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Journal articles on the topic 'Supramolecular chirality'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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1

Haberhauer, G. "Controlling Supramolecular Chirality." Synfacts 2011, no. 02 (2011): 0147. http://dx.doi.org/10.1055/s-0030-1259258.

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2

Cheng, Xiaoxiao, Tengfei Miao, Yilin Qian, Zhengbiao Zhang, Wei Zhang, and Xiulin Zhu. "Supramolecular Chirality in Azobenzene-Containing Polymer System: Traditional Postpolymerization Self-Assembly Versus In Situ Supramolecular Self-Assembly Strategy." International Journal of Molecular Sciences 21, no. 17 (2020): 6186. http://dx.doi.org/10.3390/ijms21176186.

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Recently, the design of novel supramolecular chiral materials has received a great deal of attention due to rapid developments in the fields of supramolecular chemistry and molecular self-assembly. Supramolecular chirality has been widely introduced to polymers containing photoresponsive azobenzene groups. On the one hand, supramolecular chiral structures of azobenzene-containing polymers (Azo-polymers) can be produced by nonsymmetric arrangement of Azo units through noncovalent interactions. On the other hand, the reversibility of the photoisomerization also allows for the control of the supr

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3

Kurouski, Dmitry, Joseph D. Handen, Rina K. Dukor, Laurence A. Nafie, and Igor K. Lednev. "Supramolecular chirality in peptide microcrystals." Chemical Communications 51, no. 1 (2015): 89–92. http://dx.doi.org/10.1039/c4cc05002a.

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VCD reveals supramolecular chirality in microcrystals of two peptide segments from human islet amyloid (IAPP, amylin). Previously such supramolecular chirality has been observed by VCD only for amyloid fibrils.

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4

Hembury, Guy A., Victor V. Borovkov, and Yoshihisa Inoue. "Chirality-Sensing Supramolecular Systems." Chemical Reviews 108, no. 1 (2008): 1–73. http://dx.doi.org/10.1021/cr050005k.

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5

Rusanov, Anatoly I., and Aleksandr G. Nekrasov. "Supramolecular chirality of surfactants." Mendeleev Communications 21, no. 1 (2011): 15–16. http://dx.doi.org/10.1016/j.mencom.2011.01.006.

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6

WANG, Xiu-Feng, Li ZHANG, and Ming-Hua LIU. "supramolecular Gels: Structural Diversity and supramolecular Chirality." Acta Physico-Chimica Sinica 32, no. 1 (2016): 227–38. http://dx.doi.org/10.3866/pku.whxb201511181.

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7

Wang, Qiuling, Li Zhang, Dong Yang, Tiesheng Li, and Minghua Liu. "Chiral signs of TPPS co-assemblies with chiral gelators: role of molecular and supramolecular chirality." Chemical Communications 52, no. 84 (2016): 12434–37. http://dx.doi.org/10.1039/c6cc05668g.

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8

Yin, Lu, Meng Liu, Yin Zhao, et al. "Supramolecular chirality induced by chiral solvation in achiral cyclic Azo-containing polymers: topological effects on chiral aggregation." Polymer Chemistry 9, no. 6 (2018): 769–76. http://dx.doi.org/10.1039/c7py02002c.

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The supramolecular chirality of linear and cyclic Azo aggregates was successfully induced by chiral limonene, demonstrating that the topological structural constraint and molecular mass of cyclic polymers have clear effects on the supramolecular chirality driven by a chiral solvent.

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9

Zhu, Zexi, Mingfeng Wei, Bao Li, and Lixin Wu. "Constructing chiral polyoxometalate assemblies via supramolecular approaches." Dalton Transactions 50, no. 15 (2021): 5080–98. http://dx.doi.org/10.1039/d1dt00182e.

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Chirality generation, induced chirality transfer, and the functionalization of polyoxometalate-based complexes and their self-assembly constructed through supramolecular approach are systematically reviewed.

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10

Wang, Ke-Rang, Dan Han, Guo-Jing Cao, and Xiao-Liu Li. "Link spacer controlled supramolecular chirality of perylene bisimide-carbohydrate conjugate." RSC Advances 5, no. 59 (2015): 47728–31. http://dx.doi.org/10.1039/c5ra06255a.

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Controllable supramolecular chirality based on the self-assembly of the perylene bisimide-carbohydrate conjugates was achieved, exhibiting right-handed chirality with triazole as linker and left-handed chirality with the amide bond as linker.

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11

Borovkov, Victor. "Supramolecular Chirality in Porphyrin Chemistry." Symmetry 6, no. 2 (2014): 256–94. http://dx.doi.org/10.3390/sym6020256.

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12

Luo, Jun, and Yan-Song Zheng. "Supramolecular Chirality Based on Calixarenes." Current Organic Chemistry 16, no. 4 (2012): 483–506. http://dx.doi.org/10.2174/138527212799499813.

