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Статті в журналах з теми "Stimuli-responsive emission"

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Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 28 січня 2023

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1

Moscardi, Liliana, Guglielmo Lanzani, Giuseppe M. Paternò, and Francesco Scotognella. "Stimuli-Responsive Photonic Crystals." Applied Sciences 11, no. 5 (February 27, 2021): 2119. http://dx.doi.org/10.3390/app11052119.

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Анотація:

Recently, tunable photonic crystals (PhCs) have received great research interest, thanks to the wide range of applications in which they can be employed, such as light emission and sensing, among others. In addition, the versatility and ease of fabrication of PhCs allow for the integration of a large range of responsive elements that, in turn, can permit active tuning of PhC optical properties upon application of external stimuli, e.g., physical, chemical or even biological triggers. In this work, we summarize the most employed theoretical tools used for the design of optical properties of responsive PhCs and the most used fabrication techniques. Furthermore, we collect the most relevant results related to this field, with particular emphasis on electrochromic devices.

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2

Hirose, Amane, Kazuo Tanaka, Ryousuke Yoshii, and Yoshiki Chujo. "Film-type chemosensors based on boron diiminate polymers having oxidation-induced emission properties." Polymer Chemistry 6, no. 31 (2015): 5590–95. http://dx.doi.org/10.1039/c5py00055f.

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3

Kim, Joo-Ho, Dajeong Yim, and Woo-Dong Jang. "Thermo-responsive poly(2-isopropyl-2-oxazoline) and tetraphenylethene hybrids for stimuli-responsive photoluminescence control." Chemical Communications 52, no. 22 (2016): 4152–55. http://dx.doi.org/10.1039/c6cc00722h.

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Анотація:

Poly(2-isopropyl-2-oxazoline) (POx), a typical thermo-responsive polymer, was conjugated with a tetraphenylethene derivative, having aggregation induced emission behavior, towards the thermal control of their fluorescence emission.

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4

Yu, Huli, Biao Zhao, Jinbao Guo, Kai Pan, and Jianping Deng. "Stimuli-responsive circularly polarized luminescent films with tunable emission." Journal of Materials Chemistry C 8, no. 4 (2020): 1459–65. http://dx.doi.org/10.1039/c9tc06105c.

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5

Chen, Weijie, Yingle Pan, Jianhua Chen, Fengying Ye, Sheng Hua Liu, and Jun Yin. "Stimuli-responsive organic chromic materials with near-infrared emission." Chinese Chemical Letters 29, no. 10 (October 2018): 1429–35. http://dx.doi.org/10.1016/j.cclet.2018.08.011.

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6

Kazantsev, Maxim S., Alina A. Sonina, Igor P. Koskin, Peter S. Sherin, Tatyana V. Rybalova, Enrico Benassi, and Evgeny A. Mostovich. "Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals." Materials Chemistry Frontiers 3, no. 8 (2019): 1545–54. http://dx.doi.org/10.1039/c9qm00198k.

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7

Li, Changhua, and Shiyong Liu. "Polymeric assemblies and nanoparticles with stimuli-responsive fluorescence emission characteristics." Chemical Communications 48, no. 27 (2012): 3262. http://dx.doi.org/10.1039/c2cc17695e.

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8

Wang, Jie, Fu Tang, Yue Wang, Shuqi Liu, and Lidong Li. "Tunable Single‐Molecule White‐Light Emission in Stimuli‐Responsive Hydrogel." Advanced Optical Materials 8, no. 6 (March 2020): 1901571. http://dx.doi.org/10.1002/adom.201901571.

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9

DONG, YONG QIANG, CHENYU LI, WEIJUN ZHAO, YUPING DONG, and BEN ZHONG TANG. "STIMULUS RESPONSIVE LUMINESCENT MATERIALS: CRYSTALLIZATION-INDUCED EMISSION ENHANCEMENT." Journal of Molecular and Engineering Materials 01, no. 03 (September 2013): 1340010. http://dx.doi.org/10.1142/s2251237313400108.

