Constructing Crystalline Covalent Organic Frameworks from Chiral Building Blocks
Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality...
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Published in | Journal of the American Chemical Society Vol. 138; no. 36; pp. 11489 - 11492 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
14.09.2016
Amer Chemical Soc |
Subjects | |
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Abstract | Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality. We report herein a facile strategy for the direct construction of chiral-functionalized COFs from chiral building blocks. The key design is to use the rigid scaffold 4,4′-(1H-benzo[d]imidazole-4,7-diyl)dianiline (2) for attaching a variety of chiral moieties. As a first example, the chiral pyrrolidine-embedded building block (S)-4,4′-(2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole-4,7-diyl)dianiline (3) was accordingly synthesized and applied for the successful construction of two chiral COFs, LZU-72 and LZU-76. Our experimental results further showed that these chiral COFs are structurally robust and highly active as heterogeneous organocatalysts. |
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AbstractList | Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality. We report herein a facile strategy for the direct construction of chiral-functionalized COFs from chiral building blocks. The key design is to use the rigid scaffold 4,4′-(1H-benzo[d]imidazole-4,7-diyl)dianiline (2) for attaching a variety of chiral moieties. As a first example, the chiral pyrrolidine-embedded building block (S)-4,4′-(2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole-4,7-diyl)dianiline (3) was accordingly synthesized and applied for the successful construction of two chiral COFs, LZU-72 and LZU-76. Our experimental results further showed that these chiral COFs are structurally robust and highly active as heterogeneous organocatalysts. Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality. We report herein a facile strategy for the direct construction of chiral-functionalized COFs from chiral building blocks. The key design is to use the rigid scaffold 4,4′-(1H-benzo[d]imidazole-4,7-diyl)dianiline (2) for attaching a variety of chiral moieties. As a first example, the chiral pyrrolidine-embedded building block (S)-4,4′-(2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole-4,7-diyl)dianiline (3) was accordingly synthesized and applied for the successful construction of two chiral COFs, LZU-72 and LZU-76. Our experimental results further showed that these chiral COFs are structurally robust and highly active as heterogeneous organocatalysts. Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality. We report herein a facile strategy for the direct construction of chiral-functionalized COFs from chiral building blocks. The key design is to use the rigid scaffold 4,4'-(1H-benzo[d]imidazole-4,7-diyl)dianiline (2) for attaching a variety of chiral moieties. As a first example, the chiral pyrrolidine-embedded building block (S)-4,4'-(2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole-4,7-diyl)dianiline (3) was accordingly synthesized and applied for the successful construction of two chiral COFs, LZU-72 and LZU-76. Our experimental results further showed that these chiral COFs are structurally robust and highly active as heterogeneous organocatalysts.Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks. Construction of functional COFs is, however, a difficult task because it has to meet simultaneously the requirements for crystallinity and functionality. We report herein a facile strategy for the direct construction of chiral-functionalized COFs from chiral building blocks. The key design is to use the rigid scaffold 4,4'-(1H-benzo[d]imidazole-4,7-diyl)dianiline (2) for attaching a variety of chiral moieties. As a first example, the chiral pyrrolidine-embedded building block (S)-4,4'-(2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole-4,7-diyl)dianiline (3) was accordingly synthesized and applied for the successful construction of two chiral COFs, LZU-72 and LZU-76. Our experimental results further showed that these chiral COFs are structurally robust and highly active as heterogeneous organocatalysts. |
