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Journal articles on the topic 'Fluorescence'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Sona, B. Warrier and Prashant S. Kharkar*. "DESIGN, SYNTHESIS AND CHARACTERIZATION OF FLUORESCENT PROBES BASED ON SCHIFF BASES." Indo American Journal of Pharmaceutical Sciences 04, no. 06 (2017): 1505–10. https://doi.org/10.5281/zenodo.815365.

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Abstract: Schiff bases of fluorescein were synthesized from fluorescein hydrazide using different aromatic aldehydes. These compounds show bright fluorescence different from that of starting material, fluorescein. The compounds were characterised by spectroscopic methods. Absorption and fluorescence spectra of the compounds were also recorded. Keywords: Fluorescein, Schiff bases, Fluorescein hydrazide, fluorescent probes, fluorescence

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2

MATSUMOTO, TAKURO, ATSUSHI SUETSUGU, KOSUKE HASEGAWA, et al. "A Mouse Model of Fluorescent Protein-expressing Disseminated Peritoneal Lymphoma for Fluorescence-guided Surgery." Anticancer Research 36, no. 9 (2016): 4483–88. http://dx.doi.org/10.21873/anticanres.10993.

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3

Pawley, James B. "Fluorescence Microscopy and Fluorescence Probes." Microscopy and Microanalysis 4, no. 2 (1998): 164–65. http://dx.doi.org/10.1017/s1431927698000166.

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Fluorescence Microscopy and Fluorescence Probes, edited by Jan Slavik, 1996. Plenum Press, New York and London. 306 pages. (hardback, $95)This volume is a compilation of abstracts of papers presented at the Fluorescence Microscopy and Fluorescence Probes Conference held in Prague in June 1995. This conference was one of the first tangible results of the end of the Cold War in the field of microscopy. As such, it attracted a great many of those who constitute the vanguard of progress in the field of fluorescence microscopy, on both sides of the old East-West divide. About one-third of the 127 c

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4

Sessions, S. K. "Fluorescence Microscopy; Quantitative Fluorescence Microscopy." Systematic Biology 42, no. 2 (1993): 224–25. http://dx.doi.org/10.1093/sysbio/42.2.224.

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5

Heldt, Józef, Janina R. Heldt, and Jerzy Kamiński. "Steady-state and Time-resolved Spectroscopic Studies of Benzanilides." Zeitschrift für Naturforschung A 54, no. 8-9 (1999): 495–502. http://dx.doi.org/10.1515/zna-1999-8-909.

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Steady-state and time-resolved spectroscopic studies of benzanilide (I) and jV-methylbenzanilide (II)were performed at 298 and 77 K in various solvents. The results indicate that benzanilide fluorescencein non-polar solvents at room temperature involves three independent modes of emission: F1 (LE) normalfluorescence from the initially excited state S1 (LE) with λmax = 320 nm, F2´(PT) fluorescence from the proton transfer tautomer with λmax = 468 nm, F2″CT) fluorescence from the species where intramolecular charge transfer appears, with λmax = 510 nm. At 77 K in MCH a new fluorescence band, Fag

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6

Ravinson, Daniel Sylvinson Muthiah, and Mark E. Thompson. "Thermally assisted delayed fluorescence (TADF): fluorescence delayed is fluorescence denied." Materials Horizons 7, no. 5 (2020): 1210–17. http://dx.doi.org/10.1039/d0mh00276c.

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Thermally assisted delayed fluorescence (TADF) allows for efficient collection of both singlet and triplet excitons with both emitting through the singlet channel. TADF opens the door to photo- and electroluminescence efficiencies close to 100%.

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7

Ma, Xiben, Jimeng Cheng, Sijun Fan, et al. "Silver-Neodymium Codoped Lithium Aluminum Metaphosphate Glasses for Radio-Photoluminescence Dosimeter." Materials 15, no. 16 (2022): 5527. http://dx.doi.org/10.3390/ma15165527.

