Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford St, Cambridge, MA, 02138, USA.
Department of Chemistry, University of California, Berkeley, 535 Latimer Hall, Berkeley, CA, 94720, USA.
Angew Chem Int Ed Engl. 2016 Oct 4;55(41):12596-624. doi: 10.1002/anie.201600547. Epub 2016 Jun 22.
Catalysis by small molecules (≤1000 Da, 10(-9) m) that are capable of binding and activating substrates through attractive, noncovalent interactions has emerged as an important approach in organic and organometallic chemistry. While the canonical noncovalent interactions, including hydrogen bonding, ion pairing, and π stacking, have become mainstays of catalyst design, the cation-π interaction has been comparatively underutilized in this context since its discovery in the 1980s. However, like a hydrogen bond, the cation-π interaction exhibits a typical binding affinity of several kcal mol(-1) with substantial directionality. These properties render it attractive as a design element for the development of small-molecule catalysts, and in recent years, the catalysis community has begun to take advantage of these features, drawing inspiration from pioneering research in molecular recognition and structural biology. This Review surveys the burgeoning application of the cation-π interaction in catalysis.
小分子催化(≤1000Da,10(-9)m)通过吸引力、非共价相互作用结合和激活底物,已成为有机和金属有机化学中的重要方法。虽然经典的非共价相互作用,包括氢键、离子配对和π堆叠,已成为催化剂设计的主要支柱,但自 20 世纪 80 年代发现以来,阳离子-π相互作用在这方面的应用相对较少。然而,与氢键一样,阳离子-π相互作用表现出典型的几个千卡每摩尔(kcal/mol)的结合亲和力,具有很大的方向性。这些特性使其成为小分子催化剂开发的设计元素具有吸引力,近年来,催化界开始利用这些特性,从分子识别和结构生物学的开创性研究中汲取灵感。这篇综述调查了阳离子-π相互作用在催化中的新兴应用。