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Journal articles on the topic 'Cyanostilbene'

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Gopinath, A., K. Ramamurthy, Mamangam Subaraja, Chellappan Selvaraju, and A. Sultan Nasar. "A3-Type star stilbene and cyanostilbene molecules: synthesis, fluorescence properties and bio-imaging application." New Journal of Chemistry 42, no. 12 (2018): 10243–53. http://dx.doi.org/10.1039/c8nj00676h.

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In this article, we report star-like stilbene and cyanostilbene molecules exhibiting strong fluorescence, ICT and AIE properties. Star cyanostilbene was found to be an excellent fluorophore for bio-imaging application.

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2

Palakollu, Veerabhadraiah, Anuji K. Vasu, Vijay Thiruvenkatam, and Sriram Kanvah. "A sensitive AIEE probe for amphiphilic compounds." New Journal of Chemistry 40, no. 5 (2016): 4588–94. http://dx.doi.org/10.1039/c5nj02398j.

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3

Arivazhagan, C., Partha Malakar, R. Jagan, Edamana Prasad, and Sundargopal Ghosh. "Dimesitylboryl-functionalised cyanostilbene derivatives of phenothiazine: distinctive polymorphism-dependent emission and mechanofluorochromism." CrystEngComm 20, no. 23 (2018): 3162–66. http://dx.doi.org/10.1039/c8ce00250a.

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4

Liu, Jin, Weijun Li, Minjie Liu, et al. "Photo-irradiated E/Z isomerization reaction of star-shaped isomers containing two cyanostilbene arms with charge transfer excited states." Physical Chemistry Chemical Physics 20, no. 44 (2018): 28279–86. http://dx.doi.org/10.1039/c8cp05581e.

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5

Wang, Aizhi, Yunxu Yang, Feifei Yu, et al. "Switching the recognition preference of thiourea derivative by replacing Cu2+: spectroscopic characteristics of aggregation-induced emission and mechanism studies for recognition of Hg(ii) in aqueous solution." Analytical Methods 7, no. 6 (2015): 2839–47. http://dx.doi.org/10.1039/c4ay02916j.

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6

Kamiya, Yukiko, Kazuki Iishiba, Tetsuya Doi, Kouki Tsuda, Hiromu Kashida, and Hiroyuki Asanuma. "Terminus-free siRNA prepared by photo-crosslinking activated via slicing by Ago2." Biomaterials Science 3, no. 12 (2015): 1534–38. http://dx.doi.org/10.1039/c5bm00231a.

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7

Liao, Junqiu, Ming Yang, Zui Liu та Hailiang Zhang. "Fast photoinduced deformation of hydrogen-bonded supramolecular polymers containing α-cyanostilbene derivative". Journal of Materials Chemistry A 7, № 5 (2019): 2002–8. http://dx.doi.org/10.1039/c8ta12030g.

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8

Zhang, Yuyang, Huifang Li, Gaobin Zhang та ін. "Aggregation-induced emission enhancement and mechanofluorochromic properties of α-cyanostilbene functionalized tetraphenyl imidazole derivatives". Journal of Materials Chemistry C 4, № 14 (2016): 2971–78. http://dx.doi.org/10.1039/c5tc03348a.

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9

Wu, Yijin, Shasha Zhang, Jiwei Pei та Xiao-Fang Chen. "Photochromic fluorescence switching in liquid crystalline polynorbornenes with α-cyanostilbene side-chains". Journal of Materials Chemistry C 8, № 19 (2020): 6461–69. http://dx.doi.org/10.1039/d0tc00069h.

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10

Yu, Feifei, Yunxu Yang, Aizhi Wang, et al. "Quantitative and highly selective sensing of sodium houttuyfonate via long-aliphatic chains hydrophobic assembly and aggregation-induced emission." New Journal of Chemistry 39, no. 12 (2015): 9743–51. http://dx.doi.org/10.1039/c5nj01036e.

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11

Zhang, Yuping, Chunshuang Liang, and Shimei Jiang. "A solvatochromic cyanostilbene derivative as an intensity and wavelength-based fluorescent sensor for water in organic solvents." New Journal of Chemistry 41, no. 16 (2017): 8644–49. http://dx.doi.org/10.1039/c7nj01361b.

