Literature DB >> 22310886

Dynamic imine chemistry.

Matthew E Belowich1, J Fraser Stoddart.   

Abstract

Formation of an imine--from an amine and an aldehyde--is a reversible reaction which operates under thermodynamic control such that the formation of kinetically competitive intermediates are, in the fullness of time, replaced by the thermodynamically most stable product(s). For this fundamental reason, the imine bond has emerged as an extraordinarily diverse and useful one in the hands of synthetic chemists. Imine bond formation is one of a handful of reactions which define a discipline known as dynamic covalent chemistry (DCC), which is now employed widely in the construction of exotic molecules and extended structures on account of the inherent 'proof-reading' and 'error-checking' associated with these reversible reactions. While both supramolecular chemistry and DCC operate under the regime of reversibility, DCC has the added advantage of constructing robust molecules on account of the formation of covalent bonds rather than fragile supermolecules resulting from noncovalent bonding interactions. On the other hand, these products tend to require more time to form--sometimes days or even months--but their formation can often be catalysed. In this manner, highly symmetrical molecules and extended structures can be prepared from relatively simple precursors. When DCC is utilised in conjunction with template-directed protocols--which rely on the use of noncovalent bonding interactions between molecular building blocks in order to preorganise them into certain relative geometries as a prelude to the formation of covalent bonds under equilibrium control--an additional level of control of structure and topology arises which offers a disarmingly simple way of constructing mechanically-interlocked molecules, such as rotaxanes, catenanes, Borromean rings, and Solomon knots. This tutorial review focuses on the use of dynamic imine bonds in the construction of compounds and products formed with and without the aid of additional templates. While synthesis under thermodynamic control is giving the field of chemical topology a new lease of life, it is also providing access to an endless array of new materials that are, in many circumstances, simply not accessible using more traditional synthetic methodologies where kinetic control rules the roost. One of the most endearing qualities of chemistry is its ability to reinvent itself in order to create its own object, as Berthelot first pointed out a century and a half ago.

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Year:  2012        PMID: 22310886     DOI: 10.1039/c2cs15305j

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  82 in total

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2.  Biomimetic Generation and Remodeling of Phospholipid Membranes by Dynamic Imine Chemistry.

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Authors:  Olga A Mukhina; Dmitry M Kuznetsov; Teresa M Cowger; Andrei G Kutateladze
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Journal:  Nat Chem       Date:  2012-08-05       Impact factor: 24.427

6.  Dynamic covalent chemistry of bisimines at the solid/liquid interface monitored by scanning tunnelling microscopy.

Authors:  Artur Ciesielski; Mohamed El Garah; Sébastien Haar; Petr Kovaříček; Jean-Marie Lehn; Paolo Samorì
Journal:  Nat Chem       Date:  2014-09-14       Impact factor: 24.427

7.  Template-guided selection of RNA ligands using imine-based dynamic combinatorial chemistry.

Authors:  Aline Umuhire Juru; Zhengguo Cai; Adina Jan; Amanda E Hargrove
Journal:  Chem Commun (Camb)       Date:  2020-03-24       Impact factor: 6.222

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Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-01       Impact factor: 11.205

10.  On the formation and properties of interstrand DNA-DNA cross-links forged by reaction of an abasic site with the opposing guanine residue of 5'-CAp sequences in duplex DNA.

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Journal:  J Am Chem Soc       Date:  2013-01-11       Impact factor: 15.419

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