Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190 (P.R. China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072 (P.R. China).
Angew Chem Int Ed Engl. 2015 Mar 27;54(14):4334-7. doi: 10.1002/anie.201411593. Epub 2015 Feb 11.
An aza-crown ether, modified phosphoramidite ligand, has been designed and synthesized. The ON/OFF reversible switch of catalytic activity for its rhodium catalyst was thoroughly investigated in the asymmetric hydrogenation of dehydroamino acid esters modulated by host-guest interactions. In the OFF state, the catalyst is almost inactive (less than 1% conversion) because of the formation of an intermolecular sandwich complex by two aza-crown ether moities and the cationic rhodium metal center. In using alkali-metal-cations as the trigger, the catalytic activity was turned ON and consequently resulted in full conversions and excellent enantioselectivities (up to 98% ee).
一种氮杂冠醚修饰的膦酰胺配体已被设计和合成。通过主客体相互作用调控去氢氨基酸酯的不对称氢化反应,深入研究了其铑催化剂的催化活性的开/关可逆开关。在关闭状态下,由于两个氮杂冠醚部分和阳离子铑金属中心形成了分子间夹心配合物,催化剂几乎没有活性(转化率小于 1%)。使用碱金属阳离子作为触发剂,将催化活性打开,从而导致完全转化和优异的对映选择性(高达 98%ee)。