Superbases in Confined Space: Control of the Basicity and Reactivity of the Proton Transfer

被引:33
作者
Chatelet, Bastien [1 ]
Gornitzka, Heinz [2 ,3 ]
Dufaud, Veronique [4 ]
Jeanneau, Erwann [5 ]
Dutasta, Jean-Pierre [1 ]
Martinez, Alexandre [1 ]
机构
[1] UCBL, Chim Lab, Ecole Normale Super Lyon, CNRS, F-69364 Lyon, France
[2] CNRS, Chim Coordinat Lab, F-31077 Toulouse 4, France
[3] Univ Toulouse, UPS, INPT, F-31077 Toulouse 4, France
[4] Univ Lyon 1, Lab Chim Catalyse Polymere Procedes C2P2, CNRS, CPE Lyon, F-69616 Villeurbanne, France
[5] Univ Lyon 1, Ctr Diffractometrie Henri Longchambon, F-69100 Villeurbanne, France
关键词
LEWIS-BASE CATALYST; ALPHA; BETA-UNSATURATED ESTERS; H BOND; PROAZAPHOSPHATRANES; P(I-PRNCH2CH2)(3)N; COORDINATION; FLUORIDES; CAPSULES; CAGES;
D O I
10.1021/ja409444s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Endohedral functionalization of the molecular cavity of host molecules is in high demand in many areas of supramolecular chemistry. When highly reactive species are incarcerated in the confined space of a molecular cavity, deep changes of their chemical properties are expected. Here, we show that the superbasic properties of proazaphosphatranes can be improved in the confined space of the molecular cavity of hemicryptophane hosts. A general and modular procedure is described to prepare supramolecular superbases with various cavity sizes. The rate of proton transfer is strongly dependent on the shape and size of the inner cavity of the designed superbasic structure. Kinetic and thermodynamic data are strongly correlated to the space available around the basic center as revealed by the X-ray molecular structures analyses.
引用
收藏
页码:18659 / 18664
页数:6
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