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Commercial radio-photoluminescence (RPL) glass dosimeters generally use Ag single-doped phosphate glass as a single-wavelength sensor. Now, a novel type of Ag–Nd-codoped phosphate glass has been developed, which can be applied to dual-wavelength or multi-wavelength RPL sensors, and can thus improve the accuracy and stability of RPL dosimeters. An anhydrous 99.5 (0.7LiPO3–0.3Al (PO3)3) −0.25Ag2O–0.25Nd2O3 glass was prepared and irradiated at different doses, and then the absorption, fluorescence, infrared transmission spectra, as well as fluorescence lifetimes were tested and analyzed. The resu

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8

BEARDER, E. ARTHUR. "Fluorescence." Journal of the Society of Dyers and Colourists 27, no. 12 (2008): 270–79. http://dx.doi.org/10.1111/j.1478-4408.1911.tb00530.x.

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9

Inoue, S., O. Shimomura, M. Goda, M. Shribak, and P. T. Tran. "Fluorescence polarization of green fluorescence protein." Proceedings of the National Academy of Sciences 99, no. 7 (2002): 4272–77. http://dx.doi.org/10.1073/pnas.062065199.

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10

Gardner, Craig M., Steven L. Jacques, and Ashley J. Welch. "Fluorescence spectroscopy of tissue: recovery of intrinsic fluorescence from measured fluorescence." Applied Optics 35, no. 10 (1996): 1780. http://dx.doi.org/10.1364/ao.35.001780.

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11

Han, Zhengang, and Kefeng Xie. "Abnormally aggregation-induced emissions observed from hydrogen- and silyl-substituted siloles." Main Group Metal Chemistry 43, no. 1 (2020): 125–31. http://dx.doi.org/10.1515/mgmc-2020-0015.

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AbstractSilacyclopentadienes (siloles) are currently of great interest because of their intriguing aggregation-induced emission (AIE) characteristics. In this work, abnormally AIE phenomena were observed from silyl- and hydrogen-substituted siloles respectively. We propose silyl-substituent and hydrogen atom effects to explain this via both experiments and theoretical calculations. It was discovered that trimethylsilyl substituents destroyed the p-interactions with the silole core and resulted in the non-fluorescence. Additionally, 1-chloro-1-H-2,3,4,5-tetraphenylsilole featuring strong fluore

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12

Ping Tang, Ping Tang, and Luping Lyu and Yujin Li Luping Lyu and Yujin Li. "Fluorescence and Theoretical Calculation of Phenylhydrazone Derivatives and Fluorine Boron Complex: Synthesis and Fluorescence Characteristics." Journal of the chemical society of pakistan 42, no. 1 (2020): 10. http://dx.doi.org/10.52568/000623.

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A sereis of phenylhydrazone-based derivatives and their corresponding BF2 complexes were synthesized efficiently by a three-step reaction. Photophysical performance was investigated in different organic solvents and in the solid state. Although these compounds exhibited feeble fluorescent intensity in solution-state, BF2 complexes showed weaker fluorescence in solid state compared to precursors 2, which were caused by slight geometry relaxation of upon photo excitation. Density Functional Theory calculations was carried out to confirm above inference.

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13

Ping Tang, Ping Tang, and Luping Lyu and Yujin Li Luping Lyu and Yujin Li. "Fluorescence and Theoretical Calculation of Phenylhydrazone Derivatives and Fluorine Boron Complex: Synthesis and Fluorescence Characteristics." Journal of the chemical society of pakistan 42, no. 1 (2020): 10. http://dx.doi.org/10.52568/000623/jcsp/42.01.2020.

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A sereis of phenylhydrazone-based derivatives and their corresponding BF2 complexes were synthesized efficiently by a three-step reaction. Photophysical performance was investigated in different organic solvents and in the solid state. Although these compounds exhibited feeble fluorescent intensity in solution-state, BF2 complexes showed weaker fluorescence in solid state compared to precursors 2, which were caused by slight geometry relaxation of upon photo excitation. Density Functional Theory calculations was carried out to confirm above inference.

