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Artykuły w czasopismach na temat „Photoresponsive systems”

Autor: Grafiati
Data publikacji: 26 października 2024
Data aktualizacji: 31 lipca 2025

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1

Park, Hea-Lim, Min-Hoi Kim, and Hyeok Kim. "Improvement of Photoresponse in Organic Phototransistors through Bulk Effect of Photoresponsive Gate Insulators." Materials 13, no. 7 (2020): 1565. http://dx.doi.org/10.3390/ma13071565.

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In this study, we investigate the bulk effect of photoresponsive gate insulators on the photoresponse of organic phototransistors (OPTs), using OPTs with poly(4-vinylphenol) layers of two different thicknesses. For the photoresponse, the interplay between the charge accumulation (capacitance) and light-absorbance capabilities of a photoresponsive gate insulator was investigated. Although an OPT with a thicker gate insulator exhibits a lower capacitance and hence a lower accumulation capability of photogenerating charges, a thicker poly(4-vinylphenol) layer, in contrast to a thinner one, absorb
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2

Kinoshita, Takatoshi. "Photoresponsive membrane systems." Journal of Photochemistry and Photobiology B: Biology 42, no. 1 (1998): 12–19. http://dx.doi.org/10.1016/s1011-1344(97)00099-7.

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3

Desvergne, Jean-Pierre, Frédéric Fages, Henri Bouas-Laurent, and P. Marsau. "Tunable photoresponsive supramolecular systems." Pure and Applied Chemistry 64, no. 9 (1992): 1231–38. http://dx.doi.org/10.1351/pac199264091231.

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4

Qu, Da-Hui, Qiao-Chun Wang, Qi-Wei Zhang, Xiang Ma, and He Tian. "Photoresponsive Host–Guest Functional Systems." Chemical Reviews 115, no. 15 (2015): 7543–88. http://dx.doi.org/10.1021/cr5006342.

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Zhou, Yang, Huan Ye, Yongbing Chen, Rongying Zhu, and Lichen Yin. "Photoresponsive Drug/Gene Delivery Systems." Biomacromolecules 19, no. 6 (2018): 1840–57. http://dx.doi.org/10.1021/acs.biomac.8b00422.

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Abueva, Celine DG, Phil-Sang Chung, Hyun-Seok Ryu, So-Young Park, and Seung Hoon Woo. "Photoresponsive Hydrogels as Drug Delivery Systems." Medical Lasers 9, no. 1 (2020): 6–11. http://dx.doi.org/10.25289/ml.2020.9.1.6.

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Revilla-López, Guillem, Adele D. Laurent, Eric A. Perpète, et al. "Key Building Block of Photoresponsive Biomimetic Systems." Journal of Physical Chemistry B 115, no. 5 (2011): 1232–42. http://dx.doi.org/10.1021/jp108341a.

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8

Qu, Da-Hui, Qiao-Chun Wang, Qi-Wei Zhang, Xiang Ma, and He Tian. "ChemInform Abstract: Photoresponsive Host-Guest Functional Systems." ChemInform 46, no. 38 (2015): no. http://dx.doi.org/10.1002/chin.201538291.

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9

Menon, Sajith, Rahul M. Ongungal, and Suresh Das. "Photoresponsive Glycopolymer Aggregates as Controlled Release Systems." Macromolecular Chemistry and Physics 215, no. 23 (2014): 2365–73. http://dx.doi.org/10.1002/macp.201400365.

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10

Chen, Hengjun, Min Li, Guiming Zheng, et al. "Molecular packing, crystal to crystal transformation, electron transfer behaviour, and photochromic and fluorescent properties of three hydrogen-bonded supramolecular complexes containing benzenecarboxylate donors and viologen acceptors." RSC Adv. 4, no. 81 (2014): 42983–90. http://dx.doi.org/10.1039/c4ra07471h.

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11

Xue, Xiaonan, Huarui Wang, Yanbing Han, and Hongwei Hou. "Photoswitchable nonlinear optical properties of metal complexes." Dalton Transactions 47, no. 1 (2018): 13–22. http://dx.doi.org/10.1039/c7dt03989a.

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12

Wang, Huan, and Dong Ha Kim. "Perovskite-based photodetectors: materials and devices." Chemical Society Reviews 46, no. 17 (2017): 5204–36. http://dx.doi.org/10.1039/c6cs00896h.

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13

IKEDA, Tomiki, Seiji KURIHARA, and Shigeo TAZUKE. "Photoresponsive function in biological membranes and artificial systems." membrane 11, no. 6 (1986): 314–25. http://dx.doi.org/10.5360/membrane.11.314.

