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Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation

1 : 1 mixtures of aminomethylenehelicene (P)-tetramer and (M)-pentamer with terminal C(16) alkyl groups in fluorobenzene showed structural changes between hetero-double-helices B and C and random-coils 2A. Figure-eight thermal hysteresis appeared when the solution was cooled and heated at a constant...

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Detalles Bibliográficos
Autores principales: Sawato, Tsukasa, Iwamoto, Rina, Yamaguchi, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157274/
https://www.ncbi.nlm.nih.gov/pubmed/34122836
http://dx.doi.org/10.1039/c9sc06496f
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author Sawato, Tsukasa
Iwamoto, Rina
Yamaguchi, Masahiko
author_facet Sawato, Tsukasa
Iwamoto, Rina
Yamaguchi, Masahiko
author_sort Sawato, Tsukasa
collection PubMed
description 1 : 1 mixtures of aminomethylenehelicene (P)-tetramer and (M)-pentamer with terminal C(16) alkyl groups in fluorobenzene showed structural changes between hetero-double-helices B and C and random-coils 2A. Figure-eight thermal hysteresis appeared when the solution was cooled and heated at a constant rate and involved the crossing of cooling and heating curves in Δε/temperature profiles. This unusual thermal hysteresis emerged in the intermediate state between counterclockwise and clockwise thermal hystereses. This phenomenon arose from the competition between self-catalytic reactions to form B and C from 2A. Significant effects of terminal C(16) alkyl groups on the thermodynamic and kinetic phenomena are also described.
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spelling pubmed-81572742021-06-11 Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation Sawato, Tsukasa Iwamoto, Rina Yamaguchi, Masahiko Chem Sci Chemistry 1 : 1 mixtures of aminomethylenehelicene (P)-tetramer and (M)-pentamer with terminal C(16) alkyl groups in fluorobenzene showed structural changes between hetero-double-helices B and C and random-coils 2A. Figure-eight thermal hysteresis appeared when the solution was cooled and heated at a constant rate and involved the crossing of cooling and heating curves in Δε/temperature profiles. This unusual thermal hysteresis emerged in the intermediate state between counterclockwise and clockwise thermal hystereses. This phenomenon arose from the competition between self-catalytic reactions to form B and C from 2A. Significant effects of terminal C(16) alkyl groups on the thermodynamic and kinetic phenomena are also described. The Royal Society of Chemistry 2020-02-26 /pmc/articles/PMC8157274/ /pubmed/34122836 http://dx.doi.org/10.1039/c9sc06496f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Sawato, Tsukasa
Iwamoto, Rina
Yamaguchi, Masahiko
Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title_full Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title_fullStr Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title_full_unstemmed Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title_short Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C(16) alkyl groups during hetero-double-helix formation
title_sort figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal c(16) alkyl groups during hetero-double-helix formation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157274/
https://www.ncbi.nlm.nih.gov/pubmed/34122836
http://dx.doi.org/10.1039/c9sc06496f
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