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12

Xing, Pengyao, Hongzhong Chen, Linyi Bai, and Yanli Zhao. "Photo-triggered transformation from vesicles to branched nanotubes fabricated by a cholesterol-appended cyanostilbene." Chemical Communications 51, no. 45 (2015): 9309–12. http://dx.doi.org/10.1039/c5cc02816g.

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13

Huang, Guangxi, Xiaoyong Chang, Yuqing Jiang, Bei Lin, Bing Shi Li, and Ben Zhong Tang. "Multi-stimuli responsive cyanostilbene derivatives: pH, amine vapor sensing and mechanoluminescence." Materials Chemistry Frontiers 4, no. 6 (2020): 1720–28. http://dx.doi.org/10.1039/d0qm00113a.

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14

Liu, Zui, Junqiu Liao, Lifang He, Qin Gui, Yongjie Yuan та Hailiang Zhang. "Preparation, photo-induced deformation behavior and application of hydrogen-bonded crosslinked liquid crystalline elastomers based on α-cyanostilbene". Polymer Chemistry 11, № 37 (2020): 6047–55. http://dx.doi.org/10.1039/d0py01060j.

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15

Dhinakaran, Manivannan Kalavathi, Weitao Gong, Yue Yin, et al. "Configuration-independent AIE-active supramolecular polymers of cyanostilbene through the photo-stable host–guest interaction of pillar[5]arene." Polymer Chemistry 8, no. 35 (2017): 5295–302. http://dx.doi.org/10.1039/c7py00845g.

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16

Wang, Xiao, Zongchun Gao, Junlong Zhu, Zhao Gao, and Feng Wang. "Aggregation induced emission of a cyanostilbene amphiphile as a novel platform for FRET-based ratiometric sensing of mercury ions in water." Polymer Chemistry 7, no. 33 (2016): 5217–20. http://dx.doi.org/10.1039/c6py01109h.

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17

Martínez-Abadía, M., B. Robles-Hernández, B. Villacampa, M. R. de la Fuente, R. Giménez, and M. B. Ros. "Cyanostilbene bent-core molecules: a route to functional materials." Journal of Materials Chemistry C 3, no. 13 (2015): 3038–48. http://dx.doi.org/10.1039/c5tc00201j.

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18

Wei, Yabo, Weiben Chen, Xiaoyu Zhao, Sanyuan Ding, Sheng Han, and Long Chen. "Solid-state emissive cyanostilbene based conjugated microporous polymers via cost-effective Knoevenagel polycondensation." Polymer Chemistry 7, no. 24 (2016): 3983–88. http://dx.doi.org/10.1039/c6py00614k.

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Solid-state emissive cyanostilbene-based conjugated porous polymers with different topological structure and photophysical properties were newly synthesized via cost-effective Knoevenagel polycondensation.

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19

Guo, Shengmei, Jianting Pan, Jianyan Huang, Lin Kong та Jiaxiang Yang. "Two AIEE-active α-cyanostilbene derivatives containing BF2 unit for detecting explosive picric acid in aqueous medium". RSC Advances 9, № 45 (2019): 26043–50. http://dx.doi.org/10.1039/c9ra05116c.

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20

Ding, Zeyang, Yuping Zhang, Yu Gao, Bing Yang, and Shimei Jiang. "Tunable morphologies and emission of photosensitive supramolecular self-assemblies through positional and trans–cis isomerization." Nanoscale 12, no. 3 (2020): 2071–80. http://dx.doi.org/10.1039/c9nr09155f.

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21

Cao, Xinhua, Yiran Li, Qingqing Han та ін. "Design of large π-conjugated α-cyanostilbene derivatives as colorimetric sensors for volatile acids and organic amine gases". Journal of Materials Chemistry C 8, № 12 (2020): 4058–64. http://dx.doi.org/10.1039/c9tc06148g.

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22

Seo, Jangwon, Jong Won Chung, Ji Eon Kwon, and Soo Young Park. "Photoisomerization-induced gel-to-sol transition and concomitant fluorescence switching in a transparent supramolecular gel of a cyanostilbene derivative." Chem. Sci. 5, no. 12 (2014): 4845–50. http://dx.doi.org/10.1039/c4sc02170c.

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23

Ji, Lukang, Qianwen He, Dian Niu, Jiajing Tan, Guanghui Ouyang, and Minghua Liu. "Host–guest interaction enabled chiroptical photo-switching and enhanced circularly polarized luminescence." Chemical Communications 55, no. 78 (2019): 11747–50. http://dx.doi.org/10.1039/c9cc06305f.

