Actinide–Pnictide (An−Pn) Bonds Spanning Non‐Metal, Metalloid, and Metal Combinations (An=U, Th; Pn=P, As, Sb, Bi). (29th December 2017)

• Record Type: Journal Article
• Authors: Rookes, Thomas M.; Wildman, Elizabeth P.; Balázs, Gábor; Gardner, Benedict M.; Wooles, Ashley J.; Gregson, Matthew; Tuna, Floriana; Scheer, Manfred; Liddle, Stephen T.
• Is Part Of: Angewandte Chemie. Volume 130:Number 5(2018)
• Page Start: 1346
• Page End: 1350
• Publication Date: 2017-12-29
• Subjects: Metall-Metall-Bindungen -- Metalloide -- Pniktide -- Thorium -- Uran; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201711824
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: The synthesis and characterisation is presented of the compounds [An(Tren DMBS ){Pn(SiMe3 )2 }] and [An(Tren TIPS ){Pn(SiMe3 )2 }] [Tren DMBS =N(CH2 CH2 NSiMe2 Bu t )3, An=U, Pn=P, As, Sb, Bi; An=Th, Pn=P, As; Tren TIPS =N(CH2 CH2 NSiPr i 3 )3, An=U, Pn=P, As, Sb; An=Th, Pn=P, As, Sb]. The U−Sb and Th−Sb moieties are unprecedented examples of any kind of An−Sb molecular bond, and the U−Bi bond is the first two‐centre‐two‐electron (2c–2e) one. The Th−Bi combination was too unstable to isolate, underscoring the fragility of these linkages. However, the U−Bi complex is the heaviest 2c–2e pairing of two elements involving an actinide on a macroscopic scale under ambient conditions, and this is exceeded only by An−An pairings prepared under cryogenic matrix isolation conditions. Thermolysis and photolysis experiments suggest that the U−Pn bonds degrade by homolytic bond cleavage, whereas the more redox‐robust thorium compounds engage in an acid–base/dehydrocoupling route.