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Journal articles on the topic 'Fluorescence properties'

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Published: 20 April 2024

Last updated: 25 July 2025

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1

A, nil K. Singh, and Manjula D. "A fluorescence study of 1-p-aminophenyl-4-phenylbuta-1£,3£-diene m organic solvents, 1,4-dioxane-water binary mixtures and micelles." Journal of Indian Chemistry Society Vol. 78, October-December 2001 (2001): 635–41. https://doi.org/10.5281/zenodo.5892587.

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Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai-400 076, India <em>Fax</em> : 91-22-5767152 <em>Manuscript received 2 April 2001</em> 1-<em>p</em>-Aminophenyl-4-phenylbuta-1<em>E</em>,3<em>E</em>-diene (I) has been synthesied and its uv-vis absorption and fluorescence emission and euitation spectral properties in a variety of media including organic solvents and 1,4-dioxane-water binary mixtures of varying relative permittivity, and microheterogeneous media of SDS, CTAB and Triton-X-100 micelles have been namined. In contrast to a largely solvent polarity insensi

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2

Li, Yanlei, Yi Cai, Zhe Yang, et al. "Comparison of the Fluorescence Properties of Biological Solutions and Aerosols." International Journal of Engineering and Technology 15, no. 3 (2023): 115–18. http://dx.doi.org/10.7763/ijet.2023.v15.1231.

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The identification of biological aerosols is a subject of worldwide interest because of the potential for biological terrorism and the increase in public health emergencies. Laser-induced fluorescence is widely used to investigate the fluorescence properties of biomolecules and spores in solution; however, data on the fluorescence properties of the aerosolized forms are lacking. In this study, we report the fluorescence properties of tryptophan, serotonin, tyrosine, vitamin B6, and Bacillus thuringiensis and Bacillus subtilis spores in solution and aerosol form. Our results show that the shape

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3

Kravchenko, V. M. "SPECTRAL PROPERTIES OF TWO WATER-SOLUBLE MELANINS." Biotechnologia Acta 17, no. 6 (2024): 28–34. https://doi.org/10.15407/biotech17.06.028.

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Aim. The work was purposed to study the spectral properties of two types of water-soluble melanins to clarify the nature of the optical absorption and emission centers in them. Materials and methods. Studied are the spectral properties of two types of water-soluble melanins: melanin obtained from black yeast-like fungi Pseudonadsoniella brunnea 470 FCKU, dissolved in water with pH 11, and plant melanin obtained from black tea according to German patent DE102004003801A1, which is added to drinking water for medicinal purposes. In the spectral region of 200–900 nm, optical absorption spectra at

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4

Das, Joydip, Rosalie K. Crouch, and Parkson Lee-Gau Chong. "Fluorescence Properties of Pyrylretinol." Photochemistry and Photobiology 72, no. 3 (2007): 415–20. http://dx.doi.org/10.1562/0031-8655(2000)0720415fpop2.0.co2.

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5

Das, Joydip, Rosalie K. Crouch, and Parkson Lee-Gau Chong. "Fluorescence Properties of Pyrylretinol." Photochemistry and Photobiology 72, no. 3 (2000): 415. http://dx.doi.org/10.1562/0031-8655(2000)072<0415:fpop>2.0.co;2.

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6

Nakashima, Nobuaki, Stephen R. Meech, Andrew R. Auty, Anita C. Jones, and David Phillips. "Fluorescence properties of ergosterol." Journal of Photochemistry 30, no. 2 (1985): 207–14. http://dx.doi.org/10.1016/0047-2670(85)85025-5.

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7

Amteghy, Ali H. "Synthesis, Fluorescence and Thermal Properties of Some Benzidine Schiff Base." NeuroQuantology 20, no. 3 (2022): 135–49. http://dx.doi.org/10.14704/nq.2022.20.3.nq22053.

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A series of Schiff bases derived from benzidine and various aromatic aldehydes were prepared and characterized by spectroscopic methods. Fluorescence properties of prepared Schiff bases were studied in DMF solution. The thermo kinetic parameters. E, Δ H, Δ S and Δ G were calculated following Coats-Redfern method.

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8

Ren, Pan Pan, Ren Jie Wang, and Shou Zhi Pu. "Photochromism Properties of a New Unsymmetrical Diarylethene Bearing a Benzene Unit." Advanced Materials Research 830 (October 2013): 266–69. http://dx.doi.org/10.4028/www.scientific.net/amr.830.266.

