A Chiral Metal—Organic Framework Prepared on Large-Scale for Sensitive and Enantioselective Fluorescence Recognition

MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s...

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Published inMolecules (Basel, Switzerland) Vol. 28; no. 12; p. 4593
Main Authors Zhang, Xin-Mei, Bai, Yan-Mei, Ai, Lu-Lu, Wu, Fang-Hui, Shan, Wei-Long, Kang, Yan-Shang, Luo, Li, Chen, Kai, Xu, Fan
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 07.06.2023
MDPI
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ISSN1420-3049
1420-3049
DOI10.3390/molecules28124593

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Abstract MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s-L)](NO3)2 (MOF-1), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF-1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF-1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
AbstractList MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s-L)](NO3)2 (MOF-1), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF-1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF-1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd( s - L )](NO 3 ) 2 (MOF- 1 ), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF- 1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF- 1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s-L)](NO3)2 (MOF-1), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF-1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF-1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s-L)](NO3)2 (MOF-1), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF-1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF-1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd(s-L)](NO[sub.3])[sub.2] (MOF-1), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF-1 has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF-1 exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity, and fast response in the last decades. Herein, this work describes the bulk preparation of a novel luminescent homochiral MOF, namely, [Cd( - )](NO ) (MOF- ), from an enantiopure pyridyl-functionalized ligand with rigid binaphthol skeleton under mild synthetic condition. Except for the features of porosity and crystallinity, the MOF- has also been characterized with water-stability, luminescence, and homochirality. Most important, the MOF- exhibits highly sensitive molecular recognition toward the4-nitrobenzoic acid (NBC) and moderate enantioselective detection of proline, arginine, and 1-phenylethanol.
Audience Academic
Author Kang, Yan-Shang
Wu, Fang-Hui
Zhang, Xin-Mei
Xu, Fan
Luo, Li
Chen, Kai
Bai, Yan-Mei
Ai, Lu-Lu
Shan, Wei-Long
AuthorAffiliation 2 School of Chemistry and Life Sciences, Suzhou University of Science and Technology, Suzhou 215009, China
3 Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, Nanjing University of Information Science & Technology, Nanjing 210044, China; catqchen@163.com
4 SJTU SMSE—Mingguang Joint Research Center for Advanced Palygoskite Materials, Mingguang Mingyao Attapulgite Industry Technology Co., Ltd., Chuzhou 239400, China; xufan921222@163.com
1 School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002, China; zxm13295603905@163.com (X.-M.Z.); bym1101074898@163.com (Y.-M.B.); a8156162496158@163.com (L.-L.A.); wfhwfh@ahut.edu.cn (F.-H.W.); wlshan@ahut.edu.cn (W.-L.S.)
AuthorAffiliation_xml – name: 2 School of Chemistry and Life Sciences, Suzhou University of Science and Technology, Suzhou 215009, China
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– name: 1 School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002, China; zxm13295603905@163.com (X.-M.Z.); bym1101074898@163.com (Y.-M.B.); a8156162496158@163.com (L.-L.A.); wfhwfh@ahut.edu.cn (F.-H.W.); wlshan@ahut.edu.cn (W.-L.S.)
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CitedBy_id crossref_primary_10_1016_j_microc_2024_110974
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Cites_doi 10.1039/b806203j
10.1016/j.ica.2020.119926
10.1002/slct.201701741
10.1039/D2TC04016F
10.1016/j.ccr.2021.214061
10.1039/D1CC06872E
10.1039/C5CC06453H
10.1021/acs.chemrev.9b00648
10.1021/acs.chemrev.1c00740
10.1039/C8DT04091E
10.1021/cr5005524
10.1039/C5SC03839A
10.1021/jacs.6b11422
10.1021/ja212132r
10.1039/C9TA07022B
10.1039/C6CS00930A
10.1021/jacs.2c06680
10.1039/D0DT04276E
