作者:Wenxian Ma、Tingting Cheng、Fang‐Zi Liu、Yan Liu、KaKing Yan
DOI:10.1002/anie.202202213
日期:2022.4.25
Analogous to allosteric enzymes, guest binding introduces a directional pulling or pushing force that acts on the reverse side of a Zn salen complex. This tunable intramolecular force promotes various degrees of conformational and torsional strain, as predicted by both classical conformational analysis and DFT. This strain energy can be further applied to cleave chemical bonds, and the efficiency can
与变构酶类似,客体结合引入了作用于 Zn salen 复合物反面的定向拉力或推力。正如经典构象分析和 DFT 所预测的,这种可调节的分子内力促进了不同程度的构象和扭转应变。这种应变能可以进一步应用于切割化学键,并且可以通过变构客体的身份来调整效率。