Computational study of the effect of Lewis base additives and molecular spin state in SmI2-chemistry

TL;DR

This paper uses computational methods to explore how Lewis base additives affect SmI2 chemistry, influencing reactivity and reaction pathways.

Contribution

The study reveals how Lewis base additives modulate SmI2's reducing power and reaction mechanisms through coordination and electronic effects.

Findings

Lewis base additives influence SmI2's reducing power via coordination geometry and basicity.

LB additives reshape reaction profiles by altering rate-determining steps in SmI2-catalyzed reactions.

A novel septet pathway was identified as more efficient than the conventional quintet route in coupling reactions.

Abstract

SmI2 has become a crucial reagent in organic chemistry due to its ability to facilitate single-electron transfer (SET) reactions under mild conditions, enabling the construction of complex molecular architectures. Its versatility can be further enhanced by the use of additives, particularly Lewis base (LB) additives. In this study, we provide a computational understanding of the multifaceted role of LB additives in SmI2 chemistry. We first identify the critical interplay between the basicity of the LB and the coordination geometry, which together dictate the reducing power of SmI2(LB)n complexes. For example, the relatively weak LB tetrahydrofuran (THF), a less bulky ligand than analogous ethers such as tetrahydropyran (THP), can achieve tight coordination to Sm, thereby enhancing electron donation and the reducing power of SmI2. Additionally, we investigate the SET reduction of various ketones by SmI2, showing that both steric and electronic effects from the LB and the substrate play pivotal roles in governing the SET reduction reactivity of SmI2, suggesting that SET reactivity cannot be solely determined by the commonly used reduction power of SmI2. In the final part of our study, we examine the influence of LB additives on practical SmI2-catalysed coupling reactions, finding a revised reaction mechanism that proceeds along a novel septet pathway that outperforms the conventional quintet route. We find that strongly coordinating additives can markedly reshape the reaction profile by accelerating key steps and altering the rate-determining stationary points. These results highlight how LB additives can intricately modulate reactivity and selectivity, offering valuable insights for the rational design of more efficient and selective SmI2-mediated transformations.

Computational study reveals the role of Lewis bases in SmI2 chemistry, from tuning reducing power and modulating single-electron transfer to shaping reaction potential energy surfaces.

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