The Cation-π Interaction in Small-Molecule Catalysis

被引:207
|
作者
Kennedy, C. Rose [1 ]
Lin, Song [2 ]
Jacobsen, Eric N. [1 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, 12 Oxford St, Cambridge, MA 02138 USA
[2] Univ Calif Berkeley, Dept Chem, 535 Latimer Hall, Berkeley, CA 94720 USA
关键词
cation-; interaction; homogeneous catalysis; noncovalent interactions; reaction mechanisms; stereoselective catalysis; DYNAMIC KINETIC RESOLUTION; ENANTIOSELECTIVE CLAISEN REARRANGEMENTS; HEXAMERIC RESORCINARENE CAPSULE; ASYMMETRIC CONJUGATE ADDITION; CHIRAL ALLYL CATIONS; NONCOVALENT INTERACTIONS; SUPRAMOLECULAR CATALYSIS; RING-CLOSURE; BIOMIMETIC CATALYSIS; ORGANIC CATALYSIS;
D O I
10.1002/anie.201600547
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalysis by small molecules (1000Da, 10(-9)m) that are capable of binding and activating substrates through attractive, noncovalent interactions has emerged as an important approach in organic and organometallic chemistry. While the canonical noncovalent interactions, including hydrogen bonding, ion pairing, and stacking, have become mainstays of catalyst design, the cation- interaction has been comparatively underutilized in this context since its discovery in the 1980s. However, like a hydrogen bond, the cation- interaction exhibits a typical binding affinity of several kcalmol(-1) with substantial directionality. These properties render it attractive as a design element for the development of small-molecule catalysts, and in recent years, the catalysis community has begun to take advantage of these features, drawing inspiration from pioneering research in molecular recognition and structural biology. This Review surveys the burgeoning application of the cation- interaction in catalysis.
引用
收藏
页码:12596 / 12624
页数:29
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