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1

Jacobsen, NW, and A. Philippides. "The Unambiguous Syntheses of the 2,5-Diphenyloxazole Metabolites." Australian Journal of Chemistry 38, no. 9 (1985): 1335. http://dx.doi.org/10.1071/ch9851335.

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2

Agbaria, Rezik A., and David Gill. "Extended 2,5-diphenyloxazole-.gamma.-cyclodextrin aggregates emitting 2,5-diphenyloxazole excimer fluorescence." Journal of Physical Chemistry 92, no. 5 (1988): 1052–55. http://dx.doi.org/10.1021/j100316a012.

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3

Banciu, Mircea, Daniela Istrati, Dan Mihaiescu, and Constantin Draghici. "Flash Vacuum Pyrolysis of 2,5-Diphenyloxazole." Molecules 5, no. 12 (2000): 1004–10. http://dx.doi.org/10.3390/50801004.

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4

Dharamsi, A. N., and Shawpin Jong. "Triplet-State Kinetics of 2,5 Diphenyloxazole (PPO)." Applied Spectroscopy 42, no. 1 (1988): 27–31. http://dx.doi.org/10.1366/0003702884428473.

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Time-resolved excited-state triplet-triplet absorption spectra were measured for solutions of 2,5 diphenyloxazole (PPO) in various solvents, with the use of a pump and probe technique. The rate constants for intersystem crossing, triplet deactivation by oxygen, and triplet-triplet self-quenching are obtained. The latter two rate constants are substantially larger than the corresponding rate constants for 2-(1 naphthyl)-5-phenyloxazole-αNPO.
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5

Meanwell, Nicholas A., Michael J. Rosenfeld, Ashok K. Trehan, et al. "Nonprostanoid prostacyclin mimetics. 2. 4,5-diphenyloxazole derivatives." Journal of Medicinal Chemistry 35, no. 19 (1992): 3483–97. http://dx.doi.org/10.1021/jm00097a006.

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6

Losytskyy, Mykhaylo, Lyudmyla Vretik, Olena Nikolaeva, Daryna Getya, Andrii Marynin, and Valeriy Yashchuk. "Energy Transfer in Polystyrene Nanoparticles with Encapsulated 2,5-Diphenyloxazole." French-Ukrainian Journal of Chemistry 3, no. 2 (2015): 119–24. http://dx.doi.org/10.17721/fujcv3i2p119-124.

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As the first step to design nanosystems for X-ray excited sensitising of singlet oxygen, nanoparticles of polystyrene (PS NP) and polystyrene with encapsulated diphenyloxazole molecules (PS-PPO NP) were synthesized. Inside the PS-PPO NP, the electronic excitation energy transfer from polystyrene matrix to encapsulated PPO molecules takes place; efficiency of such transfer was roughly estimated to be about 0.37. X-ray stimulated luminescence of PS-PPO NP was registered.
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7

Hariharan, Chithra, V. Vijaysree, and A. K. Mishra. "Quenching of 2,5-diphenyloxazole (PPO) fluorescence by metal ions." Journal of Luminescence 75, no. 3 (1997): 205–11. http://dx.doi.org/10.1016/s0022-2313(97)00126-9.

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8

KrishnaMurthy, N. V., A. R. Reddy, and B. Bhudevi. "Wavelength Dependant Quenching of 2,5-Diphenyloxazole Fluorescence by Nucleotides." Journal of Fluorescence 18, no. 1 (2007): 29–34. http://dx.doi.org/10.1007/s10895-007-0231-z.

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9

Losytskyy, M. Yu, L. O. Vretik, O. A. Nikolaeva, A. I. Marynin, N. F. Gamaleya, and V. M. Yashchuk. "Polystyrene-diphenyloxazole-chlorin e6 nanosystem for PDT: Energy transfer study." Molecular Crystals and Liquid Crystals 639, no. 1 (2016): 169–76. http://dx.doi.org/10.1080/15421406.2016.1255072.

