School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K.
Department of Chemistry, University of Southampton, Highfield Campus, Southampton SO17 2BJ, U.K.
J Am Chem Soc. 2022 Dec 21;144(50):23127-23133. doi: 10.1021/jacs.2c10742. Epub 2022 Dec 12.
Hydrogen-bonded supramolecular systems are usually characterized in solution through analysis of NMR data such as complexation-induced shifts and nuclear Overhauser effects (nOe). Routine direct detection of hydrogen bonding particularly in multicomponent mixtures, even with the aid of 2D NMR experiments for full assignment, is more challenging. We describe an elementary rapid H-N HMQC NMR experiment which addresses these challenges without the need for complex pulse sequences. Under readily accessible conditions (243/263 K, 50 mM solutions) and natural N abundance, unambiguous assignment of N resonances facilitates direct detection of intra- and intermolecular hydrogen bonds in mechanically interlocked structures and quadruply hydrogen-bonded dimers─of dialkylaminoureidopyrimidinones, ureidopyrimidinones, and diamidonaphthyridines─in single or multicomponent mixtures to establish tautomeric configuration, conformation, and, to resolve self-sorted speciation.
氢键超分子体系通常通过分析 NMR 数据(如络合诱导位移和核 Overhauser 效应(nOe))在溶液中进行表征。即使借助二维 NMR 实验进行全分配,在多组分混合物中常规直接检测氢键也更具挑战性。我们描述了一种基本的快速 H-N HMQC NMR 实验,该实验无需复杂的脉冲序列即可解决这些挑战。在易于实现的条件下(243/263 K,50 mM 溶液)和天然 N 丰度下,N 共振的明确分配有助于直接检测机械互锁结构和四氢键二聚体中的分子内和分子间氢键——二烷基氨基脲嘧啶酮、脲嘧啶酮和二酰胺萘啶——在单组分或多组分混合物中建立互变异构体构型、构象,并解析自分类物种。