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Crystallization of a luminogen normally red-shifts and weakens its emission. During investigation of some luminogens exhibiting aggregation-induced emission (AIE), we first noticed that some AIE active luminogens display higher photoluminescence (PL) intensity and bluer emission in the crystalline state than in their amorphous phase, which is termed as crystallization induced emission enhancement (CIEE). The twisted conformations of CIEE active molecules afford loose packing patterns and rule out any detrimental strong interaction. Molecular conformations are locked more tightly in crystals than those in amorphous solid due to the regular weak interactions in crystals, which affords the CIEE effect. The loose packing patterns facilitate emission switching through morphology modulation. Many AIE active molecules have been developed based on restriction of intramolecular rotation (RIR) mechanism, and we obtained many CIEE compounds from those AIE active luminogens and investigated their utilities as stimuli responsive functional materials, especially as chemosensors, thermosensor, mechanosensors and solid-state emitters. Thus, we provide a possible design strategy for the stimuli responsive solid luminescent materials.

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10

Wang, Jing, Bingbing Yue, Xiaoyong Jia, Ruirui Cao, Xiling Niu, Huimin Zhao, Juntan Li, and Liangliang Zhu. "Mechanical stimuli-induced multiple photophysical responsive AIEgens with high contrast properties." Chemical Communications 58, no. 21 (2022): 3517–20. http://dx.doi.org/10.1039/d1cc06931d.

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A new cyano-distyrylbenzene derivative with mechano-induced high contrast change in color and emission was demonstrated. Under mechanical stimuli, the emission peak can redshift from 440 nm to 650 nm, while the appearance can switch from white to pink.

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11

Wang, Meiyao, Lili Xu, Min Lin, Zhibo Li, and Jing Sun. "Fabrication of reversible pH-responsive aggregation-induced emission luminogens assisted by a block copolymer via a dynamic covalent bond." Polymer Chemistry 12, no. 19 (2021): 2825–31. http://dx.doi.org/10.1039/d1py00312g.

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12

Johnstone, Mark D., Chien-Wei Hsu, Nicolas Hochbaum, Joakim Andréasson, and Henrik Sundén. "Multi-color emission with orthogonal input triggers from a diarylethene pyrene-OTHO organogelator cocktail." Chemical Communications 56, no. 6 (2020): 988–91. http://dx.doi.org/10.1039/c9cc08994b.

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13

Zuo, Yunfei, Xing Wang, and Decheng Wu. "Uniting aggregation-induced emission and stimuli-responsive aggregation-caused quenching, single molecule achieved multicolour luminescence." Journal of Materials Chemistry C 7, no. 46 (2019): 14555–62. http://dx.doi.org/10.1039/c9tc05258e.

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14

Han, Tianyu, Xiao Feng, Didi Chen, and Yuping Dong. "A diethylaminophenol functionalized Schiff base: crystallization-induced emission-enhancement, switchable fluorescence and application for security printing and data storage." Journal of Materials Chemistry C 3, no. 28 (2015): 7446–54. http://dx.doi.org/10.1039/c5tc00891c.

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15

Liu, Hao, Wentao Liu, Naoki Ando, Shigehiro Yamaguchi, and Hongyu Zhang. "Organic phosphorescent polymorphs induced by various halogen bonds with stimuli-responsive single/dual phosphorescence switching." Journal of Materials Chemistry C 9, no. 8 (2021): 2738–43. http://dx.doi.org/10.1039/d0tc05468b.

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Анотація:

Cry-A displays pure single RTP emission while Cry-B displays pure dual RTP emission. These two polymorphs could exhibit stimuli-responsive single/dual RTP switching by heating or under solvent vapor conditions.

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16

Liang, Enxiang, Fang Su, Yan Liang, Guoxiang Wang, Wenyuan Xu, Shan Li, Caixia Yang, Jianxin Tang, and Ningbo Zhou. "Dissipative aggregation-induced emission behaviour of an amino-functionalized tetraphenylethene using a pH oscillator." Chemical Communications 56, no. 96 (2020): 15169–72. http://dx.doi.org/10.1039/d0cc06923j.