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10

Dereka, Bogdan, Denis Svechkarev, and Andrey Doroshenko. "Facile ultrasensitive monitoring of mercury ions in water by fluorescent ratiometric detection." Open Chemistry 11, no. 4 (2013): 584–93. http://dx.doi.org/10.2478/s11532-012-0193-0.

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AbstractProspects for analytical application of 2,5-diphenyloxazole-substituted 3-hydroxychromone for detection of mercury ions are presented. Sensitivity and selectivity for a number of metal ions both in methanol solution and in the plasticized polymer are outlined. Ultrasensitive and highly selective fluorescent ratiometric response of the polymer film containing the title compound for mercury ions in water media is revealed. Reversibility of ratiometric response to mercury ions and influence of plasticizer’s content in the polymer film on the optical feedback are also discussed.
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11

Wieczorek, Anna, Bożena Zgardzińska, Bożena Jasińska, et al. "PALS investigations of free volumes thermal expansion of J-PET plastic scintillator synthesized in polystyrene matrix." Nukleonika 60, no. 4 (2015): 777–81. http://dx.doi.org/10.1515/nuka-2015-0140.

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Abstract The polystyrene doped with 2,5-diphenyloxazole as a primary fluor and 2-(4-styrylphenyl)benzoxazole as a wavelength shifter prepared as a plastic scintillator was investigated using positronium probe in wide range of temperatures from 123 to 423 K. Three structural transitions at 260, 283, and 370 K were found in the material. In the o-Ps intensity dependence on temperature, the significant hysteresis is observed. Heated to 370 K, the material exhibits the o-Ps intensity variations in time.
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12

Polacki, Zenon, and Krzysztof Sienicki. "Photoluminescence and radioluminescence of 1,4-dioxane-water solutions of 2,5-diphenyloxazole." Journal of Photochemistry 33, no. 2 (1986): 181–86. http://dx.doi.org/10.1016/0047-2670(86)87032-0.

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13

Biddau, M., M. Massacesi, R. Pinna, and G. Ponticelli. "Zinc(II), cadmium(II) and mercury(II) complexes with 2,5-diphenyloxazole." Recueil des Travaux Chimiques des Pays-Bas 98, no. 6 (2010): 405–8. http://dx.doi.org/10.1002/recl.19790980608.

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14

Kawski, A., P. Bojarski, and A. Kubicki. "The Inertial Effect in Rotational Fluorescence Depolarization." Zeitschrift für Naturforschung A 47, no. 9 (1992): 971–73. http://dx.doi.org/10.1515/zna-1992-0907.

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Abstract The influence of the moment of inertia on the rotational fluorescence depolarization is discussed. Based on experimental results obtained for five luminescent compounds: 2,5-diphenyloxazole (PPO), 2,2'-p-phenylene-bis(5-phenyloxazole) (POPOP), p-bis[2-(5-α-naphthyloxazolyl)]-benzene (α-NOPON), 4-dimethylamino-ω-methylsulphonyl-trans-styrene (3a) in n-parafines at low viscosity (from 0.22 x 10-3 Pa • s to 0.993 x 10-3 Pa • s) and diphenylenestilbene (DPS) in different solvents, a semi-empirical equation is proposed, yielding moments of inertia that are only two to five times higher tha
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15

Gryczynski, Ignacy, Henryk Malak, and Joseph R. Lakowicz. "Three-photon induced fluorescence of 2,5-diphenyloxazole with a femtosecond Ti:sapphire laser." Chemical Physics Letters 245, no. 1 (1995): 30–35. http://dx.doi.org/10.1016/0009-2614(95)00958-7.

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16

Lim, Allison, Griselda Hernandez, Joseph Latta, et al. "Methacrylate-Functionalized 2,5-Diphenyloxazole for Use as Fluorescent Monomers in Plastic Scintillators." ACS Applied Polymer Materials 1, no. 6 (2019): 1420–29. http://dx.doi.org/10.1021/acsapm.9b00188.

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17

Hamai, Sanyo. "Inclusion of 2,4- and 2,5-Diphenyloxazole by γ-Cyclodextrin in Aqueous Solution". Bulletin of the Chemical Society of Japan 81, № 5 (2008): 574–82. http://dx.doi.org/10.1246/bcsj.81.574.