Author | An, Wan-Kai Wu, Han Xu, Hai-Sen Wang, Wei Ding, San-Yuan |
AuthorAffiliation | Lanzhou University Collaborative Innovation Center of Chemical Science and Engineering State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering |
AuthorAffiliation_xml | – name: State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering – name: Lanzhou University – name: Collaborative Innovation Center of Chemical Science and Engineering |
Author_xml | – sequence: 1 givenname: Hai-Sen surname: Xu fullname: Xu, Hai-Sen – sequence: 2 givenname: San-Yuan surname: Ding fullname: Ding, San-Yuan email: dingsy@lzu.edu.cn – sequence: 3 givenname: Wan-Kai surname: An fullname: An, Wan-Kai – sequence: 4 givenname: Han surname: Wu fullname: Wu, Han – sequence: 5 givenname: Wei surname: Wang fullname: Wang, Wei email: wang_wei@lzu.edu.cn |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27585120$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1002/anie.200803405 10.1039/C5CC10221A 10.1021/ja212132r 10.1039/b804136a 10.1002/anie.201004736 10.1002/anie.200705710 10.1007/978-3-642-14613-8 10.1021/ja109069k 10.1039/C3CC48813F 10.1039/C3CC47652A 10.1021/cr2003147 10.1002/anie.201206438 10.1021/jacs.5b10708 10.1038/ncomms5503 10.1039/C0CS00002G 10.1002/anie.201504934 10.1039/b800704g 10.1021/jacs.5b09487 10.1002/anie.201109072 10.1021/ja502212v 10.1038/nchem.2444 10.1021/acs.chemrev.5b00317 10.1021/jacs.6b00652 10.1039/C4SC02305F 10.1021/acs.accounts.5b00369 10.1021/ol802766u 10.1126/science.1120411 10.1039/9781782622611 10.1021/ma071453s 10.1039/B920113K 10.1038/ncomms9508 10.1021/jacs.5b02034 10.1039/c2cs35157a 10.1002/anie.201310500 10.1038/nchem.628 10.1021/jacs.5b10754 10.1021/ja305367j 10.1039/C2CS35222B 10.1039/C2CS35072F 10.1021/ja308278w 10.1021/ar400243m 10.1038/ncomms10487 10.1021/cr800200t 10.1021/ja101208s 10.1021/ja057395c 10.1021/ja310640b 10.1021/ja8096256 10.1126/science.aac8343 10.1002/9783527619566 10.1021/ja405088c 10.1021/jacs.5b07529 10.1021/ja409421d 10.1021/cs200131g 10.1038/nchem.1628 10.1021/ja204728y 10.1021/jacs.5b05327 10.1021/ja4129795 10.1002/anie.200504212 10.1002/chem.201403002 10.1021/ja206242v 10.1039/C5CC04680G 10.1002/chem.201200753 10.1021/ja5092936 10.1038/nchem.2352 10.1021/cr200440z 10.1126/science.aaa8075 10.1002/adma.201000197 10.1002/asia.201402682 10.1021/ja510926w 10.1021/cr500671p 10.1002/anie.200503075 10.1002/ejoc.200600664 10.1021/jacs.5b13490 10.1021/ja202223d 10.1021/jacs.6b04204 10.1038/nchem.738 10.1021/ja302110d 10.1039/c2cs35072f 10.1039/b920113k 10.1039/c3cc48813f 10.1039/c0cs00002g 10.1039/c4sc02305f 10.1039/c5cc04680g 10.1038/NCHEM.2352 10.1039/c5cc10221a 10.1038/NCHEM.738 10.1038/NCHEM.628 10.1007/128_2009_21 10.1039/c3cc47652a 10.1038/NCHEM.2444 10.1039/c2cs35222b |
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References | ref9/cit9 ref17/cit17b ref17/cit17c ref17/cit17d ref17/cit17a ref2/cit2g ref2/cit2f ref2/cit2e ref2/cit2d ref13/cit13a ref2/cit2k ref13/cit13b ref2/cit2j ref13/cit13c ref13/cit13d ref2/cit2h ref13/cit13e ref2/cit2c ref2/cit2b ref2/cit2a ref20/cit20 ref5/cit5b ref5/cit5a ref21/cit21 ref3/cit3b ref22/cit22a ref3/cit3c ref11/cit11b ref3/cit3a Schröder M. (ref2/cit2i) 2010 ref3/cit3f Mahrwald R. (ref23/cit23) 2004 ref3/cit3g ref3/cit3d ref11/cit11a ref3/cit3e ref22/cit22b ref7/cit7b ref7/cit7a ref19/cit19a Hofmann K. (ref16/cit16a) 1953; 6 ref19/cit19b Preedy V. R. (ref16/cit16b) 2015 ref8/cit8a ref10/cit10a ref10/cit10b ref8/cit8b ref18/cit18d ref18/cit18e ref18/cit18b ref4/cit4a ref18/cit18c ref4/cit4b ref4/cit4c ref18/cit18a ref14/cit14a ref12/cit12 ref14/cit14c ref14/cit14b ref15/cit15 ref14/cit14e ref14/cit14d ref14/cit14g ref14/cit14f ref14/cit14i Eliel E. L. (ref1/cit1) 1994 ref14/cit14h ref14/cit14k ref14/cit14j ref14/cit14m ref14/cit14l ref14/cit14o ref14/cit14n ref4/cit4d ref4/cit4e ref6/cit6a ref14/cit14p ref6/cit6b ref6/cit6c Ding, SY (WOS:000371945800035) 2016; 138 Cote, AP (WOS:000233437300040) 2005; 310 Ma, LQ (WOS:000282091300016) 2010; 2 Slater, AG (WOS:000355276600037) 2015; 348 An, WK (WOS:000340902800021) 2014; 20 Wu, DC (WOS:000306298800010) 2012; 112 Mahrwald, R (000383410700017.42) 2004 Wu, PY (WOS:000308574800057) 2012; 134 Wang, CA (WOS:000304347600002) 2012; 18 MacLean, MWA (WOS:000346736100005) 