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17

Xu, Bingjia, Haozhong Wu, Junru Chen, Zhan Yang, Zhiyong Yang, Yuan-Chun Wu, Yi Zhang, et al. "White-light emission from a single heavy atom-free molecule with room temperature phosphorescence, mechanochromism and thermochromism." Chemical Science 8, no. 3 (2017): 1909–14. http://dx.doi.org/10.1039/c6sc03038f.

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18

Li, Junfeng, Chenglong Yang, Xuelei Peng, Ying Chen, Qi Qi, Xiaoyan Luo, Wen-Yong Lai, and Wei Huang. "Stimuli-responsive solid-state emission from o-carborane–tetraphenylethene dyads induced by twisted intramolecular charge transfer in the crystalline state." Journal of Materials Chemistry C 6, no. 1 (2018): 19–28. http://dx.doi.org/10.1039/c7tc03780e.

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19

Shi, Peijun, Xunxue Zhang, Yang Liu, Yuai Duan, Yaping Li, Zhongfeng Li, and Tianyu Han. "A multi-stimuli-responsive AIE material switching among three emission states." Materials Letters 263 (March 2020): 127214. http://dx.doi.org/10.1016/j.matlet.2019.127214.

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20

Yuan, Jin, Ling Wang, Yitong Wang, and Jingcheng Hao. "Stimuli‐Responsive Fluorescent Nanoswitches: Solvent‐Induced Emission Enhancement of Copper Nanoclusters." Chemistry – A European Journal 26, no. 16 (March 18, 2020): 3545–54. http://dx.doi.org/10.1002/chem.201905094.

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21

Wang, Fang, Christopher A. DeRosa, Margaret L. Daly, Daniel Song, Michal Sabat та Cassandra L. Fraser. "Multi-stimuli responsive luminescent azepane-substituted β-diketones and difluoroboron complexes". Materials Chemistry Frontiers 1, № 9 (2017): 1866–74. http://dx.doi.org/10.1039/c7qm00137a.

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Анотація:

Multi-stimuli responsive properties were found for azepane-substituted β-diketones and difluoroboron complexes, including solvatochromism, viscochromism, aggregation-induced emission, mechanochromic luminescence and halochromism.

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22

Hariharan, P. S., M. Baby Mariyatra, E. M. Mothi, Antonia Neels, Georgina Rosair, and Savarimuthu Philip Anthony. "Polymorphism and benzene solvent controlled stimuli responsive reversible fluorescence switching in triphenylphosphoniumfluorenylide crystals." New Journal of Chemistry 41, no. 11 (2017): 4592–98. http://dx.doi.org/10.1039/c7nj01136a.

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Анотація:

Triphenylphosphoniumfluorenylide (TPPFY), a fluorescent fluorene attached molecule, showed polymorphism, benzene solvent induced aggregation enhanced emission (AEE) and external stimuli responsive on–off fluorescence switching.

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23

Jiang, Guoshan, Yu Hai, Hebo Ye, and Lei You. "Dynamic covalent chemistry constrained diphenylethenes: control over reactivity and luminescence both in solution and in the solid state." Organic Chemistry Frontiers 9, no. 5 (2022): 1343–53. http://dx.doi.org/10.1039/d2qo00057a.

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Анотація:

A combination of diphenylethene and dynamic covalent chemistry for the modulation of reactivity and luminescence, stimuli-responsive multistate emission, and mechanochemical reactions in the solid state.

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24

Hu, Liangyu, Yuai Duan, Zhenzhen Xu, Jing Yuan, Yuping Dong, and Tianyu Han. "Stimuli-responsive fluorophores with aggregation-induced emission: implication for dual-channel optical data storage." Journal of Materials Chemistry C 4, no. 23 (2016): 5334–41. http://dx.doi.org/10.1039/c6tc01179a.

