Mirror symmetry breaking and chiral amplification in foldamer-based supramolecular helical aggregates

2012 ◽  
Vol 48 (17) ◽  
pp. 2292 ◽  
Author(s):  
Simon Azeroual ◽  
Jamie Surprenant ◽  
Thomas D. Lazzara ◽  
Marta Kocun ◽  
Ye Tao ◽  
...  
Keyword(s):  
Symmetry Breaking ◽  
Mirror Symmetry ◽  
Chiral Amplification

scholarly journals Chiral Oscillations and Spontaneous Mirror Symmetry Breaking in a Simple Polymerization Model

Symmetry ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1388
Author(s):  
William Bock ◽  
Enrique Peacock-López
Keyword(s):  
Symmetry Breaking ◽  
Mirror Symmetry ◽  
Chiral Symmetry Breaking ◽  
Enantiomeric Excess ◽  
Chemical Species ◽  
Preferential Formation ◽  
Chiral Amplification ◽  
Sustained Oscillations ◽  
Wide Range ◽  
The Origin Of Life

The origin of biological homochirality—defined as the preference of biological systems for only one enantiomer—has widespread implications in the study of chemical evolution and the origin of life. The activation—polymerization—epimerization—depolymerization (APED) model is a theoretical model originally proposed to describe chiral symmetry breaking in a simple dimerization system. It is known that the model produces chiral and chemical oscillations for certain system parameters, in particular, the preferential formation of heterochiral polymers. In order to investigate the effect of higher oligomers, our model adds trimers, tetramers, and pentamers. We report sustained oscillations of all chemical species and the enantiomeric excess for a wide range of parameter sets as well as the periodic chiral amplification of a small initial enantiomeric excess to a nearly homochiral state.

scholarly journals Spontaneous and directed symmetry breaking in the formation of chiral nanocrystals

2019 ◽  
Vol 116 (23) ◽  
pp. 11159-11164 ◽  
Author(s):  
Uri Hananel ◽  
Assaf Ben-Moshe ◽  
Haim Diamant ◽  
Gil Markovich
Keyword(s):  
Symmetry Breaking ◽  
Mirror Symmetry ◽  
Natural World ◽  
Colloidal Synthesis ◽  
Aqueous Environment ◽  
Chemical Systems ◽  
Chiral Amplification ◽  
Circularly Polarized Luminescence ◽  
Left And Right ◽  
Crucial Part

Symmetry plays a crucial part in our understanding of the natural world. Mirror symmetry breaking is of special interest as it is related to life as we know it. Studying systems which display chiral amplification, therefore, could further our understanding of symmetry breaking in chemical systems, in general, and thus also of the asymmetry in Nature. Here, we report on strong chiral amplification in the colloidal synthesis of intrinsically chiral lanthanide phosphate nanocrystals, measured via circularly polarized luminescence. The amplification involves spontaneous symmetry breaking into either left- or right-handed nanocrystals below a critical temperature. Furthermore, chiral tartaric acid molecules in the solution direct the amplified nanocrystal handedness through a discontinuous transition between left- and right-handed excess. We analyze the observations based on the statistical thermodynamics of critical phenomena. Our results demonstrate how chiral minerals with high enantiopurity can form in a racemic aqueous environment.

2,6-Dibromogallates as a new building block for controlling π-stacking, network formation and mirror symmetry breaking

2021 ◽  
Author(s):  
Ohjin Kwon ◽  
Xiaoqian Cai ◽  
Azhar Saeed ◽  
Feng Liu ◽  
Silvio Poppe ◽  
...  
Keyword(s):  
Symmetry Breaking ◽  
Building Block ◽  
Mirror Symmetry ◽  
Network Formation ◽  
Network Structures ◽  
Π Stacking ◽  
Bicontinuous Cubic ◽  
Substituted 1 ◽  
End Group

Achiral multi-chain (polycatenar) compounds based on the 2,7-diphenyl substituted [1]benzothieno[3,2-b]benzothiophene (BTBT) unit and a 2,6-dibromo-3,4,5-trialkoxybenzoate end group lead to materials forming bicontinuous cubic liquid crystaline phases with helical network structures...

Reply to “Mirror Symmetry Breaking” of the Centrosymmetric CaCO3 Crystals with Amino Acids

2008 ◽  
Vol 120 (20) ◽  
pp. 3741-3744
Author(s):  
Niklas Loges ◽  
Stephan E. Wolf ◽  
Martin Panthöfer ◽  
Lars Müller ◽  
Marc-Christopher Reinnig ◽  
...  
Keyword(s):  
Amino Acids ◽  
Symmetry Breaking ◽  
Mirror Symmetry

scholarly journals Entropic Analysis of Mirror Symmetry Breaking in Chiral Hypercycles

Life ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 28 ◽  
Author(s):  
David Hochberg ◽  
Josep Ribó
Keyword(s):  
Symmetry Breaking ◽  
Entropy Production ◽  
Mirror Symmetry ◽  
Flow Reactor ◽  
Evolutionary Selection ◽  
Replicator System ◽  
Stoichiometric Network Analysis ◽  
Underlying Mechanisms ◽  
The Individual ◽  
Origin Of Homochirality

Replicators are fundamental to the origin of life and evolvability. Biology exhibits homochirality: only one of two enantiomers is used in proteins and nucleic acids. Thermodynamic studies of chemical replicators able to lead to homochirality shed valuable light on the origin of homochirality and life in conformity with the underlying mechanisms and constraints. In line with this framework, enantioselective hypercyclic replicators may lead to spontaneous mirror symmetry breaking (SMSB) without the need for additional heterochiral inhibition reactions, which can be an obstacle for the emergence of evolutionary selection properties. We analyze the entropy production of a two-replicator system subject to homochiral cross-catalysis which can undergo SMSB in an open-flow reactor. The entropy exchange with the environment is provided by the input and output matter flows, and is essential for balancing the entropy production at the non-equilibrium stationary states. The partial entropy contributions, associated with the individual elementary flux modes, as defined by stoichiometric network analysis (SNA), describe how the system’s internal currents evolve, maintaining the balance between entropy production and exchange, while minimizing the entropy production after the symmetry breaking transition. We validate the General Evolution Criterion, stating that the change in the chemical affinities proceeds in a way as to lower the value of the entropy production.

Sign in / Sign up

Export Citation Format

Share Document