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Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules

[Image: see text] Asymmetric amplification induced in the Soai autocatalytic reaction by chiral initiators that are enantiomeric only by virtue of an isotope, e.g., −CH(3) vs CD(3)–, is examined by spectroscopic, kinetic, and DFT modeling studies to help understand requirements for the emergence of...

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Autores principales: Hawbaker, Neil A., Blackmond, Donna G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026777/
https://www.ncbi.nlm.nih.gov/pubmed/29974074
http://dx.doi.org/10.1021/acscentsci.8b00297
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author Hawbaker, Neil A.
Blackmond, Donna G.
author_facet Hawbaker, Neil A.
Blackmond, Donna G.
author_sort Hawbaker, Neil A.
collection PubMed
description [Image: see text] Asymmetric amplification induced in the Soai autocatalytic reaction by chiral initiators that are enantiomeric only by virtue of an isotope, e.g., −CH(3) vs CD(3)–, is examined by spectroscopic, kinetic, and DFT modeling studies to help understand requirements for the emergence of biological homochirality. We find that the initiator inhibits the autocatalytic pathway at the outset of the reaction but ultimately provides the imbalance required for asymmetric amplification. This work provides clues in the ongoing search for prebiotically plausible versions of asymmetric autocatalysis.
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spelling pubmed-60267772018-07-04 Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules Hawbaker, Neil A. Blackmond, Donna G. ACS Cent Sci [Image: see text] Asymmetric amplification induced in the Soai autocatalytic reaction by chiral initiators that are enantiomeric only by virtue of an isotope, e.g., −CH(3) vs CD(3)–, is examined by spectroscopic, kinetic, and DFT modeling studies to help understand requirements for the emergence of biological homochirality. We find that the initiator inhibits the autocatalytic pathway at the outset of the reaction but ultimately provides the imbalance required for asymmetric amplification. This work provides clues in the ongoing search for prebiotically plausible versions of asymmetric autocatalysis. American Chemical Society 2018-06-06 2018-06-27 /pmc/articles/PMC6026777/ /pubmed/29974074 http://dx.doi.org/10.1021/acscentsci.8b00297 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Hawbaker, Neil A.
Blackmond, Donna G.
Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title_full Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title_fullStr Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title_full_unstemmed Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title_short Rationalization of Asymmetric Amplification via Autocatalysis Triggered by Isotopically Chiral Molecules
title_sort rationalization of asymmetric amplification via autocatalysis triggered by isotopically chiral molecules
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026777/
https://www.ncbi.nlm.nih.gov/pubmed/29974074
http://dx.doi.org/10.1021/acscentsci.8b00297
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