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Relevant bibliographies by topics / Perfluorophenyl derivatives

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Journal articles

Academic literature on the topic 'Perfluorophenyl derivatives'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Perfluorophenyl derivatives"

1

Kwiczak-Yiğitbaşı, Joanna, Jean-Luc Pirat, David Virieux, et al. "Synthesis, structural studies and biological properties of some phosphono-perfluorophenylalanine derivatives formed by SNAr reactions." RSC Advances 9, no. 42 (2019): 24117–33. http://dx.doi.org/10.1039/c9ra03982a.

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Several novel phosphono-perfluorophenylalanine derivatives, as mimetics of phenylalanine, were synthesized by subjecting diethyl (2-(perfluorophenyl)-1-(phenylamino)ethyl)-phosphonate to S<sub>N</sub>Ar reactions with thiols, amines and phenols.

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2

Syutkina, O. P., L. F. Rybakova, E. S. Petrov, and I. P. Beletskaya. "Thienyl and perfluorophenyl derivatives of divalent lanthanides." Journal of Organometallic Chemistry 280, no. 3 (1985): c67—c69. http://dx.doi.org/10.1016/0022-328x(85)88124-9.

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3

Askerova, Ulviyya F. "Prediction of Acute Toxicity of (Z) -N, N-Dimethyl-2- (perfluorophenyl) -2- (2-phenylhydrazinylidine)acetamide for Rats using the GUSAR Program." Pharmaceutical and Chemical Journal 8, no. 5 (2021): 63–66. https://doi.org/10.5281/zenodo.13963658.

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It is known that the determination of the values of half-lethal doses (LD<sub>50</sub>) for rodents is a necessary stage of preclinical experimental studies for putative physiologically active substances. To calculate (<em>in silico</em>) the LD<sub>50</sub> value for 4 methods of substance administration (oral, intraperitoneal, intravenous, subcutaneous), we used the GUSAR (General Unrestricted Structure-Activity Relationships) computer program as a web service. When making a forecast of the LD<sub>50</sub> value for the analyzed compound, it is assessed that it falls within the range of appl

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4

Petrova, T. D., and V. E. Platonov. "Reactions of N-(Perfluorophenyl)carbonimidoyl Dichloride with Aromatic Acids and Their Derivatives in the Presence of AlCl3. Formation of 2-(Perfluorophenyl)isoindoline-1,3-dione and Its Derivatives." Russian Journal of Organic Chemistry 41, no. 2 (2005): 218–26. http://dx.doi.org/10.1007/s11178-005-0147-5.

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5

Wyrębek, Przemysław, Anna Osuch-Kwiatkowska, Zbigniew Pakulski, Sławomir Jarosz, and Stanisław Ostrowski. "The synthesis of sugar-decorated hydrophilic porphyrins." Journal of Porphyrins and Phthalocyanines 17, no. 05 (2013): 384–91. http://dx.doi.org/10.1142/s1088424613500703.

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The synthesis of porphyrins conjugated with sugar moieties is described. meso-Aminophenyl-substituted and β-amino-substituted porphyrin derivatives reacted with benzyl protected glucuronic acid leading to gluco-conjugated hybrids, which after reductive deprotection of OH groups ( H2, 10% Pd/C ) gave the desired target products of increased hydrophilicity. Alternatively, this type of similar conjugates were obtained through SNAr reaction of meso-tetrakis(pentafluorophenyl)porphyrin with aminomethyl sacharides. The substitution took place selectively in para-position of meso-perfluorophenyl ring

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6

Chen, Yang, Jiao He, Hang Lin, et al. "Efficient synthesis of fluorinated triphenylenes with enhanced arene–perfluoroarene interactions in columnar mesophases." Beilstein Journal of Organic Chemistry 20 (December 16, 2024): 3263–73. https://doi.org/10.3762/bjoc.20.270.

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The high potential of non-covalent arene–fluoroarene intermolecular interactions in the design of liquid crystals lies in their ability to strongly promote self-assembly, improve the order and stability of the supramolecular mesophases, and enable tuneability of the optical and electronic properties, which can potentially be exploited for advanced applications in display technologies, photonic devices, sensors, and organic electronics. We recently successfully reported the straightforward synthesis of several mesogens containing four lateral aliphatic chains and derived from the classical trip

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7

Aivali, Stefania, Sofia Kakogianni, Charalampos Anastasopoulos, Aikaterini Andreopoulou, and Joannis Kallitsis. "Copolymers and Hybrids Based on Carbazole Derivatives and Their Nanomorphology Investigation." Nanomaterials 9, no. 2 (2019): 133. http://dx.doi.org/10.3390/nano9020133.

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Oligomers of the low-band-gap PCDTBT polymer, based on either 3,6 or 2,7 carbazole units, were modified with vinyl ω-chain end functionalities. The vinyl-functionalized oligomers were used as comonomers in free radical polymerizations with quinoline-based monomers such as 6-vinylphenyl-(2-pyridinyl)-4-phenyl-quinoline (vinyl-QPy), and 6-vinylphenyl-(2-perfluorophenyl)-4-phenyl quinoline (vinyl-5FQ). The co-polymeric materials bearing the vinyl-QPy moiety were developed as potential compatibilizers in polymer electron donor–fullerene acceptor blends for non-covalent interactions with the fuller

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8

Sivý, Július, Dušan Bortňák, Daniel Végh, and Erik Rakovský. "Two novel potent perfluorophenylhydrazone derivatives, 1-((4-bromothiophen-2-yl)methylene)-2-(perfluorophenyl) hydrazine, and 1-((4-bromo-5-methylthiophen-2-yl)methylene)-2-(perfluorophenyl)hydrazine as multi-target compounds to combat Alzheimer disease and their crystal, molecular, and electronic properties." Acta Chimica Slovaca 16, no. 1 (2023): 81–91. http://dx.doi.org/10.2478/acs-2023-0008.

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Abstract Two potent novel perfluorophenylhydrazone derivatives are presented as multi-target compounds to combat Alzheimer disease C11H4BrF5N2S, 1-((4-bromothiophen-2-yl)methylene)-2-(perfluorophenyl) hydrazine, (I) and C12H6BrF5N2S, 1-((4-bromo-5-methylthiophen-2-yl)methylene)-2-(perfluorophenyl) hydrazine, (II), which can potentially be improved by further design. Their multi-target structures and features have been combined as potential AD therapeutics. Crystals (I), and (II), are molecules with two rings and a hydrazone part as a centre of the molecule. The compounds have been synthesised

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9

Ileri, Merve, Serife O. Hacioglu, Ali Cirpan, and Levent Toppare. "Syntheses and Optical Properties of Perfluorophenyl Containing Benzimidazole Derivatives: The Effect of Donor Units." Journal of Macromolecular Science, Part A 52, no. 7 (2015): 510–16. http://dx.doi.org/10.1080/10601325.2015.1039321.

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10

Khan, Momin, Ghulam Ahad, Abdul Manaf, et al. "Synthesis, in vitro urease inhibitory activity, and molecular docking studies of (perfluorophenyl)hydrazone derivatives." Medicinal Chemistry Research 28, no. 6 (2019): 873–83. http://dx.doi.org/10.1007/s00044-019-02341-5.

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