Difference between revisions of "Chelation"

Latest revision as of 19:14, 21 September 2010

Chelation (pronounced /kiːˈleɪʃən/) is the formation or presence of two or more separate bindings between a polydentate (multiple bonded) ligand and a single central atom.^[1] Usually these ligands are organic compounds, and are called chelants, chelators, chelating agents, or sequestering agents.

The ligand forms a chelate complex with the substrate. Chelate complexes are contrasted with coordination complexes with monodentate ligands, which form only one bond with the central atom.

Chelants, according to ASTM-A-380, are "chemicals that form soluble, complex molecules with certain metal ions, inactivating the ions so that they cannot normally react with other elements or ions to produce precipitates or scale."

The word chelation is derived from Greek χηλή, chelè, meaning claw; the ligands lie around the central atom like the claws of a lobster.^[2]

The chelate effect

The chelate effect describes the enhanced affinity of chelating ligands for a metal ion compared to the affinity of a collection of similar nonchelating (monodentate) ligands for the same metal.

Consider the two equilibria, in aqueous solution, between the copper(II) ion, Cu²⁺ and ethylenediamine (en) on the one hand and methylamine, MeNH₂ on the other.

Cu²⁺ + en 15px [Cu(en)]²⁺ (1)

Cu²⁺ + 2 MeNH₂ 15px [Cu(MeNH₂)₂]²⁺ (2)

In (1) the bidentate ligand ethylene diamine forms a chelate complex with the copper ion. Chelation results in the formation of a five–membered ring. In (2) the bidentate ligand is replaced by two monodentate methylamine ligands of approximately the same donor power, meaning that the enthalpy of formation of Cu—N bonds is approximately the same in the two reactions. Under conditions of equal copper concentrations and when the concentration of methylamine is twice the concentration of ethylenediamine, the concentration of the complex (1) will be greater than the concentration of the complex (2). The effect increases with the number of chelate rings so the concentration of the EDTA complex, which has six chelate rings, is much much higher than a corresponding complex with two monodentate nitrogen donor ligands and four monodentate carboxylate ligands. Thus, the phenomenon of the chelate effect is a firmly established empirical fact.

The thermodynamic approach to explaining the chelate effect considers the equilibrium constant for the reaction: the larger the equilibrium constant, the higher the concentration of the complex.

[Cu(en)] =β₁₁[Cu][en]

[Cu(MeNH₂)₂]= β₁₂[Cu][MeNH₂]²

Electrical charges have been omitted for simplicity of notation. The square brackets indicate concentration, and the subscripts to the stability constants, β, indicate the stoichiometry of the complex. When the analytical concentration of methylamine is twice that of ethylenediamine and the concentration of copper is the same in both reactions, the concentration [Cu(en)] is much higher than the concentration [Cu(MeNH₂)₂] because β₁₁ >> β₁₂.

An equilibrium constant, K, is related to the standard Gibbs free energy, ΔG^{File:StrikeO.png} by

ΔG^{File:StrikeO.png} = −RT ln K = ΔH^{File:StrikeO.png} − TΔS^{File:StrikeO.png}

where R is the gas constant and T is the temperature in kelvins. ΔH^{File:StrikeO.png} is the standard enthalpy change of the reaction and ΔS^{File:StrikeO.png} is the standard entropy change. It has already been posited that the enthalpy term should be approximately the same for the two reactions. Therefore the difference between the two stability constants is due to the entropy term. In equation (1) there are two particles on the left and one on the right, whereas in equation (2) there are three particles on the left and one on the right. This means that less entropy of disorder is lost when the chelate complex is formed than when the complex with monodentate ligands is formed. This is one of the factors contributing to the entropy difference. Other factors include solvation changes and ring formation. Some experimental data to illustrate the effect are shown in the following table.^[3]

Equilibrium	log β	ΔGFile:StrikeO.png	ΔHFile:StrikeO.png /kJ mol−1	−TΔSFile:StrikeO.png /kJ mol−1
Cd2+ + 4 MeNH2 15px Cd(MeNH2)42+	6.55	-37.4	-57.3	19.9
Cd2+ + 2 en 15px Cd(en)22+	10.62	-60.67	-56.48	-4.19

These data show that the standard enthalpy changes are indeed approximately equal for the two reactions and that the main reason why the chelate complex is so much more stable is that the standard entropy term is much less unfavourable, indeed, it is favourable in this instance. In general it is difficult to account precisely for thermodynamic values in terms of changes in solution at the molecular level, but it is clear that the chelate effect is predominantly an effect of entropy.

Other explanations, Including that of Schwarzenbach,^[4] are discussed in Greenwood and Earnshaw (loc.cit).

In nature

Virtually all biochemicals exhibit the ability to dissolve certain metal cations. Thus, proteins, polysaccharides, and polynucleic acids are excellent polydentate ligands for many metal ions. In addition to these adventitious chelators, several biomolecules are produced to specifically bind certain metals (see next section). Histidine, malate and phytochelatin are typical chelators used by plants.^[5][6][7]

In biochemistry and microbiology

Virtually all metalloenzymes feature metals that are chelated, usually to peptides or cofactors and prosthetic groups.^[8] Such chelating agents include the porphyrin rings in hemoglobin and chlorophyll. Many microbial species produce water-soluble pigments that serve as chelating agents, termed siderophores. For example, species of Pseudomonas are known to secrete pycocyanin and pyoverdin that bind iron. Enterobactin, produced by E. coli, is the strongest chelating agent known.