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13

Rusanov, A. I., and A. G. Nekrasov. "Supramolecular chirality of sodium dodecylsulfate." Russian Journal of General Chemistry 80, no. 8 (2010): 1568–69. http://dx.doi.org/10.1134/s1070363210080050.

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14

Wang, Yu-Xuan, Qi-Feng Zhou, Shu-Ting Jiang, et al. "Photoresponsive Chirality-Tunable Supramolecular Metallacycles." Macromolecular Rapid Communications 39, no. 22 (2018): 1800454. http://dx.doi.org/10.1002/marc.201800454.

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15

Arteaga, Oriol, Adolf Canillas, Joaquim Crusats, et al. "Flow Effects in Supramolecular Chirality." Israel Journal of Chemistry 51, no. 10 (2011): 1007–16. http://dx.doi.org/10.1002/ijch.201100043.

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16

Li, Shuai, Tengfei Miao, Xiaoxiao Cheng, Yin Zhao, Wei Zhang, and Xiulin Zhu. "Different phase-dominated chiral assembly of polyfluorenes induced by chiral solvation: axial and supramolecular chirality." RSC Advances 9, no. 65 (2019): 38257–64. http://dx.doi.org/10.1039/c9ra08354e.

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17

Wei, Chengpeng, Mingyang Liu, Yifei Han, Hua Zhong, and Feng Wang. "Supramolecular Chirogenesis Engineered by Pt(II)···Pt(II) Metal–Metal Interactions." Organic Materials 03, no. 02 (2021): 274–80. http://dx.doi.org/10.1055/a-1512-5965.

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Supramolecular chirogenesis represents an effective way to induce chirality at the supramolecular level. For the previous host–guest chirogenic systems, metal–ligand coordination, hydrogen bonding, π–π stacking and hydrophobic interactions have been mainly employed as the non-covalent driving forces. In this study, Pt(II)···Pt(II) metal–metal interactions have been engineered to induce supramolecular chirogenesis, by forming non-covalent clipping structures between chiral platinum receptors and achiral platinum guests together. This results in the emergence of Cotton effects in the metal–metal

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18

Yang, Li, Fang Wang, Dang-i. Y. Auphedeous, and Chuanliang Feng. "Achiral isomers controlled circularly polarized luminescence in supramolecular hydrogels." Nanoscale 11, no. 30 (2019): 14210–15. http://dx.doi.org/10.1039/c9nr05033g.

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19

Duan, Pengfei, Hai Cao, Li Zhang, and Minghua Liu. "Gelation induced supramolecular chirality: chirality transfer, amplification and application." Soft Matter 10, no. 30 (2014): 5428. http://dx.doi.org/10.1039/c4sm00507d.

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20

de Jong, J. J. D. "Reversible Optical Transcription of Supramolecular Chirality into Molecular Chirality." Science 304, no. 5668 (2004): 278–81. http://dx.doi.org/10.1126/science.1095353.

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21

YUAN, JING, and MINGHUA LIU. "SUPRAMOLECULAR CHIRALITY OF THE LANGMUIR-BLODGETT FILMS OF AN ACHIRAL 2-(HEPTADECYL)PHENANTHRO[9, 10-d]IMIDAZOLE." International Journal of Nanoscience 05, no. 06 (2006): 689–95. http://dx.doi.org/10.1142/s0219581x06005005.

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A novel amphiphilic compound, 2-(heptadecyl)phenanthro[9, 10-d]imidazole (PhImC17), was synthesized and its assembly at the air/water interface was investigated. It has been found that although the compound was achiral, it can form a chiral Langmuir–Blodgett film through the interfacial organization. The larger aromatic ring of the compound, which caused the cooperative arrangement of the chromophore in the assembled ultrathin film, was suggested to play an important role in forming such supramolecular chirality. A comparison between the supramolecular chirality of the PhImC17 film with that o

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22

Boer, Stephanie A., and David R. Turner. "Self-selecting homochiral quadruple-stranded helicates and control of supramolecular chirality." Chemical Communications 51, no. 98 (2015): 17375–78. http://dx.doi.org/10.1039/c5cc07422c.

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23

Huan, Jinwen, Xuemei Zhang, and Qingdao Zeng. "Two-dimensional supramolecular crystal engineering: chirality manipulation." Physical Chemistry Chemical Physics 21, no. 22 (2019): 11537–53. http://dx.doi.org/10.1039/c9cp02207d.

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24

McAulay, Kate, Bart Dietrich, Hao Su, et al. "Using chirality to influence supramolecular gelation." Chemical Science 10, no. 33 (2019): 7801–6. http://dx.doi.org/10.1039/c9sc02239b.