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25

Park, Y. I., O. Postupna, A. Zhugayevych, H. Shin, Y. S. Park, B. Kim, H. J. Yen, et al. "A new pH sensitive fluorescent and white light emissive material through controlled intermolecular charge transfer." Chemical Science 6, no. 1 (2015): 789–97. http://dx.doi.org/10.1039/c4sc01911c.

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26

Aschmann, Dennis, Steffen Riebe, Thorben Neumann, Dennis Killa, Jan-Erik Ostwaldt, Christoph Wölper, Carsten Schmuck, and Jens Voskuhl. "A stimuli responsive two component supramolecular hydrogelator with aggregation-induced emission properties." Soft Matter 15, no. 36 (2019): 7117–21. http://dx.doi.org/10.1039/c9sm01513b.

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A dual pH-responsive two component hydrogelator with aggregation-induced emission properties is described. The orchestration of supramolecular guadiniumcarbonylpyrrole dimerisation and the recognition of carboxylic acid is reason for the gelation.

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27

Ohtani, Shunsuke, Natsumi Yamada, Masayuki Gon, Kazuo Tanaka, and Yoshiki Chujo. "The effect of alkyl chain lengths on the red-to-near-infrared emission of boron-fused azomethine conjugated polymers and their film-state stimuli-responsivities." Polymer Chemistry 12, no. 18 (2021): 2752–59. http://dx.doi.org/10.1039/d1py00213a.

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Анотація:

We present systematic studies of the dependence of the red-to-near-infrared emission and stimuli-responsive properties of boron-fused azomethine conjugated copolymers on the lengths of the alkyl chains.

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28

Bhuin, Shouvik, Suman Bhattacharya, and Manab Chakravarty. "Acceptor–donor–acceptor-linked triphenylamine and phenothiazine motifs as cousin molecules: the methyl effect on stimuli-responsiveness, crystallochromism, and dual-state emission." New Journal of Chemistry 45, no. 45 (2021): 21236–47. http://dx.doi.org/10.1039/d1nj04190h.

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Bulky/twisted triphenylamine or phenothiazine linked dicyanoaniline is synthesized to achieve dual-state emitters with crystallochromic and multi-stimuli responsive behaviour. The effect of methyl group on emission is also identified.

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29

Yang, Chaoqing, Flavia Artizzu, Karel Folens, Gijs Du Laing, and Rik Van Deun. "Excitation dependent multicolour luminescence and colour blue-shifted afterglow at room-temperature of europium incorporated hydrogen-bonded multicomponent frameworks." Journal of Materials Chemistry C 9, no. 22 (2021): 7154–62. http://dx.doi.org/10.1039/d1tc01627j.

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Анотація:

Multicoloured luminescence and long-lived blue-shifted afterglow have been obtained in a europium-doped hydrogen-bonded organic framework (HOF). The material displays multi-stimuli responsive emission with anticounterfeiting application potential.

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30

Zhan, Yong, Peng Gong, Peng Yang, Zhe Jin, Ying Bao, Ying Li, and Yongnan Xu. "Aggregation-induced emission and reversible mechanochromic luminescence of carbazole-based triphenylacrylonitrile derivatives." RSC Advances 6, no. 39 (2016): 32697–704. http://dx.doi.org/10.1039/c6ra03310e.

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Анотація:

Conjugated organic molecules exhibiting AIE are characterized by the strongly twisted conjugated skeleton, which could provide loose intermolecular stacking and weak π–π interactions in the solid state to generate stimuli-responsive materials.

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31

Jobbágy, Csaba, Péter Baranyai, Gábor Marsi, Barbara Rácz, Liang Li, Panče Naumov, and Andrea Deák. "Novel gold(i) diphosphine-based dimers with aurophilicity triggered multistimuli light-emitting properties." Journal of Materials Chemistry C 4, no. 43 (2016): 10253–64. http://dx.doi.org/10.1039/c6tc01427e.

