Department of Chemistry, Indian Institute of Science Education and Research (IISER) Pune, Dr. Homi Bhabha Road, Pashan, Pune-411008, India.
Phys Chem Chem Phys. 2022 Sep 28;24(37):22371-22389. doi: 10.1039/d2cp02070j.
Herein, a perspective on the recent understanding of weak n → π* interaction obtained using different experimental and theoretical approaches is presented. This interaction is purely an orbital interaction that involves the delocalization of the lone pair electrons (n) on nitrogen, oxygen, and sulfur to the π* orbitals of CO, CN, and aromatic rings. The n → π* interaction has been found to profoundly influence the stabilization of peptides, proteins, drugs, and various small molecules. Although the functional properties of this non-covalent interaction are still quite underestimated, there are recent demonstrations of applying this interaction to the regulation of synthetic chemistry, catalysis, and molecular recognition. However, the identification and quantification of the n → π* interaction remain a demanding task as this interaction is quite weak and based on the electron delocalization between the two orbitals, while hyperconjugation interactions between neighboring atoms and the group involved in the n → π* interaction are simultaneously present. This review provides a comprehensive picture of understanding the n → π* interaction using different experimental approaches such as the X-ray diffraction technique, and electronic, NMR, microwave, and IR spectroscopy, in addition to quantum chemistry calculations. A detailed understanding of the n → π* interaction can help in modulating the strength of this interaction, which will be further helpful in designing efficient drugs, synthetic peptides, peptidomimetics,
本文介绍了使用不同实验和理论方法对弱 n→π* 相互作用的最新理解。这种相互作用纯粹是一种轨道相互作用,涉及氮、氧和硫上的孤对电子(n)的离域到 C=O、C=N 和芳环的π轨道。已经发现 n→π相互作用对肽、蛋白质、药物和各种小分子的稳定有深远的影响。尽管这种非共价相互作用的功能性质仍然被低估,但最近有应用这种相互作用来调节合成化学、催化和分子识别的例子。然而,n→π相互作用的识别和量化仍然是一项具有挑战性的任务,因为这种相互作用非常弱,基于两个轨道之间的电子离域,同时存在相邻原子和参与 n→π相互作用的基团之间的超共轭相互作用。本综述提供了使用不同实验方法(如 X 射线衍射技术以及电子、NMR、微波和红外光谱)和量子化学计算来理解 n→π相互作用的全面图景。对 n→π相互作用的详细了解有助于调节这种相互作用的强度,这将有助于设计高效的药物、合成肽、肽模拟物。