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14

Xue, Hongyan, Youmei Han, Guanglei Liu, Wenjing Chen, Zhihang Wang, and Nong Wang. "Photoresponsive surfactants for controllable and reversible emulsion systems." Colloids and Surfaces A: Physicochemical and Engineering Aspects 705 (January 2025): 135669. http://dx.doi.org/10.1016/j.colsurfa.2024.135669.

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15

Seki, Takahiro. "Smart Photoresponsive Polymer Systems Organized in Two Dimensions." Bulletin of the Chemical Society of Japan 80, no. 11 (2007): 2084–109. http://dx.doi.org/10.1246/bcsj.80.2084.

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16

Schulze, Michael, Manuel Utecht, Thomas Moldt, et al. "Nonlinear optical response of photochromic azobenzene-functionalized self-assembled monolayers." Physical Chemistry Chemical Physics 17, no. 27 (2015): 18079–86. http://dx.doi.org/10.1039/c5cp03093e.

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Incorporating photochromic molecules into organic–inorganic hybrid materials may lead to photoresponsive systems. In such systems, the second-order nonlinear properties can be controlled via external stimulation with light at appropriate wavelengths.
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17

Cieślak, Anna M., Emma-Rose Janeček, Kamil Sokołowski, et al. "Photo-induced interfacial electron transfer of ZnO nanocrystals to control supramolecular assembly in water." Nanoscale 9, no. 42 (2017): 16128–32. http://dx.doi.org/10.1039/c7nr03095a.

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18

Akamatsu, Masaaki, Mayu Shiina, Rekha Goswami Shrestha, Kenichi Sakai, Masahiko Abe, and Hideki Sakai. "Photoinduced viscosity control of lecithin-based reverse wormlike micellar systems using azobenzene derivatives." RSC Advances 8, no. 42 (2018): 23742–47. http://dx.doi.org/10.1039/c8ra04690e.

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19

Chen, Shaoyu, Liang Fei, Fangqing Ge, and Chaoxia Wang. "Photoresponsive aqueous foams with controllable stability from nonionic azobenzene surfactants in multiple-component systems." Soft Matter 15, no. 41 (2019): 8313–19. http://dx.doi.org/10.1039/c9sm01379b.

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20

Aya, Satoshi, Junichi Kougo, Fumito Araoka, Osamu Haba, and Koichiro Yonetake. "Nontrivial topological defects of micro-rods immersed in nematics and their phototuning." Physical Chemistry Chemical Physics 24, no. 5 (2022): 3338–47. http://dx.doi.org/10.1039/d1cp03363h.

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The paper presents the experimental observation of nontrivial zigzag-like topology in many-body micro-rod systems, where photoresponsive surfaces can switch the topology. Simulation results are compared with the experimental ones.
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21

Palma, Matteo. "(Invited) Solution-Processable Carbon Nanotube Nanohybrids for Multiplexed Photoresponsive Devices." ECS Meeting Abstracts MA2022-01, no. 9 (2022): 743. http://dx.doi.org/10.1149/ma2022-019743mtgabs.

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In this talk, we will present assembly strategies for the construction in aqueous solution of hybrid nanostructures comprising inorganic semiconducting nanoparticles (CdS and PbS) grown on DNA-wrapped carbon nanotubes employed as templates. The organization of these hybrids in nanoscale devices, including ones employed for multiplexed photoinduced electrical response, will be discussed. In particular, solution-processed multiplexed photoresponsive devices were fabricated from CdS-CNT and PbS-CNT nanohybrids,[1] displaying a sensitivity to a broad range of illumination wavelengths (405,532, and
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22

Zhu, Jiajia, Wei Zhao, and Biao Wu. "Photoresponsive Phosphate Coordination Using Azobenzene-Spaced Bis-tris(urea) Ligand." Advances in Engineering Technology Research 6, no. 1 (2023): 241. http://dx.doi.org/10.56028/aetr.6.1.241.2023.

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Given the nondestructive nature and high spatiotemporal resolution of the light source, studies of photoresponsive systems have gained great attention and made considerable progresses in the past decades. By incoporationg photoswitch molecules with noncovalent interaction, photoresoive, supramolecular systems can be designed for tailored properties, e.g., guest delivery, catalysis, sensing, and information processing. Here, we introduced a new photoresponsive ligand (L) comprised of azobenzene spacer and two tris(urea) binding moiety. The latter component displayed characteristic coordination
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23

Gutiérrez-Arzaluz, Luis, Fatima López-Salazar, Bernardo Salcido-Santacruz, et al. "Bisindole caulerpin analogues as nature-inspired photoresponsive molecules." Journal of Materials Chemistry C 8, no. 20 (2020): 6680–88. http://dx.doi.org/10.1039/c9tc05889c.