10.1021/ja302110d
10.1016/S0040-4020(01)00482-3
10.1002/anie.202104111
10.1021/acs.inorgchem.8b01903
10.1002/cplu.201600137
10.1007/s10895-016-1893-1
10.1002/anie.201406501
10.1039/D0DT03049J
10.1039/C4CS00003J
10.1016/j.dyepig.2020.108741
10.1021/acs.inorgchem.8b03001
10.1002/chem.201304606
10.1016/j.ccr.2021.213793
10.1039/D0CS00955E
10.1039/C9CS00778D
10.1021/acs.inorgchem.0c00307
10.1039/C8NJ06549G
10.1021/acssuschemeng.8b04429
10.1039/D0AN01225D
10.1021/acsami.8b19815
10.1039/C8DT04558E
10.1039/C8CC06274A
10.1016/j.poly.2020.114639
10.1039/D0CS01463J
10.1016/j.inoche.2018.09.029
10.1002/asia.202100039
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Issue 12
Keywords enantioselectivity
chiral recognition
luminescence
chiral metal-organic framework
amino acid
Language English
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References Thoonen (ref_7) 2021; 16
Chandrasekhar (ref_29) 2016; 7
Kursunlu (ref_10) 2016; 26
Mukhopadhyay (ref_25) 2020; 59
Lee (ref_8) 2022; 10
Dong (ref_33) 2014; 20
Dong (ref_11) 2019; 7
Zhao (ref_13) 2021; 50
Jiao (ref_30) 2021; 60
Li (ref_16) 2019; 11
Zhao (ref_27) 2019; 58
Mukherjee (ref_42) 2019; 7
Gong (ref_35) 2022; 122
Wang (ref_32) 2019; 48
Crassous (ref_6) 2009; 38
Lu (ref_23) 2014; 43
Wanderley (ref_37) 2012; 134
Morohashi (ref_44) 2001; 57
Karmakar (ref_38) 2020; 187
Xin (ref_41) 2018; 97
Lin (ref_15) 2015; 51
Xu (ref_24) 2019; 48
Wang (ref_26) 2021; 50
Huang (ref_20) 2021; 50
Xuan (ref_36) 2012; 134
Nanjan (ref_12) 2021; 435
Karmakar (ref_39) 2019; 43
Kalidindi (ref_22) 2015; 54
Thoonen (ref_31) 2022; 58
Alizada (ref_9) 2021; 184
Umapathi (ref_3) 2021; 446
Dong (ref_34) 2017; 139
Gao (ref_1) 2021; 50
You (ref_2) 2015; 115
Xu (ref_4) 2018; 57
Yu (ref_5) 2020; 145
Qiao (ref_43) 2022; 144
Gomez (ref_14) 2020; 513
Chen (ref_21) 2020; 120
Dasgupta (ref_40) 2017; 2
Yi (ref_17) 2016; 81
Li (ref_19) 2020; 49
Zhang (ref_28) 2018; 54
Lustig (ref_18) 2017; 46
References_xml – volume: 38
  start-page: 830
  year: 2009
  ident: ref_6
  article-title: Chiral transfer in coordination complexes: Towards molecular materials
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b806203j
– volume: 513
  start-page: 119926
  year: 2020
  ident: ref_14
  article-title: Photofunctional metal-organic framework thin films for sensing, catalysis and device fabrication
  publication-title: Inorg. Chim. Acta
  doi: 10.1016/j.ica.2020.119926
– volume: 2
  start-page: 1
  year: 2017
  ident: ref_40
  article-title: A Comparative Study on “Turn-off” Fluorimetric Nitro Aromatic Detection Using a Class of Dinulear Zinc (II) Schiff Base Complexes
  publication-title: ChemistrySelect
  doi: 10.1002/slct.201701741
– volume: 10
  start-page: 17127
  year: 2022
  ident: ref_8
  article-title: Chiral coordination compounds with exceptional enantioselectivity
  publication-title: J. Mater. Chem. C
  doi: 10.1039/D2TC04016F
– volume: 446
  start-page: 214061
  year: 2021
  ident: ref_3
  article-title: Colorimetric based on-site sensing strategies for the rapid detection of pesticides in agricultural foods: New horizons, perspectives, and challenges
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2021.214061
– volume: 58
  start-page: 4512
  year: 2022
  ident: ref_31
  article-title: A chiral binaphthyl-based coordination polymer as an enantioselective fluorescence sensor
  publication-title: Chem.Commun.
  doi: 10.1039/D1CC06872E
– volume: 51
  start-page: 16996
  year: 2015
  ident: ref_15
  article-title: Pre-Concentration and energy transfer enable the efficient luminescence sensing of transition metal ions by metal-organic frameworks
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC06453H
– volume: 120
  start-page: 8039
  year: 2020
  ident: ref_21
  article-title: Reticular chemistry 3.2: Typical minimal edge-transitive derived and related nets for the design and synthesis of metal-organic frameworks
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.9b00648
– volume: 122
  start-page: 9078
  year: 2022
  ident: ref_35
  article-title: Chiral metal-organic frameworks
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.1c00740
– volume: 48
  start-page: 602
  year: 2019
  ident: ref_32
  article-title: A pillared-layer strategy to construct water-stable Zn-organic frameworks for iodine capture and luminescence sensing of Fe3+
  publication-title: Dalton Trans.
