A relativistic DFT probe for small-molecule activation mediated by low-valent uranium metallocenes. (17th February 2021)

• Record Type: Journal Article
• Authors: Shen, Yong-Peng; Cai, Hong-Xue; Chen, Fang-Yuan; Guo, Yuan-Ru; Pan, Qing-Jiang
• Is Part Of: New journal of chemistry. Volume 45:Number 9(2021)
• Page Start: 4270
• Page End: 4279
• Publication Date: 2021-02-17
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/d0nj06296k
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : DFT calculations rationalize the capability of uranium metallocenes in activating small molecules, and the experimentally inaccessible CO2 adduct is addressed. Abstract : Due to the powerful reducing ability of the metal active site, low-valent uranium complexes show remarkable performance in activating thermodynamically stable and kinetically inert small molecules. In this work, experimentally known uranium metallocenes [Cp3 U] z ( z = 0 and +1) were intensively studied using relativistic density functional theory for their activation of small molecules (X = CO2, N2, CO and NO). Regardless of whether z = 0 or +1, a weak double bond was realized between uranium and NO, which is in agreement with a previous study; a weak single bond with the dative nature was assigned to other small-molecule uranium adducts. A general order for the uranium–small molecule bond strength, NO > CO > N2 > CO2, has been built, the trend being exactly the same as the computed reduction potentials. These are corroborated by energetics and experimental results that (i) analogues of the first three [Cp3 U(X)] adducts were crystallographically identified but the one of [Cp3 U(CO2 )] was not, and (ii) much higher X gas pressure was required to synthesize [Cp3 U(N2 )] than for [Cp3 U(CO)]. Additionally, the experimentally inaccessible CO2 adduct was rationalized using thermodynamic and kinetic calculations as well as geometric/electronic properties and bonding analyses.