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...

Full description

Saved in:
Bibliographic Details
Published inChirality (New York, N.Y.) Vol. 36; no. 9; pp. e23717 - n/a
Main Authors Belonogov, Eduard, Ermolaeva, Ekaterina, Zinoviev, Ilya, Zhang, Zhi‐hui, Guskov, Vladimir
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.09.2024
Subjects
Online AccessGet full text

Cover

Loading…
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.
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
BookMark eNp90UFLHTEQAOBQlPq0vfQHlEAvRVidTbLJ7lG2VgVBeLbQW8hmJzWyL_ua7CLv3zfr04uUniZDvhmGmWNyEMaAhHwq4awEYOf2wcczxlWp3pFVWTEoJJe_DsgK6qYpAAQ7IscpPQJAI7l4T454wyRjjVoRfRlMmPy4wUjXaMffwecs0G5Hpwek37xzGDFYpD7Qiz6Ncfv8vzYTJpofi7qfozN2yR1t8zBmoG3cpckM6QM5dDngx5d4Qn5-v_zRXhe3d1c37cVtYXmlVNFVvWt43xlrgAlVQy9dzQxyIXvZY91LYbtMGg6OoXJgDRO8YpUyRilT8hPydd93G8c_M6ZJb3yyOAwm4DgnzUvgQtSyUZl-eUMfxzmGPN2iRJ1JtajPL2ruNtjrbfQbE3f6dXUZwB7YOKYU0WnrJ7MsZ4rGD7oEvVxHL9fRz9fJJadvSl67_hOXe_zkB9z9R-r2-ma9r_kLq7GfdA
CitedBy_id crossref_primary_10_1021_acs_langmuir_4c04695
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
ContentType Journal Article
Copyright 2024 Wiley Periodicals LLC.
2024 Wiley Periodicals LLC
Copyright_xml – notice: 2024 Wiley Periodicals LLC.
– notice: 2024 Wiley Periodicals LLC
DBID AAYXX
CITATION
NPM
7QO
7QR
7U7
8FD
C1K
FR3
P64
7X8
DOI 10.1002/chir.23717
DatabaseName CrossRef
PubMed
Biotechnology Research Abstracts
Chemoreception Abstracts
Toxicology Abstracts
Technology Research Database
Environmental Sciences and Pollution Management
Engineering Research Database
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitle CrossRef
PubMed
Biotechnology Research Abstracts
Technology Research Database
Toxicology Abstracts
Chemoreception Abstracts
Engineering Research Database
Biotechnology and BioEngineering Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList CrossRef
PubMed

Biotechnology Research Abstracts
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
Chemistry
EISSN 1520-636X
EndPage n/a
ExternalDocumentID 39262297
10_1002_chir_23717
CHIR23717
Genre article
Journal Article
GrantInformation_xml – fundername: Russian Science Foundation
  funderid: 19‐73‐10079
– fundername: Russian Science Foundation
  grantid: 19-73-10079
GroupedDBID ---
.3N
.GA
.GJ
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
29B
31~
33P
3SF
3WU
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
6J9
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AAHQN
AAMNL
AANHP
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABDBF
ABEML
ABIJN
ABOCM
ABPVW
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACIWK
ACPOU
ACPRK
ACRPL
ACSCC
ACUHS
ACXBN
ACXQS
ACYXJ
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AI.
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AUFTA
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BTSUX
BY8
CS3
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DRFUL
DRSTM
DU5
EBD
EBS
EJD
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M21
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2W
P2X
P4D
PALCI
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RWI
RWK
RX1
RYL
SAMSI
SUPJJ
TUS
UB1
UPT
V2E
V8K
VH1
W8V
W99
WBFHL
WBKPD
WIB
WIH
WIK
WJL
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XV2
YCJ
ZZTAW
~02
~IA
~WT
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
NPM
7QO
7QR
7U7
8FD
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
C1K
FR3
P64
7X8
ID FETCH-LOGICAL-c3577-b5df93dbaca024780d6f82ae346d6de8d64cbdf9930f2e7f0ca2435257aa77a13
IEDL.DBID DR2
ISSN 0899-0042
1520-636X
IngestDate Thu Jul 10 18:42:11 EDT 2025
Fri Jul 25 10:21:07 EDT 2025
Wed Feb 19 02:02:55 EST 2025
Tue Jul 01 02:50:55 EDT 2025
Thu Apr 24 23:10:48 EDT 2025
Wed Jan 22 17:16:39 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 9
Keywords enantioselectivity
adsorption
kinetic curve
chiral crystal
supramolecular chirality
Language English
License 2024 Wiley Periodicals LLC.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3577-b5df93dbaca024780d6f82ae346d6de8d64cbdf9930f2e7f0ca2435257aa77a13
Notes Funding
This work was supported by the Russian Science Foundation (Project No. 19‐73‐10079).