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18

Birch, D. J. S., A. D. Dutch, R. E. Imhof, B. Nadolski, and I. Soutar. "The effect of transient quenching on the excimer kinetics of 2,5-diphenyloxazole." Journal of Photochemistry 38 (June 1987): 239–54. http://dx.doi.org/10.1016/0047-2670(87)87020-x.

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19

Ahokas, J. T., C. Davies, N. Jacobsen, N. T. Kärki, A. Philippides, and A. M. Treston. "The Metabolism of 2,5-Diphenyloxazole (PPO) in Human Lymphocytes and Rat Liver Microsomes." Pharmacology & Toxicology 61, no. 3 (1987): 184–90. http://dx.doi.org/10.1111/j.1600-0773.1987.tb01800.x.

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20

Fan, Guoling, Xiaogang Yang, Ruizheng Liang, Jingwen Zhao, Shuzhen Li, and Dongpeng Yan. "Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties." CrystEngComm 18, no. 2 (2016): 240–49. http://dx.doi.org/10.1039/c5ce02019k.

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21

DiCesare, Nicolas, and Joseph R. Lakowicz. "A new highly fluorescent probe for monosaccharides based on a donor–acceptor diphenyloxazole." Chemical Communications, no. 19 (2001): 2022–23. http://dx.doi.org/10.1039/b106763j.

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22

Bentoumi, G., X. Dai, E. Pruszkowski, L. Li, and B. Sur. "A Novel Boron-Loaded Liquid Scintillator for Neutron Detection." AECL Nuclear Review 1, no. 1 (2012): 57–59. http://dx.doi.org/10.12943/anr.2012.00008.

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A boron-loaded liquid scintillator (LS) has been optimized for neutron detection application in a high gamma field environment. It is composed of the solvent linear alkylbenzene (LAB), a boroncontaining material, o-carborane (C2B10H12); a fluor, 2,5-diphenyloxazole (PPO); and a wavelength shifter, 1,4-bis[2-methylstyryl] benzene (bis-MSB). Preparation of the liquid scintillator and optimization of its chemical composition are described. The boronloaded LS has been tested with a neutron beam at the National Research Universal (NRU) reactor. A peak at an equivalent energy of 60 keV is observed i
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23

Mutch, Elaine, K. W. Woodhouse, Faith M. Williams, D. Lambert, O. F. W. James, and M. D. Rawlins. "2,5-Diphenyloxazole as a probe for microsomal mono-oxygenation in human and rat liver." Xenobiotica 15, no. 7 (1985): 599–603. http://dx.doi.org/10.3109/00498258509045889.

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24

Balamurugan, N., A. Arulchakkaravarthi, and P. Ramasamy. "Growth of 2,5-diphenyloxazole-doped naphthalene crystal by Bridgman method and its fluorescence studies." Journal of Crystal Growth 310, no. 7-9 (2008): 2115–19. http://dx.doi.org/10.1016/j.jcrysgro.2007.10.047.

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25

Agnew, Kimberly A., Tracy D. McCarley, Rezik A. Agbaria та Isiah M. Warner. "Phase transition pattern of 2,5-diphenyloxazole/γ-cyclodextrin (PPO/γ-CD) self-assembly aggregates". Journal of Photochemistry and Photobiology A: Chemistry 91, № 3 (1995): 205–10. http://dx.doi.org/10.1016/1010-6030(95)04118-9.

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26

Luchowski, Rafal. "Two-photon excitation of 2,5-diphenyloxazole using a low power green solid state laser." Chemical Physics Letters 501, no. 4-6 (2011): 572–74. http://dx.doi.org/10.1016/j.cplett.2010.11.038.

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27

Pimpha, Nuttaporn, Supawan Tantayanon, and Frank Harris. "Synthesis and Characterization of a Novel Poly(aryl ether) Containing 4-Chloro-2,5-diphenyloxazole." Macromolecular Symposia 216, no. 1 (2004): 109–16. http://dx.doi.org/10.1002/masy.200451212.

