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Antiparallel Dynamic Covalent Chemistries
[Image: see text] The ability to design reaction networks with high, but addressable complexity is a necessary prerequisite to make advanced functional chemical systems. Dynamic combinatorial chemistry has proven to be a useful tool in achieving complexity, however with some limitations in controlli...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438195/ https://www.ncbi.nlm.nih.gov/pubmed/28440073 http://dx.doi.org/10.1021/jacs.7b02575 |
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author | Matysiak, Bartosz M. Nowak, Piotr Cvrtila, Ivica Pappas, Charalampos G. Liu, Bin Komáromy, Dávid Otto, Sijbren |
author_facet | Matysiak, Bartosz M. Nowak, Piotr Cvrtila, Ivica Pappas, Charalampos G. Liu, Bin Komáromy, Dávid Otto, Sijbren |
author_sort | Matysiak, Bartosz M. |
collection | PubMed |
description | [Image: see text] The ability to design reaction networks with high, but addressable complexity is a necessary prerequisite to make advanced functional chemical systems. Dynamic combinatorial chemistry has proven to be a useful tool in achieving complexity, however with some limitations in controlling it. Herein we introduce the concept of antiparallel chemistries, in which the same functional group can be channeled into one of two reversible chemistries depending on a controllable parameter. Such systems allow both for achieving complexity, by combinatorial chemistry, and addressing it, by switching from one chemistry to another by controlling an external parameter. In our design the two antiparallel chemistries are thiol–disulfide exchange and thio-Michael addition, sharing the thiol as the common building block. By means of oxidation and reduction the system can be reversibly switched from predominantly thio-Michael chemistry to predominantly disulfide chemistry, as well as to any intermediate state. Both chemistries operate in water, at room temperature, and at mildly basic pH, which makes them a suitable platform for further development of systems chemistry. |
format | Online Article Text |
id | pubmed-5438195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54381952017-05-22 Antiparallel Dynamic Covalent Chemistries Matysiak, Bartosz M. Nowak, Piotr Cvrtila, Ivica Pappas, Charalampos G. Liu, Bin Komáromy, Dávid Otto, Sijbren J Am Chem Soc [Image: see text] The ability to design reaction networks with high, but addressable complexity is a necessary prerequisite to make advanced functional chemical systems. Dynamic combinatorial chemistry has proven to be a useful tool in achieving complexity, however with some limitations in controlling it. Herein we introduce the concept of antiparallel chemistries, in which the same functional group can be channeled into one of two reversible chemistries depending on a controllable parameter. Such systems allow both for achieving complexity, by combinatorial chemistry, and addressing it, by switching from one chemistry to another by controlling an external parameter. In our design the two antiparallel chemistries are thiol–disulfide exchange and thio-Michael addition, sharing the thiol as the common building block. By means of oxidation and reduction the system can be reversibly switched from predominantly thio-Michael chemistry to predominantly disulfide chemistry, as well as to any intermediate state. Both chemistries operate in water, at room temperature, and at mildly basic pH, which makes them a suitable platform for further development of systems chemistry. American Chemical Society 2017-04-25 2017-05-17 /pmc/articles/PMC5438195/ /pubmed/28440073 http://dx.doi.org/10.1021/jacs.7b02575 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Matysiak, Bartosz M. Nowak, Piotr Cvrtila, Ivica Pappas, Charalampos G. Liu, Bin Komáromy, Dávid Otto, Sijbren Antiparallel Dynamic Covalent Chemistries |
title | Antiparallel
Dynamic Covalent Chemistries |
title_full | Antiparallel
Dynamic Covalent Chemistries |
title_fullStr | Antiparallel
Dynamic Covalent Chemistries |
title_full_unstemmed | Antiparallel
Dynamic Covalent Chemistries |
title_short | Antiparallel
Dynamic Covalent Chemistries |
title_sort | antiparallel
dynamic covalent chemistries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438195/ https://www.ncbi.nlm.nih.gov/pubmed/28440073 http://dx.doi.org/10.1021/jacs.7b02575 |
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