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0003-4814-5180
0000-0002-1053-5565
PMID 39262297
PQID 3104897357
PQPubID 986330
PageCount 7
ParticipantIDs proquest_miscellaneous_3103448697
proquest_journals_3104897357
pubmed_primary_39262297
crossref_citationtrail_10_1002_chir_23717
crossref_primary_10_1002_chir_23717
wiley_primary_10_1002_chir_23717_CHIR23717
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate September 2024
2024-09-00
2024-Sep
20240901
PublicationDateYYYYMMDD 2024-09-01
PublicationDate_xml – month: 09
  year: 2024
  text: September 2024
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Chichester
PublicationTitle Chirality (New York, N.Y.)
PublicationTitleAlternate Chirality
PublicationYear 2024
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2017; 40
2010; 11
2023; 14
2021; 23
2023; 15
2012; 1269
2005; 117
2006; 7
1999; 121
2022; 24
2015; 448
2004; 1
2024; 36
2009; 48
1969; 8
2020; 5
2023; 24
2013; 14
2023; 23
2015; 115
2023
1984; 310
2011; 51
2013; 52
2008; 47
2020; 26
2018; 30
2015
2018; 73
2020; 22
2020; 44
2005; 94
1975; 6
2014; 10
2014; 53
e_1_2_7_6_1
e_1_2_7_5_1
e_1_2_7_4_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_8_1
e_1_2_7_7_1
e_1_2_7_19_1
e_1_2_7_18_1
e_1_2_7_17_1
e_1_2_7_16_1
e_1_2_7_2_1
e_1_2_7_15_1
e_1_2_7_14_1
e_1_2_7_13_1
e_1_2_7_12_1
e_1_2_7_11_1
e_1_2_7_10_1
e_1_2_7_26_1
e_1_2_7_27_1
e_1_2_7_28_1
e_1_2_7_29_1
Belonogov E. V. (e_1_2_7_34_1) 2023; 23
e_1_2_7_30_1
e_1_2_7_25_1
e_1_2_7_31_1
e_1_2_7_24_1
e_1_2_7_23_1
e_1_2_7_33_1
e_1_2_7_22_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_20_1
e_1_2_7_36_1
e_1_2_7_37_1
Sparks D. L. (e_1_2_7_32_1) 2023
References_xml – volume: 52
  start-page: 10545
  year: 2013
  end-page: 10548
  article-title: Enantiomer‐Specific Oriented Attachment: Formation of Macroscopic Homochiral Crystal Aggregates From a Racemic System
  publication-title: Angewandte Chemie
– volume: 11
  start-page: 1446
  issue: 7
  year: 2010
  end-page: 1451
  article-title: Supramolecular Organization and Chiral Resolution of p‐Terphenyl‐m‐Dicarbonitrile on the Ag(111) Surface
  publication-title: ChemPhysChem
– volume: 24
  issue: 3
  year: 2023
  article-title: Chirality Transfer From an Innately Chiral Nanocrystal Core to a Nematic Liquid Crystal 2: Lyotropic Chromonic Liquid Crystals
  publication-title: ChemPhysChem
– volume: 1269
  start-page: 52
  year: 2012
  end-page: 68
  article-title: Recent Development of Cyclodextrin Chiral Stationary Phases and Their Applications in Chromatography
  publication-title: Journal of Chromatography A
– volume: 14
  start-page: 4480
  year: 2023
  end-page: 4484
  article-title: Chirally and Chemically Reversible Strecker Reaction
  publication-title: Chemical Science
– volume: 40
  start-page: 124
  issue: 1
  year: 2017
  end-page: 137
  article-title: Recent Progress of Chiral Stationary Phases for Separation of Enantiomers in gas Chromatography
  publication-title: Journal of Separation Science
– volume: 22
