Enantiomer Recognition by the Difference in Adsorption Rates on the Surfaces of Chiral Crystals
ABSTRACT The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this...
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Published in | Chirality (New York, N.Y.) Vol. 36; no. 9; pp. e23717 - n/a |
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Abstract | ABSTRACT
The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ‐glycine and NiSO4•6H2O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ‐glycine crystals and 2.12 for NiSO4•6H2O crystals. Even if no differences in adsorption were observed under adsorption–desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing.
A nontrivial phenomenon was discovered: enantioselectivity of menthol enantiomer adsorption on the surfaces of NiSO4•6H2O and γ‐glycine was determined both by differences in thermodynamics and by the different adsorption rates. Even in the absence of enantioselectivity in equilibrium state, the non‐equal rates of enantiomer adsorption have observed. |
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AbstractList | The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ‐glycine and NiSO
4
•6H
2
O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ‐glycine crystals and 2.12 for NiSO
4
•6H
2
O crystals. Even if no differences in adsorption were observed under adsorption–desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing. The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ-glycine and NiSO •6H O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ-glycine crystals and 2.12 for NiSO •6H O crystals. Even if no differences in adsorption were observed under adsorption-desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing. ABSTRACT The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ‐glycine and NiSO4•6H2O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ‐glycine crystals and 2.12 for NiSO4•6H2O crystals. Even if no differences in adsorption were observed under adsorption–desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing. A nontrivial phenomenon was discovered: enantioselectivity of menthol enantiomer adsorption on the surfaces of NiSO4•6H2O and γ‐glycine was determined both by differences in thermodynamics and by the different adsorption rates. Even in the absence of enantioselectivity in equilibrium state, the non‐equal rates of enantiomer adsorption have observed. The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ‐glycine and NiSO4•6H2O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ‐glycine crystals and 2.12 for NiSO4•6H2O crystals. Even if no differences in adsorption were observed under adsorption–desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing. The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ-glycine and NiSO4•6H2O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ-glycine crystals and 2.12 for NiSO4•6H2O crystals. Even if no differences in adsorption were observed under adsorption-desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing.The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can be recognized by the adsorption on surfaces with SMC. However, the mechanisms of such chiral recognition are still unknown. In this work, the adsorption kinetics of menthol test enantiomers on the surfaces of γ-glycine and NiSO4•6H2O chiral crystals was studied. It was found that the difference in adsorption was observed in nonequilibrium state more often than in equilibrium. If the enantioselectivity in equilibrium state was observed, the enantioselectivity coefficient α at nonequilibrium conditions was higher. The maximum α in nonequilibrium state was 2.44 for γ-glycine crystals and 2.12 for NiSO4•6H2O crystals. Even if no differences in adsorption were observed under adsorption-desorption equilibrium conditions, a significant enantioselectivity at nonequilibrium conditions was found. This has proved the possibility of chiral recognition on surfaces with SMC by the differences in adsorption rates. Such novel chiral recognition mechanism can provide enhanced enantioselectivity in adsorption, catalysis, chromatographic separation, and chemical sensing. |
Author | Guskov, Vladimir Ermolaeva, Ekaterina Zinoviev, Ilya Zhang, Zhi‐hui Belonogov, Eduard |
Author_xml | – sequence: 1 givenname: Eduard orcidid: 0000-0002-1053-5565 surname: Belonogov fullname: Belonogov, Eduard organization: Ufa University of Science and Technology – sequence: 2 givenname: Ekaterina surname: Ermolaeva fullname: Ermolaeva, Ekaterina organization: Ufa University of Science and Technology – sequence: 3 givenname: Ilya surname: Zinoviev fullname: Zinoviev, Ilya organization: Ufa University of Science and Technology – sequence: 4 givenname: Zhi‐hui surname: Zhang fullname: Zhang, Zhi‐hui organization: Changzhou University – sequence: 5 givenname: Vladimir orcidid: 0000-0003-4814-5180 surname: Guskov fullname: Guskov, Vladimir email: guscov@mail.ru organization: Ufa University of Science and Technology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39262297$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1002/jssc.201600808 10.1016/j.jphotochemrev.2006.11.002 10.1002/ange.200462963 10.1039/D2CP01212J 10.1007/BF01732291 10.1002/cphc.201300321 10.1007/978-4-431-55555-1_20 10.1002/ijch.201100066 10.1002/anie.196906082 10.1039/D1CP01265G 10.1039/D3SC00359K 10.1002/chem.202000126 10.1080/10610278.2018.1489541 10.1103/PhysRevLett.94.065504 10.1021/cr500671p 10.1039/D0CP02827D 10.1002/anie.200703634 10.3390/sym15020498 10.1016/j.jcis.2015.02.053 10.1002/chir.23617 10.1023/B:SCIE.0000013305.99473.cf 10.1039/C9ME00146H 10.1002/cphc.202200685 10.1002/anie.201407223 10.1038/310161a0 10.1002/anie.201303915 10.1016/j.chroma.2012.08.049 10.1002/anie.200803578 10.1002/cphc.201000658 10.1002/cphc.200900938 10.1134/S1061934818100027 10.1039/C3SM52322E 10.1039/D0NJ03912H 10.1021/ja993128t |
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The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital.... The chirality of biopolymers remains one of the mysteries of Life. For such objects, the phenomenon of supramolecular chirality (SMC) is vital. Enantiomers can... |
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SubjectTerms | Adsorption Biopolymers Catalysis Chemical perception Chemoreception chiral crystal Chirality Crystals Enantiomers enantioselectivity Equilibrium Equilibrium conditions Glycine kinetic curve Menthol Nonequilibrium conditions Object recognition supramolecular chirality |
Title | Enantiomer Recognition by the Difference in Adsorption Rates on the Surfaces of Chiral Crystals |
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