Stabilization of the Oxidation State +IV in Siloxide‐Supported Terbium Compounds. Issue 9 (23rd January 2020)

• Record Type: Journal Article
• Authors: Willauer, Aurélien R.; Palumbo, Chad T.; Scopelliti, Rosario; Zivkovic, Ivica; Douair, Iskander; Maron, Laurent; Mazzanti, Marinella
• Is Part Of: Angewandte Chemie international edition. Volume 59:Issue 9(2020)
• Page Start: 3549
• Page End: 3553
• Publication Date: 2020-01-23
• Subjects: lanthanides -- metal-ion-coupled electron transfer -- rare earths -- siloxides -- terbium; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201914733
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: The synthesis of lanthanides other than cerium in the oxidation state +IV has remained a desirable but unmet target until recently, when two examples of Tb IV with saturated coordination spheres were isolated. Here we report the third example of an isolated molecular complex of terbium(IV), where the supporting siloxide ligands do not saturate the coordination sphere. The fully characterized six‐coordinate complex [Tb IV (OSiPh3 )4 (MeCN)2 ], 2 ‐Tb Ph, shows high stability and the labile MeCN ligands can be replaced by phosphinoxide ligands. Computational studies suggest that the stability is due to a strong π(O−Tb) interaction which is stronger than in the previously reported Tb IV complexes. Cyclic‐voltammetry experiments demonstrate that non‐binding counterions contribute to the stability of Tb IV in solution by destabilizing the +III oxidation state, while alkali ions promote Tb IV /Tb III electron transfer. Abstract : Tb IV is here to stay : The terbium(IV) complex [Tb(OSiPh3 )4 (MeCN)2 ] contains labile ligands but shows high stability as a result of a strong π(O−Tb) interaction. Non‐binding counterions contribute to the stability of Tb IV in solution by destabilizing the oxidation state +III, while alkali ions promote Tb IV /Tb III electron transfer.