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A new photochromic diarylethene compound 1-[(2-methyl-5-(4-trifluoromethyphenyl)-3-thienyl)]-2-{2-methyl-5-[2-(1,3-dioxolane)]-3-thienyl} perfluorocyclopentene 1O was synthesized. Its optoelectronic properties, such as photochromism in solution as well as in poly-methylmethacrylate (PMMA) amorphous films, fluorescences switch were investigated in detail. Upon irradiated UV light it changes from colorless to purple in solution and PMMA amorphous film, respectively. Finally, the diarylethene 1O was exhibited remarkable fluorescence switch properties along with the cyclization reactions. When the

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9

Yan, Qicheng, Ziyuan Liu, and Ying Guo. "Study on Fluorescence Properties of Green-Blue Apatite." Crystals 12, no. 6 (2022): 866. http://dx.doi.org/10.3390/cryst12060866.

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The fluorescence phenomenon of apatite is an important feature. In this paper, three apatites with uniform transition from green to blue were selected, and the fluorescence color characteristics of the samples were observed under UV fluorescent lamp and DiamondView. With 3D fluorescence technology, combined with LA-ICP-MS, this paper aims to comprehensively test the fluorescence phenomenon of apatite to explore the relationship between apatite fluorescence and elements and analyze the fluorescence color characteristics. With the experiments mentioned above, this paper explores the fluorescent

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10

Chen Maofu, 陈茂福, 吴静 Wu Jing, 律严励 Lü Yanli, and 陈庆俊 Chen Qingjun. "Fluorescence Properties of Municipal Wastewater." Acta Optica Sinica 28, no. 3 (2008): 578–82. http://dx.doi.org/10.3788/aos20082803.0578.

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11

Leung, A. F., L. Hayashibara, and J. Spadaro. "Fluorescence properties of uranyl nitrates." Journal of Physics and Chemistry of Solids 60, no. 3 (1999): 299–304. http://dx.doi.org/10.1016/s0022-3697(98)00294-7.

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12

Nutiu, Razvan, and Yingfu Li. "Aptamers with fluorescence-signaling properties." Methods 37, no. 1 (2005): 16–25. http://dx.doi.org/10.1016/j.ymeth.2005.07.001.

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13

Anstead, Gregory M., and John A. Katzenellenbogen. "Fluorescence properties of 2,3-diarylindenes." Journal of Physical Chemistry 92, no. 22 (1988): 6249–58. http://dx.doi.org/10.1021/j100333a017.

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14

Wolfbeis, Otto S., Monowara Begum, and Hans Geiger. "The fluorescence properties of luteolines." Monatshefte f�r Chemie Chemical Monthly 118, no. 12 (1987): 1403–11. http://dx.doi.org/10.1007/bf00810645.

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15

Gupta, Iti, and M. Ravikanth. "Fluorescence properties of meso-tetrafurylporphyrins." Journal of Chemical Sciences 117, no. 2 (2005): 161–66. http://dx.doi.org/10.1007/bf03356111.

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16

Kapinus, E. I. "Fluorescence properties of nanosized sulfides." Russian Journal of Physical Chemistry A 85, no. 4 (2011): 668–71. http://dx.doi.org/10.1134/s003602441104011x.

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17

Macías, Pedro, Rosario Zamora, M. Carmen Pinto, and Carlos Gutiérrez-Merino. "Comparative fluorescence properties of lipoxygenases." Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 89, no. 3 (1988): 531–37. http://dx.doi.org/10.1016/0305-0491(88)90170-8.

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18

Birch, D. J. S., G. Hungerford, R. E. Imhof, and A. S. Holmes. "The fluorescence properties of DCM." Chemical Physics Letters 178, no. 2-3 (1991): 177–84. http://dx.doi.org/10.1016/0009-2614(91)87053-e.

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19

Farkas, É., M. Hilbert, I. Ketskeméty, and L. Gáti. "Fluorescence properties of bichromophoric molecules." Spectrochimica Acta Part A: Molecular Spectroscopy 48, no. 1 (1992): 95–99. http://dx.doi.org/10.1016/0584-8539(92)80202-8.

