PNNL

Abstract

Predicting accurate NMR chemical shieldings relies upon cancellation of different types of error between the theoretically calculated shielding constant of the analyte of interest and the reference. Often the intrinsic error in computed shieldings due to basis sets, approximations in the Hamiltonian, description of the wave function, and dynamic effects, is nearly identical between the analyte and reference, yet if the electronic structure or sensitivity to local environment differs dramatically, this cannot be taken for granted. Detailed prior work has examined the octahedral trivalent cation Al(H2O)36+ , accounting for ab initio intrinsic errors. However, the use of this species as a reference for the chemically distinct tetrahedral anion Al(OH)4- requires an understanding of how these errors cancel, in order to define the limits of accurately predicting 27Al chemical shielding in Al(OH)4- . In this work, we estimate the absolute shielding of the 27Al nucleus in Al(OH)4- at the coupled cluster level (515.1 _ 5.3 ppm). Shielding sensitivity to the choice of method approximation and atomic basis sets used has been evaluated. Solvent and thermal effects are assessed through ensemble averaging techniques using ab-initio molecular dynamics. The contribution of each type of intrinsic error is assessed for the Al(H2O)36+ and Al(OH)4- ions, revealing significant differences that fundamentally hamper the ability to accurately calculate the 27Al chemical shift of Al(OH)4- from first principles.