2015; 10 Hofmann, K. (000383410700017.23) 1953; 6 Fang, QR (WOS:000332270000006) 2014; 53 Ye, Y (WOS:000361930000011) 2015; 137 Xu, H (WOS:000363468600012) 2015; 7 Zhou, TY (WOS:000344906100020) 2014; 136 Wanderley, MM (WOS:000304837800008) 2012; 134 Shen, J (WOS:000370216000009) 2016; 116 Zeng, YF (WOS:000348690100004) 2015; 137 Du, X (WOS:000274070800038) 2010; 46 Trindade, AF (WOS:000263562900006) 2009; 109 Liu, Y (WOS:000283392000002) 2010; 22 Zhu, YL (WOS:000344376400052) 2014; 5 Liu, MH (WOS:000359613600007) 2015; 115 Waller, PJ (WOS:000366871400008) 2015; 48 Bonnefoy, J (WOS:000358896600035) 2015; 137 Zhang, ZF (WOS:000284202200035) 2010; 132 Lin, S (WOS:000360968400039) 2015; 349 Kuschel, A (WOS:000261484200028) 2008; 47 Van der Voort, P (WOS:000317596100019) 2013; 42 Uribe-Romo, FJ (WOS:000293872800021) 2011; 133 Spitler, EL (WOS:000297606500034) 2011; 133 Lin, XA (WOS:000282018800002) 2010; 293 Fracaroli, AM (WOS:000379794400009) 2016; 138 Li, YH (WOS:000263299000031) 2009; 11 Yoon, M (WOS:000300472300017) 2012; 112 Zhang, B (WOS:000312552900051) 2012; 51 DeBlase, CR (WOS:000327103600020) 2013; 135 Vyas, VS (WOS:000363149200001) 2015; 6 Lun, DJ (WOS:000290358200051) 2011; 133 Kaur, P (WOS:000292479400019) 2011; 1 Eliel, E. L. (000383410700017.14) 1994 Fang, QR (WOS:000340625100006) 2014; 5 Kaushik, M (WOS:000355053100004) 2015; 137 Hoffmann, F (WOS:000237762800003) 2006; 45 Yashima, E (WOS:000252045600002) 2008; 41 Wei, H (WOS:000358228300004) 2015; 51 Lacoste, E (WOS:000243303000019) 2007; 2007 Kuhn, P (WOS:000255489500036) 2008; 47 Qiu, HB (WOS:000287585000008) 2011; 40 Xu, H (WOS:000329469800003) 2014; 50 Uribe-Romo, FJ (WOS:000264806300009) 2009; 131 Gross, E (WOS:000316244200030) 2013; 135 Weng, XL (WOS:000363389400041) 2015; 54 Kandambeth, S (WOS:000311869600007) 2012; 134 Colson, JW (WOS:000319404900007) 2013; 5 Rojas, A (WOS:000323241200051) 2013; 135 Ascherl, L (WOS:000372505500008) 2016; 8 Bass, JD (WOS:000236299700057) 2006; 128 Ding, SY (WOS:000312460600010) 2013; 42 Xuan, WM (WOS:000303139800005) 2012; 134 Smith, BJ (WOS:000371008500023) 2016; 52 Preedy, V. R. (000383410700017.44) 2015 Dang, DB (WOS:000283276800001) 2010; 132 Tanabe, KK (WOS:000285211000033) 2010; 49 Heitbaum, M (WOS:000239284500005) 2006; 45 Kelly, JA (WOS:000334658200011) 2014; 47 Kundu, DS (WOS:000304345800036) 2012; 51 Calik, M (WOS:000369558000026) 2016; 138 Zhu, YL (WOS:000364355900013) 2015; 137 Li, P (WOS:000330018600002) 2014; 136 Yu, JH (WOS:000258737900002) 2008; 18 Chandra, S (WOS:000335720200011) 2014; 136 Feng, X (WOS:000307779600011) 2012; 41 Morris, RE (WOS:000276977300009) 2010; 2 Lin, GQ (WOS:000372477700011) 2016; 138 Gruttadauria, M (WOS:000257839100018) 2008; 37 Ma, HP (WOS:000375889100031) 2016; 138 Song, JR (WOS:000328884500006) 2014; 50 Wu, K (WOS:000371134900001) 2016; 7 |
References_xml | – ident: ref8/cit8a doi: 10.1002/anie.200803405 – ident: ref22/cit22b doi: 10.1039/C5CC10221A – ident: ref5/cit5b doi: 10.1021/ja212132r – ident: ref2/cit2e doi: 10.1039/b804136a – ident: ref18/cit18d doi: 10.1002/anie.201004736 – ident: ref14/cit14p doi: 10.1002/anie.200705710 – volume-title: Functional Metal-Organic Frameworks: Gas Storage, Separation and Catalysis year: 2010 ident: ref2/cit2i doi: 10.1007/978-3-642-14613-8 – ident: ref17/cit17a doi: 10.1021/ja109069k – ident: ref3/cit3f doi: 10.1039/C3CC48813F – ident: ref14/cit14m doi: 10.1039/C3CC47652A – ident: ref3/cit3d doi: 10.1021/cr2003147 – volume: 6 volume-title: Imidazole and its derivatives year: 1953 ident: ref16/cit16a – ident: ref17/cit17d doi: 10.1002/anie.201206438 – ident: ref22/cit22a doi: 10.1021/jacs.5b10708 – ident: ref14/cit14e doi: 10.1038/ncomms5503 – ident: ref2/cit2g doi: 10.1039/C0CS00002G – ident: ref4/cit4c doi: 10.1002/anie.201504934 – ident: ref7/cit7a doi: 10.1039/b800704g – ident: ref14/cit14i doi: 10.1021/jacs.5b09487 – ident: ref3/cit3b doi: 10.1002/anie.201109072 – ident: ref20/cit20 doi: 10.1021/ja502212v – ident: ref14/cit14f doi: 10.1038/nchem.2444 – ident: ref4/cit4a doi: 10.1021/acs.chemrev.5b00317 – ident: ref14/cit14k doi: 10.1021/jacs.6b00652 – ident: ref15/cit15 doi: 10.1039/C4SC02305F – ident: ref13/cit13a doi: 10.1021/acs.accounts.5b00369 – ident: ref17/cit17b doi: 10.1021/ol802766u – ident: ref12/cit12 doi: 