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14

Mohanty, N., and HY Yamamoto. "Mechanism of Non-Photochemical Chlorophyll Fluorescence Quenching. I. The Role of De-Epoxidised Xanthophylls and Sequestered Thylakoid Membrane Protons as Probed by Dibucaine." Functional Plant Biology 22, no. 2 (1995): 231. http://dx.doi.org/10.1071/pp9950231.

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Dibucaine reportedly inhibits the light-induced transthylakoid proton gradient of chloroplasts without inhibiting energy-dependent non-photochemical chlorophyll fluorescence quenching (Laasch, H. and Weis, E. (1989). Photosynthesis Research 22, 137-146). We show that dibucaine can inhibit fluorescence quenching, depending on the de-epoxidation state of the xanthophyll cycle. Whereas dibucaine (20-40 μM) had little effect on fluorescence quenching in pre-illuminated-type thylakoids (loaded with zeaxanthin and antheraxanthin), it strongly inhibited quenching in dark-adapted-type thylakoids (no p

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15

Fukushima, Shuichiro, Takashi Yasui, Tetsuo Iwata, Pasuk Mahakkanukrauh, and Tsutomu Araki. "P-25 Distribution of fluorescence lifetime of human dentin measured by nanosecond time-resolved fluorescence microscopy." Abstracts of ATEM : International Conference on Advanced Technology in Experimental Mechanics : Asian Conference on Experimental Mechanics 2007.6 (2007): _P—25–1_—_P—25–3_. http://dx.doi.org/10.1299/jsmeatem.2007.6._p-25-1_.

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16

MI, Cheng. "Does Anti Stokes Fluorescence Belong to Fluorescence." University Chemistry 31, no. 11 (2016): 81–82. http://dx.doi.org/10.3866/pku.dxhx201603019.

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17

Sakurai, Takeki, Shigeru Kobayashi, Jun Ogura, Yukio Inoue, and Hirokazu Hori. "Dissociation Processes of SiCl4 and Plasma Parameters measured by Transient Spectroscopy at the Beginning of a SiCl4?Helium dc Discharge." Australian Journal of Physics 48, no. 3 (1995): 515. http://dx.doi.org/10.1071/ph950515.

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We propose that the excitation or the dissociation mechanism and plasma parameters in a discharge can be estimated by. spectroscopic methods, such as the measurement of the transient behaviour of fluorescences at the beginning of a pulsed de discharge. Fluorescences emitted from excited atoms and dissociated fragments from 270 to 640 nm in wavelength are measured as a function of time at the beginning of a discharge of a He-SiCl4 gas mixture. The transient waveform of fluorescence is calculated by considering the experimental results of discharge current and voltage between electrodes measured

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18

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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19

Raabe, Andreas, and Robert F. Spetzler. "Fluorescence Angiography." Journal of Neurosurgery 108, no. 2 (2008): 429–30. http://dx.doi.org/10.3171/jns/2008/108/2/0429.

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20

Bollinger, A. "Fluorescence videomicroscopy." Clinical Hemorheology and Microcirculation 8, no. 3-4 (2016): 379–83. http://dx.doi.org/10.3233/ch-1988-83-414.

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21

Yilmaz, Ibrahim. "Fluorescence Sensors." Current Analytical Chemistry 18, no. 2 (2022): 143–44. http://dx.doi.org/10.2174/1573411018666220104214202.

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22

OHYANAGI, Hiroyuki. "Fluorescence EXAFS." Nihon Kessho Gakkaishi 27, no. 2 (1985): 106–12. http://dx.doi.org/10.5940/jcrsj.27.106.

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23

Evanko, Daniel. "Intelligent fluorescence." Nature Methods 2, no. 5 (2005): 324–25. http://dx.doi.org/10.1038/nmeth0505-324b.

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24

Bilenca, Alberto, Jing Cao, Max Colice, et al. "Fluorescence Interferometry." Annals of the New York Academy of Sciences 1130, no. 1 (2008): 68–77. http://dx.doi.org/10.1196/annals.1430.038.

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25

Stiel, Laure, Xavier Delabranche, Anne-Cécile Galoisy, et al. "Neutrophil Fluorescence." Critical Care Medicine 44, no. 11 (2016): e1132-e1136. http://dx.doi.org/10.1097/ccm.0000000000001851.

