Academic literature on the topic 'Diphenylamine derivatives'

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Journal articles on the topic "Diphenylamine derivatives"

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Ito, Akihiro, Ken-ichi Ota, Kazunari Yoshizawa, Kazuyoshi Tanaka, and Tokio Yamabe. "Ab initio MO study of diphenylamine derivatives: diphenylamine, diphenylaminium, diphenylaminyl and diphenylnitroxide." Chemical Physics Letters 223, no. 1-2 (1994): 27–34. http://dx.doi.org/10.1016/0009-2614(94)00416-1.

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Begunov, Roman S., and Alexander I. Khlopotinin. "BENZOTRIAZOLE DERIVATIVES OF DIPHENYLAMINE ARE NEW UV RADIATION ABSORBERS." ChemChemTech 68, no. 5 (2025): 112–20. https://doi.org/10.6060/ivkkt.20256805.7200.

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In order to develop UV absorbers with improved extinction coefficients, previously obtained UV absorbers 1-(2-aminophenyl)-1H- and 2-(2-aminophenyl)-2H-benzotriazoles functionalization was carried out through aromatic nucleophilic substitution reaction with nitrohalogenarenes and followed reduction of the obtained nitrodiphenylamines. The conditions for these reactions were selected to synthesize target products with high yield. As a result, 10 new diphenylamine derivatives containing 1H- or 2H-benzotriazole cycles were synthesized. The structures of the obtained multifunctional compounds were
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Rudell, David, James Mattheis, and John Fellman. "Diphenylamine and Diphenylamine Derivative Content of `Granny Smith' Peel: Influence of Ethylene Action and Regular or Controlled Atmosphere Storage Duration." HortScience 40, no. 4 (2005): 1144B—1144. http://dx.doi.org/10.21273/hortsci.40.4.1144b.

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Diphenylamine (DPA) is used for superficial scald control in apple fruit. A number of DPA derivatives resulting from C-nitration, C-hydroxylation, O-methylation, and N-nitrosation can be present in DPA-treated apple fruit after storage. The presence of the compounds may be indicative of metabolic processes that lead to scald development. Therefore, apple peel DPA and DPA derivative content in fruit treated at harvest with DPA or DPA plus 1-methylcyclopropene (1-MCP) was assayed upon removal of fruit from controlled atmosphere (CA) and regular atmosphere (RA) storage and during a 14-d post-stor
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Huang, Tai-Hsiang, and Jiann T. Lin. "Tunable Dipolar Acenaphthopyrazine Derivatives Containing Diphenylamine." Chemistry of Materials 16, no. 25 (2004): 5387–93. http://dx.doi.org/10.1021/cm049069m.

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Janovec, Ladislav, Jana Janočková, Mária Matejová, et al. "Proliferation inhibition of novel diphenylamine derivatives." Bioorganic Chemistry 83 (March 2019): 487–99. http://dx.doi.org/10.1016/j.bioorg.2018.10.063.

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Kumar, Arvind, and Arun K. Mishra. "Synthesis, Toxicity Profile and Pharmacological Evaluation of Some New N,N-Diphenyl Amine Derivatives with Special Reference to Analgesic and Anti-inflammatory Activity." Letters in Organic Chemistry 17, no. 7 (2020): 560–70. http://dx.doi.org/10.2174/1570178617666191220150024.

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The present work was aimed to synthesize eight new diphenylamine derivatives by the reactions of 2-chloro-N-(4-(diphenyl amino) thiazol-2-yl)acetamide with substituted phenols in the chloroform along with anhydrous potassium carbonate and potassium iodide. The structures of newly synthesized compounds were characterized by IR, NMR, Mass and elemental analysis techniques. Toxicity profile (acute and subacute oral toxicity) and biological activity (analgesic and anti-inflammatory activity) of the synthesized derivatives was performed. Findings of the present work suggested that the synthesized c
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Tretiakov, I. V., and J. R. Cable. "Electronic spectroscopy and molecular structure of jet-cooled diphenylamine and diphenylamine derivatives." Journal of Chemical Physics 107, no. 23 (1997): 9715–25. http://dx.doi.org/10.1063/1.475268.