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28

Hamerton, Ian, John N. Hay, John R. Jones, and Shui-Yu Lu. "Covalent Incorporation of 2,5-Diphenyloxazole in Sol−Gel Matrices and Their Application in Radioanalytical Chemistry." Chemistry of Materials 12, no. 2 (2000): 568–72. http://dx.doi.org/10.1021/cm991157x.

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29

DiCesare, Nicolas, and Joseph R. Lakowicz. "ChemInform Abstract: A New Highly Fluorescent Probe for Monosaccharides Based on a Donor-Acceptor Diphenyloxazole." ChemInform 33, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.200206134.

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30

Hamerton, Ian, John N. Hay, John R. Jones, and Shui-Yu Lu. "Preparation of 2,5-diphenyloxazole doped sol-gel glasses and their application to radio-analytical chemistry." Journal of Materials Chemistry 8, no. 11 (1998): 2429–32. http://dx.doi.org/10.1039/a804267e.

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31

Hattori, Kouji, Osamu Okitsu, Seiichiro Tabuchi, et al. "Discovery of new diphenyloxazole derivatives containing a pyrrolidine ring: Orally active prostacyclin mimetics. Part 2." Bioorganic & Medicinal Chemistry Letters 15, no. 13 (2005): 3279–83. http://dx.doi.org/10.1016/j.bmcl.2005.04.042.

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32

Zhai, Xiaoyu, Siqi Li, Yufeng Ding, et al. "Fabrication and Investigation of Two-Component Film of 2,5-Diphenyloxazole and Octafluoronaphthalene Exhibiting Tunable Blue/Bluish Violet Fluorescence Based on Low Vacuum Physical Vapor Deposition Method." Journal of Nanomaterials 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/4363541.

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Organic luminescent materials play an important role in the fields of light-emitting diodes and fluorescent imaging. Moreover, new synthetic approaches towardsπ-conjugated molecular systems with high fluorescence quantum efficiency are highly desired. Herein, different 2,5-diphenyloxazole-octafluoronaphthalene (DPO-OFN) films with tunable fluorescence have been prepared by Low Vacuum Physical Vapor Deposition (LVPVD) method. DPO-OFN films showed some changed properties, such as molecular vibration and fluorescence. All films exhibited blue/bluish violet fluorescence and showed blue shift, in c
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33

Hattori, Kouji, Akira Tanaka, Naoaki Fujii та ін. "Discovery of Diphenyloxazole and Nδ-Z-Ornithine Derivatives as Highly Potent and Selective Human Prostaglandin EP4Receptor Antagonists". Journal of Medicinal Chemistry 48, № 9 (2005): 3103–6. http://dx.doi.org/10.1021/jm050085k.

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34

Zhang, Liang, Qingfeng Xu, Jianmei Lu, Xuewei Xia, and Lihua Wang. "ATRP of MMA initiated by 2-bromomethyl-4,5-diphenyloxazole at room temperature and study of fluorescent property." European Polymer Journal 43, no. 6 (2007): 2718–24. http://dx.doi.org/10.1016/j.eurpolymj.2007.02.032.

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35

Dudko, E. V., I. I. Kalosha, and V. A. Tolkachev. "Collisional quenching and depolarization of the fluorescence of the 2,5-diphenyloxazole and 2-phenylbenzoxazole vapors by oxygen." Journal of Applied Spectroscopy 72, no. 1 (2005): 43–48. http://dx.doi.org/10.1007/s10812-005-0029-1.

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36

Min, Sujung, Hara Kang, Bumkyung Seo, Changhyun Roh, Sangbum Hong, and Jaehak Cheong. "Integrated and Portable Probe Based on Functional Plastic Scintillator for Detection of Radioactive Cesium." Applied Sciences 11, no. 11 (2021): 5210. http://dx.doi.org/10.3390/app11115210.

