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Journal articles on the topic 'Chiroptical switch'

Author: Grafiati

Published: 25 May 2024

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1

Feringa, Ben L., Wolter F. Jager, Ben De Lange, and Egbert W. Meijer. "Chiroptical molecular switch." Journal of the American Chemical Society 113, no. 14 (July 1991): 5468–70. http://dx.doi.org/10.1021/ja00014a057.

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2

Opačak, Saša, Darko Babić, Berislav Perić, Željko Marinić, Vilko Smrečki, Barbara Pem, Ivana Vinković Vrček, and Srećko I. Kirin. "A ferrocene-based pseudopeptide chiroptical switch." Dalton Transactions 50, no. 13 (2021): 4504–11. http://dx.doi.org/10.1039/d1dt00508a.

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3

Westermeier, Christian, Hans-Christoph Gallmeier, Markus Komma, and Jörg Daub. "Bispyrene based chiroptical molecular redox switch." Chemical Communications, no. 23 (1999): 2427–28. http://dx.doi.org/10.1039/a907454f.

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4

van Delden, Richard A., Matthijs K. J. ter Wiel, and Ben L. Feringa. "A chiroptical molecular switch with perfect stereocontrol." Chemical Communications, no. 2 (2004): 200. http://dx.doi.org/10.1039/b312170d.

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5

Isla, Helena, Monika Srebro-Hooper, Marion Jean, Nicolas Vanthuyne, Thierry Roisnel, Jamie L. Lunkley, Gilles Muller, J. A. Gareth Williams, Jochen Autschbach, and Jeanne Crassous. "Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn2+ binding." Chemical Communications 52, no. 35 (2016): 5932–35. http://dx.doi.org/10.1039/c6cc01748g.

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6

Takaishi, Kazuto, Makoto Yasui, and Tadashi Ema. "Binaphthyl–Bipyridyl Cyclic Dyads as a Chiroptical Switch." Journal of the American Chemical Society 140, no. 16 (April 13, 2018): 5334–38. http://dx.doi.org/10.1021/jacs.8b01860.

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7

Haridas, V., Sandhya Sadanandan, Sameer Dhawan, Rituraj Mishra, Ishani Jain, Gaurav Goel, Yuan Hu, and Sandeep Patel. "Synthetic minimalistic tryptophan zippers as a chiroptical switch." Organic & Biomolecular Chemistry 15, no. 7 (2017): 1661–69. http://dx.doi.org/10.1039/c6ob02617f.

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Supramolecular helices with left and right handed chirality were designed and synthesized based on l-tryptophan that undergo helical inversion upon addition of H₂PO₄⁻.

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8

Lu, Jinjie, Ganquan Jiang, Zhengbiao Zhang, Wei Zhang, Yonggang Yang, Yong Wang, Nianchen Zhou, and Xiulin Zhu. "A cyclic azobenzenophane-based smart polymer for chiroptical switches." Polymer Chemistry 6, no. 47 (2015): 8144–49. http://dx.doi.org/10.1039/c5py01301a.

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Polymers based on cyclic azobenzenophanes as pendants with different methylene spacers (n = 2, 6, 11) have been synthesized. And the one with a six-methylene spacer is a good candidate for a chiroptical switch.

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9

Rodríguez, Rafael, Emilio Quiñoá, Ricardo Riguera, and Félix Freire. "Multistate Chiroptical Switch Triggered by Stimuli-Responsive Chiral Teleinduction." Chemistry of Materials 30, no. 8 (April 11, 2018): 2493–97. http://dx.doi.org/10.1021/acs.chemmater.8b00800.

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10

Guo, P., L. Zhang, and M. Liu. "A Supramolecular Chiroptical Switch Exclusively from an Achiral Amphiphile." Advanced Materials 18, no. 2 (January 19, 2006): 177–80. http://dx.doi.org/10.1002/adma.200501047.

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11

Kim, M. J., S. J. Yoo, and D. Y. Kim. "A Supramolecular Chiroptical Switch Using an Amorphous Azobenzene Polymer." Advanced Functional Materials 16, no. 16 (October 20, 2006): 2089–94. http://dx.doi.org/10.1002/adfm.200600130.

