Chen Haonan, Chen Wang, Wang Dongmin, Chen Yizhen, Liu Zheng, Ye Shengfa, Tan Gengwen, Gao Song
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-sen University, Guangzhou, 510275, China.
Innovation Center for Chemical Sciences, Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China.
Angew Chem Int Ed Engl. 2024 May 13;63(20):e202402093. doi: 10.1002/anie.202402093. Epub 2024 Apr 10.
Lead-based radicals in the oxidation state of +1 are elusive species and are highly challenging to isolate in the condensed phase. In this study, we present the synthesis and characterization of the first isolable free plumbylyne radical 2 bearing a one-coordinate Pb(I) atom. It reacts with an N-heterocyclic carbene (NHC) to afford a two-coordinate NHC-ligated Pb(I) radical 3. 2 and 3 represent the first isolable Pb(I)-based radicals. Theoretical calculations and electron paramagnetic resonance analysis revealed that the unpaired electron mainly resides at the Pb 6p orbital in both radicals. Owing to the unique one-coordinate nature of the Pb atom in 2, it possesses two-fold orbital pseudo-degeneracy and substantial unquenched orbital angular momentum, and exhibits hitherto strongest g-factor anisotropy (g=1.496, 1.166, 0.683) amongst main group radicals. Preliminary investigations into the reactivity of 2 unveiled its Pb-centered radical nature, and plumbylenes were isolated as products.
氧化态为 +1 的铅基自由基是难以捉摸的物种,在凝聚相中分离极具挑战性。在本研究中,我们展示了首个可分离的含单配位 Pb(I) 原子的游离铅炔自由基 2 的合成与表征。它与 N - 杂环卡宾(NHC)反应生成二配位的 NHC 配位 Pb(I) 自由基 3。2 和 3 代表了首个可分离的基于 Pb(I) 的自由基。理论计算和电子顺磁共振分析表明,两个自由基中的未成对电子主要位于 Pb 的 6p 轨道。由于 2 中 Pb 原子独特的单配位性质,它具有双重轨道准简并性和大量未淬灭的轨道角动量,并且在主族自由基中表现出迄今最强的 g 因子各向异性(g = 1.496, 1.166, 0.683)。对 2 的反应性的初步研究揭示了其以 Pb 为中心的自由基性质,并分离得到了铅炔作为产物。