‐κ2‐O,O’)Ln [[EQUATION]] [Au2(Lcat)2]} in the cases of La3+ and Nd3+ or as the ‘ion‐pair’ {Yb [[EQUATION]] [Au2(Lcat)2]}+(NO3)‐ for the Yb(III) compound. The cationic complexes can be isolated in higher yields as the PF6‐ salts {M [[EQUATION]] [Au2(Lcat)2]}+(PF6)‐ (M3+ = Yb3+ or In3+) by treatment of reaction mixtures with (n‐Bu4N)(PF6).","PeriodicalId":23934,"journal":{"name":"Zeitschrift für anorganische und allgemeine Chemie","volume":"31 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für anorganische und allgemeine Chemie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/zaac.202400012","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
One‐pot reactions of a catechol‐scaffolding aroylbis(N,N‐diethylthiourea) H2Lcat and mixtures of lanthanide nitrates Ln(NO3)3 (Ln3+ = La3+, Nd3+ or Yb3+) or indium(III) chloride InCl3 and [Au(tht)Cl] in methanol in the presence of the supporting base Et3N result in gold(I) {2}‐metallacoronates. Depending on radii of the trivalent metal ions, the corresponding complexes are separated either in the neutral form with the composition {(NO3‐κ2‐O,O’)Ln [[EQUATION]] [Au2(Lcat)2]} in the cases of La3+ and Nd3+ or as the ‘ion‐pair’ {Yb [[EQUATION]] [Au2(Lcat)2]}+(NO3)‐ for the Yb(III) compound. The cationic complexes can be isolated in higher yields as the PF6‐ salts {M [[EQUATION]] [Au2(Lcat)2]}+(PF6)‐ (M3+ = Yb3+ or In3+) by treatment of reaction mixtures with (n‐Bu4N)(PF6).