[1] Shen J,Okamoto Y.Efficient separation of enantiomers using stereoregular chiral polymers.Chemical Reviews,2015,116(8):1094-1138.
[2] Kotelnikova E,Isakov A,Kryuchkova L,et al.Acids with chiral molecules as essential organic compounds of biogenic-abiogenic systems[J].Processes and Phenomena on the Boundary Between Biogenic and Abiogenic Nature,2020,10(6):69-72.
[3] Navarrosanchez J,Argentegarcia A,Molinermartinez Y,et al.Peptide metal-organic frameworks for enantioselective separation of chiral drugs[J].Journal of the American Chemical Society,2017,139(12):4294-4297.
[4] Gu L,Chen Q,Li X,et al.Amino acid modified carbon nanotubes with optimal pore size for chiral separation[J].Molecular Simulation,2019,45(13):1051-1057.
[5] Gao B,Li Y,Cui K,et al.Molecularly imprinted membrane with innovative structure and high performance for chiral separation of amino acids[J].International Journal of Polymeric Materials,2018,67(8):517-527.
[6] Zang Y,Qu Y,Aoki T.Simultaneous improvement of permeability and selectivity in enantioselective permeation through solid chiral membranes from a newly synthesized one-handed helical polyphenylacetylene with aldehyde pendant groups by enantioselective reaction[J].Polymer,2019,171(34):45-49.
[7] Yuan L M,Ma W,Xu M,et al.Optical resolution and mechanism using enantioselective cellulose,sodium alginate and hydroxypropyl-β-cyclodextrin membranes[J].Chirality,2017,29(5):315-324.
[8] Amarajothi D,Zhaohui L,Hermenegildo G.Catalysis and photocatalysis by metal organic frameworks[J].Chemical Society Reviews,2018,47(10):62-65.
[9] Kashani T,Jahanshahi M,Rahimpour A,et al.Nanopore molecularly imprinted polymer membranes for environmental usage:selective separation of 2,4-dichlorophenoxyacetic acid as a toxic herbicide from water[J].Polymer-Plastics Technology and Engineering,2016,55(16):1700-1712.
[10] Gao B,Cui K,Li Y,et al.Preparation of molecule imprinted membrane of single enantiomer of amino acid with an innovative strategy and study on its chiral recognition and resolution properties[J].Journal of Chemical Technology & Biotechnology,2017,92(7):1566-1576.
[11] Zhang J,Lu H,Lu H,et al.Porous bimetallic Mo-W oxide nanofibers fabricated by electrospinning with enhanced acetone sensing performances[J].Journal of Alloys and Compounds,2019,779(13):531-542.
[12] Xiong C,Li B,Lin X,et al.The recent progress on three-dimensional porous graphene-based hybrid structure for supercapacitor[J].Composites Part B-Engineering,2019,165(4):10-46.
[13] Roy S,Bandyopadhyay A,Das M,et al.Redox-active and semi-conducting donor-acceptor conjugated microporous polymers as metal-free ORR catalysts[J].Journal of Materials Chemistry,2018,6(14):5587-5591.
[14] Yulia F,Zulys A,Ruliandini R.Metal-organic framework based chromium terephthalate (MIL-101 Cr) growth for carbon dioxide capture:a review[J].Journal of Advanced Research in Fluid Mechanics and Thermal Sciences,2019,57(4):158-174.
[15] Liu Z,Yang X,Lu B,et al.Delicate topotactic conversion of coordination polymers to Pd porous nanosheets for high-efficiency electrocatalysis[J].Applied Catalysis B-Environmental,2019,243(12):86-93.
[16] Chaoui N,Trunk M,Dawson R,et al.Trends and challenges for microporous polymers[J].Chemical Society Reviews,2017,46(6):3302-3321.
[17] Ji X,Yao Y,Li J,et al.A Supramolecular cross-linked conjugated polymer network for multiple fluorescent sensing[J].Journal of the American Chemical Society,2013,135(1):74-77.