  start-page: 16571
  year: 2020
  end-page: 16578
  article-title: Theoretical Investigation of Amino‐Acid Adsorption on Hydroxylated Quartz Surfaces: Dispersion Can Determine Enantioselectivity
  publication-title: Physical Chemistry Chemical Physics
– volume: 53
  start-page: 13424
  year: 2014
  end-page: 13428
  article-title: Macroscopic Chirality of Supramolecular Gels Formed From Achiral Tris (Ethyl Cinnamate) Benzene‐1,3,5‐Tricarboxamides
  publication-title: Angewandte Chemie International Edition
– volume: 47
  start-page: 496
  year: 2008
  end-page: 499
  article-title: Achiral Nucleobase Cytosine Acts as an Origin of Homochirality of Biomolecules in Conjunction With Asymmetric Autocatalysis
  publication-title: Angewandte Chemie
– start-page: 393
  year: 2015
  end-page: 420
– volume: 310
  start-page: 161
  year: 1984
  end-page: 164
  article-title: Spontaneous Generation and Amplification of Optical Activity in α‐Amino Acids by Enantioselective Occlusion Into Centrosymmetric Crystals of Glycine
  publication-title: Nature
– volume: 30
  start-page: 940
  issue: 11
  year: 2018
  end-page: 948
  article-title: Chiral Recognition Capabilities of Melamine and Cyanuric Acid Supramolecular Structures
  publication-title: Supramolecular Chemistry
– volume: 15
  start-page: 498
  year: 2023
  end-page: 512
  article-title: Manifestation of Supramolecular Chirality During Adsorption on CsCuCl and γ‐Glycine Crystals
  publication-title: Symmetry
– volume: 117
  start-page: 2834
  year: 2005
  end-page: 2837
  article-title: Asymmetric Amplification Using Chiral Cocrystals Formed From Achiral Organic Molecules by Asymmetric Autocatalysis
  publication-title: Angewandte Chemie
– volume: 5
  start-page: 376
  year: 2020
  end-page: 384
  article-title: Engineering Porous Two‐Dimensional Lattices via Self‐Assembly of Non‐convex Hexagonal Platelets
  publication-title: Molecular Systems Design and Engineering
– volume: 48
  start-page: 314
  year: 2009
  end-page: 317
  article-title: Heteroatom‐Stabilized Chiral Framework of Aluminophosphate Molecular Sieves
  publication-title: Angewandte Chemie, International Edition
– volume: 23
  start-page: 11968
  year: 2021
  end-page: 11979
  article-title: Mechanism of Chiral Recognition by Enantiomorphous Cytosine Crystals During Enantiomer Adsorption
  publication-title: Physical Chemistry Chemical Physics
– volume: 448
  start-page: 437
  year: 2015
  end-page: 450
  article-title: The Range of Validity of Sorption Kinetic Models
  publication-title: Journal of Colloid and Interface Science
– volume: 23
  start-page: 657
  issue: 4
  year: 2023
  end-page: 666
  article-title: Kinetic Features of the Adsorption of Menthol Enantiomers on o‐Toluylic Acid and CsCuCl3 Crystals With Supramolecular Chirality
  publication-title: Sorbtsionnye i Khromatograficheskie Protsessy
– volume: 24
  start-page: 26785
  year: 2022
  end-page: 26794
