Crystal structure, DFT and HF calculations and radical scavenging activities of (E)-4,6-dibromo-3-methoxy-2-[(3-methoxyphenylimino)methyl]phenol.

doi:10.1016/j.saa.2014.01.104

Paper

Crystal structure, DFT and HF calculations and radical scavenging activities of (E)-4,6-dibromo-3-methoxy-2-[(3-methoxyphenylimino)methyl]phenol.

Published May 5, 2014 · C. Alaşalvar, M. S. Soylu, A. Güder

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

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Study Snapshot

(E)-4,6-dibromo-3-methoxy-2-[(3-methoxyphenylimino)methyl]phenol exhibits effective radical scavenging activities compared to standard antioxidants BHA, rutin, and trolox.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Crystal structure, DFT and HF calculations and radical scavenging activities of (E)-4,6-dibromo-3-methoxy-2-[(3-methoxyphenylimino)methyl]phenol.

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References

Citations

Molecular structure determination, spectroscopic, quantum computational studies and molecular docking of 4-(E)-[2-(benzylamino)phenylimino) methyl-2]ethoxy phenol

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Synthesis, In Vitro, and In Silico Analysis of the Antioxidative Activity of Dapsone Imine Derivatives

Dapsone imine derivatives 2, 3, and 4 show good antioxidant properties, while derivatives 4, 9, and 10 show the best reducing capacity activity, making them the best antireductants in our series.

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The novel molecule TTBM, synthesized using thieno[3,2-b]thiophene fragment, shows good agreement between experimental and theoretical results in UV-Vis and FTIR spectra.

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Substituted phenols and anilines show potential antioxidant activity, with their structure-activity relationship (SAR) influenced by energetic and structural properties.

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Copper complexes [CuII(sal-ppzH)Cl2] (1) and [CuII(hyap-ppzH)Cl2] (2) effectively catalyze the oxidation of 3,5-di-tert-butylcatechol and oxidative bromination