[18] Fuoco A,Rizzuto C,Tocci E,et al.The origin of size-selective gas transport through polymers of intrinsic microporosity[J].Journal of Materials Chemistry A,2019,7(36):20121-20126.
[19] Jansen J C,Esposito E,Fuoco A,et al.Microporous organic polymers:synthesis,aharacterization,and applications[J].Polymers,2019,11(54):844-847.
[20] Wang H,Zeng Z,Xu P,et al.Recent progress in covalent organic framework thin films:fabrications,applications and perspectives[J].Chemical Society Reviews,2019,48(28):488-516.
[21] Wei J,Zhang X,Zhao Y,et al.Chiral conjugated microporous polymers as novel chiral fluorescence sensors for amino alcohols[J].Macromolecular Chemistry & Physics,2013,214(19):2232-2238.
[22] Li C,Liu Y,Li J,et al.Conjugated microporous polymers with chiral BINAP ligand built-in as efficient catalysts for asymmetric hydrogenation[J].Catalysis Science & Technology,2015,23(6):45-47.
[23] Huang H,Miao Q,Kang Y,et al.Synthesis and fluorescent properties of a chiral conjugated polymer based on (S)-2,2′-binaphtho-20-crown-6[J].Bulletin of the Chemical Society of Japan,2008,23(4):22-25.
[24] Kokado Kenta,Tokoro Yuichiro,Chujo Yoshiki.Luminescent and axially chiral π-conjugated polymers linked by carboranes in the main chain[J].Macromolecules,2009,45(6):444-446.
[25] Wang L,Zhou J,Lan Y,et al.Divergent synthesis of chiral covalent organic frameworks[J].Angewandte Chemie,2019,58(28):9443-9447.
[26] Ma H C,Zhao C C,Chen G J,et al.Photothermal conversion triggered thermal asymmetric catalysis within metal nanoparticles loaded homochiral covalent organic framework[J].Nature Communications,2019,10(1):3368-3370.
[27] Fang L,Qian H,Cheng Y,et al.Room-temperature preparation of a chiral covalent organic framework for the selective adsorption of amino acid enantiomers[J].RSC Advances,2010,65(6):121-124.
[28] Wang X,Han X,Jie Z,et al.Homochiral 2D porous covalent organic frameworks for heterogeneous asymmetric catalysis[J].Journal of the American Chemical Society,2016,23(5):164-166.
[29] Xu H,Chen X,Gao J,et al.Catalytic covalent organic frameworks via pore surface engineering[J].Chemical Communications,2014,50(11):1292-1294.
[30] Xu S,Wang Y,Li W,et al.Covalent organic framework incorporated chiral polymer monoliths for capillary electrochromatography[J].Journal of Chromatography A,2019,1602:481-488.
[31] Chen X,Qiao Z,Hou B,et al.Chiral metal-organic frameworks with tunable catalytic selectivity in asymmetric transfer hydrogenation reactions[J].Nano Research,2020,23(4):34-36.
[32] Guo J,Zhang Y,Zhu Y,et al.Ultrathin chiral metal-organic-framework nanosheets for efficient enantioselective separation[J].Angewandte Chemie International Edition,2018,57(23):6873-6877.
[33] Das S,Xu S,Ben T,et al.Chiral recognition and separation by chirality-enriched metal-organic frameworks[J].Angewandte Chemie,2018,130(28):8765-8769.
[34] Zhang J,Chen S,Wu T,et al.Homochiral crystallization of microporous framework materials from achiral precursors by chiral catalysis[J].Journal of the American Chemical Society,2016,130(39):12882-12883.
[35] Zhang S Y,Li D,Guo D,et al.Synthesis of a chiral crystal form of MOF-5,CMOF-5,by chiral induction[J].Journal of the American Chemical Society,2015,137(49):15406-15409.
