Dynamic Covalent Chemistry
Top Cited Papers
- 15 March 2002
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 41 (6), 898-952
- https://doi.org/10.1002/1521-3773(20020315)41:6<898::aid-anie898>3.0.co;2-e
Abstract
Dynamic covalent chemistry relates to chemical reactions carried out reversibly under conditions of equilibrium control. The reversible nature of the reactions introduces the prospects of "error checking" and "proof-reading" into synthetic processes where dynamic covalent chemistry operates. Since the formation of products occurs under thermodynamic control, product distributions depend only on the relative stabilities of the final products. In kinetically controlled reactions, however, it is the free energy differences between the transition states leading to the products that determines their relative proportions. Supramolecular chemistry has had a huge impact on synthesis at two levels: one is noncovalent synthesis, or strict self-assembly, and the other is supramolecular assistance to molecular synthesis, also referred to as self-assembly followed by covalent modification. Noncovalent synthesis has given us access to finite supermolecules and infinite supramolecular arrays. Supramolecular assistance to covalent synthesis has been exploited in the construction of more-complex systems, such as interlocked molecular compounds (for example, catenanes and rotaxanes) as well as container molecules (molecular capsules). The appealing prospect of also synthesizing these types of compounds with complex molecular architectures using reversible covalent bond forming chemistry has led to the development of dynamic covalent chemistry. Historically, dynamic covalent chemistry has played a central role in the development of conformational analysis by opening up the possibility to be able to equilibrate configurational isomers, sometimes with base (for example, esters) and sometimes with acid (for example, acetals). These stereochemical "balancing acts" revealed another major advantage that dynamic covalent chemistry offers the chemist, which is not so easily accessible in the kinetically controlled regime: the ability to re-adjust the product distribution of a reaction, even once the initial products have been formed, by changing the reaction's environment (for example, concentration, temperature, presence or absence of a template). This highly transparent, yet tremendously subtle, characteristic of dynamic covalent chemistry has led to key discoveries in polymer chemistry. In this review, some recent examples where dynamic covalent chemistry has been demonstrated are shown to emphasise the basic concepts of this area of science.Keywords
This publication has 522 references indexed in Scilit:
- Polymerization of Ethylene Terephthalate Cyclic Oligomers with Antimony TrioxideMacromolecules, 2000
- Polymerization of Ethylene Terephthalate Cyclic Oligomers with a Cyclic Dibutyltin InitiatorMacromolecules, 2000
- Zirconium-Mediated Metathesis of Imines: A Study of the Scope, Longevity, and Mechanism of a Complicated Catalytic SystemJournal of the American Chemical Society, 2000
- Equilibrium Polymerization of 7-(Alkoxycarbonyl)-7-cyano-1,4-benzoquinone Methides, Substituent Effect on Polymerizability, and Copolymerization with StyreneMacromolecules, 1998
- Slippage—an alternative method for assembling [2]rotaxanesJournal of the Chemical Society, Chemical Communications, 1993
- Preparation and polymerization of bisphenol A cyclic oligomeric carbonatesMacromolecules, 1991
- Use of cyclic carbonate oligomers in the synthesis of bisphenol-a polycarbonate-polydimethylsiloxane copolymersMakromolekulare Chemie. Macromolecular Symposia, 1991
- The self-assembly of [n]pseudorotaxanesJournal of the Chemical Society, Chemical Communications, 1991
- Synthesis, structure, and ring-opening polymerisation of strained macrocyclic biaryls: a new route to high-performance materialsJournal of the Chemical Society, Chemical Communications, 1990
- The effect of ring size on threading reactions of macrocyclesJournal of the Chemical Society, Chemical Communications, 1972