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26

Fitzgerald, Richard J. "Frog fluorescence." Physics Today 70, no. 5 (2017): 23. http://dx.doi.org/10.1063/pt.3.3549.

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27

Dowell, L. Jonathan. "Fluorescence Thermometry." Applied Mechanics Reviews 45, no. 7 (1992): 253–60. http://dx.doi.org/10.1115/1.3119756.

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The fluorescence of rare-earth-doped ceramic phosphors depends on temperature. Particularly, the fluorescence lifetime is decreased by temperature. This dependence makes the fluorescence suitable for measuring temperature. This paper describes the physics of the fluorescence of these ceramics, noting the works of Forster, Dexter, Inokuti, Hirayama, and others. Next, it outlines the several advantages of fluorescence thermometry. These advantages include (a) measurement of temperature by transfer to measurement standards for time, (b) remote sensing for surface thermometry, (c) high speed of me

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28

Lichtman, Jeff W., and José-Angel Conchello. "Fluorescence microscopy." Nature Methods 2, no. 12 (2005): 910–19. http://dx.doi.org/10.1038/nmeth817.

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29

Rakovan, John. "Green Fluorescence." Rocks & Minerals 100, no. 1 (2024): 98–102. https://doi.org/10.1080/00357529.2024.2398402.

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30

Pile, David. "Resonance fluorescence." Nature Photonics 10, no. 9 (2016): 565. http://dx.doi.org/10.1038/nphoton.2016.168.

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31

Muyskens, Mark. "pHantastic Fluorescence." Journal of Chemical Education 83, no. 5 (2006): 768A. http://dx.doi.org/10.1021/ed083p768a.

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32

Sanderson, M. J., I. Smith, I. Parker, and M. D. Bootman. "Fluorescence Microscopy." Cold Spring Harbor Protocols 2014, no. 10 (2014): pdb.top071795. http://dx.doi.org/10.1101/pdb.top071795.

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33

Diamandis, Eleftherios P. "Fluorescence Spectroscopy." Analytical Chemistry 65, no. 12 (1993): 454–59. http://dx.doi.org/10.1021/ac00060a616.

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34

Stanley, P. E. "Practical fluorescence." TrAC Trends in Analytical Chemistry 11, no. 6 (1992): XIV—XV. http://dx.doi.org/10.1016/0165-9936(92)80048-b.

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35

Morgan, C. G. "Fluorescence spectroscopy." TrAC Trends in Analytical Chemistry 13, no. 1 (1994): xiii—xiv. http://dx.doi.org/10.1016/0165-9936(94)85060-7.

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36

Cohen, Bruce E. "Beyond fluorescence." Nature 467, no. 7314 (2010): 407–8. http://dx.doi.org/10.1038/467407a.

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37

Foley, J. F. "Sensitive Fluorescence." Science Signaling 1, no. 50 (2008): ec432-ec432. http://dx.doi.org/10.1126/scisignal.150ec432.

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38

Khanizadeh, Shahrokh, and Jennifer Deell. "Chlorophyll Fluorescence." Small Fruits Review 1, no. 3 (2001): 61–67. http://dx.doi.org/10.1300/j301v01n03_06.

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39

Baeyens, Willy R. G. "Practical fluorescence." Analytica Chimica Acta 254, no. 1-2 (1991): 253. http://dx.doi.org/10.1016/0003-2670(91)90038-7.

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40

Gillbro, Tomas, and Richard J. Cogdell. "Carotenoid fluorescence." Chemical Physics Letters 158, no. 3-4 (1989): 312–16. http://dx.doi.org/10.1016/0009-2614(89)87342-7.

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41

Herman, Brian. "Fluorescence Microscopy." Current Protocols in Cell Biology 00, no. 1 (1998): 4.2.1–4.2.10. http://dx.doi.org/10.1002/0471143030.cb0402s13.