[36] Bai J,Zhang W,Ma X,et al.Synthesis of novel hyper-cross-linked chiral porous polymers and their applications in enantioselective adsorption of amino acids[J].Microporous and Mesoporous Materials,2019,65(1):23-25.
[37] Kenta K,Yuichiro T,Yoshiki C.Luminescent and axially chiral π-conjugated polymers linked by carboranes in the main chain[J].Macromolecules,2009,13(4):12-15.
[38] Bai J,Zhang W,Ma X,et al.Synthesis of novel hyper-cross-linked chiral porous polymers and their applications in enantioselective adsorption of amino acids[J].Microporous and Mesoporous Materials,2020,10(9):111-114.
[39] Ma L,Wanderley M M,Lin W,et al.Highly porous cross-linked polymers for catalytic asymmetric diethylzinc addition to aldehydes[J].ACS Catalysis,2011,1(7):691-697.
[40] Liu Y,Li P,Xie L,et al.β-cyclodextrin modified silica nanochannel membrane for chiral separation[J].Journal of Membrane Science,2014,453(12):12-17.
[41] Shiomi K,Yoshikawa M.Multi-stage chiral separation with electrospun chitin nanofiber membranes[J].Separation and Purification Technology,2013,65(1):300-304.
[42] Kashani T,Jahanshahi M,Rahimpour A,et al.Nano pore molecularly imprinted polymer membranes for environmental usage:selective separation of 2,4-dichlorophenoxyacetic acid as a toxic herbicide from water[J].Polymer-Plastics Technology and Engineering,2016,65(3):19-23.
[43] Gao B,Cui K,Li Y,et al.Preparation of molecule imprinted membrane of single enantiomer of amino acid with an innovative strategy and study on its chiral recognition and resolution properties[J].Journal of Chemical Technology & Biotechnology,2017,92(7):1566-1576.
[44] Wang W J,Dong X L,Nan J P,et al.A homochiral metal-organic framework membrane for enantioselective separation[J].Chemical Communications,2012,48(56):7022-7024.
[45] Gu Z G,Grosjean S,Brse S,et al.Enantioselective adsorption in homochiral metal-organic frameworks:the pore size influence[J].Chemical Communications,2015,51(7):19-23.
[46] Seo J S,Whang D,Lee H,et al.A homochiral metal-organic porous material for enantioselective separation and catalysis[J].Nature,2000,404(6781):982-986.
[47] Kang Z,Xue M,Fan L,et al.‘Single nickel source’ in situ fabrication of a stable homochiral MOF membrane with chiral resolution properties[J].Chemical Communications,2013,49(90):10569-10571.
[48] Huang K,Dong X,Ren R,et al.Fabrication of homochiral metal-organic framework membrane for enantioseparation of racemic Diols[J].Aiche Journal,2013,59(11):65-68.
[49] Guo J,Zhang Y,Zhu Y,et al.Ultrathin chiral metal-organic-framework nanosheets for efficient enantioselective separation[J].Angewandte Chemie International Edition,2018,56(3):25-28.
[50] Lu Y,Zhang H,Chan J Y,et al.Homochiral mOF-polymer mixed matrix membranes for efficient separation of chiral molecules[J].Angewandte Chemie,2019,131(47):69-72.
[51] Chan J Y,Zhang H,Nolvachai Y.Incorporation of homochirality into zeolitic imidazole framework membrane for efficient chiral separation[J].Angewandte Chemie International Edition,2018,57(6):96-100.
[52] Gu Z,Fu W,Liu M,et al.Surface-Mounted MOF templated fabrication of homochiral polymer thin film for enantioselective adsorption of drug[J].Chemical Communications,2017,53(9):1470-1473.
[53] Weng X,Baez J E,Khiterer M,et al.Chiral polymers of intrinsic microporosity:selective membrane permeation of enantiomers[J].Angewandte Chemie,2015,54(38):11214-11218.