10.1126/science.1120411 – volume-title: Imidazole Dipeptides: Chemistry, Analysis, Function and Effects year: 2015 ident: ref16/cit16b doi: 10.1039/9781782622611 – ident: ref2/cit2h doi: 10.1021/ma071453s – ident: ref9/cit9 doi: 10.1039/B920113K – ident: ref14/cit14j doi: 10.1038/ncomms9508 – ident: ref2/cit2d doi: 10.1021/jacs.5b02034 – ident: ref13/cit13c doi: 10.1039/c2cs35157a – ident: ref19/cit19b doi: 10.1002/anie.201310500 – ident: ref2/cit2j doi: 10.1038/nchem.628 – ident: ref14/cit14l doi: 10.1021/jacs.5b10754 – ident: ref18/cit18b doi: 10.1021/ja305367j – ident: ref6/cit6c doi: 10.1039/C2CS35222B – ident: ref13/cit13b doi: 10.1039/C2CS35072F – volume-title: Stereochemistry of Organic Compounds year: 1994 ident: ref1/cit1 – ident: ref14/cit14d doi: 10.1021/ja308278w – ident: ref2/cit2k doi: 10.1021/ar400243m – ident: ref4/cit4e doi: 10.1038/ncomms10487 – ident: ref6/cit6a doi: 10.1021/cr800200t – ident: ref3/cit3c doi: 10.1021/ja101208s – ident: ref18/cit18c doi: 10.1021/ja057395c – ident: ref3/cit3a doi: 10.1021/ja310640b – ident: ref14/cit14a doi: 10.1021/ja8096256 – ident: ref14/cit14c doi: 10.1126/science.aac8343 – volume-title: Modern Aldol Reactions year: 2004 ident: ref23/cit23 doi: 10.1002/9783527619566 – ident: ref2/cit2c doi: 10.1021/ja405088c – ident: ref2/cit2b doi: 10.1021/jacs.5b07529 – ident: ref19/cit19a doi: 10.1021/ja409421d – ident: ref11/cit11b doi: 10.1021/cs200131g – ident: ref13/cit13e doi: 10.1038/nchem.1628 – ident: ref14/cit14b doi: 10.1021/ja204728y – ident: ref3/cit3e doi: 10.1021/jacs.5b05327 – ident: ref4/cit4d doi: 10.1021/ja4129795 – ident: ref6/cit6b doi: 10.1002/anie.200504212 – ident: ref10/cit10b doi: 10.1002/chem.201403002 – ident: ref21/cit21 doi: 10.1021/ja206242v – ident: ref14/cit14n doi: 10.1039/C5CC04680G – ident: ref10/cit10a doi: 10.1002/chem.201200753 – ident: ref14/cit14g doi: 10.1021/ja5092936 – ident: ref3/cit3g doi: 10.1038/nchem.2352 – ident: ref11/cit11a doi: 10.1021/cr200440z – ident: ref13/cit13d doi: 10.1126/science.aaa8075 – ident: ref4/cit4b doi: 10.1002/adma.201000197 – ident: ref2/cit2f doi: 10.1002/asia.201402682 – ident: ref14/cit14h doi: 10.1021/ja510926w – ident: ref2/cit2a doi: 10.1021/cr500671p – ident: ref7/cit7b doi: 10.1002/anie.200503075 – ident: ref17/cit17c doi: 10.1002/ejoc.200600664 – ident: ref14/cit14o doi: 10.1021/jacs.5b13490 – ident: ref18/cit18a doi: 10.1021/ja202223d – ident: ref18/cit18e doi: 10.1021/jacs.6b04204 – ident: ref8/cit8b doi: 10.1038/nchem.738 – ident: ref5/cit5a doi: 10.1021/ja302110d – volume: 128 start-page: 3737 year: 2006 ident: WOS:000236299700057 article-title: Acid-base bifunctional and dielectric outer-sphere effects in heterogeneous catalysis: A comparative investigation of model primary amine catalysts publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja057395c – volume: 42 start-page: 548 year: 2013 ident: WOS:000312460600010 article-title: Covalent organic frameworks (COFs): from design to applications publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c2cs35072f – volume: 115 start-page: 7304 year: 2015 ident: WOS:000359613600007 article-title: Supramolecular Chirality in Self-Assembled Systems publication-title: CHEMICAL REVIEWS doi: 10.1021/cr500671p – volume: 138 start-page: 3031 year: 2016 ident: WOS:000371945800035 article-title: Thioether-Based Fluorescent Covalent Organic Framework for Selective Detection and Facile Removal of Mercury(II) publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b10754 – volume: 46 start-page: 970 year: 2010 ident: WOS:000274070800038 article-title: Troger's base-functionalised organic nanoporous polymer for heterogeneous catalysis publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/b920113k – volume: 138 start-page: 5897 year: 2016 ident: WOS:000375889100031 article-title: Cationic Covalent Organic Frameworks: A Simple Platform of Anionic Exchange for Porosity Tuning and Proton Conduction publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b13490 – volume: 135 start-page: 16821 year: 2013 ident: WOS:000327103600020 article-title: beta-Ketoenamine-Linked Covalent Organic Frameworks Capable of Pseudocapacitive Energy Storage publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja409421d – volume: 51 start-page: 5456 year: 2012 ident: