Theoretical elucidation of the multi-functional synthetic methodology for switchable Ni(0)-catalyzed C–H allylations, alkenylations and dienylations with allenes. Issue 13 (11th June 2020)

• Record Type: Journal Article
• Authors: Liu, Yuxia; Wang, Kaifeng; Ling, Baoping; Chen, Guang; Li, Yulin; Liu, Lingjun; Bi, Siwei
• Is Part Of: Catalysis science & technology. Volume 10:Issue 13(2020)
• Page Start: 4219
• Page End: 4228
• Publication Date: 2020-06-11
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/d0cy00965b
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : The mechanisms and origins of switchable Ni(0)-catalyzed C–H allylations, alkenylations and dienylations with allenes are theoretically elucidated. Abstract : The Ni(0)-catalyzed coupling of benzimidazole with 1, 1-disubstituted allenes represents a new strategy for achieving controllable C–H allylations, alkenylations and dienylations. To understand the detailed mechanisms and origins of the switchable selectivities, density functional theory (DFT) calculations were conducted. The results using a t Bu-substituted allene demonstrate that the formation of the allylated product involves a Ni-catalyzed C–H activation mechanism through ligand-to-ligand-hydrogen transfer (LLHT) under base-free conditions. In contrast, a Ni/NaO t Bu co-promoted C–H activation mechanism is newly proposed in the presence of NaO t Bu, which is remarkably different from the previously reported literature. The novel mechanism emphasizes that NaO t Bu abstracts the Ni-activated heterocyclic ( ipso -C)H atom followed by turnover limiting Ni slippage, and subsequently the allylated product is generated after alkene insertion and protonation. The strong electrostatic attraction between Ni and heterocyclic ipso -C in the Ni slippage pre-intermediate is critical for facilitating the Ni slippage. Once formed, the allylated product, assisted by NaO t Bu, further evolves into a more stable alkenylated isomer. Employing a ( tert -butyldimethylsilyl)-ether substituted allene as the substrate, the NaO t Bu-induced chemoselectivity for dienylation vs. alkenylation was also probed and it was found that the O( t Bu)–H⋯O(Si) hydrogen bonding interaction in the C–O(Si) cleavage pre-intermediate remarkably weakens the adjacent C–O(Si) σ-bond, thereby resulting in an exclusive C–O(Si) cleaved dienylation product. Further theoretical predictions suggest that the chemoselectivity might be reversed by replacing t Bu in NaO t Bu by the withdrawing C(CF3 )3 group.