Mirror-symmetry breaking in the Soai reaction: a kinetic understanding.

Proc Natl Acad Sci U S A

Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos, Avenida Universidad 1001, Colonia Chamilpa, 62209 Cuernavaca, Morelos, Mexico.

Published: September 2005

Kinetic modeling using nonlinear differential equations is proposed to analyze the spontaneous generation of enantiomeric excess in the autocatalytic addition of diisopropylzinc to prochiral pyrimidine carbaldehydes (Soai reaction). Our approach reproduces experimentally observed giant chiral amplification from an initial enantiomeric excess of <10(-6)% to >60%, high sensitivity and positive response to the presence of minute amounts of chiral initiator at concentrations <10(-14) M, and spontaneous absolute asymmetric synthesis from achiral starting conditions. From our numerical simulations using kinetic schemes derived from the Frank model, including stereospecific autocatalysis and mutual inhibition, we have shown that it is possible to reproduce the mirror-symmetry-breaking behavior of the Soai reaction under batch conditions leading to a bimodal enantiomeric product distribution. Mirror-symmetry breaking was found to be resistant to a loss of stereoselectivity up to 30%. While the mutual inhibition between enantiomers seems to originate from the presence of dimerization equilibria, the exact nature of the autocatalytic stereoselective process still remains to be revealed. From the kinetic viewpoint, simple autocatalysis involving monomers as the catalytic species is consistent with all reported experimental effects of the Soai reaction.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1236534PMC
http://dx.doi.org/10.1073/pnas.0503171102DOI Listing

Publication Analysis

Top Keywords

soai reaction
8
enantiomeric excess
8
mirror-symmetry breaking
4
breaking soai
4
reaction kinetic
4
kinetic understanding
4
understanding kinetic
4
kinetic modeling
4
modeling nonlinear
4
nonlinear differential
4

Similar Publications

A previously unknown reduction of carbonyl compounds with dicyclopentylzinc is reported. Aldehydes react in mild conditions yielding corresponding primary alcohols and cyclopentene. Although cyclohexanone and acetophenone are inert to dicyclopentylzinc, a variety of heterocyclic ketones reacted readily, yielding reasonable to high yields of corresponding secondary alcohols.

View Article and Find Full Text PDF
Article Synopsis
  • - Achiral 2-pyridone and 4-aminopyridine crystals acted as sources of chirality in a reaction involving 5-pyrimidyl alkanol, promoting asymmetric autocatalysis known as the Soai reaction.
  • - During this process, diisopropylzinc was added to pyrimidine-5-carbaldehyde, leading to the creation of enantioenriched products.
  • - The reaction resulted in a significant increase in enantiomeric excess, with the final 5-pyrimidyl alkanol mirroring the configurations of the original chiral crystals.
View Article and Find Full Text PDF

Biological homochirality of essential components such as L-amino acids and D-sugars is prerequisite for the emergence, evolution and the maintenance of life. Implication of biological homochirality is described. Considerable interest has been focused on the origin and the process leading to the homochirality.

View Article and Find Full Text PDF

Spontaneous Emergence of Transient Chirality in Closed, Reversible Frank-like Deterministic Models.

Orig Life Evol Biosph

September 2022

Laboratoire des IMRCP, Université Paul Sabatier, UMR au CNRS No. 5623, F-31062, Toulouse Cedex, France.

To explore abiotic theories related to the origin of biomolecular homochirality, we analyze two entirely reversible kinetic models composed of an enantioselective autocatalysis with limited stereoselectivity that is coupled to an enantiomeric mutual inhibition (Frank-like models). The two models differ in their autocatalytic steps in respect to the formation of monomer species in one model and of dimer species in the other. While fully reversible and running in a closed system, spontaneous mirror symmetry breaking (SMSB) gives rise to transient chiral excursions, even when starting from a strictly achiral situation.

View Article and Find Full Text PDF

Possible chemical and physical scenarios towards biological homochirality.

Chem Soc Rev

May 2022

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, Equipe Chimie des Polymères, 4 Place Jussieu, 75005 Paris, France.

The single chirality of biological molecules in terrestrial biology raises more questions than certitudes about its origin. The emergence of biological homochirality (BH) and its connection with the appearance of life have elicited a large number of theories related to the generation, amplification and preservation of a chiral bias in molecules of life under prebiotically relevant conditions. However, a global scenario is still lacking.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!