Mechanistic Insights into H–H Bond Cleavage and [1 + 2] Cycloaddition of Ethylene Mediated by Triplet Pnictinidenes

作者：Zhengfeng Zhang, Ming‐Der Su · 发表于：Inorganic Chemistry · 年份：2026 · DOI：10.1021/acs.inorgchem.6c00182 · 被引用次数：1 · 研究领域：Cyclization and Aryne Chemistry、Synthesis and characterization of novel inorganic/organometallic compounds、Organic Chemistry Cycloaddition Reactions

This study presents a theoretical investigation of the mechanistic pathways for H–H bond cleavage and [1 + 2] cycloaddition with ethylene mediated by triplet monomeric pnictinidenes ( [G15] 3; G15 = Group 15 element). Our results demonstrate that sterically congested singlet dipnictenes ( [G15] 1 2 ) can thermally dissociate into two triplet [G15] 3 monomers, with the dissociation energy decreasing systematically from N to Bi. M06-2X-D3 calculations indicate that triplet [G15] 3 activates H 2 via a transition state on the triplet surface, followed by intersystem crossing to form singlet products, with the reactivity decreasing as the atomic number of G15 increases. Similarly, triplet [G15] 3 undergoes [1 + 2] cycloaddition with ethylene through a triplet transition state, ultimately producing singlet three-membered heterocycles after intersystem crossing. Activation strain model (ASM) analyses reveal that the atomic radius of the central G15 atom provides a consistent explanation for the origins of the activation barriers in both H–H bond cleavage and [1 + 2] cycloaddition reactions. This study offers qualitative rationalization based on the activation barrier and assesses the feasibility of the proposed experimental observations.