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Artigos de revistas sobre o tema "Chiroptical switch"

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Autor: Grafiati
Publicado: 25 de maio de 2024

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1

Feringa, Ben L., Wolter F. Jager, Ben De Lange e Egbert W. Meijer. "Chiroptical molecular switch". Journal of the American Chemical Society 113, n.º 14 (julho de 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 e Srećko I. Kirin. "A ferrocene-based pseudopeptide chiroptical switch". Dalton Transactions 50, n.º 13 (2021): 4504–11. http://dx.doi.org/10.1039/d1dt00508a.

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3

Westermeier, Christian, Hans-Christoph Gallmeier, Markus Komma e Jörg Daub. "Bispyrene based chiroptical molecular redox switch". Chemical Communications, n.º 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 e Ben L. Feringa. "A chiroptical molecular switch with perfect stereocontrol". Chemical Communications, n.º 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 e Jeanne Crassous. "Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn2+ binding". Chemical Communications 52, n.º 35 (2016): 5932–35. http://dx.doi.org/10.1039/c6cc01748g.

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6

Takaishi, Kazuto, Makoto Yasui e Tadashi Ema. "Binaphthyl–Bipyridyl Cyclic Dyads as a Chiroptical Switch". Journal of the American Chemical Society 140, n.º 16 (13 de abril de 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 e Sandeep Patel. "Synthetic minimalistic tryptophan zippers as a chiroptical switch". Organic & Biomolecular Chemistry 15, n.º 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 e Xiulin Zhu. "A cyclic azobenzenophane-based smart polymer for chiroptical switches". Polymer Chemistry 6, n.º 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 e Félix Freire. "Multistate Chiroptical Switch Triggered by Stimuli-Responsive Chiral Teleinduction". Chemistry of Materials 30, n.º 8 (11 de abril de 2018): 2493–97. http://dx.doi.org/10.1021/acs.chemmater.8b00800.

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10

Guo, P., L. Zhang e M. Liu. "A Supramolecular Chiroptical Switch Exclusively from an Achiral Amphiphile". Advanced Materials 18, n.º 2 (19 de janeiro de 2006): 177–80. http://dx.doi.org/10.1002/adma.200501047.

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11

Kim, M. J., S. J. Yoo e D. Y. Kim. "A Supramolecular Chiroptical Switch Using an Amorphous Azobenzene Polymer". Advanced Functional Materials 16, n.º 16 (20 de outubro de 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 e Jian Ping Gao. "Dual Modulation of a Molecular Switch with Exceptional Chiroptical Properties". Journal of the American Chemical Society 127, n.º 33 (agosto de 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 e 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, n.º 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 e Pengfei Yan. "A light triggered optical and chiroptical switch based on a homochiral Eu2L3 helicate". Journal of Materials Chemistry C 8, n.º 20 (2020): 6788–96. http://dx.doi.org/10.1039/d0tc01044h.

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A pair of homochiral triple-stranded helicates [Eu2(o-LRR)3](TOf)6 and [Eu2(o-LSS)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 e Martin Putala. "A chiroptical binaphthopyran switch: amplified CD response in a polystyrene film". New Journal of Chemistry 34, n.º 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 e Shuxian Shi. "A Chiroptical Switch Based on DNA/Layered Double Hydroxide Ultrathin Films". Langmuir 30, n.º 43 (20 de outubro de 2014): 12916–22. http://dx.doi.org/10.1021/la502968z.

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17

Liao, Bo, Ruigang Liu e Yong Huang. "A Supramolecular Chiroptical Switch Based on Chitosan and Anionic Porphyrin Complex Film". Polymer Journal 39, n.º 10 (4 de setembro de 2007): 1071–77. http://dx.doi.org/10.1295/polymj.pj2007036.

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18

Gomar-Nadal, E., J. Veciana, C. Rovira e D. B. Amabilino. "Chiral Teleinduction in the Formation of a Macromolecular Multistate Chiroptical Redox Switch". Advanced Materials 17, n.º 17 (5 de setembro de 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 e James P. Parakka. "Dynamic NMR Studies of a Potential Chiroptical Switch Based on Dithiocarbamate−Iminodithiolane Interconversion". Organic Letters 3, n.º 21 (outubro de 2001): 3413–16. http://dx.doi.org/10.1021/ol016671z.

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20

Agati, Giovanni, e Antony F. McDonagh. "Chiroptical Switch Based on Photoisomerization of Bilirubin-III.alpha. Bound to Human Serum Albumin". Journal of the American Chemical Society 117, n.º 15 (abril de 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 e Xiang-An Yan. "Electronic transport properties of a single chiroptical molecular switch with graphene nanoribbons electrodes". Optik 127, n.º 11 (junho de 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 e 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, n.º 1 (1 de junho de 2000): 1–6. http://dx.doi.org/10.1080/10587250008023807.

