Results 101 to 110 of about 24,479 (307)

Novel aroylated phenylenediamine compounds enhance antimicrobial defense and maintain airway epithelial barrier integrity

open access: yesScientific Reports, 2019
Aroylated phenylenediamines (APDs) are novel inducers of innate immunity enhancing cathelicidin gene expression in human bronchial epithelial cell lines.
Iwona T. Myszor   +6 more
doaj   +1 more source

Primary coloured electrochromism of aromatic diesters and phenylenediamines

open access: yes, 2015
Thirteen aromatic oxygen and thioic S,S'-diesters were synthesized and investigated using electrochemical (cyclic voltammetry and controlled potential electrolysis) and UV-vis spectroscopic techniques over a range of temperatures.
Xu, Xiuhui
core  

Aminophenols and Phenylenediamines as Corrosion Inhibitors for 70/30 Brass in Nitric Acid

open access: yes, 1975
Chemistry Department University School of Sciences, Gujarat University, Ahmedabad-9 Manuscript received 17 July 1974; revised 10 May 1975; accepted 19 May 1975 Aminophenols and phenylenediamines are reported as inhibitors for the corrosion of 70/30 ...
M. N. DESAI, B. C. THAKER, P. M. CHHAYA
core   +1 more source

Tailored for Binding: Alanine‐Modified Poly(1‐Naphthylamine) Targets Serum Albumins

open access: yesPolymer Engineering &Science, EarlyView.
Alanine modified poly(1‐naphthylamine). ABSTRACT This study presents a new approach for modifying the structural and functional properties of poly(1‐naphthylamine) (PNA) by incorporating the amino acid alanine (Ala) in different molar proportions (80/20, 50/50, and 20/80 for PNA/Ala) through an ultrasound‐assisted polymerization process.
Nuzhat Nabi, Ufana Riaz
wiley   +1 more source

Redox Potential Inversion by Ionic Hydrogen Bonding between Phenylenediamines and Pyridines

open access: yes, 2014
In electrochemical oxidations, the second oxidation potential of phenylenediamines (PD) varies because of hydrogen-bonding formation for PD(+center dot) with pyridines.
Chung, Y.C.   +5 more
core   +1 more source

Hypervalent iodine(III)-induced oxidative [4+2] annulation of o-phenylenediamines and electron-deficient alkynes: direct synthesis of quinoxalines from alkyne substrates under metal-free conditions.

open access: yesChemical Communications, 2013
Hypervalent iodine(III)-induced oxidative [4+2] annulation of o-phenylenediamines and electron-deficient alkynes under metal-free conditions has been developed. The reaction allows for direct access to quinoxalines bearing two electron-withdrawing groups
Sota Okumura   +3 more
semanticscholar   +1 more source

Liquid Crystals: Low Melting Nematic 4, 4\u27-Bis-(Alkylbenzal)-2-Chloro-1,4-Phenylenediamines [PDF]

open access: yes, 1973
Several homologues of the 4,4\u27-bis-(alkoxybenzal)-2-chloro-1,4-phenylene series were synthesized and their mesomorphic behavior characterized.
Cole, Herbert S., Jr.
core  

Machine learning‐driven advances in carbon‐based quantum dots: Opportunities accompanied by challenges

open access: yesResponsive Materials, EarlyView.
Machine learning provides a unifying framework to connect structure, fluorescence properties, and applications of carbon‐based quantum dots. This review highlights how data‐driven strategies enable fluorescence regulation, reveal underlying mechanisms, and accelerate the rational design of functional carbon dots.
Liangfeng Chen   +8 more
wiley   +1 more source

P-phenylenediamines and their quinones in estuarine-coastal sediments of Zhejiang Province: Occurrence, prioritization, and risk assessment

open access: yesEmerging Contaminants
As emerging contaminants of concern, p-phenylenediamines (PPDs) and their quinone transformation products (PPD-Qs) serve as critical indicators of pollutant inputs from urban runoff and tire wear to coastal ecosystems.
Zhou Wu   +12 more
doaj   +1 more source

NITROSUBSTITUTED 1,2-PHENYLENEDIAMINES

open access: yesProceedings of The 14th International Electronic Conference on Synthetic Organic Chemistry, 2010
The 1H, 13C and 15N NMR spectra, both in solution and in the solid state, of five 1,2-phenylenediamines have been recorded. Assignment of all the signals has been achieved and chemical shifts and coupling constants determined. When necessary homo- and heteronuclear 2D NMR experiments have been performed.
Concepción López   +5 more
openaire   +1 more source

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