  doi: 10.1039/C8DT04091E
– volume: 115
  start-page: 7840
  year: 2015
  ident: ref_2
  article-title: Recent advances in supramolecular analytical chemistry using optical sensing
  publication-title: Chem. Rev.
  doi: 10.1021/cr5005524
– volume: 7
  start-page: 3085
  year: 2016
  ident: ref_29
  article-title: Remarkably selective and enantio differentiating sensing of histidine by a fluorescent homochiral Zn-MOF based on pyrene-tetralactic acid
  publication-title: Chem. Sci.
  doi: 10.1039/C5SC03839A
– volume: 139
  start-page: 1554
  year: 2017
  ident: ref_34
  article-title: Chiral NH-controlled supra molecular metallacycles
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b11422
– volume: 134
  start-page: 6904
  year: 2012
  ident: ref_36
  article-title: A chiral quadruple-stranded helicate cage for enantioselective recognition and separation
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja212132r
– volume: 7
  start-page: 22744
  year: 2019
  ident: ref_11
  article-title: Photoluminescent metal-organic frameworks and their application for sensing biomolecules
  publication-title: J. Mater. Chem. A
  doi: 10.1039/C9TA07022B
– volume: 46
  start-page: 3242
  year: 2017
  ident: ref_18
  article-title: Metal-organic frameworks: Functional luminescent and photonic materials for sensing applications
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C6CS00930A
– volume: 144
  start-page: 17054
  year: 2022
  ident: ref_43
  article-title: Unique Fluorescence Turn-On and Turn-Off−On Responses to Acids by a Carbazole-Based Metal−Organic Framework and Theoretical Studies
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.2c06680
– volume: 50
  start-page: 3429
  year: 2021
  ident: ref_20
  article-title: Luminescent metal-organic frameworks as chemical sensors based on “mechanism-response”: A review
  publication-title: Dalton Trans.
  doi: 10.1039/D0DT04276E
– volume: 134
  start-page: 9050
  year: 2012
  ident: ref_37
  article-title: A chiral porous metal-organic framework for highly sensitive and enantioselective fluorescence sensing of amino alcohols
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja302110d
– volume: 57
  start-page: 5557
  year: 2001
  ident: ref_44
  article-title: Selective oxidation of thiacalix[4]arenes to the sulfinyl and sulfonyl counterparts and their complexation abilities toward metal ions as studied by solvent extraction
  publication-title: Tetrahedron
  doi: 10.1016/S0040-4020(01)00482-3
– volume: 60
  start-page: 16568
  year: 2021
  ident: ref_30
  article-title: Fine-tuning of chiral microenvironments within triple-stranded helicates for enhanced enantioselectivity
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.202104111
– volume: 57
  start-page: 13330
  year: 2018
  ident: ref_4
  article-title: A novel magnesium metal-organic framework as a multiresponsive luminescent sensor for Fe(III) ions, pesticides, and antibiotics with high selectivity and sensitivity
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.8b01903
– volume: 81
  start-page: 675
  year: 2016
  ident: ref_17
  article-title: Chemical sensors based on metal-organic frameworks
  publication-title: Chempluschem
  doi: 10.1002/cplu.201600137
– volume: 26
  start-page: 1997
  year: 2016
  ident: ref_10
  article-title: Cu(II) chemo sensor based on a fluorogenic bodipy-salophen combination: Sensitivity and selectivtity studies
  publication-title: J. Fluoresc.
  doi: 10.1007/s10895-016-1893-1
– volume: 54
  start-page: 221
  year: 2015
  ident: ref_22
  article-title: Chemical and structural stability of zirconium-based metal-organic frameworks with large three-dimensional pores by linker engineering
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201406501
– volume: 50
  start-page: 3816
  year: 2021
  ident: ref_26
  article-title: A water-stable multi-responsive luminescent Zn-MOF sensor for detecting TNP, NZF and Cr2O72− in aqueous media
  publication-title: Dalton Trans.
  doi: 10.1039/D0DT03049J
– volume: 43
  start-page: 5561
  year: 2014
  ident: ref_23
  article-title: Tuning the structure and function of metal-organic frameworks via linker design
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C4CS00003J
– volume: 184
  start-page: 108741
  year: 2021
  ident: ref_9
  article-title: Ion sensing of sister sensors based-on calix[4]arene in aqueous medium and their bioimaging applications
  publication-title: Dyes. Pigment.
  doi: 10.1016/j.dyepig.2020.108741
– volume: 58
  start-page: 2444
  year: 2019
  ident: ref_27
  article-title: 8-Hydroxyquinolinate-based metal-organic frameworks: Synthesis, tunable luminescent properties, and highly sensitive detection of small molecules and metal ions
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.8b03001
– volume: 20
  start-page: 6455
  year: 2014
  ident: ref_33
  article-title: A highly fluorescent metallosalalen-based chiral cage for enantioselective recognition and sensing
  publication-title: Chem. Eur. J.