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24

Martínez-Abadía, Marta, Shinto Varghese, Begoña Milián-Medina, Johannes Gierschner, Raquel Giménez, and M. Blanca Ros. "Bent-core liquid crystalline cyanostilbenes: fluorescence switching and thermochromism." Physical Chemistry Chemical Physics 17, no. 17 (2015): 11715–24. http://dx.doi.org/10.1039/c5cp00696a.

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25

Zhu, Liangliang, and Yanli Zhao. "Cyanostilbene-based intelligent organic optoelectronic materials." J. Mater. Chem. C 1, no. 6 (2013): 1059–65. http://dx.doi.org/10.1039/c2tc00593j.

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26

Chen, Sin-Yu, Ya-Wen Chiu та Guey-Sheng Liou. "Substituent effects of AIE-active α-cyanostilbene-containing triphenylamine derivatives on electrofluorochromic behavior". Nanoscale 11, № 17 (2019): 8597–603. http://dx.doi.org/10.1039/c9nr02692d.

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Four aggregation-induced emission- and electro-active cyanostilbene-based diphenylamine-containing derivatives were synthesized to investigate the photoluminescence properties, and electrochromic and electrofluorochromic behavior of gel-type devices.

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27

Gao, Zhao, Ze Chen, Yifei Han, and Feng Wang. "Cyanostilbene-based vapo-fluorochromic supramolecular assemblies for reversible 3D code encryption." Nanoscale Horizons 5, no. 7 (2020): 1081–87. http://dx.doi.org/10.1039/d0nh00186d.

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Vapo-fluorochromic 3D code encryption systems have been constructed on the basis of cyanostilbene-based supramolecular assemblies, which open up a new avenue toward smart information protection materials.

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28

Bhaumik, Shubhra Kanti, and Supratim Banerjee. "Tunable multi-color luminescence from a self-assembled cyanostilbene and cucurbit[7]uril in aqueous media." Chemical Communications 56, no. 4 (2020): 655–58. http://dx.doi.org/10.1039/c9cc09277c.

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A tunable multicolor luminescent supramolecular system was designed in aqueous media employing the self-assembly of a cationic amphiphilic cyanostilbene and the host–guest chemistry of cucurbit[7]uril.

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29

Gopinath, A., N. Manivannan, Sudip Mandal, N. Mathivanan та A. Sultan Nasar. "Substituent enhanced fluorescence properties of star α-cyanostilbenes and their application in bioimaging". Journal of Materials Chemistry B 7, № 39 (2019): 6010–23. http://dx.doi.org/10.1039/c9tb01452g.

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In this paper, we report the fluorescence properties of new star α-cyanostilbene molecules. Fungus cell imaging studies using one of the molecules allowed observing nuclear movement in the live mycelium.

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30

Kondo, Mizuho, Yuya Morita, Jun-ichi Nishida, Takeshi Kawase, and Nobuhiro Kawatsuki. "Mechano-induced photoluminescence colour change in an alkyltolane-terminated cyanostilbene." CrystEngComm 23, no. 34 (2021): 5869–75. http://dx.doi.org/10.1039/d1ce00456e.

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A novel alkyltolane-terminated cyanostilbene is synthesized. The photoluminescence colour changed depending on the precipitation method, with either a red shift or blue shift in the photoluminescence spectra observed upon mechanical grinding.

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31

Chen, Sin-Yu, Min-Hao Pai та Guey-Sheng Liou. "Effects of alkyl chain length and anion on the optical and electrochemical properties of AIE-active α-cyanostilbene-containing triphenylamine derivatives". Journal of Materials Chemistry C 8, № 22 (2020): 7454–62. http://dx.doi.org/10.1039/d0tc00683a.

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A series of AIE-active and redox-active α-cyanostilbene-containing triphenylamine derivatives with different alkyl chain lengths and anions were successfully synthesized, and their optical, photoluminescent and electrochromic behaviors were investigated.

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32

Xing, Pengyao, Hongzhong Chen, Mingfang Ma, Xingdong Xu, Aiyou Hao, and Yanli Zhao. "Light and cucurbit[7]uril complexation dual-responsiveness of a cyanostilbene-based self-assembled system." Nanoscale 8, no. 4 (2016): 1892–96. http://dx.doi.org/10.1039/c5nr07873c.