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25

van Dijken, Derk Jan, John M. Beierle, Marc C. A. Stuart, Wiktor Szymański, Wesley R. Browne, and Ben L. Feringa. "Autoamplification of Molecular Chirality through the Induction of Supramolecular Chirality." Angewandte Chemie 126, no. 20 (2014): 5173–77. http://dx.doi.org/10.1002/ange.201311160.

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26

Hattori, Shingo, Stefaan Vandendriessche, Guy Koeckelberghs, Thierry Verbiest, and Kazuyuki Ishii. "Evaporation rate-based selection of supramolecular chirality." Chemical Communications 53, no. 21 (2017): 3066–69. http://dx.doi.org/10.1039/c6cc09842h.

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27

Kurata, Misaki, and Atsushi Yoshizawa. "The formation of a chiral supramolecular structure acting as a template for chirality transfer." Chemical Communications 56, no. 59 (2020): 8289–92. http://dx.doi.org/10.1039/d0cc02413a.

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Spontaneous mirror symmetry breaking in self-assembled achiral trimers under a nonequilibrium state induces supramolecular chirality, which is amplified to produce a homochiral material acting as a template for chirality transfer.

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28

Hemraz, Usha D., Mounir El-Bakkari, Takeshi Yamazaki, Jae-Young Cho, Rachel L. Beingessner, and Hicham Fenniri. "Chiromers: conformation-driven mirror-image supramolecular chirality isomerism identified in a new class of helical rosette nanotubes." Nanoscale 6, no. 16 (2014): 9421–27. http://dx.doi.org/10.1039/c4nr00340c.

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29

Miyake, Hiroyuki. "Supramolecular Chirality in Dynamic Coordination Chemistry." Symmetry 6, no. 4 (2014): 880–95. http://dx.doi.org/10.3390/sym6040880.

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30

Dong, Jinqiao, Yan Liu, and Yong Cui. "Supramolecular Chirality in Metal–Organic Complexes." Accounts of Chemical Research 54, no. 1 (2020): 194–206. http://dx.doi.org/10.1021/acs.accounts.0c00604.

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31

Shen, Jiang-Shan, Guo-Juan Mao, Yu-Hua Zhou, Yun-Bao Jiang, and Hong-Wu Zhang. "A ligand-chirality controlled supramolecular hydrogel." Dalton Transactions 39, no. 30 (2010): 7054. http://dx.doi.org/10.1039/c0dt00364f.

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32

Roche, Cécile, Hao-Jan Sun, Pawaret Leowanawat, et al. "A supramolecular helix that disregards chirality." Nature Chemistry 8, no. 1 (2015): 80–89. http://dx.doi.org/10.1038/nchem.2397.

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33

Pop, Anca, Myroslav O. Vysotsky, Mohamed Saadioui, and Volker Böhmer. "Self-assembled dimers with supramolecular chirality." Chemical Communications, no. 10 (April 14, 2003): 1124–25. http://dx.doi.org/10.1039/b301418e.

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34

Liu, Minghua, Li Zhang, and Tianyu Wang. "Supramolecular Chirality in Self-Assembled Systems." Chemical Reviews 115, no. 15 (2015): 7304–97. http://dx.doi.org/10.1021/cr500671p.

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35

Terraneo, G., S. Biella, P. Metrangolo, T. Pilati, and G. Resnati. "Chirality in halogen-bonded supramolecular architectures." Acta Crystallographica Section A Foundations of Crystallography 67, a1 (2011): C190—C191. http://dx.doi.org/10.1107/s0108767311095250.

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36

Arteaga, Oriol, Adolf Canillas, Joaquim Crusats, et al. "Emergence of Supramolecular Chirality by Flows." ChemPhysChem 11, no. 16 (2010): 3511–16. http://dx.doi.org/10.1002/cphc.201000658.

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37

Simonyi, Miklós, Zsolt Bikádi, Ferenc Zsila, and József Deli. "Supramolecular exciton chirality of carotenoid aggregates." Chirality 15, no. 8 (2003): 680–98. http://dx.doi.org/10.1002/chir.10282.

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38

Katzenelson, Omer, Hagit Zabrodsky Hel-Or, and David Avnir. "Chirality of Large Random Supramolecular Structures." Chemistry - A European Journal 2, no. 2 (1996): 174–81. http://dx.doi.org/10.1002/chem.19960020209.

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39

Rizzo, Paola, Eugenia Lepera, and Gaetano Guerra. "Enantiomeric guests with the same signs of chiral optical responses." Chem. Commun. 50, no. 60 (2014): 8185–88. http://dx.doi.org/10.1039/c4cc02853h.

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The chiral response of non-racemic molecules, being guests of s-PS co-crystalline films, does not depend on their R or S molecular chirality but essentially only on the polymer host supramolecular chirality.

