| Literature DB >> 33913186 |
Wei Su1, Yanshun Ma2, Libo Xiang1, Junyi Wang1, Shuao Wang3, Lili Zhao2, Gernot Frenking2,4, Qing Ye1.
Abstract
Low-valent uranium-element multiple bond complexes remain scarce, though there is burgeoning interest regarding to their bonding and reactivity. Herein, isolation of a uranium(III)-carbon double bond complex [(Cp*)2 U(CDP)](BPh4 ) (1) comprising a tridentate carbodiphosphorane (CDP) was reported for the first time. Oxidation of 1 afforded the corresponding U(IV) complex [(Cp*)2 U(CDP)](BPh4 )2 (2). The distance between U and C in 2 is 2.481 Å, indicating the existence of a typical U=C double bond, which is further confirmed by quantum chemical calculations. Bonding analysis suggested that the CDP also serves as both σ- and π-donor in complex 1, though a longer U-C bond (2.666(3) Å) is observed. It implies that 1 is the first isolable mononuclear uranium(III) carbene complex. Moreover, these results suggest that CDPs are promising ligands to establish other low-valent f-block metal-carbon multiple bond complexes.Entities:
Keywords: carbodiphosphorane; low-valent; multiple bond; quantum chemical calculation; uranium
Year: 2021 PMID: 33913186 DOI: 10.1002/chem.202100699
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236