  article-title: Possibility of Chiral Recognition by Adsorption on Enantiomorphous Crystals: The Impact of Crystal Surface Polarity
  publication-title: Physical Chemistry Chemical Physics
– start-page: 305
  year: 2023
  end-page: 348
– volume: 44
  start-page: 17769
  year: 2020
  end-page: 17779
  article-title: Supramolecular Chiral Surface of Nickel Sulfate Hexahydrate Crystals and Its Ability to Chirally Recognize Enantiomers by Adsorption Data
  publication-title: New Journal of Chemistry
– volume: 7
  start-page: 183
  year: 2006
  end-page: 196
  article-title: Spontaneous Chiral Crystallization of Achiral Materials and Absolute Asymmetric Photochemical Transformation Using the Chiral Crystalline Environment
  publication-title: Journal of Photochemistry and Photobiology C: Photochemistry Reviews
– volume: 10
  start-page: 44
  year: 2014
  end-page: 47
  article-title: Supramolecular Chirality Induced by a Weak Thermal Force
  publication-title: Soft Matter
– volume: 115
  start-page: 7304
  issue: 15
  year: 2015
  end-page: 7397
  article-title: Supramolecular Chirality in Self‐Assembled Systems
  publication-title: Chemical Reviews
– volume: 73
  start-page: 937
  issue: 10
  year: 2018
  end-page: 945
  article-title: New Chiral Stationary Phases: Preparation, Properties and Applications in gas Chromatography
  publication-title: Journal of Analytical Chemistry
– volume: 36
  year: 2024
  article-title: Achiral 2‐Pyridone and 4‐Aminopyridine act as Chiral Inducers of Asymmetric Autocatalysis With Amplification of Enantiomeric Excess via the Formation of Chiral Crystals
  publication-title: Chirality
– volume: 51
  start-page: 1017
  year: 2011
  end-page: 1033
  article-title: Achiral Organic, Inorganic, and Metal Crystals as Auxiliaries for Asymmetric Transformations
  publication-title: Israel Journal of Chemistry
– volume: 26
  start-page: 3515
  year: 2020
  end-page: 3518
  article-title: Long‐Range Chiral Induction by a Fully Noncovalent Approach in Supramolecular Porphyrin–Calixarene Assemblies
  publication-title: Chemistry ‐ A European Journal
– volume: 11
  start-page: 3511
  issue: 16
  year: 2010
  end-page: 3516
  article-title: Emergence of Supramolecular Chirality by Flows
  publication-title: ChemPhysChem
– volume: 121
  start-page: 11235
  year: 1999
  end-page: 11236
  article-title: d‐ and l‐Quartz‐Promoted Highly Enantioselective Synthesis of a Chiral Organic Compound
  publication-title: Journal of the American Chemical Society
– volume: 14
  start-page: 3294
  issue: 14
  year: 2013
  end-page: 3302
  article-title: Onset of Chiral Adenine Surface Growth
  publication-title: ChemPhysChem
– volume: 94
  year: 2005
  article-title: Chiral Symmetry Breaking During Crystallization: Complete Chiral Purity Induced by Nonlinear Autocatalysis and Recycling
  publication-title: Physical Review Letters
– volume: 6
  start-page: 99
  year: 1975
  end-page: 115
  article-title: Crystallization and Solid‐State Reaction as a Route to Asymmetric Synthesis From Achiral Starting Materials
