Acceleration of a Diels–Alder reaction by a self-assembled molecular capsule
- 1 January 1997
- journal article
- Published by Springer Nature in Nature
- Vol. 385 (6611) , 50-52
- https://doi.org/10.1038/385050a0
Abstract
The interior of cage-like molecules can be considered to provide a new phase of matter, in which it becomes possible to stabilize reactive intermediates and to observe new forms of stereoisomerism. Cage-like molecular complexes that self-assemble through weak intermolecular forces are dynamic species, encapsulating guest molecules reversibly. They can persist over timescales ranging from microseconds to hours, long enough for chemical processes to take place within them. Here we report the acceleration of a Diels-Alder reaction by encapsulation of the reactants in a self-assembling molecular capsule. Although product inhibition (lack of dissociation) prevents the system from showing true catalytic behaviour, there is clear evidence for a rate increase of over two orders of magnitude owing to the effective enhancement of concentration inside the capsule.Keywords
This publication has 19 references indexed in Scilit:
- Entropically driven binding in a self-assembling molecular capsuleNature, 1996
- Autoencapsulation Through Intermolecular Forces: A Synthetic Self-Assembling Spherical ComplexScience, 1995
- Synthesis and Self-Assembly of Pseudo-Spherical Homo- and Heterodimeric CapsulesJournal of the American Chemical Society, 1995
- A Novel Type of Stereoisomerism in Calix[4]arene‐Based CarceplexesAngewandte Chemie International Edition in English, 1994
- A Synthetic Cavity Assembles Through Self‐Complementary Hydrogen BondsAngewandte Chemie International Edition in English, 1993
- Complexation of Methane and Chlorofluorocarbons by Cryptophane‐A in Organic SolutionAngewandte Chemie International Edition in English, 1993
- The Taming of CyclobutadieneAngewandte Chemie International Edition in English, 1991
- Diels-alder reactions: Rate acceleration promoted by a biphenylenediolTetrahedron Letters, 1990
- Catalysis by cucurbituril. The significance of bound-substrate destabilization for induced triazole formationThe Journal of Organic Chemistry, 1989
- Carcerand interiors provide a new phase of matterJournal of the American Chemical Society, 1989