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12

Wang, Zhi Yuan, Erin K. Todd, Xian Sheng Meng, and Jian Ping Gao. "Dual Modulation of a Molecular Switch with Exceptional Chiroptical Properties." Journal of the American Chemical Society 127, no. 33 (August 2005): 11552–53. http://dx.doi.org/10.1021/ja0526721.

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13

Pascal, Simon, Céline Besnard, Francesco Zinna, Lorenzo Di Bari, Boris Le Guennic, Denis Jacquemin, and Jérôme Lacour. "Zwitterionic [4]helicene: a water-soluble and reversible pH-triggered ECD/CPL chiroptical switch in the UV and red spectral regions." Organic & Biomolecular Chemistry 14, no. 20 (2016): 4590–94. http://dx.doi.org/10.1039/c6ob00752j.

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14

Zhang, Jianpeng, Yanyan Zhou, Yuan Yao, Zhenyu Cheng, Ting Gao, Hongfeng Li, and Pengfei Yan. "A light triggered optical and chiroptical switch based on a homochiral Eu2L3 helicate." Journal of Materials Chemistry C 8, no. 20 (2020): 6788–96. http://dx.doi.org/10.1039/d0tc01044h.

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A pair of homochiral triple-stranded helicates [Eu₂(o-L^RR)₃](TOf)₆ and [Eu₂(o-L^SS)₃](TOf)₆ show light-responsive optical (UV and PL) and chiroptical (ECD and CPL) switching properties upon alternating UV and visible light irradiation.

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15

Kicková, Anna, Jana Donovalová, Peter Kasák, and Martin Putala. "A chiroptical binaphthopyran switch: amplified CD response in a polystyrene film." New Journal of Chemistry 34, no. 6 (2010): 1109. http://dx.doi.org/10.1039/c0nj00102c.

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16

Shi, Wenying, Yankun Jia, Simin Xu, Zhixiong Li, Yi Fu, Min Wei, and Shuxian Shi. "A Chiroptical Switch Based on DNA/Layered Double Hydroxide Ultrathin Films." Langmuir 30, no. 43 (October 20, 2014): 12916–22. http://dx.doi.org/10.1021/la502968z.

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17

Liao, Bo, Ruigang Liu, and Yong Huang. "A Supramolecular Chiroptical Switch Based on Chitosan and Anionic Porphyrin Complex Film." Polymer Journal 39, no. 10 (September 4, 2007): 1071–77. http://dx.doi.org/10.1295/polymj.pj2007036.

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18

Gomar-Nadal, E., J. Veciana, C. Rovira, and D. B. Amabilino. "Chiral Teleinduction in the Formation of a Macromolecular Multistate Chiroptical Redox Switch." Advanced Materials 17, no. 17 (September 5, 2005): 2095–98. http://dx.doi.org/10.1002/adma.200500348.

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19

Aubin, Lauren B., Tracy M. Wagner, John D. Thoburn, Brenda S. Kesler, Katherine A. Hutchison, Robert R. Schumaker, and James P. Parakka. "Dynamic NMR Studies of a Potential Chiroptical Switch Based on Dithiocarbamate−Iminodithiolane Interconversion." Organic Letters 3, no. 21 (October 2001): 3413–16. http://dx.doi.org/10.1021/ol016671z.

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20

Agati, Giovanni, and Antony F. McDonagh. "Chiroptical Switch Based on Photoisomerization of Bilirubin-III.alpha. Bound to Human Serum Albumin." Journal of the American Chemical Society 117, no. 15 (April 1995): 4425–26. http://dx.doi.org/10.1021/ja00120a036.

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21

Xia, Cai-Juan, Bo-Qun Zhang, Yao-Heng Su, Zhe-Yan Tu, and Xiang-An Yan. "Electronic transport properties of a single chiroptical molecular switch with graphene nanoribbons electrodes." Optik 127, no. 11 (June 2016): 4774–77. http://dx.doi.org/10.1016/j.ijleo.2016.02.018.