  doi: 10.1002/chem.201304606
– volume: 435
  start-page: 213793
  year: 2021
  ident: ref_12
  article-title: Recent advances in luminescent metal-organic frameworks (LMOFs) based fluorescent sensors for antibiotics
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2021.213793
– volume: 50
  start-page: 4484
  year: 2021
  ident: ref_13
  article-title: Metal-organic frameworks as photo luminescent biosensing platforms: Mechanisms and applications
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/D0CS00955E
– volume: 49
  start-page: 6364
  year: 2020
  ident: ref_19
  article-title: Functional metal-organic frameworks as effective sensors of gases and volatile compounds
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00778D
– volume: 59
  start-page: 6202
  year: 2020
  ident: ref_25
  article-title: Temperature-dependent emission and turn-off fluorescence sensing of hazardous “Quat” herbicides in water by a Zn-MOF based on a semi-rigid dibenzochrysenetetra acetic acid linker
  publication-title: Inorg. Chem.
  doi: 10.1021/acs.inorgchem.0c00307
– volume: 43
  start-page: 4432
  year: 2019
  ident: ref_39
  article-title: penta-nuclear zinc(II) complex with a reduced Schiff base ligand: Assessment of its ability to sense nitroaromatics
  publication-title: New J. Chem.
  doi: 10.1039/C8NJ06549G
– volume: 7
  start-page: 819
  year: 2019
  ident: ref_42
  article-title: Green Synthesis of Self Assembled Nanospherical Dysprosium MOFs: Selective and Efficient Detection of Picric Acid in Aqueous and Gas Phase
  publication-title: ACS Sustain. Chem. Eng.
  doi: 10.1021/acssuschemeng.8b04429
– volume: 145
  start-page: 6769
  year: 2020
  ident: ref_5
  article-title: Recent advances of BINOL-based sensors for enantioselective fluorescence recognition
  publication-title: Analyst
  doi: 10.1039/D0AN01225D
– volume: 11
  start-page: 8227
  year: 2019
  ident: ref_16
  article-title: Facile fabrication of a multifunctional metal-organic framework-based sensor exhibiting exclusive solvochromic behaviors toward ketone molecules
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.8b19815
– volume: 48
  start-page: 2683
  year: 2019
  ident: ref_24
  article-title: A carbazole-functionalized metal-organic framework for efficient detection of antibiotics, pesticides and nitroaromatic compounds
  publication-title: Dalton Trans.
  doi: 10.1039/C8DT04558E
– volume: 54
  start-page: 10901
  year: 2018
  ident: ref_28
  article-title: A water-stable homochiral luminescent MOF constructed from an achiral acylamide-containing dicarboxylate ligand for enantioselective sensing of penicillamine
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC06274A
– volume: 187
  start-page: 114639
  year: 2020
  ident: ref_38
  article-title: Synthesis, structure and nitroaromatic sensing ability of a trinuclear zinc complex with a reduced Schiff base ligand: Assessment of the ability of the ligand to sense zinc ion
  publication-title: Polyhedron
  doi: 10.1016/j.poly.2020.114639
– volume: 50
  start-page: 5564
  year: 2021
  ident: ref_1
  article-title: Recent advances in persistent luminescence based on molecular hybrid materials
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/D0CS01463J
– volume: 97
  start-page: 129
  year: 2018
  ident: ref_41
  article-title: A luminescent barium-based metal-organic framework: Synthesis, structure and efficient detection of 4-nitrobenzoic acid
  publication-title: Inorg. Chem. Commun.
  doi: 10.1016/j.inoche.2018.09.029
– volume: 16
  start-page: 890
  year: 2021
  ident: ref_7
  article-title: Chiral detection with coordination polymers
  publication-title: Chem.-Asian J.
  doi: 10.1002/asia.202100039
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Snippet MOF-based luminescent sensors have garnered considerable attention due to their potential in recognition and discrimination with high sensitivity, selectivity,...
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SubjectTerms amino acid
Aqueous solutions
chiral metal-organic framework
chiral recognition
Communication
enantioselectivity
Fluorescence
Ligands
luminescence
Pollutants
Single crystals
Solvents
Spectrum analysis
Water pollution
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Title A Chiral Metal—Organic Framework Prepared on Large-Scale for Sensitive and Enantioselective Fluorescence Recognition
URI https://www.ncbi.nlm.nih.gov/pubmed/37375148
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https://doaj.org/article/4e70e69d597a496ea552ef2eed669f79
Volume 28
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