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40

Garifullin, Ruslan, and Mustafa O. Guler. "Supramolecular chirality in self-assembled peptide amphiphile nanostructures." Chemical Communications 51, no. 62 (2015): 12470–73. http://dx.doi.org/10.1039/c5cc04982b.

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41

Vyborna, Y., S. Altunbas, M. Vybornyi, and R. Häner. "Morphological diversity of supramolecular polymers of DNA-containing oligopyrenes – formation of chiroptically active nanosheets." Chemical Communications 53, no. 89 (2017): 12128–31. http://dx.doi.org/10.1039/c7cc07511a.

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Supramolecular polymerization of chimeric DNA-pyrene oligomers leads to 1D and 2D objects depending on the length of the DNA. A single guanosine induces supramolecular chirality in the self-assembled nanosheets.

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42

Imai, Yuki, and Junpei Yuasa. "Supramolecular chirality transformation driven by monodentate ligand binding to a coordinatively unsaturated self-assembly based on C3-symmetric ligands." Chemical Science 10, no. 15 (2019): 4236–45. http://dx.doi.org/10.1039/c9sc00399a.

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A supramolecular chirality transition driven by monodentate ligand binding, the present strategy shows promise for the rational design of dynamic coordination chirality capable of alternating between chiral objects of different shapes driven by a specific external stimulus.

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43

Cooper, James A., Stefan Borsley, Paul J. Lusby, and Scott L. Cockroft. "Discrimination of supramolecular chirality using a protein nanopore." Chemical Science 8, no. 7 (2017): 5005–9. http://dx.doi.org/10.1039/c7sc01940h.

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44

Fujiki, Michiya. "Supramolecular Chirality: Solvent Chirality Transfer in Molecular Chemistry and Polymer Chemistry." Symmetry 6, no. 3 (2014): 677–703. http://dx.doi.org/10.3390/sym6030677.

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45

Bystrov, Vladimir, Alla Sidorova, Aleksey Lutsenko, et al. "Modeling of Self-Assembled Peptide Nanotubes and Determination of Their Chirality Sign Based on Dipole Moment Calculations." Nanomaterials 11, no. 9 (2021): 2415. http://dx.doi.org/10.3390/nano11092415.

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The chirality quantification is of great importance in structural biology, where the differences in proteins twisting can provide essentially different physiological effects. However, this aspect of the chirality is still poorly studied for helix-like supramolecular structures. In this work, a method for chirality quantification based on the calculation of scalar triple products of dipole moments is suggested. As a model structure, self-assembled nanotubes of diphenylalanine (FF) made of L- and D-enantiomers were considered. The dipole moments of FF molecules were calculated using semi-empiric

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46

Zhao, Lizhi, Manman Liu, Sensen Li, et al. "Aggregation and supramolecular chirality of 5,10,15,20-tetrakis-(4-sulfonatophenyl)-porphyrin on an achiral poly(2-(dimethylamino)ethyl methylacrylate)-grafted ethylene-vinyl alcohol membrane." Journal of Materials Chemistry C 3, no. 15 (2015): 3650–58. http://dx.doi.org/10.1039/c5tc00037h.

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47

Zong, Zhaohui, Peng Zhang, Hongwei Qiao, Aiyou Hao, and Pengyao Xing. "Chiral toroids and tendril superstructures from integrated ternary species with consecutively tunable supramolecular chirality and circularly polarized luminescence." Journal of Materials Chemistry C 8, no. 45 (2020): 16224–33. http://dx.doi.org/10.1039/d0tc04373g.

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48

Patera, Laerte L., Zhiyu Zou, Carlo Dri, Cristina Africh, Jascha Repp, and Giovanni Comelli. "Imaging on-surface hierarchical assembly of chiral supramolecular networks." Physical Chemistry Chemical Physics 19, no. 36 (2017): 24605–12. http://dx.doi.org/10.1039/c7cp01341h.

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49

Ikbal, Sk Asif, Sanfaori Brahma, and Sankar Prasad Rath. "Step-wise induction, amplification and inversion of molecular chirality through the coordination of chiral diamines with Zn(ii) bisporphyrin." Chemical Communications 51, no. 5 (2015): 895–98. http://dx.doi.org/10.1039/c4cc07955h.

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A clear structural rationalization of the origin of chirality transfer from an optically active diamine guest to an achiral Zn(ii) bisporphyrin host in a 1 : 1 and 2 : 3 host–guest supramolecular complex has been demonstrated for the first time. During the process, chirality inversion along with amplification was observed.

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50

WEI, XueHong, DianSheng LIU, Jin CAI, Jing ZHANG, and Hong YUAN. "Dynamic control and functionalization of supramolecular chirality." Chinese Science Bulletin 61, no. 6 (2016): 630–41. http://dx.doi.org/10.1360/n972015-01216.

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