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24

Muraoka, Takahiro, and Kazushi Kinbara. "Development of photoresponsive supramolecular machines inspired by biological molecular systems." Journal of Photochemistry and Photobiology C: Photochemistry Reviews 13, no. 2 (2012): 136–47. http://dx.doi.org/10.1016/j.jphotochemrev.2012.04.001.

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25

Liu, Ming, Xuzhou Yan, Menglong Hu, et al. "Photoresponsive Host−Guest Systems Based on a New Azobenzene-Containing Crytpand." Organic Letters 12, no. 11 (2010): 2558–61. http://dx.doi.org/10.1021/ol100770j.

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26

Chiu, Chun‐Wei, та Jye‐Shane Yang. "Photoluminescent and Photoresponsive Iptycene‐Incorporated π‐Conjugated Systems: Fundamentals and Applications". ChemPhotoChem 4, № 8 (2020): 538–63. http://dx.doi.org/10.1002/cptc.201900300.

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27

刘, 傲冉. "Research Progress on Photoresponsive Host-Guest Supramolecular Systems Based on Pillararenes." Advances in Analytical Chemistry 15, no. 01 (2025): 22–33. https://doi.org/10.12677/aac.2025.151003.

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28

Tyutyulkov, Nikolai, та Fritz Dietz. "Photoswitching of the Optical and Electrical Properties of One-dimensional π-Electron Systems". Zeitschrift für Naturforschung A 57, № 1-2 (2002): 89–93. http://dx.doi.org/10.1515/zna-2002-1-214.

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The photoswitching of the energy gap width of the isomeric forms of photoresponsive polymers with homomiclear photochrome diaryletheue elementary units is investigated theoretically, taking into account the correlation correction. It is shown that a real switching of electrical conductivity (insulator ⇔ semiconductor or conductor) can not be realized with polymers with alternant homomiclear π -electron systems within the elementary unit. A change and tuning-in of the light absorption is possible in most cases.
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29

Tyutyulkov, Nikolai, та Fritz Dietz Wilhelm-Ostwald. "Photoswitching of the Optical and Electrical Properties of One-dimensional π-Electron Systems". Zeitschrift für Naturforschung A 57, № 9-10 (2002): 89–93. http://dx.doi.org/10.1515/zna-2002-9-1014.

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The photoswitching of the energy gap width of the isomeric forms of photoresponsive polymers with homonuclear photochromic diarylethene elementary units is investigated theoretically, taking into account the correlation correction. It is shown that a real switching of electrical conductivity (insulator ⇔ semiconductor or conductor) can not be realized with polymers with alternant homonuclear π-electron systems within the elementary unit. A change and tuning-in of the light absorption is possible in most cases.
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30

Kuzuya, Akinori, Keita Tanaka, and Makoto Komiyama. "Photoswitching of Site-Selective RNA Scission by Sequential Incorporation of Azobenzene and Acridine Residues in a DNA Oligomer." Journal of Nucleic Acids 2011 (2011): 1–8. http://dx.doi.org/10.4061/2011/162452.

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Photoresponsive systems for site-selective RNA scission have been prepared by combining Lu(III) ions with acridine/azobenzene dual-modified DNA. The modified DNA forms a heteroduplex with substrate RNA, and the target phosphodiester linkages in front of the acridine residue is selectively activated so that Lu(III) ion rapidly cleaves the linkage. Azobenzene residue introduced adjacent to the acridine residue acts as a photoresponsive switch, which triggers the site-selective scission upon UV irradiation. Atransisomer of azobenzene efficiently suppresses the scission, whereas the cis isomer for
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31

Seki, Takahiro. "Dynamic Photoresponsive Functions in Organized Layer Systems Comprised of Azobenzene-containing Polymers." Polymer Journal 36, no. 6 (2004): 435–54. http://dx.doi.org/10.1295/polymj.36.435.

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32

Hong, Bo. "Photoresponsive and Redox-Active Supramolecular Systems with Rigid Sp Carbon Chain Spacers." Comments on Inorganic Chemistry 20, no. 4-6 (1999): 177–207. http://dx.doi.org/10.1080/02603599908021443.