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20

Bakalova, Sn, L. Biczók, I. Kavrakova, and T. Bérces. "Photophysical and Photochemical Properties of 2,3-Dihydro-4(l H)-quinolinones. Part I. Fluorescence Properties." Zeitschrift für Naturforschung C 45, no. 9-10 (1990): 980–86. http://dx.doi.org/10.1515/znc-1990-9-1009.

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Abstract Absorption spectra and fluorescence properties of 2,3-dihydro-4(1 H)-quinolinone derivatives were studied at room temperature in different solvents. It has been found that the fluorescence quantum yields and fluorescence decay times strongly depend on the molecular structure and solvent polarity. The character and the energy of excited states were determined by PPP and CNDO/S quantum-chemical calculations.

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21

Van, Nguyen Thi Khanh, Nguyen Dinh Hoang, Nguyen Thanh Binh, Nguyen Cong Thanh, and Pham Kim Binh. "Fluorescent Properties of Cancerous Liver Tissue." Communications in Physics 24, no. 3S2 (2014): 130–34. http://dx.doi.org/10.15625/0868-3166/24/3s2/5058.

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Fluorescence spectroscopy is a technology used fruitfully for biomedical diagnostics as well as for therapeutic purposes. The fluorescent analysis method are applied in biomedical diagnosticsbases on fluorescence of endogenous or exogenous fluorophores. We initially applied fluorescence spectroscopy for the study of human liver cancer (hepatocellular carcinoma) with an exogenous fluorophores, Radachlorin\(^{\circledR }\) 0.35%. The main aim of this study is to determine the spectral variation between normal and malignant liver tissues in 2 cases: the samples expose and non-expose to Radachlori

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22

Diac, Andreea Petronela, Ana-Maria Ţepeş, Albert Soran, et al. "Indenopyrans – synthesis and photoluminescence properties." Beilstein Journal of Organic Chemistry 12 (April 27, 2016): 825–34. http://dx.doi.org/10.3762/bjoc.12.81.

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New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significantly higher fluorescence quantum yields (relative to 9,10-diphenylanthracene) as compared to the corresponding cis isomers. The solid-state fluorescence spectra revealed an important red shift of λmax due to intermolecular interactions in the lattice, along with an emission-band broadening, as compared to the solution fluorescence spectra.

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23

Li, Renjie, Junyuan Li, Jiangtao Shi, et al. "Fluorescence Properties of Pterocarpus Wood Extract." Forests 14, no. 6 (2023): 1094. http://dx.doi.org/10.3390/f14061094.

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The water immersion of Pterocarpus wood produces strong blue fluorescence, which comes from the extract. The fluorescence contained in the extract is of interest for the identification of Pterocarpus wood. We conducted an investigation into the extraction solution of Pterocarpus wood and analyzed the mechanism of fluorescence in this species. Possible species of the fluorescent molecules are discussed based on the mixture. Liquid chromatography mass spectrometry (LC-MS) is used for an analysis of the extract, the obtained substances that may be fluorescent in Pterocarpus wood. In addition, the

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24

Ibrayev, N. Kh. "HOTOVOLTAIC PROPERTIES OF FUNCTIONALIZED INDODICARBOCYANINE DYE." Eurasian Physical Technical Journal 19, no. 3 (41) (2022): 55–59. http://dx.doi.org/10.31489/2022no3/55-59.

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The effect of the chemical structure of polymethine dyes on their spectral-luminescent and photovoltaic properties has been studied. It has been shown that the introduction of hydroxyl functional groups into the dye structure leads to a bathochromic shift of the absorption and fluorescence bands. During the adsorption of dyes on the surface of titanium dioxide, a shift of their spectra to the red wavelength region was recorded with a simultaneous broadening of the bands caused by dye aggregation on the semiconductor surface. A decrease in the lifetimes of the excited state of molecules by 64 a

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25

SHIMONO, Isao, Takumi TAKAMURA, and Motokazu NISHINO. "Fluorescence Properties of Firing Scallop Shell." Journal of the Ceramic Society of Japan 112, no. 1303 (2004): 184–88. http://dx.doi.org/10.2109/jcersj.112.184.

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26

Kovář, Jan, Karel Šimek, Eva Kožoušková, Hana Klukanová, and Jiří Slavík. "Fluorescence properties of some isoquinoline alkaloids." Collection of Czechoslovak Chemical Communications 50, no. 6 (1985): 1312–28. http://dx.doi.org/10.1135/cccc19851312.