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Анотація:

We report a design strategy for the preparation of stimuli-responsive materials with multicolour emission that is based on a single type of luminophore molecule comprising gold(i) and a flexible diphosphine ligand.

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32

Mardani, Hanieh, Hossein Roghani-Mamaqani, Sina Shahi, and Mehdi Salami-Kalajahi. "Stimuli-responsive block copolymers as pH chemosensors by fluorescence emission intensification mechanism." European Polymer Journal 162 (January 2022): 110928. http://dx.doi.org/10.1016/j.eurpolymj.2021.110928.

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33

Zhang, Yujian, Jingwei Sun, Gaofeng Bian, Yiyi Chen, Mi Ouyang, Bin Hu, and Cheng Zhang. "Cyanostilben-based derivatives: mechanical stimuli-responsive luminophors with aggregation-induced emission enhancement." Photochemical & Photobiological Sciences 11, no. 9 (2012): 1414. http://dx.doi.org/10.1039/c2pp05404c.

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34

Wang, Sheng, Teng Li, Xiaoduo Zhang, Liangwei Ma, Chenpeng Li, Xuyang Yao, Derong Cao, and Xiang Ma. "Stimuli‐Responsive Copolymer and Uniform Polymeric Nanoparticles with Photochromism and Switchable Emission." ChemPhotoChem 3, no. 7 (April 23, 2019): 568–74. http://dx.doi.org/10.1002/cptc.201900042.

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35

Butler, Tristan, Fang Wang, Michal Sabat, and Cassandra L. Fraser. "Controlling solid-state optical properties of stimuli responsive dimethylamino-substituted dibenzoylmethane materials." Materials Chemistry Frontiers 1, no. 9 (2017): 1804–17. http://dx.doi.org/10.1039/c7qm00157f.

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Анотація:

Dimethylamino β-diketones with electron donating and withdrawing substituents displayed solvatochromism and aggregation induced emission. In the solid state, a blue to orange color range and thermal and mechanoresponsive properties were achieved.

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36

Das, Sabya Sachi, Priyanshu Bharadwaj, Muhammad Bilal, Mahmood Barani, Abbas Rahdar, Pablo Taboada, Simona Bungau, and George Z. Kyzas. "Stimuli-Responsive Polymeric Nanocarriers for Drug Delivery, Imaging, and Theragnosis." Polymers 12, no. 6 (June 22, 2020): 1397. http://dx.doi.org/10.3390/polym12061397.

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Анотація:

In the past few decades, polymeric nanocarriers have been recognized as promising tools and have gained attention from researchers for their potential to efficiently deliver bioactive compounds, including drugs, proteins, genes, nucleic acids, etc., in pharmaceutical and biomedical applications. Remarkably, these polymeric nanocarriers could be further modified as stimuli-responsive systems based on the mechanism of triggered release, i.e., response to a specific stimulus, either endogenous (pH, enzymes, temperature, redox values, hypoxia, glucose levels) or exogenous (light, magnetism, ultrasound, electrical pulses) for the effective biodistribution and controlled release of drugs or genes at specific sites. Various nanoparticles (NPs) have been functionalized and used as templates for imaging systems in the form of metallic NPs, dendrimers, polymeric NPs, quantum dots, and liposomes. The use of polymeric nanocarriers for imaging and to deliver active compounds has attracted considerable interest in various cancer therapy fields. So-called smart nanopolymer systems are built to respond to certain stimuli such as temperature, pH, light intensity and wavelength, and electrical, magnetic and ultrasonic fields. Many imaging techniques have been explored including optical imaging, magnetic resonance imaging (MRI), nuclear imaging, ultrasound, photoacoustic imaging (PAI), single photon emission computed tomography (SPECT), and positron emission tomography (PET). This review reports on the most recent developments in imaging methods by analyzing examples of smart nanopolymers that can be imaged using one or more imaging techniques. Unique features, including nontoxicity, water solubility, biocompatibility, and the presence of multiple functional groups, designate polymeric nanocues as attractive nanomedicine candidates. In this context, we summarize various classes of multifunctional, polymeric, nano-sized formulations such as liposomes, micelles, nanogels, and dendrimers.