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33

Ameerunisha, Sardar, and Panthappally S. Zacharias. "Characterization of simple photoresponsive systems and their applications to metal ion transport." Journal of the Chemical Society, Perkin Transactions 2, no. 8 (1995): 1679. http://dx.doi.org/10.1039/p29950001679.

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34

Zhou, Fang, Shaohua Wu, Chris Rader, et al. "Crosslinked Ionic Alginate and Cellulose-based Hydrogels for Photoresponsive Drug Release Systems." Fibers and Polymers 21, no. 1 (2020): 45–54. http://dx.doi.org/10.1007/s12221-020-9418-6.

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35

Saccone, Marco, Giancarlo Terraneo, Tullio Pilati, et al. "Azobenzene-based difunctional halogen-bond donor: towards the engineering of photoresponsive co-crystals." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 70, no. 1 (2013): 149–56. http://dx.doi.org/10.1107/s205252061302622x.

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Halogen bonding is emerging as a powerful non-covalent interaction in the context of supramolecular photoresponsive materials design, particularly due to its high directionality. In order to obtain further insight into the solid-state features of halogen-bonded photoactive molecules, three halogen-bonded co-crystals containing an azobenzene-based difunctional halogen-bond donor molecule, (E)-bis(4-iodo-2,3,5,6-tetrafluorophenyl)diazene, C12F8I2N2, have been synthesized and structurally characterized by single-crystal X-ray diffraction. The crystal structure of the non-iodinated homologue (E)-b
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36

Klajn, Rafal. "Immobilized azobenzenes for the construction of photoresponsive materials." Pure and Applied Chemistry 82, no. 12 (2010): 2247–79. http://dx.doi.org/10.1351/pac-con-10-09-04.

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The immobilization of molecular switches onto inorganic supports has recently become a hot topic as it can give rise to novel hybrid materials in which the properties of the two components are mutually enhanced. Even more attractive is the concept of “transferring” the switchable characteristics of single layers of organic molecules onto the underlying inorganic components, rendering them responsive to external stimuli as well. Of the various molecular switches studied, azobenzene (AB) has arguably attracted most attention due to its simple molecular structure, and because its “trigger” (light
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37

Tamba, Masaaki, Keiji Murayama, Hiroyuki Asanuma, and Takashi Nakakuki. "Renewable DNA Proportional-Integral Controller with Photoresponsive Molecules." Micromachines 13, no. 2 (2022): 193. http://dx.doi.org/10.3390/mi13020193.

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A molecular robot is an intelligent molecular system. A typical control problem of molecular robots is to maintain the concentration of a specific DNA strand at the desired level, which is typically attained by a molecular feedback control mechanism. A molecular feedback system can be constructed in a bottom-up method by transforming a nonlinear chemical reaction system into a pseudo-linear system. This method enables the implementation of a molecular proportional-integral (PI) controller on a DNA reaction system. However, a DNA reaction system is driven by fuel DNA strand consumption, and wit
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38

Nagasaki, Takeshi. "Photoresponsive polymeric materials for drug delivery systems: double targeting with photo-responsive polymers." Drug Delivery System 23, no. 6 (2008): 637–43. http://dx.doi.org/10.2745/dds.23.637.

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Santamaria-Garcia, Vivian J., Domingo R. Flores-Hernandez, Flavio F. Contreras-Torres, Rodrigo Cué-Sampedro, and José Antonio Sánchez-Fernández. "Advances in the Structural Strategies of the Self-Assembly of Photoresponsive Supramolecular Systems." International Journal of Molecular Sciences 23, no. 14 (2022): 7998. http://dx.doi.org/10.3390/ijms23147998.

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Photosensitive supramolecular systems have garnered attention due to their potential to catalyze highly specific tasks through structural changes triggered by a light stimulus. The tunability of their chemical structure and charge transfer properties provides opportunities for designing and developing smart materials for multidisciplinary applications. This review focuses on the approaches reported in the literature for tailoring properties of the photosensitive supramolecular systems, including MOFs, MOPs, and HOFs. We discuss relevant aspects regarding their chemical structure, action mechan
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40

Yamamoto, Hiroyuki, and Ayako Nishida. "Photoresponsive Peptide and Polypeptide Systems. VI. Reversible Solubility Change of Azo Aromatic Lysine." Bulletin of the Chemical Society of Japan 61, no. 6 (1988): 2201–2. http://dx.doi.org/10.1246/bcsj.61.2201.

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41

Higuchi, Masahiro, та Takatoshi Kinoshita. "Photoresponsive behavior of self-assembling systems by amphiphilic α-helix with azobenzene unit". Journal of Photochemistry and Photobiology B: Biology 42, № 2 (1998): 143–50. http://dx.doi.org/10.1016/s1011-1344(98)00066-9.

