Department of Applied Chemistry, School of Engineering, The University of Tokyo, and CREST, Japan Science and Technology Agency (JST), 7-3-1 Hongo, Tokyo 113-8656, Japan.
J Am Chem Soc. 2012 Jan 11;134(1):162-4. doi: 10.1021/ja210068f. Epub 2011 Dec 12.
A cationic coordination cage dramatically accelerates the Knoevenagel condensation of aromatic aldehydes in water under neutral conditions. The addition of a nucleophile to the aldehyde to generate anionic intermediates seems to be facilitated by the cationic environment of the cavity. The products are ejected from the cage as a result of the host-guest size discrepancy. As a result, the condensation is promoted by a catalytic amount of the cage.
一种正离子配位笼在中性条件下显著加速了芳香醛的 Knoevenagel 缩合反应。醛中亲核试剂的添加似乎是由于空腔的正离子环境而得到促进,生成了阴离子中间体。由于主客体尺寸差异,产物从笼中被逐出。因此,少量的笼即可促进缩合反应。