WOS:000304345800036 article-title: A Microporous Binol-Derived Phosphoric Acid publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201109072 – volume: 50 start-page: 1292 year: 2014 ident: WOS:000329469800003 article-title: Catalytic covalent organic frameworks via pore surface engineering publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c3cc48813f – volume: 37 start-page: 1666 year: 2008 ident: WOS:000257839100018 article-title: Supported proline and proline-derivatives as recyclable organocatalysts publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/b800704g – volume: 54 start-page: 11214 year: 2015 ident: WOS:000363389400041 article-title: Chiral Polymers of Intrinsic Microporosity: Selective Membrane Permeation of Enantiomers publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201504934 – volume: 137 start-page: 1020 year: 2015 ident: WOS:000348690100004 article-title: Covalent Organic Frameworks Formed with Two Types of Covalent Bonds Based on Orthogonal Reactions publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja510926w – volume: 112 start-page: 1196 year: 2012 ident: WOS:000300472300017 article-title: Homochiral Metal-Organic Frameworks for Asymmetric Heterogeneous Catalysis publication-title: CHEMICAL REVIEWS doi: 10.1021/cr2003147 – volume: 348 start-page: ARTN aaa8075 year: 2015 ident: WOS:000355276600037 article-title: Function-led design of new porous materials publication-title: SCIENCE doi: 10.1126/science.aaa8075 – volume: 133 start-page: 19416 year: 2011 ident: WOS:000297606500034 article-title: A 2D Covalent Organic Framework with 4.7-nm Pores and Insight into Its Interlayer Stacking publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja206242v – volume: 22 start-page: 4112 year: 2010 ident: WOS:000283392000002 article-title: Engineering Homochiral Metal-Organic Frameworks for Heterogeneous Asymmetric Catalysis and Enantioselective Separation publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201000197 – volume: 5 start-page: 453 year: 2013 ident: WOS:000319404900007 article-title: Rationally synthesized two-dimensional polymers publication-title: NATURE CHEMISTRY doi: 10.1038/nchem.1628 – volume: 40 start-page: 1259 year: 2011 ident: WOS:000287585000008 article-title: Chiral mesoporous silica: Chiral construction and imprinting via cooperative self-assembly of amphiphiles and silica precursors publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c0cs00002g – year: 1994 ident: 000383410700017.14 publication-title: Stereochemistry of Organic Compounds – volume: 137 start-page: 9409 year: 2015 ident: WOS:000358896600035 article-title: Enantiopure Peptide-Functionalized Metal-Organic Frameworks publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b05327 – volume: 5 start-page: ARTN 4503 year: 2014 ident: WOS:000340625100006 article-title: Designed synthesis of large-pore crystalline polyimide covalent organic frameworks publication-title: NATURE COMMUNICATIONS doi: 10.1038/ncomms5503 – volume: 6 start-page: ARTN 8508 year: 2015 ident: WOS:000363149200001 article-title: A tunable azine covalent organic framework platform for visible light-induced hydrogen generation publication-title: NATURE COMMUNICATIONS doi: 10.1038/ncomms9508 – volume: 45 start-page: 4732 year: 2006 ident: WOS:000239284500005 article-title: Asymmetric heterogeneous catalysis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200504212 – volume: 109 start-page: 418 year: 2009 ident: WOS:000263562900006 article-title: Recyclable Stereoselective Catalysts publication-title: CHEMICAL REVIEWS doi: 10.1021/cr800200t – volume: 5 start-page: 4957 year: 2014 ident: WOS:000344376400052 article-title: Reversible tuning of pore size and CO2 adsorption in azobenzene functionalized porous organic polymers publication-title: CHEMICAL SCIENCE doi: 10.1039/c4sc02305f – volume: 48 start-page: 3053 year: 2015 ident: WOS:000366871400008 article-title: Chemistry of Covalent Organic Frameworks publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.5b00369 – volume: 51 start-page: 13159 year: 2012 ident: WOS:000312552900051 article-title: The Synthesis of Chiral Isotetronic Acids with Amphiphilic Imidazole/Pyrrolidine Catalysts Assembled in Oil-in-Water Emulsion Droplets publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201206438 – volume: 135 start-page: 3881 year: 2013 ident: WOS:000316244200030 article-title: Asymmetric Catalysis at the Mesoscale: Gold Nanoclusters Embedded in Chiral Self-Assembled Monolayer as Heterogeneous Catalyst for Asymmetric Reactions publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja310640b – volume: 47 start-page: 1088 year: 2014 ident: WOS:000334658200011 article-title: The Development of Chiral Nematic Mesoporous Materials publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400243m – volume: 310 start-page: 1166 year: 2005 ident: WOS:000233437300040 article-title: Porous, crystalline, covalent organic frameworks publication-title: SCIENCE doi: 10.1126/science.1120411 – volume: 51 start-page: 12178 year: 2015 ident: WOS:000358228300004 article-title: The microwave-assisted solvothermal synthesis of a crystalline two-dimensional covalent organic framework with high CO2 capacity publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c5cc04680g – volume: 137 start-page: 13772 year: 2015 ident: WOS:000364355900013 article-title: Desymmetrized Vertex Design for the Synthesis of Covalent Organic Frameworks with Periodically Heterogeneous Pore Structures publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b09487 – volume: 349 start-page: 1208 year: 2015 ident: WOS:000360968400039 article-title: Covalent organic frameworks comprising cobalt porphyrins for catalytic CO2 reduction in water publication-title: SCIENCE doi: 10.1126/science.aac8343 – volume: 136 start-page: 547 year: 2014 ident: WOS:000330018600002 article-title: A Homochiral Microporous Hydrogen-Bonded Organic Framework for Highly Enantioselective Separation of Secondary Alcohols publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja4129795 – year: 2015 ident: 000383410700017.44 publication-title: Imidazole Dipeptides: Chemistry, Analysis, Function and Effects – volume: 7 start-page: 905 year: 2015 ident: WOS:000363468600012 article-title: Stable, crystalline, porous, covalent organic frameworks as a platform for chiral organocatalysts publication-title: NATURE CHEMISTRY doi: 10.1038/NCHEM.2352 – volume: 45 start-page: 3216 year: 2006 ident: WOS:000237762800003 article-title: Silica-based mesoporous organic-inorganic hybrid materials publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200503075 – volume: 52 start-page: 3690 year: 2016 ident: WOS:000371008500023 article-title: Insight into the crystallization of amorphous imine-linked polymer networks to 2D covalent organic frameworks publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c5cc10221a – volume: 136 start-page: 6570 year: 2014 ident: WOS:000335720200011 article-title: Phosphoric Acid Loaded Azo (-N=N-) Based Covalent Organic Framework for Proton Conduction publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja502212v – volume: 134 start-page: 14991 year: 2012 ident: WOS:000308574800057 article-title: Photoactive Chiral Metal-Organic Frameworks for Light-Driven Asymmetric alpha-Alkylation of Aldehydes publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja305367j – volume: 137 start-page: 11896 year: 2015 ident: WOS:000361930000011 article-title: Self-Assembly of Chiral Metallacycles and Metallacages from a Directionally Adaptable BINOL-Derived Donor publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b07529 – volume: 18 start-page: 6718 year: 2012 ident: WOS:000304347600002 article-title: "Bottom-Up" Embedding of the Jorgensen-Hayashi Catalyst into a Chiral Porous Polymer for Highly Efficient Heterogeneous Asymmetric Organocatalysis publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201200753 – volume: 20 start-page: 11019 year: 2014 ident: WOS:000340902800021 article-title: Insights into the Asymmetric Heterogeneous Catalysis in Porous Organic Polymers: Constructing A TADDOL-Embedded Chiral Catalyst for Studying the Structure-Activity Relationship publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201403002 – volume: 134 start-page: 9050 year: 2012 ident: WOS:000304837800008 article-title: A Chiral Porous Metal-Organic Framework for Highly Sensitive and Enantioselective Fluorescence Sensing of Amino Alcohols publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja302110d – volume: 133 start-page: 