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Benzoic acid

About: Benzoic acid is a research topic. Over the lifetime, 11832 publications have been published within this topic receiving 167127 citations. The topic is also known as: Retardex & E210.


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Journal ArticleDOI
Jinming Wang1, Ya Zheng1, Tianyou Peng1, Jing Zhang1, Renjie Li1 
TL;DR: An asymmetric zinc porphyrin derivative bearing one benzoic acid and three 3-pyridines as meso-position substituents (zinc-5-(4-carboxyphenyl)-10,15,20-tri(3-pridyl)porphyrin, ZnMT3PyP) was used to sensitize graphitic carbon nitride (g-C3N4) for visible-light-driven photocatalytic H2 production as mentioned in this paper.
Abstract: An asymmetric zinc porphyrin (ZnPy) derivative bearing one benzoic acid and three 3-pyridines as meso-position substituents (zinc-5-(4-carboxyphenyl)-10,15,20-tri(3-pridyl)porphyrin, ZnMT3PyP) was used to sensitize graphitic carbon nitride (g-C3N4) for visible-light-driven photocatalytic H2 production. It was found that ZnMT3PyP exhibits more excellent photosensitization and stability on g-C3N4 than its counterpart bearing one benzoic acid and three phenyls (zinc-5-(4-carboxyphenyl)-10,15,20-triphenylporphrin, ZnMTPP) under visible light (λ > 420 nm) irradiation even though they have very similar physicochemical properties such as optical absorption capacities and energy band structures. Especially, ZnMT3PyP-Pt/g-C3N4 gives an apparent quantum yield (AQY) up to 25.1% at λ = 420 nm light illumination, greater than that (11.6%) of ZnMTPP-Pt/g-C3N4. The differences in photosensitization and stability between ZnMT3PyP and ZnMTPP are mainly due to the substitution of 3-pyridine for the phenyls in ZnMTPP, which...

66 citations

Journal ArticleDOI
TL;DR: In this paper, Dimer structures were found in the crystals of the free acid 1 and the lithium salt 1·Li· 1 2 MeOH by X-ray crystal structure studies.

66 citations

Journal ArticleDOI
Paolo Davini1
01 Feb 1989-Fuel
TL;DR: In this article, an active commercial-grade carbon, washed with boiling 1 M HCl, to eliminate ash from its surface, was thermally treated in the presence of oxygen at temperatures between 400 and 750 °C, to produce carbon samples whose capacity to adsorb SO2 was investigated.

66 citations

Journal ArticleDOI
TL;DR: Estrogenicity assays showed that methyl paraben was more estrogenic than EP; however, parabens are slightly estrogenic compared to 17β-estradiol, and liquid chromatography-time of flight mass spectrometry revealed the formation of methylParaben, 4-hydroxybenzoic acid, benzoic Acid and phenol as primary transformation by-products.

65 citations

Journal ArticleDOI
E. Chin1, John W. Goodby1
TL;DR: In this article, a variety of synthetic pathways were employed in an attempt to increase the overall yield of the final product, and it was found that catalytic agents such as boron trifluoride-etherate (BF3 Et2O), 1,3-dicyclohexyl carbodiimide (DCC), and 4-N, N-di-methylaminopyridine (DMAP) were relatively ineffective in these processes.
Abstract: Common syntheses of phenyl benzoyloxybenzoates generally produce products in low yields. A variety of synthetic pathways were employed in an attempt to increase the overall yield of the final product. It was found that catalytic agents such as boron trifluoride-etherate (BF3 Et2O), 1,3-dicyclohexylcarbodiimide (DCC), and 4-N, N-di-methylaminopyridine (DMAP) were relatively ineffective in these processes. However. protection of the hydroxy moiety of an appropriately substituted benzoic acid with methyl chloroformate, followed by esterification under normal conditions, and deprotection with ammonia in ethanol produces the hydroxy-benzoyloxybenzoate intermediate. This material can be used in further esterifications to produce phenyl benzoyloxybenzoate compounds in good yield. Materials such as the triply reentrant compound 4-n-nonyloxyphenyl 4-nitrobenzoyloxybenzoate (DB9ONO2) can be prepared by this method.

65 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023207
2022519
2021217
2020279
2019315
2018332