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42

Rakotondradany, Felaniaina, M. A. Whitehead, Anne-Marie Lebuis, and Hanadi F. Sleiman. "Photoresponsive Supramolecular Systems: Self-Assembly of Azodibenzoic Acid Linear Tapes and Cyclic Tetramers." Chemistry - A European Journal 9, no. 19 (2003): 4771–80. http://dx.doi.org/10.1002/chem.200304864.

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43

Yu, Wentao, Sudarshana Santhosh Kumar Kothapalli, Zhiyao Yang, et al. "Light-Controlled Interconvertible Self-Assembly of Non-Photoresponsive Suprastructures." Molecules 29, no. 20 (2024): 4842. http://dx.doi.org/10.3390/molecules29204842.

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Achieving light-induced manipulation of controlled self-assembly in nanosized structures is essential for developing artificially dynamic smart materials. Herein, we demonstrate an approach using a non-photoresponsive hydrogen-bonded (H-bonded) macrocycle to control the self-assembly and disassembly of nanostructures in response to light. The present system comprises a photoacid (merocyanine, 1-MEH), a pseudorotaxane formed by two H-bonded macrocycles, dipyridinyl acetylene, and zinc ions. The operation of such a system is examined according to the alternation of self-assembly through proton t
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44

Jin, Sangrak, Yale Jeon, Min Soo Jeon, et al. "Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth." Proceedings of the National Academy of Sciences 118, no. 9 (2021): e2020552118. http://dx.doi.org/10.1073/pnas.2020552118.

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Acetogenic bacteria use cellular redox energy to convert CO2 to acetate using the Wood–Ljungdahl (WL) pathway. Such redox energy can be derived from electrons generated from H2 as well as from inorganic materials, such as photoresponsive semiconductors. We have developed a nanoparticle-microbe hybrid system in which chemically synthesized cadmium sulfide nanoparticles (CdS-NPs) are displayed on the cell surface of the industrial acetogen Clostridium autoethanogenum. The hybrid system converts CO2 into acetate without the need for additional energy sources, such as H2, and uses only light-induc
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45

Yadav, Santosh, Smriti Rekha Deka, Geeta Verma, Ashwani Kumar Sharma, and Pradeep Kumar. "Photoresponsive amphiphilic azobenzene–PEG self-assembles to form supramolecular nanostructures for drug delivery applications." RSC Advances 6, no. 10 (2016): 8103–17. http://dx.doi.org/10.1039/c5ra26658k.

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Kleine, Tristan S., Julie I. Frish, Nicholas G. Pavlopoulos, et al. "Refractive Index Contrast Polymers: Photoresponsive Systems with Spatial Modulation of Refractive Index for Photonics." ACS Macro Letters 9, no. 3 (2020): 416–21. http://dx.doi.org/10.1021/acsmacrolett.9b00919.

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47

Yamamoto, Hiroyuki, and Ayako Nishida. "Photoresponsive peptide and polypeptide systems V: Reversible photochromism of azo aromatic pentapeptide in solvents." Journal of Photochemistry and Photobiology A: Chemistry 42, no. 1 (1988): 149–55. http://dx.doi.org/10.1016/1010-6030(88)80056-x.

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48

Hong, Bo. "ChemInform Abstract: Photoresponsive and Redox-Active Supramolecular Systems with Rigid Sp Carbon Chain Spacers." ChemInform 30, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199931302.

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Thaggard, Grace, Kyoung Chul Park, and Natalia Shustova. "(Invited) Stimuli-Responsive Metal-Organic Frameworks." ECS Meeting Abstracts MA2023-01, no. 37 (2023): 2165. http://dx.doi.org/10.1149/ma2023-01372165mtgabs.

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Development of stimuli-responsive materials is crucial for the next advancements in the technology and energy sectors. For instance, reversible tuning photophysical profiles of materials or modulation of energy transfer processes are key aspects for the development of next generation of logic gates, spatially- and temporally-resolved sensors, and on-demand drug delivery systems. Our recent efforts have focused on employment of metal-organic frameworks (MOFs) as a versatile platform for the material development, which contain photochromic moieties, allowing for tailoring MOF electronic and phot
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50

White, Timothy J. "Light to work transduction and shape memory in glassy, photoresponsive macromolecular systems: Trends and opportunities." Journal of Polymer Science Part B: Polymer Physics 50, no. 13 (2012): 877–80. http://dx.doi.org/10.1002/polb.23079.

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