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Relevant bibliographies by topics / Fluorescein hydrazide

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Academic literature on the topic 'Fluorescein hydrazide'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Fluorescein hydrazide"

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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

NAKAHARA, Ryosuke, Mitsunobu DOI, Yuuki KITANI, Takako YAMAGUCHI, and Yoshikazu FUJITA. "Crystal Structure of Tetraacetyl Fluorescein Hydrazide." X-ray Structure Analysis Online 25 (2009): 21–22. http://dx.doi.org/10.2116/xraystruct.25.21.

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3

Liu, Guanhong, Peipei Ren, Fan Yang, Xuekai Dou, Jun Wang, and Youtao Song. "Two novel colorimetric probes (5-HMBA-FH and 3-HMBA-FH) based on fluorescein for copper(II) ion detection." Canadian Journal of Chemistry 96, no. 12 (2018): 1037–45. http://dx.doi.org/10.1139/cjc-2018-0105.

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Two novel isomeric colorimetric probes are established for simultaneous determination of copper ions using 2-hydroxy-5-methoxybenzaldehyde fluorescein hydrazone (5-HMBA-FH) and 2-hydroxy-3-methoxybenzaldehyde fluorescein hydrazone (3-HMBA-FH). They are synthesized by reacting fluorescein hydrazide with 2-hydroxy-5-methoxybenzaldehyde and 2-hydroxy-3-methoxybenzaldehyde, respectively, and then characterized by 1H-NMR, 13C-NMR, and infrared spectrum. The addition of copper ions to the solutions of two novel colorimetric probes can generate the obviously peaks at 498 nm in UV–vis absorption spect

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4

Zavalishin, Maksim N., Alexey N. Kiselev, Alexandra K. Isagulieva, et al. "Shedding Light on Heavy Metal Contamination: Fluorescein-Based Chemosensor for Selective Detection of Hg2+ in Water." International Journal of Molecular Sciences 25, no. 6 (2024): 3186. http://dx.doi.org/10.3390/ijms25063186.

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This article discusses the design and analysis of a new chemical chemosensor for detecting mercury(II) ions. The chemosensor is a hydrazone made from 4-methylthiazole-5-carbaldehyde and fluorescein hydrazide. The structure of the chemosensor was confirmed using various methods, including nuclear magnetic resonance spectroscopy, infrared spectroscopy with Fourier transformation, mass spectroscopy, and quantum chemical calculations. The sensor’s ability in the highly selective and sensitive discovery of Hg2+ ions in water was demonstrated. The detection limit for mercury(II) ions was determined

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Shazia Kousar, Shazia Kousar, Abdul Jabbar Abdul Jabbar, Muhammad Ahmad Mudassir Muhammad Ahmad Mudassir, et al. "Designing, Synthesis and Characterization of Fluorescent Fluorescein Hydrazides and Antibacterial Studies against Sinusitis Isolates and Hemolytic Activities." Journal of the chemical society of pakistan 46, no. 6 (2024): 560. https://doi.org/10.52568/001615/jcsp/46.06.2024.

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Fluorescein and its various derivatives show remarkable biological and bio-analytical applications because of its solubility, high degree of inertness and high fluorescent activity. To broaden the spectrum of its applications, we synthesized novel fluorescein-based hydrazides (FHJ-0.2 - FHJ-0.6) using different substituted aryl hydrazine. The newly designed and synthesized products have been monitored by thin layer chromatography and characterized by 1HNMR, IR and MS data. To find the application of these hydrazides, the biological screening is considered and screened by antimicrobial and hemo

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6

Chen, Xinqi, and Huimin Ma. "A selective fluorescence-on reaction of spiro form fluorescein hydrazide with Cu(II)." Analytica Chimica Acta 575, no. 2 (2006): 217–22. http://dx.doi.org/10.1016/j.aca.2006.05.097.

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7

Mori, I. "Selective and sensitive fluorometric determinations of cobalt(II) and hydrogen peroxide with fluorescein-hydrazide." Talanta 47, no. 3 (1998): 631–37. http://dx.doi.org/10.1016/s0039-9140(98)00118-0.