  publication-title: Journal of Molecular Evolution
– volume: 1
  start-page: 171
  issue: 59
  year: 2004
  end-page: 177
  article-title: Citation Review of Lagergren Kinetic Rate Equation on Adsorption Reactions
  publication-title: Scientometrics
– volume: 8
  start-page: 608
  issue: 8
  year: 1969
  end-page: 609
  article-title: Reactions in Chiral Crystals: An Absolute Asymmetric Synthesis
  publication-title: Angewandte Chemie, International Edition
– ident: e_1_2_7_35_1
  doi: 10.1002/jssc.201600808
– ident: e_1_2_7_20_1
  doi: 10.1016/j.jphotochemrev.2006.11.002
– ident: e_1_2_7_24_1
  doi: 10.1002/ange.200462963
– ident: e_1_2_7_28_1
  doi: 10.1039/D2CP01212J
– ident: e_1_2_7_6_1
  doi: 10.1007/BF01732291
– ident: e_1_2_7_16_1
  doi: 10.1002/cphc.201300321
– ident: e_1_2_7_2_1
  doi: 10.1007/978-4-431-55555-1_20
– ident: e_1_2_7_7_1
  doi: 10.1002/ijch.201100066
– ident: e_1_2_7_19_1
  doi: 10.1002/anie.196906082
– ident: e_1_2_7_27_1
  doi: 10.1039/D1CP01265G
– ident: e_1_2_7_21_1
  doi: 10.1039/D3SC00359K
– ident: e_1_2_7_8_1
  doi: 10.1002/chem.202000126
– ident: e_1_2_7_4_1
  doi: 10.1080/10610278.2018.1489541
– ident: e_1_2_7_17_1
  doi: 10.1103/PhysRevLett.94.065504
– ident: e_1_2_7_3_1
  doi: 10.1021/cr500671p
– ident: e_1_2_7_12_1
  doi: 10.1039/D0CP02827D
– ident: e_1_2_7_23_1
  doi: 10.1002/anie.200703634
– ident: e_1_2_7_33_1
  doi: 10.3390/sym15020498
– ident: e_1_2_7_31_1
  doi: 10.1016/j.jcis.2015.02.053
– ident: e_1_2_7_25_1
  doi: 10.1002/chir.23617
– ident: e_1_2_7_30_1
  doi: 10.1023/B:SCIE.0000013305.99473.cf
– ident: e_1_2_7_5_1
  doi: 10.1039/C9ME00146H
– ident: e_1_2_7_10_1
  doi: 10.1002/cphc.202200685
– start-page: 305
  volume-title: Kinetics of Soil Chemical Processes. Environmental Soil Chemistry
  year: 2023
  ident: e_1_2_7_32_1
– ident: e_1_2_7_14_1
  doi: 10.1002/anie.201407223
– ident: e_1_2_7_18_1
  doi: 10.1038/310161a0
– ident: e_1_2_7_29_1
  doi: 10.1002/anie.201303915
– ident: e_1_2_7_37_1
  doi: 10.1016/j.chroma.2012.08.049
– ident: e_1_2_7_9_1
  doi: 10.1002/anie.200803578
– volume: 23
  start-page: 657
  issue: 4
  year: 2023
  ident: e_1_2_7_34_1
  article-title: Kinetic Features of the Adsorption of Menthol Enantiomers on o‐Toluylic Acid and CsCuCl3 Crystals With Supramolecular Chirality
  publication-title: Sorbtsionnye i Khromatograficheskie Protsessy
– ident: e_1_2_7_15_1
  doi: 10.1002/cphc.201000658
– ident: e_1_2_7_11_1
  doi: 10.1002/cphc.200900938
– ident: e_1_2_7_36_1
  doi: 10.1134/S1061934818100027
– ident: e_1_2_7_13_1
  doi: 10.1039/C3SM52322E
– ident: e_1_2_7_26_1
  doi: 10.1039/D0NJ03912H
– ident: e_1_2_7_22_1
  doi: 10.1021/ja993128t
SSID ssj0009634
Score 2.3973212
Snippet ABSTRACT 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...
SourceID proquest
pubmed
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e23717
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchir.23717
https://www.ncbi.nlm.nih.gov/pubmed/39262297
