Electrochemical Reactions at Sacrificial Electrodes: Electrochemical Synthesis of Aluminium(III) Alkoxides and their Coordination Compounds

Authors

  • Baljit Singh Punjabi University, Patiala-147002, Punjab
  • Kanchan Bala Punjabi University, Patiala-147002, Punjab
  • Kishanpal Singh Punjabi University, Patiala-147002, Punjab
  • Sukhveer Singh Punjabi University, Patiala-147002, Punjab

DOI:

https://doi.org/10.24297/jac.v5i1.938

Keywords:

Electrochemical reactions, Sacrificial Electrode, Aluminium(III) alkoxides.

Abstract

Electrochemical   reactions of methanol, ethanol, propan-l-ol, butan-1-ol, pentan-1-ol, hexan-1-ol, heptan-1-ol, octan-1-ol, nonan-1-ol and decan-1-ol (ROH) at sacrificial aluminium anode and inert platinum cathode in the presence of tetrabutylammonium chloride as a conductive additive and acetonitrile as solvent yield aluminium(III) alkoxides. On refluxing with ligand (L) {where L = 2,2’-bipyridyl and 1,10-phenanthroline} these alkoxides don’t form coordination compounds. However, the coordination compounds have been prepared by electrolyzing the solution of above alcohols in the presence of ligand (L) at aluminium anode. These products have been characterized by microanalysis, physical measurements and IR spectral studies.General formula conform to M(OR)3 and M(OR)3.L.{where M- Aluminium and L- ligand}.All these reactions proceed with high current efficiencies.

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Author Biographies

  • Baljit Singh, Punjabi University, Patiala-147002, Punjab
    Department of Chemistry
  • Kanchan Bala, Punjabi University, Patiala-147002, Punjab
    Department of Chemistry
  • Kishanpal Singh, Punjabi University, Patiala-147002, Punjab
    Department of Chemistry
  • Sukhveer Singh, Punjabi University, Patiala-147002, Punjab
    Department of Chemistry

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Published

2009-04-29

Issue

Section

Articles

How to Cite

Electrochemical Reactions at Sacrificial Electrodes: Electrochemical Synthesis of Aluminium(III) Alkoxides and their Coordination Compounds. (2009). JOURNAL OF ADVANCES IN CHEMISTRY, 5(1), 592-597. https://doi.org/10.24297/jac.v5i1.938

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