5806 year: 2011 ident: WOS:000290358200051 article-title: A General Thermolabile Protecting Group Strategy for Organocatalytic Metal-Organic Frameworks publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja202223d – volume: 2 start-page: 838 year: 2010 ident: WOS:000282091300016 article-title: A series of isoreticular chiral metal-organic frameworks as a tunable platform for asymmetric catalysis publication-title: NATURE CHEMISTRY doi: 10.1038/NCHEM.738 – volume: 138 start-page: 3302 year: 2016 ident: WOS:000372477700011 article-title: A Pyrene-Based, Fluorescent Three-Dimensional Covalent Organic Framework publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.6b00652 – volume: 2 start-page: 353 year: 2010 ident: WOS:000276977300009 article-title: Induction of chiral porous solids containing only achiral building blocks publication-title: NATURE CHEMISTRY doi: 10.1038/NCHEM.628 – volume: 293 start-page: 35 year: 2010 ident: WOS:000282018800002 article-title: Hydrogen, Methane and Carbon Dioxide Adsorption in Metal-Organic Framework Materials publication-title: FUNCTIONAL METAL-ORGANIC FRAMEWORKS: GAS STORAGE, SEPARATION AND CATALYSIS doi: 10.1007/128_2009_21 – volume: 116 start-page: 1094 year: 2016 ident: WOS:000370216000009 article-title: Efficient Separation of Enantiomers Using Stereoregular Chiral Polymers publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.5b00317 – volume: 1 start-page: 819 year: 2011 ident: WOS:000292479400019 article-title: Porous Organic Polymers in Catalysis: Opportunities and Challenges publication-title: ACS CATALYSIS doi: 10.1021/cs200131g – volume: 50 start-page: 788 year: 2014 ident: WOS:000328884500006 article-title: Thermally/hydrolytically stable covalent organic frameworks from a rigid macrocyclic host publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c3cc47652a – volume: 135 start-page: 11975 year: 2013 ident: WOS:000323241200051 article-title: Synthesis, Structure, and Optical Activity of HPM-1, a Pure Silica Chiral Zeolite publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja405088c – volume: 132 start-page: 14321 year: 2010 ident: WOS:000283276800001 article-title: Homochiral Metal-Organic Frameworks for Heterogeneous Asymmetric Catalysis publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja101208s – volume: 47 start-page: 9513 year: 2008 ident: WOS:000261484200028 article-title: Amino Acid Silica Hybrid Materials with Mesoporous Structure and Enantiopure Surfaces publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200803405 – volume: 53 start-page: 2878 year: 2014 ident: WOS:000332270000006 article-title: 3D Microporous Base-Functionalized Covalent Organic Frameworks for Size-Selective Catalysis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201310500 – volume: 2007 start-page: 167 year: 2007 ident: WOS:000243303000019 article-title: Benzimidazole-pyrrolidine/H+ (BIP/H+), a highly reactive organocatalyst for asymmetric processes publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.200600664 – volume: 131 start-page: 4570 year: 2009 ident: WOS:000264806300009 article-title: A Crystalline Imine-Linked 3-D Porous Covalent Organic Framework publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja8096256 – volume: 10 start-page: 70 year: 2015 ident: WOS:000346736100005 article-title: Chirality in Ordered Porous Organosilica Hybrid Materials publication-title: CHEMISTRY-AN ASIAN JOURNAL doi: 10.1002/asia.201402682 – volume: 112 start-page: 3959 year: 2012 ident: WOS:000306298800010 article-title: Design and Preparation of Porous Polymers publication-title: CHEMICAL REVIEWS doi: 10.1021/cr200440z – volume: 133 start-page: 11478 year: 2011 ident: WOS:000293872800021 article-title: Crystalline Covalent Organic Frameworks with Hydrazone Linkages publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja204728y – volume: 41 start-page: 6010 year: 2012 ident: WOS:000307779600011 article-title: Covalent organic frameworks publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c2cs35157a – year: 2004 ident: 000383410700017.42 publication-title: Modern Aldol Reactions – volume: 138 start-page: 1234 year: 2016 ident: WOS:000369558000026 article-title: From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks-A Modulation