Chiral Softballs: Synthesis and Molecular Recognition Properties
Studies on the different congeners of the softball were undertaken to explore structural variants for enantioselective encapsulation. Two different spacer elements in the monomeric subunit render the dimeric softball chiral although the monomer itself is achiral. The dimers represent capsules with dissymmetric cavities with volumes ranging from 190 to 390 Å3. The cavities are distorted spheres, and asymmetric guests, such as naturally occurring terpenes, generally prefer one enantiomer of the capsule to its mirror image. The selectivities are moderate (up to 4:1). The complexation studies show that the host capsules are flexible enough to arrange themselves comfortably around a guest but still maintain enough rigidity to be influenced by the occupancy of a chiral guest. The enantiomeric capsules can interconvert (racemize) by dissociation and recombination of their subunits.
Main Authors: | Rivera, José M., Martín, Tomás, Rebek, Julius Jr. |
---|---|
Format: | artículo biblioteca |
Language: | English |
Published: |
American Chemical Society
2001-05-10
|
Subjects: | Monomers, Encapsulation, Noncovalent interactions, Cavities, Selectivity, |
Online Access: | http://hdl.handle.net/10261/211765 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Chiral Microenvironments in Self-Assembled Capsules
by: Nuckolls, Colin, et al.
Published: (1999-10-21) -
Emergent Conformational Preferences of a Self-Assembling Small Molecule: Structure and Dynamics in a Tetrameric Capsule
by: Hof, Fraser, et al.
Published: (2000-10-21) -
Enantioselective Cooperativity between Intra-Receptor Interactions and Guest Binding: Quantification of a Reinforced Chiral Recognition
by: Carrillo Fumero, Romen, et al.
Published: (2011-11-04) -
Quantification of a CH–π Interaction Responsible for Chiral Discrimination and Evaluation of Its Contribution to Enantioselectivity
by: Carrillo Fumero, Romen, et al.
Published: (2009-10) -
Design, Synthesis, and Biological Evaluation of New Type of Gemini Analogues with a Cyclopropane Moiety in Their Side Chain
by: Gómez Bouzó, Uxía, et al.
Published: (2024-06-10)