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A cyanostilbene-based amphiphile affords vesicle assembly, exhibiting dual responsiveness to photoirradiation and cucurbit[7]uril's complexation. The luminescence of the supramolecular system can be tailored via host–guest inclusion and photoisomerization.

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33

Ji, Lukang, Yiran Liu, Zujian Li, Guanghui Ouyang, and Minghua Liu. "Solvent-regulated chiral exciton coupling and CPL sign inversion of an amphiphilic glutamide-cyanostilbene." Chemical Communications 57, no. 86 (2021): 11314–17. http://dx.doi.org/10.1039/d1cc04471k.

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The chiral exciton couplings within a Y-shaped amphiphilic glutamide-cyanostilbene could be significantly biased by solvent polarity and hydration effect, which led to sign inversion of both CD and CPL of its assemblies.

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34

Zhang, Yuyang, Jianyan Huang, Lin Kong, Yupeng Tian та Jiaxiang Yang. "Two novel AIEE-active imidazole/ α-cyanostilbene derivatives: photophysical properties, reversible fluorescence switching, and detection of explosives". CrystEngComm 20, № 9 (2018): 1237–44. http://dx.doi.org/10.1039/c7ce01842h.

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Novel imidazole derivatives containing the α-cyanostilbene unit can act as reversible acid/base stimulated fluorescence switches in the solid state, as chemosensors for explosives detection in aqueous systems, and as test strip detectors.

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35

Shen, Yihao, Kun Yao, Hang Li, Zhaoran Xu, Yiwu Quan, and Yixiang Cheng. "Strong CPL-active liquid crystal materials induced by intermolecular hydrogen-bonding interaction and a chirality induction mechanism." Soft Matter 18, no. 3 (2022): 477–81. http://dx.doi.org/10.1039/d1sm01607e.

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A novel co-assembly material can emit strong CPL signals (glum = +0.076/−0.064) from an achiral AIE-active β-cyanostilbene liquid crystal through intermolecular hydrogen bond interaction and chirality induction after a rapid cooling quench treatment.

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36

Ma, Yao, Massimo Cametti, Zoran Džolić, and Shimei Jiang. "AIE-active bis-cyanostilbene-based organogels for quantitative fluorescence sensing of CO2 based on molecular recognition principles." Journal of Materials Chemistry C 6, no. 34 (2018): 9232–37. http://dx.doi.org/10.1039/c8tc01190g.

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Fluorescence sensing of CO<sub>2</sub> is achieved by the use of gel aggregates and xerogel systems made with the aggregation induced emissive bis-cyanostilbene derivative 1 reaching a detection limit as low as 4.5 ppm.

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37

Hang, Cheng, Hong-Wei Wu та Liang-Liang Zhu. "π -Conjugated cyanostilbene-based optoelectric functional materials". Chinese Chemical Letters 27, № 8 (2016): 1155–65. http://dx.doi.org/10.1016/j.cclet.2016.04.003.

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38

Martínez-Abadía, Marta, Shinto Varghese, Pilar Romero, Johannes Gierschner, Raquel Giménez, and M. Blanca Ros. "Highly Light-Sensitive Luminescent Cyanostilbene Flexible Dimers." Advanced Optical Materials 5, no. 4 (2017): 1600860. http://dx.doi.org/10.1002/adom.201600860.

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39

Il'ichev, Yurii V., Wolfgang Kühnle, and Klaas A. Zachariasse. "Photophysics of 4-dimethylamino-4′-cyanostilbene and 4-azetidinyl-4′-cyanostilbene. Time-resolved fluorescence and trans-cis photoisomerisation." Chemical Physics 211, no. 1-3 (1996): 441–53. http://dx.doi.org/10.1016/0301-0104(96)00200-5.

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40

Ma, Yao, Massimo Cametti, Zoran Džolić, and Shimei Jiang. "Selective Cu(ii) sensing by a versatile AIE cyanostilbene-based gel system." Soft Matter 15, no. 30 (2019): 6145–50. http://dx.doi.org/10.1039/c9sm00955h.

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Pyridyl-oxalamido-cyanostilbene 1 is a versatile ambidextrous gelator forming organo-, hydro-, and Cu(ii) specific metallogels. A rare organogel-to-metallogel transformation was also observed upon exposure of 1-DMSO/H<sub>2</sub>O gel to aqueous Cu(ii).

