Assembly of an A 6 L 6 Anion Trigonal Antiprism and Binding of Glucopyranosides and Polyethylene Glycols (PEGs)
Anion-coordination-driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we demonstrate that variation of the "angle" of the backbone of C -symmetric tris-bis(urea) ligands, from triphenylamine to triphenylphosphine oxide, res...
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Published in | Angewandte Chemie International Edition Vol. 62; no. 20; p. e202301300 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
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08.05.2023
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Abstract | Anion-coordination-driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we demonstrate that variation of the "angle" of the backbone of C
-symmetric tris-bis(urea) ligands, from triphenylamine to triphenylphosphine oxide, results in the change of the final construct from an A
L
tetrahedron to a higher-nuclearity, A
L
trigonal antiprism (A=anion, herein PO
; L=ligand). Most interestingly, this assembly features a huge hollow internal space that is divided into three compartments: one central cavity and two large outer pockets. This multi-cavity character enables the binding of different guests, namely monosaccharides or polyethylene glycol molecules (PEG600, PEG1000 and PEG2000), respectively. The results prove that anion coordination by multiple hydrogen bonds may provide both sufficient strength and flexibility, thus making possible the formation of complicated structures with adaptive guest binding ability. |
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AbstractList | Anion-coordination-driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we demonstrate that variation of the "angle" of the backbone of C
-symmetric tris-bis(urea) ligands, from triphenylamine to triphenylphosphine oxide, results in the change of the final construct from an A
L
tetrahedron to a higher-nuclearity, A
L
trigonal antiprism (A=anion, herein PO
; L=ligand). Most interestingly, this assembly features a huge hollow internal space that is divided into three compartments: one central cavity and two large outer pockets. This multi-cavity character enables the binding of different guests, namely monosaccharides or polyethylene glycol molecules (PEG600, PEG1000 and PEG2000), respectively. The results prove that anion coordination by multiple hydrogen bonds may provide both sufficient strength and flexibility, thus making possible the formation of complicated structures with adaptive guest binding ability. Abstract Anion‐coordination‐driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we demonstrate that variation of the “angle” of the backbone of C 3 ‐symmetric tris‐bis(urea) ligands, from triphenylamine to triphenylphosphine oxide, results in the change of the final construct from an A 4 L 4 tetrahedron to a higher‐nuclearity, A 6 L 6 trigonal antiprism (A=anion, herein PO 4 3− ; L=ligand). Most interestingly, this assembly features a huge hollow internal space that is divided into three compartments: one central cavity and two large outer pockets. This multi‐cavity character enables the binding of different guests, namely monosaccharides or polyethylene glycol molecules (PEG600, PEG1000 and PEG2000), respectively. The results prove that anion coordination by multiple hydrogen bonds may provide both sufficient strength and flexibility, thus making possible the formation of complicated structures with adaptive guest binding ability. |