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37

Zhu, Huichao, Shiyin Weng, Hong Zhang, Haizhu Yu, Lin Kong, Yulin Zhong, Yupeng Tian, and Jiaxiang Yang. "A novel carbazole derivative containing fluorobenzene unit: aggregation-induced fluorescence emission, polymorphism, mechanochromism and non-reversible thermo-stimulus fluorescence." CrystEngComm 20, no. 20 (2018): 2772–79. http://dx.doi.org/10.1039/c8ce00025e.

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38

Raichure, Pramod C., Ramprasad Bhatt, Vishal Kachwal, Tirupati Chander Sharma, and Inamur Rahaman Laskar. "Multi-stimuli distinct responsive D–A based fluorogen oligomeric tool and efficient detection of TNT vapor." New Journal of Chemistry 46, no. 14 (2022): 6560–69. http://dx.doi.org/10.1039/d1nj05314k.

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Анотація:

P1 shows distinct emission responses with multi-stimuli, i.e., quenching for TNT sensing, red shifting for acid and base vapors, blue shifting against MFC behavior, and solvent polarity-dependent emission.

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39

Li, Chenyang, Beilin Zhang, Yunhong Dong, Yawen Li, Pinpin Wang, Yang Yu, Lin Cheng, and Liping Cao. "A tetraphenylethene-based Pd2L4 metallacage with aggregation-induced emission and stimuli-responsive behavior." Dalton Transactions 49, no. 24 (2020): 8051–55. http://dx.doi.org/10.1039/d0dt00469c.

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Анотація:

A tetraphenylethene-based Pd₂L₄ metallacage was self-assembled from four TPE-pyridine ligands with two Pd²⁺ ions. This metallacage exhibited a classical aggregation-induced emission property and stimuli-responsive behaviour.

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40

Zhao, Yuming, Wen Zhu, Ying Wu, Lin Qu, Zhengping Liu, and Ke Zhang. "An aggregation-induced emission star polymer with pH and metal ion responsive fluorescence." Polymer Chemistry 7, no. 42 (2016): 6513–20. http://dx.doi.org/10.1039/c6py01488g.

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Анотація:

A one-pot strategy from ring-opening metathesis polymerization was employed to prepare AIE-active star polymers, which were designed to have multi-responsive fluorescence to varied stimuli including pH, CO₂, and metal ions.

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41

Tomashenko, Olesya A., Alexander F. Khlebnikov, Ivan P. Mosiagin, Mikhail S. Novikov, Elena V. Grachova, Julia R. Shakirova, and Sergey P. Tunik. "A new heterocyclic skeleton with highly tunable absorption/emission wavelength via H-bonding." RSC Advances 5, no. 115 (2015): 94551–61. http://dx.doi.org/10.1039/c5ra17755c.

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Анотація:

A new heterocyclic system, pyrido[2,1-a]pyrrolo[3,2-c]isoquinoline, showing stimuli responsive fluorescence, was synthesized via Pd-catalyzed intramolecular cyclization of 1-[1-benzyl-2-(2-bromophenyl)-1H-pyrrol-3-yl]pyridin-1-ium bromides.

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42

Traeger, Hanna, Alyssa Ghielmetti, Yoshimitsu Sagara, Stephen Schrettl, and Christoph Weder. "Supramolecular Rings as Building Blocks for Stimuli-Responsive Materials." Gels 8, no. 6 (June 3, 2022): 350. http://dx.doi.org/10.3390/gels8060350.

