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The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions

[Image: see text] Langmuir monolayers of chiral amphiphiles are well-controlled model systems for the investigation of phenomena related to stereochemistry. Here, we have investigated mixed monolayers of one pair of enantiomers (l and d) of the amino-acid-based amphiphile N-stearoyl-threonine. The m...

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Autores principales: Mukhina, Tetiana, Richter, Lars, Vollhardt, Dieter, Brezesinski, Gerald, Schneck, Emanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583611/
https://www.ncbi.nlm.nih.gov/pubmed/36209408
http://dx.doi.org/10.1021/acs.langmuir.2c01936
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author Mukhina, Tetiana
Richter, Lars
Vollhardt, Dieter
Brezesinski, Gerald
Schneck, Emanuel
author_facet Mukhina, Tetiana
Richter, Lars
Vollhardt, Dieter
Brezesinski, Gerald
Schneck, Emanuel
author_sort Mukhina, Tetiana
collection PubMed
description [Image: see text] Langmuir monolayers of chiral amphiphiles are well-controlled model systems for the investigation of phenomena related to stereochemistry. Here, we have investigated mixed monolayers of one pair of enantiomers (l and d) of the amino-acid-based amphiphile N-stearoyl-threonine. The monolayer characteristics were studied by pressure–area isotherm measurements and grazing incidence X-ray diffraction (GIXD) over a wide range of mixing ratios defined by the d-enantiomer mole fraction x(D). While the isotherms provide insights into thermodynamical aspects, such as transition pressure, compression/decompression hysteresis, and preferential homo- and heterochiral interactions, GIXD reveals the molecular structural arrangements on the Ångström scale. Dominant heterochiral interactions in the racemic mixture lead to compound formation and the appearance of a nonchiral rectangular lattice, although the pure enantiomers form a chiral oblique lattice. Miscibility was found to be limited to mixtures with 0.27 ≲ x(D) ≲ 0.73, as well as to both outer edges (x(D) ≲ 0.08 and x(D) ≳ 0.92). Beyond this range, coexistence of oblique and rectangular lattices occurs, as is clearly seen in the GIXD patterns. Based on the results, a complete phase diagram with two eutectic points at x(D) ≈ 0.25 and x(D) ≈ 0.75 is proposed. Moreover, N-stearoyl-threonine was found to have a strong tendency to form a hydrogen-bonding network between the headgroups, which promotes superlattice formation.
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spelling pubmed-95836112022-10-21 The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions Mukhina, Tetiana Richter, Lars Vollhardt, Dieter Brezesinski, Gerald Schneck, Emanuel Langmuir [Image: see text] Langmuir monolayers of chiral amphiphiles are well-controlled model systems for the investigation of phenomena related to stereochemistry. Here, we have investigated mixed monolayers of one pair of enantiomers (l and d) of the amino-acid-based amphiphile N-stearoyl-threonine. The monolayer characteristics were studied by pressure–area isotherm measurements and grazing incidence X-ray diffraction (GIXD) over a wide range of mixing ratios defined by the d-enantiomer mole fraction x(D). While the isotherms provide insights into thermodynamical aspects, such as transition pressure, compression/decompression hysteresis, and preferential homo- and heterochiral interactions, GIXD reveals the molecular structural arrangements on the Ångström scale. Dominant heterochiral interactions in the racemic mixture lead to compound formation and the appearance of a nonchiral rectangular lattice, although the pure enantiomers form a chiral oblique lattice. Miscibility was found to be limited to mixtures with 0.27 ≲ x(D) ≲ 0.73, as well as to both outer edges (x(D) ≲ 0.08 and x(D) ≳ 0.92). Beyond this range, coexistence of oblique and rectangular lattices occurs, as is clearly seen in the GIXD patterns. Based on the results, a complete phase diagram with two eutectic points at x(D) ≈ 0.25 and x(D) ≈ 0.75 is proposed. Moreover, N-stearoyl-threonine was found to have a strong tendency to form a hydrogen-bonding network between the headgroups, which promotes superlattice formation. American Chemical Society 2022-10-09 2022-10-18 /pmc/articles/PMC9583611/ /pubmed/36209408 http://dx.doi.org/10.1021/acs.langmuir.2c01936 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Mukhina, Tetiana
Richter, Lars
Vollhardt, Dieter
Brezesinski, Gerald
Schneck, Emanuel
The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title_full The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title_fullStr The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title_full_unstemmed The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title_short The Complete Phase Diagram of Monolayers of Enantiomeric N-Stearoyl-threonine Mixtures with Preferred Heterochiral Interactions
title_sort complete phase diagram of monolayers of enantiomeric n-stearoyl-threonine mixtures with preferred heterochiral interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583611/
https://www.ncbi.nlm.nih.gov/pubmed/36209408
http://dx.doi.org/10.1021/acs.langmuir.2c01936
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