Author | Wu, Biao Li, Boyang Wang, Yue Xu, Lizheng Wei, Tianfu Zhao, Xiaotong Yang, Xiao-Juan |
Author_xml | – sequence: 1 givenname: Boyang surname: Li fullname: Li, Boyang organization: Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China – sequence: 2 givenname: Tianfu surname: Wei fullname: Wei, Tianfu organization: Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China – sequence: 3 givenname: Xiaotong surname: Zhao fullname: Zhao, Xiaotong organization: Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China – sequence: 4 givenname: Yue surname: Wang fullname: Wang, Yue organization: Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China – sequence: 5 givenname: Lizheng surname: Xu fullname: Xu, Lizheng organization: Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China – sequence: 6 givenname: Xiao-Juan surname: Yang fullname: Yang, Xiao-Juan organization: Key Laboratory of Medicinal Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, China – sequence: 7 givenname: Biao orcidid: 0000-0002-0724-4150 surname: Wu fullname: Wu, Biao organization: Key Laboratory of Medicinal Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, China |
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Cites_doi | 10.1002/anie.200603921 10.1021/jacs.0c03798 10.1016/j.bbagen.2014.03.016 10.1021/jacs.9b05432 10.1021/jacs.6b02445 10.1039/C4DT03535F 10.1039/b517308f 10.1021/acs.chemrev.1c00763 10.1021/jacs.9b02604 10.1038/s41570-019-0085-3 10.1021/jacs.0c10346 10.1002/anie.202113914 10.1038/356325a0 10.1146/annurev-biochem-060308-102244 10.1021/ja5042397 10.1007/s11426-022-1312-5 10.1021/ja00179a028 10.1021/ma00212a039 10.1002/(SICI)1521-3773(19991004)38:19<2882::AID-ANIE2882>3.0.CO;2-T 10.1039/C8CS00768C 10.1021/jacs.8b01488 10.1021/acs.chemrev.7b00663 10.1007/978-1-4899-0703-5 10.1038/ncomms1091 10.1002/anie.201402169 10.1039/C2CC37776D 10.1021/ja710715e 10.1038/s41467-018-06458-w 10.1002/macp.1964.020730109 10.1038/nchem.2195 10.1002/anie.201209930 10.1039/D0SC00341G 10.1021/cg0342011 10.1016/j.chempr.2019.12.002 10.1021/jacs.2c02261 10.1021/cr200077m 10.1021/acs.chemrev.1c00602 10.1021/acs.inorgchem.9b02086 10.1016/j.chempr.2017.10.015 10.1021/acs.accounts.2c00435 10.1107/S0907444993011333 10.1002/1521-3765(20020118)8:2<493::AID-CHEM493>3.0.CO;2-5 10.1002/anie.200462171 10.1016/j.chempr.2021.12.017 10.1021/jacs.1c01168 10.1002/anie.201502399 10.1002/anie.200804623 10.1021/jacs.6b11982 10.1002/asia.202100768 10.1039/C9CS00391F 10.1021/ja505414x |
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Keywords | Anion-Coordination-Driven Assembly (ACDA) Host-Guest Chemistry Polyethylene Glycols Glucopyranosides Trigonal Antiprisms |
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References | e_1_2_7_5_1 e_1_2_7_3_2 e_1_2_7_9_2 e_1_2_7_7_1 e_1_2_7_19_2 e_1_2_7_17_1 e_1_2_7_62_1 e_1_2_7_60_2 e_1_2_7_15_1 e_1_2_7_41_1 e_1_2_7_64_1 e_1_2_7_1_1 e_1_2_7_13_2 e_1_2_7_43_2 e_1_2_7_11_1 e_1_2_7_45_1 e_1_2_7_66_2 e_1_2_7_47_2 e_1_2_7_26_2 e_1_2_7_28_1 e_1_2_7_49_2 e_1_2_7_50_1 e_1_2_7_25_2 e_1_2_7_52_2 e_1_2_7_31_1 e_1_2_7_54_2 e_1_2_7_23_1 e_1_2_7_21_2 e_1_2_7_33_2 e_1_2_7_56_2 e_1_2_7_35_2 e_1_2_7_58_1 e_1_2_7_37_2 e_1_2_7_39_2 e_1_2_7_6_1 e_1_2_7_4_2 e_1_2_7_2_2 e_1_2_7_8_2 e_1_2_7_18_1 e_1_2_7_61_2 e_1_2_7_16_1 e_1_2_7_40_1 e_1_2_7_14_2 e_1_2_7_63_1 e_1_2_7_12_2 e_1_2_7_42_2 e_1_2_7_65_2 e_1_2_7_10_2 e_1_2_7_44_2 e_1_2_7_46_1 e_1_2_7_48_2 e_1_2_7_27_2 e_1_2_7_29_2 e_1_2_7_53_1 e_1_2_7_24_2 e_1_2_7_30_2 e_1_2_7_51_2 e_1_2_7_32_2 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_57_1 e_1_2_7_20_2 e_1_2_7_55_2 e_1_2_7_59_1 e_1_2_7_36_2 e_1_2_7_38_2 |