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The highly reliable and direct detection of radioactive cesium has gained potential interest due to in-situ detection and monitoring in environments. In this study, we elucidated an integrated and portable probe based on functional plastic scintillator for detection of radioactive cesium. A functional plastic scintillator with improved detection efficiency was fabricated including CdTe (cadmium telluride) material. Monolith-typed functional plastic scintillator having a diameter of 50 mm and a thickness of 30 mm was manufactured by adding 2,5-diphenyloxazole (PPO, 0.4 wt%), 1,4 di[2-(5phenylox
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37

Lakowicz, J. R., I. Gryczynski, Z. Gryczynski, E. Danielsen, and M. J. Wirth. "Time-resolved fluorescence intensity and anisotropy decays of 2,5-diphenyloxazole by two-photon excitation and frequency-domain fluorometry." Journal of Physical Chemistry 96, no. 7 (1992): 3000–3006. http://dx.doi.org/10.1021/j100186a042.

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38

McCairn, Mark C., Steven J. Culliford, Roland Z. Kozlowski, and Andrew J. Sutherland. "Synthesis, evaluation and incorporation into liposomes of 4-functionalised-2,5-diphenyloxazole derivatives for application in scintillation proximity assays." Tetrahedron Letters 45, no. 10 (2004): 2163–66. http://dx.doi.org/10.1016/j.tetlet.2004.01.034.

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39

Mathew, Jessy Elizabeth, Gubba Divya, S. Dinakaran Vachala, Jesil A. Mathew, and Ramaiah Selladurai Jeyaprakash. "Synthesis and characterisation of novel 2,4-diphenyloxazole derivatives and evaluation of their in vitro antioxidant and anticancer activity." Journal of Pharmacy Research 6, no. 1 (2013): 210–13. http://dx.doi.org/10.1016/j.jopr.2012.12.001.

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40

Ludlow, J. W., K. C. L. Yuen, and R. A. Consigli. "Fluorographic detection of [3H]thymidine-labeled deoxyribonucleic acid using agarose gels infused with 2,5-diphenyloxazole prior to electrophoresis." Analytical Biochemistry 145, no. 1 (1985): 212–15. http://dx.doi.org/10.1016/0003-2697(85)90350-1.

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41

Munkittrick, K. R., C. B. Portt, G. J. Van Der Kraak, I. R. Smith, and D. A. Rokosh. "Impact of Bleached Kraft Mill Effluent on Population Characteristics, Liver MFO Activity, and Serum Steroid Levels of a Lake Superior White Sucker (Catostomus commersoni) Population." Canadian Journal of Fisheries and Aquatic Sciences 48, no. 8 (1991): 1371–80. http://dx.doi.org/10.1139/f91-164.

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White sucker (Catostomus commersoni) collected from a site receiving primary-treated bleached kraft mill effluent (BKME) were older and had a higher condition factor than fish at a reference site and grew more slowly than fish from three other areas of Lake Superior. The BKME-exposed fish also exhibited an increased age to maturity, smaller gonads, lower fecundity with age, an absence of secondary sex characteristics in males, and females failed to show an increase in egg size with age. Lower serum estradiol and testosterone concentrations and greater hepatic mixed-function oxidase (MFO) activ
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42

Kang, Hara, Sujung Min, Bumkyung Seo, Changhyun Roh, Sangbum Hong, and Jae Hak Cheong. "Preliminary Studies of Perovskite-Loaded Plastic Scintillator Prototypes for Radioactive Strontium Detection." Chemosensors 9, no. 3 (2021): 53. http://dx.doi.org/10.3390/chemosensors9030053.

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Functional plastic scintillators have attracted much attention for their usefulness in on-site monitoring and detection in environments. In this study, we elucidated a highly reliable and functional plastic scintillator for detection of radioactive strontium, which means a potent perovskite-loaded polymeric scintillation material based on epoxy and 2,5-diphenyloxazole (PPO). Moreover, Monte Carlo N-Particle (MCNP) simulation was performed to optimize the thickness of a plastic scintillator for efficient strontium detection. A thickness of 2 mm was found to be the optimum thickness for strontiu
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43

Bucciarelli, Alessio, Alberto Quaranta, and Devid Maniglio. "Imaging the Morphological Structure of Silk Fibroin Constructs through Fluorescence Energy Transfer and Confocal Microscopy." Electronic Materials 2, no. 2 (2021): 186–97. http://dx.doi.org/10.3390/electronicmat2020015.

