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Relevant bibliographies by topics / Arsonic acid derivatives

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Journal articles

Academic literature on the topic 'Arsonic acid derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Arsonic acid derivatives"

1

Dou, Mingyu, Wenli Zhao, Jie Lin, Xianqiang Huang, and Dacheng Li. "One Functionalized Polyoxovanadates Hybrid Material Based on Arsonic Acid with Highly Effective Catalytic Property of Sulfides." Science of Advanced Materials 13, no. 4 (2021): 550–55. http://dx.doi.org/10.1166/sam.2021.3871.

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In this work, a novel 4-aminophenylarsonic acid functionalized polyoxovanadates (POVs) hybrid material, namely, (Me2NH2)4 ·[(L)8(H12V16O32)] (H2L = 4-NH2C6H4AsO3H2) POVs 1 was solvothermally synthesized and fully characterized. The results revealed POVs 1 consists of four similar tetranuclear vanadium clusters bridged by eight organic 4-aminophenylarsonic acid ligands. Remarkably, functionalized hybrid POVs 1 was further investigated as a heterogeneous stable catalyst in oxidation of sulfide derivatives, and exhibited high catalytic activities (yields up to 96.7%). Additionally, the functional

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2

Gardolinski, J. E. F. C., G. Lagaly, and M. Czank. "On the destruction of kaolinite and gibbsite by phenylphosphonic, phenylphosphinic and phenylarsonic acids: evidence for the formation of new Al compounds." Clay Minerals 39, no. 4 (2004): 391–404. http://dx.doi.org/10.1180/0009855043940142.

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AbstractKaolinite and synthetic γ-Al(OH)3 (gibbsite or hydrargillite) were reacted with phenylphosphonic, phenylphosphinic and 2-nitrophenol-4-arsonic acids. The products were studied by powder X-ray diffraction, transmission electron microscopy/selected area electron diffraction/ energy dispersive X-ray/Fourier transform infrared and simultaneous thermogravimetric/differential thermal analysis. The acids were not intercalated but, instead, easily destroyed the structure of the minerals. Lamellar Al phenylphosphonate and aluminium phenylphosphinate and phenylarsonate with polymeric linear-chai

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3

Latham, Kay, James E. Downs, Colin J. Rix, and Jonathan M. White. "Interactions of guanidinium with benzene-sulphonic, -phosphonic and -arsonic acids and several of their nitro-derivatives." Journal of Molecular Structure 987, no. 1-3 (2011): 74–85. http://dx.doi.org/10.1016/j.molstruc.2010.11.062.

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4

Mourtas, Spyridon, Konstantina Papadia, Golfo G. Kordopati, Panayiotis V. Ioannou, Sophia G. Antimisiaris, and Gerasimos M. Tsivgoulis. "Synthesis of Novel Arsonolipids and Development of Novel Arsonoliposome Types." Pharmaceutics 14, no. 8 (2022): 1649. http://dx.doi.org/10.3390/pharmaceutics14081649.

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Arsonolipids represent a class of arsenic-containing compounds with interesting biological properties either as monomers or as nanostructure forming components, such as arsonoliposomes that possess selective anticancer activity as proven by in vitro and in vivo studies. In this work, we describe, for the first time, the synthesis of novel arsono-containing lipids where the alkyl groups are connected through stable ether bonds. It is expected that this class of arsonolipids, compared with the corresponding ester linked, will have higher chemical stability. To accomplish this task, a new methodo

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5

Sandhu, G. K., and H. K. Aggarwal. "Diorganotin(IV) Derivatives of Ethyl 3-[(o-Arsono-phenyl)imino]butyrate and N-(1-Methyl-3-oxobutylidene)-o-arsanilic Acid." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 20, no. 7 (1990): 875–86. http://dx.doi.org/10.1080/00945719008048181.

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