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42

ตู้จินดา, ภูวดี. "การผลิตกระดาษอ้างอิงมาตรฐานสำหรับสอบเทียบเครื่องวัดความขาวสว่างของกระดาษชนิด Fluorescence". วารสารวิทยาศาสตร์ประยุกต์ กรมวิทยาศาสตร์บริการ 1, № 1 (2022): 72–90. http://dx.doi.org/10.60136/bas.v1.2012.180.

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ค่าความขาวสว่าง (Brightness) มีความสำคัญต่ออุตสาหกรรมเยื่อและกระดาษเป็นอย่างมากเพราะเป็นค่าที่ใช้อ้างอิงในกระบวนการฟอกเยื่อและเป็นสิ่งที่มองเห็นได้ด้วยสายตา เครื่องวัดความขาวสว่างของกระดาษมีความจำเป็นจะต้องได้รับการสอบเทียบให้ถูกต้องแม่นยำอยู่เสมอ โดยใช้กระดาษอ้างอิงมาตรฐานสำหรับสอบเทียบเครื่องวัดความขาวสว่างของกระดาษ ซึ่งหนึ่งชุดประกอบด้วยกระดาษอ้างอิงมาตรฐาน 4 ชนิดคือ Fluorescence, ความขาวสว่าง 90, 70 และ 60 เพื่อให้สามารถสอบเทียบได้ครอบคลุมทุก Parameter บทความนี้กล่าวถึงการผลิตกระดาษอ้างอิงมาตรฐานชนิด Fluorescence ซึ่งใช้วิธีการผลิตตามข้อกำหนดของ ISO TC 6 (Paper, board and pulps) และ

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43

ZHANG Li-min, 张丽敏, 刘涵 LIU Han, 尹国艳 YIN Guo-yan, 李娇 LI Jiao, 周仲兴 ZHOU Zhong-xing, and 高峰 GAO Feng. "Dynamic Diffuse Fluorescence Tomography System for Fluorescence Pharmacokinetics." ACTA PHOTONICA SINICA 48, no. 6 (2019): 611002. http://dx.doi.org/10.3788/gzxb20194806.0611002.

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44

Cadoff, Evan M. "Fluorescence Assays: Fluorescence Polarization and Time-Resolved Pulse." Laboratory Medicine 21, no. 6 (1990): 347–52. http://dx.doi.org/10.1093/labmed/21.6.347.

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45

Shelar, Deepak Prakash, Sandeep R. Patil, Ramhari V. Rote, and Madhukar N. Jachak. "A Fluorescence and Fluorescence Probe Study of Benzonaphthyridines." Journal of Fluorescence 22, no. 1 (2011): 17–29. http://dx.doi.org/10.1007/s10895-011-0945-9.

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46

Cazeau-Dubroca, C., A. Peirigua, S. Ait Lyazidi, G. Nouchi, Ph Cazeau та R. Lapouyade. "Tict fluorescence in rigid matrices: α-delayed fluorescence". Chemical Physics Letters 124, № 2 (1986): 110–15. http://dx.doi.org/10.1016/0009-2614(86)85128-4.

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47

Breusegem, Sophia Y., Moshe Levi, and Nicholas P. Barry. "Fluorescence Correlation Spectroscopy and Fluorescence Lifetime Imaging Microscopy." Nephron Experimental Nephrology 103, no. 2 (2006): e41-e49. http://dx.doi.org/10.1159/000090615.

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48

Gao, Melisa, George Lewis, Gordon M. Turner, Antoine Soubret, and Vasilis Ntziachristos. "Effects of background fluorescence in fluorescence molecular tomography." Applied Optics 44, no. 26 (2005): 5468. http://dx.doi.org/10.1364/ao.44.005468.

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49

Ghauharali, Hofstraat, and Brakenhoff. "Fluorescence photobleaching-based shading correction for fluorescence microscopy." Journal of Microscopy 192, no. 2 (1998): 99–113. http://dx.doi.org/10.1046/j.1365-2818.1998.00412.x.

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50

Ghauharali and Brakenhoff. "Fluorescence photobleaching-based image standardization for fluorescence microscopy." Journal of Microscopy 198, no. 2 (2000): 88–100. http://dx.doi.org/10.1046/j.1365-2818.2000.00683.x.

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