Abstract
The mixed-ligand complexes of molybdenum(VI) with dithiolphenols (DP) {2,6-dithiol-4-methylphenol (DTMP), 2,6-dithiol-4-ethylphenol (DTEP) and 2,6-dithiol-4-tert-butylphenol (DTBP)} in the presence of hydrophobic amines have been investigated by spectrophotometric method. The condition of complexing and extraction, physical-chemical and analytical characteristics of this complex have been found. As hydrophobic amine 2(N, N-dimethylaminomethyl)-4-methylrphenol (АP1) and 2(N, N-dimethylaminomethyl)-4-xlor-phenol (AP2), 2 (N, N-dimethylamino-methyl)-4-brom-phenol (AP3) were used. It has been found that mixed-ligand complex was formed in weakly acidic medium (pH 4.1 - 5.9). The maximum analytical signal when complexing Mo(V) is observed at 516 - 534 nm. The calculated molar absorption (εmax) belongs to the range (4.16 - 5.35) × 104. The Beer’s law was applicable in the range of 0.3 - 22 μg/ml. The extraction photometric methods of the molybdenum determination were processed. The influence of diverse ions on determination of molybdenum has been studied. The proposed method was applied successfully to determine amount of molybdenum in steel and in soil.
Highlights
The mixed-ligand complexes of molybdenum(VI) with dithiolphenols (DP) {2,6-dithiol-4-methylphenol (DTMP), 2,6-dithiol-4-ethylphenol (DTEP) and 2,6-dithiol-4-tert-butylphenol (DTBP)} in the presence of hydrophobic amines have been investigated by spectrophotometric method
Molybdenum is a part of a number of enzymes that perform important physiological functions, in particular, regulation of uric acid metabolism
We report results from liquid-liquid extraction spectrophotometric experiments on 9 different systems, each of which containing Mo(VI), a dithiolphenol (DP) {2, 6-dithiol-4-methylphenol (DTMP), 2, 6-dithiol-4-ethylphenol (DTEP) and 2, 6-dithiol-4-tert-butyl-phenol (DTBP), and hydrophobic amines (Am)
Summary
Molybdenum promotes (makes more efficient) the work of antioxidants, in-. Molybdenum is a part of a number of enzymes (aldehyde oxidase, sulfite oxidase, xanthine oxidase, etc.) that perform important physiological functions, in particular, regulation of uric acid metabolism. Molybdenoenzymes catalyze the hydroxylation of various substrates. Aldehyde oxidase oxidizes and neutralizes various pyrimidines, purines, pteridins. Xanthine oxidase catalyses the conversion of hypoxanthins to xanthines, and xanthines to uric acid. The sulfite oxidase catalyses the conversion of sulfite to sulfate [1]
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Journal of Materials Science and Chemical Engineering
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