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8

Yang, Xiao-Feng, Dong-Bing Wu, and Hua Li. "Sensitive Determination of Cobalt(II) Using a Spiro Fluorescein Hydrazide as a Chemiluminogenic Reagent." Microchimica Acta 149, no. 1-2 (2004): 123–29. http://dx.doi.org/10.1007/s00604-004-0285-4.

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9

Helal, Aasif, Muhammed Naeem, Mohammed Fettouhi, and Md Hasan Zahir. "Fluorescein Hydrazide-Appended Metal–Organic Framework as a Chromogenic and Fluorogenic Chemosensor for Mercury Ions." Molecules 26, no. 19 (2021): 5773. http://dx.doi.org/10.3390/molecules26195773.

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In this work, we prepared a fluorescein hydrazide-appended Ni(MOF) (Metal–Organic Framework) [Ni3(BTC)2(H2O)3]·(DMF)3(H2O)3 composite, FH@Ni(MOF). This composite was well-characterized by PXRD (powder X-ray diffraction), FT-IR (Fourier transform infrared spectroscopy), N2 adsorption isotherm, TGA (thermogravimetric analysis), XPS (X-ray photoelectron spectroscopy), and FESEM (field emission scanning electron microscopy). This composite was then tested with different heavy metals and was found to act as a highly selective and sensitive optical sensor for the Hg2+ ion. It was found that the aque

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10

Ahn, B., S. G. Rhee, and E. R. Stadtman. "Use of fluorescein hydrazide and fluorescein thiosemicarbazide reagents for the fluorometric determination of protein carbonyl groups and for the detection of oxidized protein on polyacrylamide gels." Analytical Biochemistry 161, no. 2 (1987): 245–57. http://dx.doi.org/10.1016/0003-2697(87)90448-9.

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Dissertations / Theses on the topic "Fluorescein hydrazide"

1

Dilek, Özlem. "Synthesis and spectroscopic characterization of fluorescent boron dipyrromethene (BDP) probes for site specific bioorthogonal labeling of proteins." Diss., Online access via UMI:, 2009.

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2

Nina, Diogo Anthony. "Hétérocycles fluorescents pour la détection des protéines carbonylées associées au vieillissement et à l’inflammation." Thesis, Sorbonne université, 2018. http://www.theses.fr/2018SORUS355.

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Les travaux présentés dans ce manuscrit décrivent la synthèse de nouvelles sondes fluorescentes pour le marquage des protéines carbonylées. Dans une première partie, la synthèse de nouvelles molécules fluorescentes à base 1,2,4-triazoles 1,3,5-trisubstitués est décrite à partir des 4H-pyrido[e][1,3]oxazin-4-ones. L’étude photophysique des 1,2,4- triazoles dans plusieurs solvants a permis de mettre en évidence un mécanisme de fluorescence de type ESIPT induisant un large déplacement de Stokes (jusqu’à 250 nm). La deuxième partie de ce manuscrit est consacrée à la synthèse de nouveaux BODIPY ave

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Book chapters on the topic "Fluorescein hydrazide"

1

Moreira Pereira, Thiago, and Arthur Eugen Kümmerle. "Hydrazone-Based Small-Molecule Chemosensors." In Computational Biology and Chemistry. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.92144.

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The hydrazone functional group is widely applied in several fields. The versatility and large use of this chemotype are attributed to its easy and straightforward synthesis and unique structural characteristics which is useful for different chemical and biological purposes. Recently hydrazone scaffold has been widely adopted in the design of small-molecule fluorescent and colorimetric chemosensors for detecting metals and anions because of its corresponding non-covalent interactions. This chapter provides an overview of hydrazone-based fluorescent and colorimetric chemosensors for anions and m

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2

"1-Pyrenebutanoic acid hydrazide (PBH)." In Handbook of Fluorescent Dyes and Probes. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119007104.ch123.

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3

"Cascade Blue hydrazide trisodium salt." In Handbook of Fluorescent Dyes and Probes. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119007104.ch52.

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4

"7-Diethylaminocoumarin-3-carboxylic acid hydrazide (DCCH)." In Handbook of Fluorescent Dyes and Probes. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119007104.ch58.

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