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Анотація:

Stimuli-responsive polymers are of great interest due to their ability to translate changing environmental conditions into responses in defined materials. One possibility to impart such behavior is the incorporation of optically active molecules into a polymer host. Here, we describe how sensor molecules that consist of a πextended benzothiadiazole emitter and a naphthalene diimide quencher can be exploited in this context. The two optically active entities were connected via different spacers and, thanks to attractive intramolecular interactions between them, the new sensor molecules assembled into cyclic structures in which the fluorescence was quenched by up to 43% when compared to solutions of the individual dyes. Detailed spectroscopic investigations of the sensor molecules in solution show that the extent of donor/acceptor interactions is influenced by various factors, including solvent polarity and ion concentration. The new sensor molecule was covalently incorporated into a polyurethane; the investigation of the optical characteristics in both the solid and solvent-swollen states indicates that a stimulus-induced formation of associated dye pairs is possible in polymeric materials. Indeed, a solvatochromic quenching effect similar to the behavior in solution was observed for solvent-swollen polymer samples, leading to an effective change of the green emission color of the dye to a yellow color.

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Kundu, Anu, P. S. Hariharan, K. Prabakaran, Dohyun Moon, and Savarimuthu Philip Anthony. "Stimuli responsive reversible high contrast off–on fluorescence switching of simple aryl-ether amine based aggregation-induced enhanced emission materials." RSC Advances 5, no. 119 (2015): 98618–25. http://dx.doi.org/10.1039/c5ra17570d.

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Ren, Yuan-Yuan, Zheng Xu, Guoqiang Li, Junhai Huang, Xiaotian Fan, and Lin Xu. "Hierarchical self-assembly of a fluorescence emission-enhanced organogelator and its multiple stimuli-responsive behaviors." Dalton Transactions 46, no. 2 (2017): 333–37. http://dx.doi.org/10.1039/c6dt04182e.

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Ekbote, Anupama, Si Hyun Han, Thaksen Jadhav, Shaikh M. Mobin, Jun Yeob Lee, and Rajneesh Misra. "Stimuli responsive AIE active positional isomers of phenanthroimidazole as non-doped emitters in OLEDs." Journal of Materials Chemistry C 6, no. 8 (2018): 2077–87. http://dx.doi.org/10.1039/c7tc05450e.

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Roy, Bibhisan, Mallu Chenna Reddy, Gregor P. Jose, Felix C. Niemeyer, Jens Voskuhl, and Partha Hazra. "All in One: Stimuli-Responsive, Efficient Mitotracking, and Single Source White Light Emission." Journal of Physical Chemistry Letters 12, no. 4 (January 22, 2021): 1162–68. http://dx.doi.org/10.1021/acs.jpclett.0c03489.

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Wang, Ling, Rui Zhang, Ze Huang, Shengmei Guo, Jia-xiang Yang, and Lin Kong. "A multi-stimuli-responsive tetraphenylethene derivative with high fluorescent emission in solid state." Dyes and Pigments 197 (January 2022): 109909. http://dx.doi.org/10.1016/j.dyepig.2021.109909.

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Fedorenko, Elena V., Anatolii G. Mirochnik, and Andrey V. Gerasimenko. "o-Hydroxydibenzoylmethanate of boron difluoride: A complex with multi-stimuli-responsive emission effects." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 223 (December 2019): 117367. http://dx.doi.org/10.1016/j.saa.2019.117367.

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Yadav, Pranjalee, Ashish Kumar Singh, Chandan Upadhyay, and Vinod P. Singh. "Photoluminescence behaviour of a stimuli responsive Schiff base: Aggregation induced emission and piezochromism." Dyes and Pigments 160 (January 2019): 731–39. http://dx.doi.org/10.1016/j.dyepig.2018.08.065.

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Jia, Xiang-Rui, Hui-Juan Yu, Jian Chen, Wei-Jie Gao, Jing-Kun Fang, Yuan-Shou Qin, Xiao-Kai Hu, and Guang Shao. "Stimuli-Responsive Properties of Aggregation-Induced-Emission Compounds Containing a 9,10-Distyrylanthracene Moiety." Chemistry - A European Journal 24, no. 71 (November 16, 2018): 19053–59. http://dx.doi.org/10.1002/chem.201804315.

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