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The fluorescence properties of 28 isoquinoline alkaloids have been investigated. In most of them the chromophore responsible for fluorescence was the benzene ring with electron-donor substituents containing oxygen. The long-wave excitation peak practically coincides with the long-wave absorption peak of these substances, covering the region from 284 to 293 nm, the maximum emission being in the range 320-332 nm. With alkaloids having a number of conjugated rings, both excitation and emission were observed at higher wavelengths. Only protoberberine alkaloids behaved as hydrophobic probes, i.e. t

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27

Fujitsuka, Mamoru, Dae Won Cho, Joji Ohshita, Atsutaka Kunai, and Tetsuro Majima. "Fluorescence Properties of Si-Linked Oligothiophenes." Journal of Physical Chemistry C 111, no. 5 (2007): 1993–98. http://dx.doi.org/10.1021/jp066336y.

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28

Yu, F. P., D. R. Yuan, L. M. Kong, et al. "Fluorescence properties of Dy3+doped La3Ga5.5Nb0.5O14nanocrystals." Nanotechnology 19, no. 4 (2008): 045705. http://dx.doi.org/10.1088/0957-4484/19/04/045705.

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29

Gao, Ming, Xiqi Feng, Guanqin Hu, and Zhiwen Yin. "Fluorescence Properties of Nd:CeF 3 Crystals." Chinese Physics Letters 11, no. 7 (1994): 451–53. http://dx.doi.org/10.1088/0256-307x/11/7/014.

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30

Zhang, Fang, Yan Fang, and Xiaoling Zhang. "Fluorescence emission properties of C60 nanoparticles." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 106 (April 2013): 242–46. http://dx.doi.org/10.1016/j.saa.2013.01.004.

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31

Jian, Zhu, Huang Liqing, Wang Yongchang, and Lu Yimin. "Fluorescence spectrum properties of gold nanochains." Physica E: Low-dimensional Systems and Nanostructures 25, no. 1 (2004): 114–18. http://dx.doi.org/10.1016/j.physe.2004.06.058.

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32

Perna, G., G. Palazzo, A. Mallardi, and V. Capozzi. "Fluorescence properties of natural eumelanin biopolymer." Journal of Luminescence 131, no. 8 (2011): 1584–88. http://dx.doi.org/10.1016/j.jlumin.2011.03.055.

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33

Endo, T., A. Shibuya, T. Sato, and M. Shimada. "Synthesis and fluorescence properties of Tb2Te4O11." Journal of Solid State Chemistry 78, no. 2 (1989): 237–41. http://dx.doi.org/10.1016/0022-4596(89)90103-5.

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34

Oliveira-Campos, Ana M. F., Lígia M. Rodrigues, Ana P. Esteves, et al. "Naphthotriazole derivatives: Synthesis and fluorescence properties." Dyes and Pigments 87, no. 3 (2010): 188–93. http://dx.doi.org/10.1016/j.dyepig.2010.03.025.

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35

Tomin, V. I., and R. Jaworski. "Multiband fluorescence spectral properties of QMOM." Russian Journal of Physical Chemistry A 85, no. 2 (2011): 254–59. http://dx.doi.org/10.1134/s0036024411020348.

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36

Nordlund, T. M., R. Rigler, C. Glemarec, et al. "Fluorescence Properties of Y-Nucleoside Derivatives." Nucleosides and Nucleotides 7, no. 5-6 (1988): 805–11. http://dx.doi.org/10.1080/07328318808056334.

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37

Haroutounian, Serkos A., and John A. Katzenellenbogen. "4′-Hydroxystyryldiazines: Synthesis and fluorescence properties." Tetrahedron 51, no. 6 (1995): 1585–98. http://dx.doi.org/10.1016/0040-4020(94)01050-a.

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38

Murakami, Hiroshi, and Takashi Kushida. "Fluorescence properties of Zn-substituted myoglobin." Journal of Luminescence 58, no. 1-6 (1994): 172–75. http://dx.doi.org/10.1016/0022-2313(94)90388-3.

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39

Johansson, Lennart B. Å., Julian G. Molotkovsky, and Lev D. Bergelson. "Fluorescence properties of anthrylvinyl lipid probes." Chemistry and Physics of Lipids 53, no. 2-3 (1990): 185–89. http://dx.doi.org/10.1016/0009-3084(90)90044-r.

