z-logo
Premium
Anodic oxidation of mercury in the presence of monocyclic ligands in propylene carbonate
Author(s) -
Boudon C.,
Gisselbrecht J. P.,
Gross M.,
Hosseini M. W.
Publication year - 1989
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.1140010604
Subject(s) - heteroatom , propylene carbonate , mercury (programming language) , chemistry , carbonate , inorganic chemistry , ligand (biochemistry) , redox , electrochemistry , electrode , organic chemistry , receptor , ring (chemistry) , biochemistry , computer science , programming language
A series of 12 macrocycles containing 4, 6, or 8 N, S, and O heteroatoms (with increasing size from 14 to 24 atoms in the cycle) was studied to ascertain size and heteroatoms effects on the formation and 14 redox characteristics of their mercuric complexes. The concentration dependence of anodic currents at mercury electrodes in solutions of these ligands led to the determination of the formation constants of the complexes generated according to the folling of\documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm Hg} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {\rm Hg}^{{\rm 2 + }} {\rm + 2e}^{\rm - } {\rm,}\,{\rm Hg}^{{\rm 2 + }} {\rm + jL} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {\rm (HgL}_{\rm j} {\rm)}^{{\rm 2 + }} $$\end{document}In propylene carbonate, the resulting mercuric complexes were stable (log K s up to 40) mono‐ and dinuclear species. Their stability depends both on the nature of the heteroatoms and on the size of the macrocycle. For identical ligand sizes, the stability sequence N > S > O was established for mercuric complexes.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here