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Silk fibroin is a well-known biopolymer that is used in several applications in which interactions with biological tissue are required. Fibroin is extremely versatile and can be shaped to form several constructs that are useful in tissue engineering applications. Confocal imaging is usually performed to test cell behavior on a construct, and, in this context, the fibroin intrinsic fluorescence is regarded as a problem. In addition, the intrinsic fluorescence is not intense enough to provide useful morphological images. In fact, to study the construct’s morphology, other techniques are used (i.
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44

Yan, Dongpeng, Hejia Yang, Qingyun Meng, Heyang Lin, and Min Wei. "Two-Component Molecular Materials of 2,5-Diphenyloxazole Exhibiting Tunable Ultraviolet/Blue Polarized Emission, Pump-enhanced Luminescence, and Mechanochromic Response." Advanced Functional Materials 24, no. 5 (2013): 587–94. http://dx.doi.org/10.1002/adfm.201302072.

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45

LAKOWICZ, J. R., I. GRYCZYNSKI, Z. GRYCZYNSKI, E. DANIELSEN, and M. J. WIRTH. "ChemInform Abstract: Time-Resolved Fluorescence Intensity and Anisotropy Decays of 2,5- Diphenyloxazole by Two-Photon Excitation and Frequency-Domain Fluorometry." ChemInform 23, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199229036.

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46

Lukavenko, Oksana N., Sergey V. Eltsov, Aleksey V. Grigorovich, and Nikolay O. Mchedlov-Petrossyan. "Solubility and fluorescence lifetime of 2,5-diphenyloxazole and 1,4-bis(5-phenyl-oxazolyl-2)benzene in water–ethanol and water–acetone solvent systems." Journal of Molecular Liquids 145, no. 3 (2009): 167–72. http://dx.doi.org/10.1016/j.molliq.2008.07.011.

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47

Yan, Dongpeng, Hejia Yang, Qingyun Meng, Heyang Lin, and Min Wei. "Supramolecular Materials: Two-Component Molecular Materials of 2,5-Diphenyloxazole Exhibiting Tunable Ultraviolet/Blue Polarized Emission, Pump-enhanced Luminescence, and Mechanochromic Response (Adv. Funct. Mater. 5/2014)." Advanced Functional Materials 24, no. 5 (2014): 720. http://dx.doi.org/10.1002/adfm.201470031.

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48

Li, Xiao-Fang, Ya-Qing Feng, Xiao-Fen Hu, and Mian Xu. "1′-Benzyl-3-(2,6-dichlorophenyl)-1′′-methyl-4,4′′-diphenyloxazole-5(4H)-spiro-3′-piperidine-5′-spiro-3′′-pyrrolidine-2′′-spiro-3′′′-1H-indole-2′′′(3′′′H),4′-dione benzene hemisolvate." Acta Crystallographica Section E Structure Reports Online 59, no. 9 (2003): o1280—o1282. http://dx.doi.org/10.1107/s1600536803015423.

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49

Clapham, Bruce, and Andrew J. Sutherland. "Scintillation-based potassium signalling using 2,5-diphenyloxazole-tagged aza-18-crown-6Electronic supplementary information (ESI) available: titration of scintillant-tagged 4 against TFA. See http://www.rsc.org/suppdata/cc/b2/b209337e/." Chemical Communications, no. 1 (November 28, 2002): 84–85. http://dx.doi.org/10.1039/b209337e.

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50

Gzella, Andrzej, and Maria D. Rozwadowska. "(4S,5S)-(+)-4-Hydroxymethyl-2,5-diphenyloxazoline." Acta Crystallographica Section C Crystal Structure Communications 56, no. 8 (2000): 981–82. http://dx.doi.org/10.1107/s0108270100006818.

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