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40

Sjöback, Robert, Jan Nygren, and Mikael Kubista. "Absorption and fluorescence properties of fluorescein." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 51, no. 6 (1995): L7—L21. http://dx.doi.org/10.1016/0584-8539(95)01421-p.

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41

Bakalova, Snezhana. "Solvent Effects on the Fluorescence Properties of Methyldihydroquinolinones." Zeitschrift für Naturforschung A 46, no. 9 (1991): 823–28. http://dx.doi.org/10.1515/zna-1991-0913.

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Abstract The absorption and fluorescence spectra and the fluorescence quantum yields of two methyl-2,3- dihydro-4(1H)-quinolinones in various solvents are reported. In some solvents deuteration-induced fluorescence enhancement has been observed. The solvent effects in aprotic solvents are consistent with the general type of solvent interaction. For protic solvents, solute-solvent complexation in the excited state is suggested

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42

Rakic, Violeta, Ajda Ota, Mihaela Skrt та ін. "Investigation of fluorescence properties of cyanidin and cyanidin 3-o-β-glucopyranoside". Chemical Industry 69, № 2 (2015): 155–63. http://dx.doi.org/10.2298/hemind140203030r.

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The absorption and fluorescence emission spectra of cyanidin and cyanidin 3-O-?-glucopyranoside (Cy3Glc) at pH 5.5 in aqueous solution have been studied. The most effective fluorescence excitations of cyanidin were at the UV absorption maxima at 220 and at 230 nm and at higher wavelengths at 270 and at 280 nm. Cyanidin exhibits fluorescence emission maxima at 310 nm and in the visible range at 615 nm. For the Cy3Glc most effective fluorescence excitation was at 220 and at 230 nm and at higher wavelengths at 300 and at 310 nm. Cy3Glc has fluorescence emission spectra with the maximum at 380 nm

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43

Li, Xiao Ting, Hui Li, and Shou Zhi Pu. "Photochemistry Properties of a Novel Photochromic Diarylethene Derivative." Advanced Materials Research 763 (September 2013): 74–78. http://dx.doi.org/10.4028/www.scientific.net/amr.763.74.

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A new unsymmetrical photochromic diarylethene, 1-[2, 4-dimethyl-5-thiazoly-2-[2-methyl-5-(3-methylphenyl)-3-thienyperfluorocyclopentene (1o) were synthesized, and its properties, such as photochromism in solution as well as in poly-methylmethacrylate (PMMA) amorphous films, and fluorescence properties were investigated in detail. The results showed the compound exhibited good photochromism in hexane solution and in PMMA amorphous film, the maxima absorption of its closed-ring isomer 1c are 492 nm and 498 nm respectively. The open-ring isomer of the diarylethene 1 exhibited relatively strong fl

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44

Kalyagin, Alexander, Lubov Antina, Alexander Ksenofontov, Elena Antina, and Mikhail Berezin. "Solvent-Dependent Fluorescence Properties of CH2-bis(BODIPY)s." International Journal of Molecular Sciences 23, no. 22 (2022): 14402. http://dx.doi.org/10.3390/ijms232214402.

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Biocompatible luminophores based on organic dyes, which have fluorescence characteristics that are highly sensitive to the properties of the solvating medium, are of particular interest as highly sensitive, selective, and easy-to-use analytical agents. We found that BODIPY dimers (2,2′-, 2,3′-3,3′-CH2-bis(BODIPY) (1–3)) demonstrate fluorescence characteristics with a high sensitivity to the presence of polar solvents. The intense fluorescence of 1–3 in nonpolar/low-polarity solvents is dramatically quenched in polar media (acetone, DMF, and DMSO). It has been established that the main reason f

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45

Girgis, Adel S., Altaf H. Basta, Houssni El-Saied, Mohamed A. Mohamed, Ahmad H. Bedair, and Ahmad S. Salim. "Synthesis, quantitative structure–property relationship study of novel fluorescence active 2-pyrazolines and application." Royal Society Open Science 5, no. 3 (2018): 171964. http://dx.doi.org/10.1098/rsos.171964.

