4.2 Article

Theoretical studies on aromaticity of selected hydroxypyrones. Part 3#. Chelatoaromaticity phenomenon in metalcomplexes of hydroxypyrones

Journal

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY
Volume 24, Issue 6, Pages 499-506

Publisher

WILEY
DOI: 10.1002/poc.1794

Keywords

aromaticity; chelatocomplexes; density functional theory; hydroxypyrones; metalloaromaticity

Funding

  1. European Community [RII3-CT-2003-506079]
  2. Spanish MEC [CTQ2008-03077/BQU]
  3. Catalan DIUE [2009SGR-637]
  4. MEC for the Ramon y Cajal
  5. DIUE of the Generalitat de Catalunya
  6. Polish Ministry of Science and Higher Education [N N204 544839]

Ask authors/readers for more resources

The aim of this project is to study the aromatic properties of various forms (neutral, cationic, and anionic) of selected hydroxypyrones (pyromeconic acid, maltol, and ethylmaltol) and their metalcomplexes with aluminum, gallium, and indium ions. Aromaticity of hydroxypyrone metalcomplexes is important because it can influence the stability of such complexes, which is crucial for their applications in medicinal and environmental chemistry. Results from ten different indices of aromaticity (HOMA, NICS(0), NICS(1), NICSscan, ASE(iso), PDI, FLU, I-ring, MCI, and KMCI) show that aromaticity in hydroxypyrones decreases in the order cations > neutral molecules > anions. Performed calculations situate the aromaticities of ligands in metalcomplexes close to their respective cations. This means that complexation causes a significant increase of the aromaticity of ligands, which stabilizes formed chelatocomplexes. On the other hand, we clearly show that rings that are involved in binding metal ions are not aromatic. Copyright (C) 2010 John Wiley & Sons, Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available