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Julianto, T. S., F. J. Rachmawaty, H. A. Tamhid, and B. S. Putri. "THE POTENTIAL ANTIMALARIAL DRUG OF ARYL AMINO ALCOHOL DERIVATIVES FROM EUGENOL: SYNTHESIS, in-vitro AND in-silico ANALYSIS OF BIOACTIVITY." RASAYAN Journal of Chemistry 16, no. 03 (2023): 1425–34. http://dx.doi.org/10.31788/rjc.2023.1636940.

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Malaria is a significant cause of death in numerous countries, and the discovery of effective drugs is crucial. In this research, a new method was employed to synthesize a derivative of aryl amino alcohol using eugenol. Initially, an epoxide compound called 2-methoxy-4-(oxiran-2-ylmethyl) phenol was synthesized from eugenol by reacting it with peroxyacetic acid in dichloromethane. Subsequently, the epoxide compound was subjected to a reaction with various amine compounds, including aniline, naphthylamine, and diphenylamine for 10 minutes under 100 W microwave conditions, resulting in the produ
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Salahifar, Eslam, and Davood Nematollahi. "Electrochemical generation of a Michael acceptor: a green method for the synthesis of 4-amino-3-(phenylsulfonyl)diphenylamine derivatives." New Journal of Chemistry 39, no. 5 (2015): 3852–58. http://dx.doi.org/10.1039/c5nj00087d.

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Chen, Sin-Yu, Ya-Wen Chiu та Guey-Sheng Liou. "Substituent effects of AIE-active α-cyanostilbene-containing triphenylamine derivatives on electrofluorochromic behavior". Nanoscale 11, № 17 (2019): 8597–603. http://dx.doi.org/10.1039/c9nr02692d.

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Four aggregation-induced emission- and electro-active cyanostilbene-based diphenylamine-containing derivatives were synthesized to investigate the photoluminescence properties, and electrochromic and electrofluorochromic behavior of gel-type devices.
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Dissertations / Theses on the topic "Diphenylamine derivatives"

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Lu, Chang-Chia, and 呂長家. "Study of charge transport properties in fluorene/diphenylamine and [2,2]-paracyclophane derivatives." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/a3sshm.

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碩士<br>國立中山大學<br>光電工程學系研究所<br>107<br>In this thesis, we investigated carrier mobility of HTM4 and HJJ series by time-of-flight method. HTM4 is a fluorene/diphenylamine derivative with non-dispersive and ambipolar carrier transporting capability. Both the hole and electron mobilities are up to the order of 10-4 cm2/V·s for fields from 2.00×105 V/cm to 5.33×105 V/cm. The balancing charge transport makes HTM4 a possible candidate of host materials for organic light-emitting diodes. The HJJ series are [2,2]-paracyclophane derivatives with diphenylamine (HJJ2, HJJ3) or carbazole(HJJ5, HJJ6) as an el
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Chen, Sin-Yu, та 陳欣鈺. "Design and Synthesis of Diphenylamine-Based α-Cyanostilbene Derivatives for Electrofluorochromic Device Application". Thesis, 2018. http://ndltd.ncl.edu.tw/handle/3abbjz.

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碩士<br>國立臺灣大學<br>高分子科學與工程學研究所<br>106<br>This study has been divided into four chapters. Chapter 1 is general introduction of electrochromism, aggregation-induced emission (AIE), and electrofluorochromism (EFC). In chapter 2, four triphenylamine-based cyanostilbene derivatives with different substituents were synthesized successfully for investigating the effects on photoluminescent properties, electrochromic and electrofluorochromic (EFC) behaviors in gel-type electrochromic devices (ECDs). The photoluminescent performance of the resulted materials in the solution, aggregated and solid states,
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Conference papers on the topic "Diphenylamine derivatives"

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Piovesan, Erick, Leonardo De Boni, and Cleber Renato Mendonça. "Nonlinear Optical Properties of Phenyl Diphenylamine Derivatives and Platinum Acetylide Complexes." In Latin America Optics and Photonics Conference. OSA, 2010. http://dx.doi.org/10.1364/laop.2010.we11.

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Bhatt, Akshita B., Thomas D. Wright, Katie Anna, et al. "Abstract 4204: Structure-activity relationship of diphenylamine derivatives to target epithelial to mesenchymal transition in triple negative breast cancer." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-4204.

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