References_xml | – ident: e_1_2_7_34_1 – ident: e_1_2_7_36_2 doi: 10.1002/anie.200603921 – ident: e_1_2_7_38_2 doi: 10.1021/jacs.0c03798 – ident: e_1_2_7_54_2 doi: 10.1016/j.bbagen.2014.03.016 – ident: e_1_2_7_26_2 doi: 10.1021/jacs.9b05432 – ident: e_1_2_7_30_2 doi: 10.1021/jacs.6b02445 – ident: e_1_2_7_11_1 – ident: e_1_2_7_29_2 doi: 10.1039/C4DT03535F – ident: e_1_2_7_43_2 doi: 10.1039/b517308f – ident: e_1_2_7_4_2 doi: 10.1021/acs.chemrev.1c00763 – ident: e_1_2_7_32_2 doi: 10.1021/jacs.9b02604 – ident: e_1_2_7_41_1 – ident: e_1_2_7_48_2 doi: 10.1038/s41570-019-0085-3 – ident: e_1_2_7_40_1 doi: 10.1021/jacs.0c10346 – ident: e_1_2_7_33_2 doi: 10.1002/anie.202113914 – ident: e_1_2_7_61_2 doi: 10.1038/356325a0 – ident: e_1_2_7_2_2 doi: 10.1146/annurev-biochem-060308-102244 – ident: e_1_2_7_19_2 doi: 10.1021/ja5042397 – ident: e_1_2_7_62_1 doi: 10.1007/s11426-022-1312-5 – ident: e_1_2_7_46_1 – ident: e_1_2_7_42_2 doi: 10.1021/ja00179a028 – ident: e_1_2_7_60_2 doi: 10.1021/ma00212a039 – ident: e_1_2_7_24_2 doi: 10.1002/(SICI)1521-3773(19991004)38:19<2882::AID-ANIE2882>3.0.CO;2-T – ident: e_1_2_7_55_2 doi: 10.1039/C8CS00768C – ident: e_1_2_7_17_1 doi: 10.1021/jacs.8b01488 – ident: e_1_2_7_3_2 doi: 10.1021/acs.chemrev.7b00663 – ident: e_1_2_7_57_1 doi: 10.1007/978-1-4899-0703-5 – ident: e_1_2_7_63_1 doi: 10.1038/ncomms1091 – ident: e_1_2_7_44_2 doi: 10.1002/anie.201402169 – ident: e_1_2_7_9_2 doi: 10.1039/C2CC37776D – ident: e_1_2_7_37_2 doi: 10.1021/ja710715e – ident: e_1_2_7_58_1 doi: 10.1038/s41467-018-06458-w – ident: e_1_2_7_65_2 doi: 10.1002/macp.1964.020730109 – ident: e_1_2_7_59_1 – ident: e_1_2_7_51_2 doi: 10.1038/nchem.2195 – ident: e_1_2_7_15_1 doi: 10.1002/anie.201209930 – ident: e_1_2_7_49_2 doi: 10.1039/D0SC00341G – ident: e_1_2_7_8_2 doi: 10.1021/cg0342011 – ident: e_1_2_7_22_1 – ident: e_1_2_7_28_1 – ident: e_1_2_7_13_2 doi: 10.1016/j.chempr.2019.12.002 – ident: e_1_2_7_21_2 doi: 10.1021/jacs.2c02261 – ident: e_1_2_7_5_1 doi: 10.1021/cr200077m – ident: e_1_2_7_6_1 doi: 10.1021/acs.chemrev.1c00602 – ident: e_1_2_7_20_2 doi: 10.1021/acs.inorgchem.9b02086 – ident: e_1_2_7_1_1 – ident: e_1_2_7_7_1 – ident: e_1_2_7_12_2 doi: 10.1016/j.chempr.2017.10.015 – ident: e_1_2_7_14_2 doi: 10.1021/acs.accounts.2c00435 – ident: e_1_2_7_45_1 doi: 10.1107/S0907444993011333 – ident: e_1_2_7_25_2 doi: 10.1002/1521-3765(20020118)8:2<493::AID-CHEM493>3.0.CO;2-5 – ident: e_1_2_7_35_2 doi: 10.1002/anie.200462171 – ident: e_1_2_7_39_2 doi: 10.1016/j.chempr.2021.12.017 – ident: e_1_2_7_27_2 doi: 10.1021/jacs.1c01168 – ident: e_1_2_7_64_1 – ident: e_1_2_7_16_1 doi: 10.1002/anie.201502399 – ident: e_1_2_7_66_2 doi: 10.1002/anie.200804623 – ident: e_1_2_7_47_2 doi: 10.1021/jacs.6b11982 – ident: e_1_2_7_18_1 – ident: e_1_2_7_53_1 – ident: e_1_2_7_52_2 doi: 10.1002/asia.202100768 – ident: e_1_2_7_50_1 – ident: e_1_2_7_56_2 doi: 10.1039/C9CS00391F – ident: e_1_2_7_23_1 – ident: e_1_2_7_31_1 – ident: e_1_2_7_10_2 doi: 10.1021/ja505414x |
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Snippet | Anion-coordination-driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we demonstrate that... Abstract Anion‐coordination‐driven assembly (ACDA) has proven to be a very effective strategy for the construction of polyhedral structures. Here we... |
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Title | Assembly of an A 6 L 6 Anion Trigonal Antiprism and Binding of Glucopyranosides and Polyethylene Glycols (PEGs) |
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