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A variety of fluorescence-active fluorinated pyrazolines 13–33 was synthesized in good yields through cyclocondensation reaction of propenones 1–9 with aryl hydrazines 10–12 . Some of the synthesized compounds provided promising fluorescence properties with quantum yield ( Φ ) higher than that of quinine sulfate (standard reference). Quantitative structure–property relationship studies were undertaken supporting the exhibited fluorescence properties and estimating the parameters governing properties. Five synthesized fluorescence-active pyrazolines ( 13 , 15 , 18 , 19 and 23 ) with variable Φ

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46

Zhang, Xian-Fu, and Xiaojie Sun. "Germanium triazatetrabenzcorrole and germanium phthalocyanine: Synthesis, fluorescence and singlet oxygen generation." Journal of Porphyrins and Phthalocyanines 22, no. 09n10 (2018): 847–52. http://dx.doi.org/10.1142/s1088424618500670.

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The synthesis, fluorescence properties and singlet oxygen generation capability of germanium tetrabenzotriazacorrole (LGeTBC), germanium phthalocyanine (Cl[Formula: see text]GePc) and their derivatives are described. Measurements include UV-vis absorption spectra, fluorescence emission spectra, fluorescence quantum yields fluorescence lifetimes, and singlet delta oxygen quantum yields. LGeTBC and its derivatives exhibit quite different spectral and fluorescence properties from their phthalocyanine precursor. Both LGeTBC and Cl[Formula: see text]GePc show high singlet delta oxygen quantum yield

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47

Zhao, Xinghao. "Application of novel AIE materials in fluorescence probes." Theoretical and Natural Science 47, no. 1 (2024): 88–96. http://dx.doi.org/10.54254/2753-8818/47/20240171.

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Fluorescence bioimaging is considered an indispensable technique in biological research due to its high sensitivity, excellent spatial and temporal resolution, non-invasiveness, rapid and real-time responsiveness, as well as its ease of accessibility. Among these, fluorescence probes play a pivotal role in fluorescence imaging technology thanks to their strong specificity, high sensitivity, rapid response, and straightforward implementation. Aggregation-Induced Emission (AIE) molecules exhibit a unique phenomenon: they emit weak or no fluorescence when dissolved in a solution but become highly

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48

Zhao, Xinghao. "Application of novel AIE materials in fluorescence probes." Theoretical and Natural Science 49, no. 1 (2024): 7–15. http://dx.doi.org/10.54254/2753-8818/49/20240171.

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Fluorescence bioimaging is considered an indispensable technique in biological research due to its high sensitivity, excellent spatial and temporal resolution, non-invasiveness, rapid and real-time responsiveness, as well as its ease of accessibility. Among these, fluorescence probes play a pivotal role in fluorescence imaging technology thanks to their strong specificity, high sensitivity, rapid response, and straightforward implementation. Aggregation-Induced Emission (AIE) molecules exhibit a unique phenomenon: they emit weak or no fluorescence when dissolved in a solution but become highly

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49

Skalski, Bohdan, Stefan Paszyc, Ryszard W. Adamiak, Ronald P. Steer, and Ronald E. Verrall. "Photophysical properties of pyridinium salts derived from purine bases." Canadian Journal of Chemistry 68, no. 12 (1990): 2164–70. http://dx.doi.org/10.1139/v90-332.

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The absorption spectra, fluorescence spectra, fluorescence lifetimes, fluorescence quenching, phosphorescence spectra, phosphorescence lifetimes, and picosecond transient absorption spectra of several purinyl-pyridinium salts have been measured in several solvents at room temperature and in ethanol glasses at 77 K. It is concluded that the previously observed photochemical transformation of N-[9-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)purin-6-yl]pyridinium chloride 1 into the highly fluorescent tri-O-acetylluminarosine 6 occurs via an excited triplet state. It is also shown that intersystem c

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50

Feng, Yu Chuan, and Jie Li. "Syntheses and Properties of a Symmetrical Photochromic Diarylethene." Advanced Materials Research 830 (October 2013): 254–57. http://dx.doi.org/10.4028/www.scientific.net/amr.830.254.

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A new photochromic diarylethene compound 1,2-(2-ethyl-3-benzofuryl) perfluorocyclopentene was synthesized. And its properties including photochromism, fluorescence both in hexane and solid films were studied. And its absorption maxima were observed at 489 nm in hexane and at 499 nm in PMMA films, respectively, upon irradiation with 313 nm UV light. The fluorescence intensity of diarylethene decreased upon irradiation with 313 nm UV light. And the fluorescence modulation efficiency was better in PMMA films than that in hexane.

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