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22

Van Delden, R. A., A. M. Schoevaars, and B. L. Feringa. "A Novel Donor Acceptor Substituted Chiroptical Molecular Switch: Physical Properties and Photoisomerization Behavior." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 344, no. 1 (June 1, 2000): 1–6. http://dx.doi.org/10.1080/10587250008023807.

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23

Duan, Pengfei, Yuangang Li, Liangchun Li, Jingen Deng, and Minghua Liu. "Multiresponsive Chiroptical Switch of an Azobenzene-Containing Lipid: Solvent, Temperature, and Photoregulated Supramolecular Chirality." Journal of Physical Chemistry B 115, no. 13 (April 7, 2011): 3322–29. http://dx.doi.org/10.1021/jp110636b.

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24

Zou, Gang, Hao Jiang, Qijin Zhang, Hideki Kohn, Takaaki Manaka, and Mitsumasa Iwamoto. "Chiroptical switch based on azobenzene-substituted polydiacetylene LB films under thermal and photic stimuli." J. Mater. Chem. 20, no. 2 (2010): 285–91. http://dx.doi.org/10.1039/b913764e.

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25

van Leeuwen, Thomas, Thomas C. Pijper, Jetsuda Areephong, Ben L. Feringa, Wesley R. Browne, and Nathalie Katsonis. "Reversible photochemical control of cholesteric liquid crystals with a diamine-based diarylethene chiroptical switch." Journal of Materials Chemistry 21, no. 9 (2011): 3142. http://dx.doi.org/10.1039/c0jm03626a.

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26

Guo, Shuo, Lin-Yi Hu, Qing-Yu Meng, Yu-Ying Zhang, Cai-Cai Zhang, Li-Juan Xing, Haitao Yu, and He-Lue Sun. "Photocontrolled chiroptical switch based on the self-assembly of azobenzene-bridged bis-tryptophan enantiomers." Journal of Colloid and Interface Science 657 (March 2024): 913–20. http://dx.doi.org/10.1016/j.jcis.2023.12.052.

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27

Miao, Tengfei, Xiaoxiao Cheng, Yilin Qian, Yaling Zhuang, and Wei Zhang. "Engineering Achiral Liquid Crystalline Polymers for Chiral Self-Recovery." International Journal of Molecular Sciences 22, no. 21 (November 5, 2021): 11980. http://dx.doi.org/10.3390/ijms222111980.

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Flexible construction of permanently stored supramolecular chirality with stimulus-responsiveness remains a big challenge. Herein, we describe an efficient method to realize the transfer and storage of chirality in intrinsically achiral films of a side-chain polymeric liquid crystal system by combining chiral doping and cross-linking strategy. Even the helical structure was destroyed by UV light irradiation, the memorized chiral information in the covalent network enabled complete self-recovery of the original chiral superstructure. These results allowed the building of a novel chiroptical switch without any additional chiral source in multiple types of liquid crystal polymers, which may be one of the competitive candidates for use in stimulus-responsive chiro-optical devices.

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28

Li, Yuangang, Tianyu Wang, and Minghua Liu. "Gelating-induced supramolecular chirality of achiral porphyrins: chiroptical switch between achiral molecules and chiral assemblies." Soft Matter 3, no. 10 (2007): 1312. http://dx.doi.org/10.1039/b710165a.

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29

Liu, Wenjie, Derong Cao, Jinan Peng, Hong Zhang, and Herbert Meier. "A Dendrimer Chiroptical Switch Based on the Reversible Intramolecular Photoreaction of Anthracene and Benzene Rings." Chemistry - An Asian Journal 5, no. 8 (June 25, 2010): 1896–901. http://dx.doi.org/10.1002/asia.201000159.

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30

Lv, Kai, Long Qin, Xiufeng Wang, Li Zhang, and Minghua Liu. "A chiroptical switch based on supramolecular chirality transfer through alkyl chain entanglement and dynamic covalent bonding." Physical Chemistry Chemical Physics 15, no. 46 (2013): 20197. http://dx.doi.org/10.1039/c3cp53620c.