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41

Fang, Wenyan, Wang Zhao, Pan Pei та ін. "A Λ-shaped cyanostilbene derivative: multi-stimuli responsive fluorescence sensors, rewritable information storage and colour converter for w-LEDs". Journal of Materials Chemistry C 6, № 34 (2018): 9269–76. http://dx.doi.org/10.1039/c8tc02973c.

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A new Λ-shaped α-cyanostilbene derivative (TSA) containing an active amino group with fluorescence emission both in solution and the solid state was designed, synthesized and characterized. TSA can be used as a fluorescent sensor, a rewritable information storage material and in w-LEDs.

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42

Zhang, Yujian, Guilin Zhuang, Mi Ouyang, et al. "Mechanochromic and thermochromic fluorescent properties of cyanostilbene derivatives." Dyes and Pigments 98, no. 3 (2013): 486–92. http://dx.doi.org/10.1016/j.dyepig.2013.03.017.

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43

Huan Yuan Long, Huan Yuan Long, Jin Zhang Jin Zhang, Zi Wei Li Zi Wei Li, Peng Zhou Peng Zhou та Tian Ying Peng and Guo Wen He Tian Ying Peng and Guo Wen He. "Substituent Effect on the Solid-State Photoinduced Luminescence of α-Cyanostilbene Derivatives". Journal of the chemical society of pakistan 41, № 5 (2019): 868. http://dx.doi.org/10.52568/000791/jcsp/41.05.2019.

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A series of α-cyanostilbene derivatives with aggregation-induced enhanced emission （AIEE） was obtained. All the compounds were characterized by UV−vis spectroscopy, fluorescence and nuclear magnetic resonance. These compounds exhibited blue, green and yellow color emission in solid state but non-fluorescent in dilute solutions. The electronic characteristics were examined by GAMESS Interface software package. The results indicate that the luminescence properties are affected by the substituents.

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44

Bhaumik, Shubhra Kanti, and Supratim Banerjee. "Highly sensitive and ratiometric luminescence sensing of heparin through templated cyanostilbene assemblies." Analyst 146, no. 7 (2021): 2194–202. http://dx.doi.org/10.1039/d0an01808b.

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45

Zhao, He, Yongtao Wang, Steven Harrington, et al. "Remarkable substitution influence on the mechanochromism of cyanostilbene derivatives." RSC Advances 6, no. 71 (2016): 66477–83. http://dx.doi.org/10.1039/c6ra14707k.

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46

LU Hong-bo, 陆红波, 吴少君 WU Shao-jun, 张超 ZHANG Chao, 邱龙臻 QIU Long-zhen та 杨家祥 YANG Jia-xiang. "Synthesis and Photoluminescence Property of α-Cyanostilbene Derivatives Molecules". Chinese Journal of Luminescence 36, № 9 (2015): 983–88. http://dx.doi.org/10.3788/fgxb20153609.0983.

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47

Li, Xin, Liangliang Zhu, Sai Duan, Yanli Zhao, and Hans Ågren. "Aggregation-induced chiral symmetry breaking of a naphthalimide–cyanostilbene dyad." Phys. Chem. Chem. Phys. 16, no. 43 (2014): 23854–60. http://dx.doi.org/10.1039/c4cp04070h.

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48

Vasu, Anuji K., Mithun Radhakrishna та Sriram Kanvah. "Self-Assembly Tuning of α-Cyanostilbene Fluorogens: Aggregates to Nanostructures". Journal of Physical Chemistry C 121, № 40 (2017): 22478–86. http://dx.doi.org/10.1021/acs.jpcc.7b06225.

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49

Yang, Minmin, Pengyao Xing, Mingfang Ma, Yimeng Zhang, Yajie Wang, and Aiyou Hao. "Controlled self-organization of cyanostilbene: emission tuning and photo-responsiveness." Soft Matter 12, no. 28 (2016): 6038–42. http://dx.doi.org/10.1039/c6sm01307d.

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50

Vasu, Anuji K., Mahalingavelar Paramasivam, and Sriram Kanvah. "Carbohydrate Tethered Cyanostilbene Fluorogen: Unique Emission and Preferential Protein Binding." ChemistrySelect 2, no. 1 (2017): 405–14. http://dx.doi.org/10.1002/slct.201601709.

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