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23

Duan, Pengfei, Yuangang Li, Liangchun Li, Jingen Deng e Minghua Liu. "Multiresponsive Chiroptical Switch of an Azobenzene-Containing Lipid: Solvent, Temperature, and Photoregulated Supramolecular Chirality". Journal of Physical Chemistry B 115, n.º 13 (7 de abril de 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 e Mitsumasa Iwamoto. "Chiroptical switch based on azobenzene-substituted polydiacetylene LB films under thermal and photic stimuli". J. Mater. Chem. 20, n.º 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 e Nathalie Katsonis. "Reversible photochemical control of cholesteric liquid crystals with a diamine-based diarylethene chiroptical switch". Journal of Materials Chemistry 21, n.º 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 e He-Lue Sun. "Photocontrolled chiroptical switch based on the self-assembly of azobenzene-bridged bis-tryptophan enantiomers". Journal of Colloid and Interface Science 657 (março de 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 e Wei Zhang. "Engineering Achiral Liquid Crystalline Polymers for Chiral Self-Recovery". International Journal of Molecular Sciences 22, n.º 21 (5 de novembro de 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 e Minghua Liu. "Gelating-induced supramolecular chirality of achiral porphyrins: chiroptical switch between achiral molecules and chiral assemblies". Soft Matter 3, n.º 10 (2007): 1312. http://dx.doi.org/10.1039/b710165a.

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29

Liu, Wenjie, Derong Cao, Jinan Peng, Hong Zhang e Herbert Meier. "A Dendrimer Chiroptical Switch Based on the Reversible Intramolecular Photoreaction of Anthracene and Benzene Rings". Chemistry - An Asian Journal 5, n.º 8 (25 de junho de 2010): 1896–901. http://dx.doi.org/10.1002/asia.201000159.

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30

Lv, Kai, Long Qin, Xiufeng Wang, Li Zhang e Minghua Liu. "A chiroptical switch based on supramolecular chirality transfer through alkyl chain entanglement and dynamic covalent bonding". Physical Chemistry Chemical Physics 15, n.º 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 e 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 (dezembro de 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 e Shen Zhi-quan. "DESIGN OF AN OPTICALLY ACTIVE POLYSTYRENE BEARING IMINE PENDANTS AND ITS ACID/BASE-TRIGGERED CHIROPTICAL SWITCH PROPERTY". Acta Polymerica Sinica 013, n.º 4 (10 de maio de 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 e 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, n.º 35 (7 de setembro de 2011): 13938–41. http://dx.doi.org/10.1021/ja206546b.

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34

Jiang, Jian, Tianyu Wang e Minghua Liu. "Creating chirality in the inner walls of silica nanotubes through a hydrogel template: chiral transcription and chiroptical switch". Chemical Communications 46, n.º 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 e Zhong-Min Su. "TDDFT studies on chiral organophosphonate substituted divacant Keggin-type polyoxotungstate: diplex multistep-redox-triggered chiroptical and NLO switch". Dalton Transactions 41, n.º 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 e 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, n.º 4 (17 de abril de 2003): 319–24. http://dx.doi.org/10.1002/adfm.200304313.

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37

Kröner, Dominik, Bastian Klaumünzer e 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, n.º 40 (9 de outubro de 2008): 9924–35. http://dx.doi.org/10.1021/jp804352q.

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38

Zhang, Guocheng, e 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, n.º 10 (2009): 1471. http://dx.doi.org/10.1039/b817782a.

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39

Pijper, Dirk, Mahthild G. M. Jongejan, Auke Meetsma e 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, n.º 13 (abril de 2008): 4541–52. http://dx.doi.org/10.1021/ja711283c.

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40

Delden, Richard A. van, Tommaso Mecca, Carlo Rosini e 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, n.º 1 (5 de janeiro de 2004): 61–70. http://dx.doi.org/10.1002/chem.200305276.

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41

Nishida, Jun-ichi, Takanori Suzuki, Masakazu Ohkita e 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, n.º 17 (3 de setembro de 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 e 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, n.º 17 (3 de setembro de 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 e 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, n.º 12 (16 de junho de 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 e 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, n.º 6 (14 de maio de 2021): 807–18. http://dx.doi.org/10.1021/jacsau.1c00084.

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45

Duan, Pengfei, Long Qin e 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, n.º 4 (15 de fevereiro de 2011): 1326–31. http://dx.doi.org/10.1021/la103934g.

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46

Zhu, Xuewang, e 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, n.º 24 (2011): 11447. http://dx.doi.org/10.1039/c1sm06523h.

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47

Kerner, Lukáš, Anna Kicková, Juraj Filo, Stanislav Kedžuch e 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, n.º 32 (31 de julho de 2015): 8588–98. http://dx.doi.org/10.1021/acs.jpca.5b03474.

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48

Mori, Tadashi, e 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, n.º 12 (março de 2005): 2728–40. http://dx.doi.org/10.1021/jp044917m.

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49

Zhang, Li, Han-Xiao Wang, Shuai Li e Minghua Liu. "Supramolecular chiroptical switches". Chemical Society Reviews 49, n.º 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 e Edzard M. Geertsema. "Chiroptical Molecular Switches". Chemical Reviews 100, n.º 5 (maio de 2000): 1789–816. http://dx.doi.org/10.1021/cr9900228.

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