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31

Liu, Yiran, Menghua Du, Penghui Zhang, Hanting Wang, Xuan Dong, Zhixia Wang, Yuanyuan Wang, and Lukang Ji. "Host-guest interaction enabled chiroptical property, morphology transition, and phase switch in azobenzene-glutamide amphiphile based hydrogel." Colloids and Surfaces A: Physicochemical and Engineering Aspects 655 (December 2022): 130212. http://dx.doi.org/10.1016/j.colsurfa.2022.130212.

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32

Bei-bei, Liu, Lu Wei, Du Gan-hong, Chen Dan, Ling Jun, Jiang Li-ming, and Shen Zhi-quan. "DESIGN OF AN OPTICALLY ACTIVE POLYSTYRENE BEARING IMINE PENDANTS AND ITS ACID/BASE-TRIGGERED CHIROPTICAL SWITCH PROPERTY." Acta Polymerica Sinica 013, no. 4 (May 10, 2013): 436–42. http://dx.doi.org/10.3724/sp.j.1105.2013.13007.

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33

Suk, Jae-min, Veluru Ramesh Naidu, Xinfang Liu, Myoung Soo Lah, and Kyu-Sung Jeong. "A Foldamer-Based Chiroptical Molecular Switch That Displays Complete Inversion of the Helical Sense upon Anion Binding." Journal of the American Chemical Society 133, no. 35 (September 7, 2011): 13938–41. http://dx.doi.org/10.1021/ja206546b.

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34

Jiang, Jian, Tianyu Wang, and Minghua Liu. "Creating chirality in the inner walls of silica nanotubes through a hydrogel template: chiral transcription and chiroptical switch." Chemical Communications 46, no. 38 (2010): 7178. http://dx.doi.org/10.1039/c0cc00891e.

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35

Wang, Jian-Ping, Guo-Chun Yang, Li-Kai Yan, Wei Guan, Shi-Zheng Wen, and Zhong-Min Su. "TDDFT studies on chiral organophosphonate substituted divacant Keggin-type polyoxotungstate: diplex multistep-redox-triggered chiroptical and NLO switch." Dalton Transactions 41, no. 33 (2012): 10097. http://dx.doi.org/10.1039/c2dt30449j.

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36

van Delden, R. A., M. B. van Gelder, N. P. M. Huck, and B. L. Feringa. "Controlling the Color of Cholesteric Liquid-Crystalline Films by Photoirradiation of a Chiroptical Molecular Switch Used as Dopant." Advanced Functional Materials 13, no. 4 (April 17, 2003): 319–24. http://dx.doi.org/10.1002/adfm.200304313.

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37

Kröner, Dominik, Bastian Klaumünzer, and Tillmann Klamroth. "From Stochastic Pulse Optimization to a Stereoselective Laser Pulse Sequence: Simulation of a Chiroptical Molecular Switch Mounted on Adamantane." Journal of Physical Chemistry A 112, no. 40 (October 9, 2008): 9924–35. http://dx.doi.org/10.1021/jp804352q.

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38

Zhang, Guocheng, and Minghua Liu. "Acidichromism and chiroptical switch based on the self-assembly of a cyanine dye on the PLGA/PAH LbL film." Journal of Materials Chemistry 19, no. 10 (2009): 1471. http://dx.doi.org/10.1039/b817782a.

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39

Pijper, Dirk, Mahthild G. M. Jongejan, Auke Meetsma, and Ben L. Feringa. "Light-Controlled Supramolecular Helicity of a Liquid Crystalline Phase Using a Helical Polymer Functionalized with a Single Chiroptical Molecular Switch." Journal of the American Chemical Society 130, no. 13 (April 2008): 4541–52. http://dx.doi.org/10.1021/ja711283c.

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40

Delden, Richard A. van, Tommaso Mecca, Carlo Rosini, and Ben L. Feringa. "A Chiroptical Molecular Switch with Distinct Chiral and Photochromic Entities and Its Application in Optical Switching of a Cholesteric Liquid Crystal." Chemistry - A European Journal 10, no. 1 (January 5, 2004): 61–70. http://dx.doi.org/10.1002/chem.200305276.