Approach publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b10708 – volume: 8 start-page: 310 year: 2016 ident: WOS:000372505500008 article-title: Molecular docking sites designed for the generation of highly crystalline covalent organic frameworks publication-title: NATURE CHEMISTRY doi: 10.1038/NCHEM.2444 – volume: 41 start-page: 3 year: 2008 ident: WOS:000252045600002 article-title: Chirality-responsive helical polymers publication-title: MACROMOLECULES doi: 10.1021/ma071453s – volume: 11 start-page: 907 year: 2009 ident: WOS:000263299000031 article-title: Hybrid NH2-Benzimidazole Ligands for Efficient Ru-Catalyzed Asymmetric Hydrogenation of Aryl Ketones publication-title: ORGANIC LETTERS doi: 10.1021/ol802766u – volume: 7 start-page: ARTN 10487 year: 2016 ident: WOS:000371134900001 article-title: Homochiral D4-symmetric metal-organic cages from stereogenic Ru(II) metalloligands for effective enantioseparation of atropisomeric molecules publication-title: NATURE COMMUNICATIONS doi: 10.1038/ncomms10487 – volume: 42 start-page: 3913 year: 2013 ident: WOS:000317596100019 article-title: Periodic Mesoporous Organosilicas: from simple to complex bridges; a comprehensive overview of functions, morphologies and applications publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c2cs35222b – volume: 134 start-page: 19524 year: 2012 ident: WOS:000311869600007 article-title: Construction of Crystalline 2D Covalent Organic Frameworks with Remarkable Chemical (Acid/Base) Stability via a Combined Reversible and Irreversible Route publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja308278w – volume: 138 start-page: 8352 year: 2016 ident: WOS:000379794400009 article-title: Seven Post-synthetic Covalent Reactions in Tandem Leading to Enzyme-like Complexity within Metal-Organic Framework Crystals publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.6b04204 – volume: 132 start-page: 15939 year: 2010 ident: WOS:000284202200035 article-title: Chiral Bicycle Imidazole Nucleophilic Catalysts: Rational Design, Facile Synthesis, and Successful Application in Asymmetric Steglich Rearrangement publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja109069k – volume: 134 start-page: 6904 year: 2012 ident: WOS:000303139800005 article-title: A Chiral Quadruple-Stranded Helicate Cage for Enantioselective Recognition and Separation publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja212132r – volume: 137 start-page: 6124 year: 2015 ident: WOS:000355053100004 article-title: Cellulose Nanocrystals as Chiral Inducers: Enantioselective Catalysis and Transmission Electron Microscopy 3D Characterization publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.5b02034 – volume: 49 start-page: 9730 year: 2010 ident: WOS:000285211000033 article-title: Photochemical Activation of a Metal-Organic Framework to Reveal Functionality publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201004736 – volume: 6 year: 1953 ident: 000383410700017.23 publication-title: Imidazole and its derivatives – volume: 47 start-page: 3450 year: 2008 ident: WOS:000255489500036 article-title: Porous, covalent triazine-based frameworks prepared by ionothermal synthesis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200705710 – volume: 136 start-page: 15885 year: 2014 ident: WOS:000344906100020 article-title: One-Step Construction of Two Different Kinds of Pores in a 2D Covalent Organic Framework publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja5092936 – volume: 18 start-page: 4021 year: 2008 ident: WOS:000258737900002 article-title: Chiral zeolitic materials: structural insights and synthetic challenges publication-title: JOURNAL OF MATERIALS CHEMISTRY doi: 10.1039/b804136a |
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Snippet | Covalent organic frameworks (COFs) represent a new type of crystalline porous materials that are covalently assembled from organic building blocks.... |
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SubjectTerms | chemical reactions Chemistry Chemistry, Multidisciplinary crystal structure organic compounds Physical Sciences Science & Technology |
Title | Constructing Crystalline Covalent Organic Frameworks from Chiral Building Blocks |
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