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Mendeleev Communications, 2015, Volume 25, Issue 1, Pages 72–74
DOI: https://doi.org/10.1016/j.mencom.2015.01.027
(Mi mendc2306)
 

This article is cited in 6 scientific papers (total in 6 papers)

Communications

Self-organization and chirality in the high dilution solutions of glycoluril enantiomers with (R)- and (S)-methionine moieties

I. S. Ryzhkinaa, Yu. V. Kiselevaa, L. I. Murtazinaa, O. A. Mishinaa, A. P. Timoshevaa, S. Yu. Sergeevaa, V. V. Baranovb, A. N. Kravchenkob, A. I. Konovalova

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The high dilution (1×10-15–1×10-5 mol dm-3) solutions of glycolurils containing an (S)-methionine moiety are capable of space-time self-organization to give nanoassociates, unlike the solutions of glycolurils with an (R)-methionine moiety. The formation of supra- molecular domains in the solutions at concentrations of 1×10-3–1×10-2 mol dm-3 is responsible for a transition from molecular to supramolecular chirality.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (528.5 Kb)


Citation: I. S. Ryzhkina, Yu. V. Kiseleva, L. I. Murtazina, O. A. Mishina, A. P. Timosheva, S. Yu. Sergeeva, V. V. Baranov, A. N. Kravchenko, A. I. Konovalov, “Self-organization and chirality in the high dilution solutions of glycoluril enantiomers with (R)- and (S)-methionine moieties”, Mendeleev Commun., 25:1 (2015), 72–74
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  • https://www.mathnet.ru/eng/mendc/v25/i1/p72
  • This publication is cited in the following 6 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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