https://www.proquest.com/docview/3104897357
https://www.proquest.com/docview/3103448697
Volume 36
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3di9QwEB-Oe9EXP-78WD0loggK3WuTbNOCL0u9YxX0YfXgXqRMPsodnq10dx_Wv95J-rGciqBvgUxJOplJfkkmvwF4kcQuNomeRYYLF0m0GGGVp5EymOaKI0-1v9H98DFdnMn357PzPXgzvIXp-CHGAzfvGWG-9g6OenW8Iw01F5ftlAvajtAE7IO1PCJa7rijyLICd1Tmn9mTaY7cpPx49-n11eg3iHkdsYYl5_Q2fBk620WafJ1u1npqfvzC4_i_f3MHbvVYlM0747kLe64-gMN5Tfvwb1v2koXo0HDsfgA3iiEz3CGUJz56xr_bb9lyCEBqaqa3jOAke9vnXDGOXdZsbldNG-YltvS4llHBS33atJUPB2NNxQrqFnWkaLeEVa9W9-Ds9ORzsYj6RA2RETOlIj2zVS6sRoO05KsstmmVcXRCpja1LrOpNJpEchFX3KkqNshl4GFFVAoTcR_266Z2D4FlwsYoMTdJkktuFWZa2lzH1lQELhM7gVfDgJWmZzH3yTSuyo5_mZdek2XQ5ASej7LfO-6OP0odDeNe9v67Kgn0yixX9HcTeDZWk5r9dQrWrtkEGUGbWzLpCTzo7GVsRngaRu5rXodR_0v7ZbF4twylR_8i_BhuclJ2F-52BPvrduOeED5a66fBD34CTWAMFA
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELagHMqFRwtloS1GICSQsk1sb5wcV2mrLbQ9LK3Um-VXREVJUHb3sPx6ZpxsVi0ICW6WPJGd8Yz92R5_Q8i7JPaxTcwosoz7SGinI13maSStTnPJNEsN3uienaeTS_HpanTVxebgW5iWH6I_cEPPCPM1OjgeSB-sWUPt1-tmyDjsR-6TB5jSO-yopmv2KLCtwB6V4UN7MM6enZQdrL-9vR79BjJvY9aw6Bw_bjOrzgJXIcaafBsu5mZof95hcvzv_3lCHnVwlI5b-3lK7vlqi2yPK9iKf1_S9zQEiIaT9y2yWaySw20TdYQBNPh0v6HTVQxSXVGzpIAo6WGXdsV6el3RsZvVTZia6BShLYUCSn1ZNCVGhNG6pAV0CzpSNEuAqzezZ-Ty-OiimERdrobI8pGUkRm5MufOaKth1ZdZ7NIyY9pzkbrU-cylwhoQyXlcMi_L2GomAhWr1lLqhD8nG1Vd-ReEZtzFWujcJkkumJM6M8LlJna2BHyZuAH5sBoxZTsic8yncaNaCmamUJMqaHJA3vayP1r6jj9K7a4GXnUuPFOAe0WWS_i7AXnTV4Oa8UZFV75eBBkO-1uw6gHZaQ2mb4YjEyPDmo9h2P_SviomJ9NQevkvwq_J5uTi7FSdnpx_fkUeMlB8G_22SzbmzcLvAVyam_3gFL8A_PAQLw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3daxQxEB9qBfXFj1btadWIIijsdTfJbXbBl2Ovx9WPIqeFvsiSr8XSulv27h7Ov95J9uOoiqBvgcyS7GQm-SWZ_AbgZRTaUEdqFGjKbMClkYEs0jgQWsapoJLGyt3ofjyOZyf83enodAvedm9hGn6I_sDNeYafr52DX5riYEMaqr-d1UPKcDtyDa7zOEycTU_mG_IoNC1PHpW4d_Zomz05KT3YfHt1OfoNY16FrH7Nmd6Br11vm1CT8-FqqYb6xy9Ejv_7O3fhdgtGybixnnuwZcsd2B2XuBH_viaviA8P9efuO3Az61LD7UJ-6MJn3MP9msy7CKSqJGpNEE-SSZt0RVtyVpKxWVS1n5jI3AFbggUn9XlVFy4ejFQFybBb2JGsXiNYvVjch5Pp4ZdsFrSZGgLNRkIEamSKlBkltcQ1XyShiYuESst4bGJjExNzrVAkZWFBrShCLSn3RKxSCiEj9gC2y6q0e0ASZkLJZaqjKOXUCJkoblIVGl0guozMAF53A5brlsbcZdO4yBsCZpo7TeZekwN40cteNuQdf5Ta78Y9bx14kSPq5Ukq8O8G8LyvRjW7-xRZ2mrlZRjubtGmB_CwsZe-GeZ4GKmreeNH_S_t59nsaO5Lj_5F-Bnc-DSZ5h-Ojt8_hlsU9d6Evu3D9rJe2SeIlZbqqXeJn-EqDuc
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Enantiomer+Recognition+by+the+Difference+in+Adsorption+Rates+on+the+Surfaces+of+Chiral+Crystals&rft.jtitle=Chirality+%28New+York%2C+N.Y.%29&rft.au=Belonogov%2C+Eduard&rft.au=Ermolaeva%2C+Ekaterina&rft.au=Zinoviev%2C+Ilya&rft.au=Zhang%2C+Zhi-Hui&rft.date=2024-09-01&rft.eissn=1520-636X&rft.volume=36&rft.issue=9&rft.spage=e23717&rft_id=info:doi/10.1002%2Fchir.23717&rft_id=info%3Apmid%2F39262297&rft.externalDocID=39262297
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0899-0042&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0899-0042&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0899-0042&client=summon