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41

Nishida, Jun-ichi, Takanori Suzuki, Masakazu Ohkita, and Takashi Tsuji. "A Redox Switch Based on Dihydro[5]helicene: Drastic Chiroptical Response Induced by Reversible C−C Bond Making/Breaking upon Electron Transfer." Angewandte Chemie 113, no. 17 (September 3, 2001): 3351–54. http://dx.doi.org/10.1002/1521-3757(20010903)113:17<3351::aid-ange3351>3.0.co;2-l.

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42

Nishida, Jun-ichi, Takanori Suzuki, Masakazu Ohkita, and Takashi Tsuji. "A Redox Switch Based on Dihydro[5]helicene: Drastic Chiroptical Response Induced by Reversible C−C Bond Making/Breaking upon Electron Transfer." Angewandte Chemie International Edition 40, no. 17 (September 3, 2001): 3251–54. http://dx.doi.org/10.1002/1521-3773(20010903)40:17<3251::aid-anie3251>3.0.co;2-p.

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43

van Delden, Richard A., Johannes H. Hurenkamp, and Ben L. Feringa. "Photochemical and Thermal Isomerization Processes of a Chiral Auxiliary Based Donor–Acceptor Substituted Chiroptical Molecular Switch: Convergent Synthesis, Improved Resolution and Switching Properties." Chemistry - A European Journal 9, no. 12 (June 16, 2003): 2845–53. http://dx.doi.org/10.1002/chem.200204660.

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44

Yen-Pon, Expédite, Floris Buttard, Lucas Frédéric, Pierre Thuéry, Frédéric Taran, Grégory Pieters, Pier Alexandre Champagne, and Davide Audisio. "Heterohelicenes through 1,3-Dipolar Cycloaddition of Sydnones with Arynes: Synthesis, Origins of Selectivity, and Application to pH-Triggered Chiroptical Switch with CPL Sign Reversal." JACS Au 1, no. 6 (May 14, 2021): 807–18. http://dx.doi.org/10.1021/jacsau.1c00084.

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45

Duan, Pengfei, Long Qin, and Minghua Liu. "Langmuir−Blodgett Films and Chiroptical Switch of an Azobenzene-Containing Dendron Regulated by the in Situ Host−Guest Reaction at the Air/Water Interface†." Langmuir 27, no. 4 (February 15, 2011): 1326–31. http://dx.doi.org/10.1021/la103934g.

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46

Zhu, Xuewang, and Minghua Liu. "Layer-by-layer assembly of a new l-glutamic acid based polymer with PAH: formation of hollow sphere during deposition, dye loading and chiroptical switch." Soft Matter 7, no. 24 (2011): 11447. http://dx.doi.org/10.1039/c1sm06523h.

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47

Kerner, Lukáš, Anna Kicková, Juraj Filo, Stanislav Kedžuch, and Martin Putala. "Elucidation of Photoisomerization-Related Structural Changes in an Acrylamide-Bridged Binaphthalene–Diazene Macrocyclic Chiroptical Switch by Experimental Electronic Circular Dichroism Spectra Simulation: Role of Dispersion Corrections." Journal of Physical Chemistry A 119, no. 32 (July 31, 2015): 8588–98. http://dx.doi.org/10.1021/acs.jpca.5b03474.

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48

Mori, Tadashi, and Yoshihisa Inoue. "Chiral Organic Radical Cation and Dication. A Reversible Chiroptical Redox Switch Based on Stepwise Transformation of Optically Active Tetrakis(p-alkoxyphenyl)ethylenes to Radical Cations and Dications." Journal of Physical Chemistry A 109, no. 12 (March 2005): 2728–40. http://dx.doi.org/10.1021/jp044917m.

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49

Zhang, Li, Han-Xiao Wang, Shuai Li, and Minghua Liu. "Supramolecular chiroptical switches." Chemical Society Reviews 49, no. 24 (2020): 9095–120. http://dx.doi.org/10.1039/d0cs00191k.

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50

Feringa, Ben L., Richard A. van Delden, Nagatoshi Koumura, and Edzard M. Geertsema. "Chiroptical Molecular Switches." Chemical Reviews 100, no. 5 (May 2000): 1789–816. http://dx.doi.org/10.1021/cr9900228.

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