In geology

In earth science, chemical weathering is attributed to organic chelating agents, e.g. peptides and sugars, that extract metal ions from minerals and rocks.^[9] Most metal complexes in the environment and in nature are bound in some form of chelate ring, e.g. with a humic acid or a protein. Thus, metal chelates are relevant to the mobilization of metals in the soil, the uptake and the accumulation of metals into plants and micro-organisms. Selective chelation of heavy metals is relevant to bioremediation, e.g. removal of ¹³⁷Cs from radioactive waste.^[10]

Applications

Chelators are used in chemical analysis, as water softeners, and are ingredients in many commercial products such as shampoos and food preservatives. Citric acid is used to soften water in soaps and laundry detergents. A common synthetic chelator is EDTA. Phosphonates are also well known chelating agents. Chelators are used in water treatment programs and specifically in steam engineering, e.g., boiler water treatment system: Chelant Water Treatment system.

Heavy metal detoxification

Chelation therapy is the use of chelating agents to detoxify poisonous metal agents such as mercury, arsenic, and lead by converting them to a chemically inert form that can be excreted without further interaction with the body, and was approved by the U.S. Food and Drug Administration in 1991. In alternative medicine, chelation is used as a treatment for autism, though this practice is controversial due to no scientific plausibility, lack of FDA approval, and its potentially deadly side-effects.^[11]

Though they can be beneficial in cases of heavy metal poisoning, chelating agents can also be dangerous. The U.S. CDC reports that use of disodium EDTA instead of calcium EDTA has resulted in fatalities due to hypocalcemia.^[12]

Other medical applications

Antibiotic drugs of the tetracycline family are chelators of Ca²⁺ and Mg²⁺ ions.

EDTA is also used in root canal treatment as a way to irrigate the canal. EDTA softens the dentin facilitating access to the entire canal length and to remove the smear layer formed during instrumentation.

Chelate complexes of gadolinium are often used as contrast agents in MRI scans.

Chemical applications

Homogeneous catalysts are often chelated complexes. A typical example is the ruthenium(II) chloride chelated with BINAP (a bidentate phosphine) used in e.g. Noyori asymmetric hydrogenation and asymmetric isomerization. The latter has the practical use of manufacture of synthetic (–)-menthol.

Products such as Evapo-Rust are chelating agents sold for the removal of rust from iron and steel.

References

ca:Quelat cs:Chelatace da:Chelat de:Chelatligand et:Kelaatumine es:Agente quelante fa:کیلات fr:Chélation ko:킬레이트 io:Kel-ionuro it:Chelazione he:קלאציה lt:Chelatas nl:Chelatie ja:キレート pl:Chelat pt:Quelato ru:Хелаты fi:Kelaatio uk:Хелати

1. ↑ IUPAC definition of chelation.
2. ↑ The term chelate was first applied in 1920 by Sir Gilbert T. Morgan and H. D. K. Drew, who stated: "The adjective chelate, derived from the great claw or chele (Greek) of the lobster or other crustaceans, is suggested for the caliperlike groups which function as two associating units and fasten to the central atom so as to produce heterocyclic rings."
   Morgan, Gilbert T.; Drew, Harry D. K. (1920). "CLXII.—Researches on residual affinity and co-ordination. Part II. Acetylacetones of selenium and tellurium". J. Chem. Soc., Trans. 117: 1456. doi:10.1039/CT9201701456. CS1 maint: Multiple names: authors list (link) (nonfree access)
3. ↑ Greenwood, Norman N.; Earnshaw, A. (1997), Chemistry of the Elements (2nd ed.), Oxford: Butterworth-Heinemann, ISBN 0080379419 CS1 maint: Multiple names: authors list (link) p 910
4. ↑ Schwarzenbach, G (1952). "Der Chelateffekt". Helv. Chim. Acta. 35: 2344–2359. doi:10.1002/hlca.19520350721. 
5. ↑ U Krämer, J D Cotter-Howells, J M Charnock, A H J M Baker, J A C Smith (1996). "Free histidine as a metal chelator in plants that accumulate nickel". Nature. 379: 635–638. doi:10.1038/379635a0. CS1 maint: Multiple names: authors list (link)
6. ↑ Jurandir Vieira Magalhaes (2006). "Aluminum tolerance genes are conserved between monocots and dicots". Proc Natl Acad Sci USA. 103 (26): 9749–9750. doi:10.1073/pnas.0603957103. PMC 1502523 Freely accessible. PMID 16785425.  More than one of |pages= and |page= specified (help)
7. ↑ Suk-Bong Ha, Aaron P. Smith, Ross Howden, Wendy M. Dietrich, Sarah Bugg, Matthew J. O'Connell, Peter B. Goldsbrough, and Christopher S. Cobbett (1999). "Phytochelatin synthase genes from arabidopsis and the yeast Schizosaccharomyces pombe". Plant Cell. 11 (6): 1153–1164. doi:10.1105/tpc.11.6.1153. PMC 144235 Freely accessible. PMID 10368185. CS1 maint: Multiple names: authors list (link)
8. ↑ S. J. Lippard, J. M. Berg “Principles of Bioinorganic Chemistry” University Science Books: Mill Valley, CA; 1994. ISBN 0-935702-73-3.
9. ↑ Dr. Michael Pidwirny, University of British Columbia Okanagan, http://www.physicalgeography.net/fundamentals/10r.html
10. ↑ Prasad (ed). Metals in the Environment. University of Hyderabad. Dekker, New York, 2001
11. ↑ Doja A, Roberts W (2006). "Immunizations and autism: a review of the literature". Can J Neurol Sci. 33 (4): 341–46. PMID 17168158. 
12. ↑ U.S. Centers for Disease Control, "Deaths Associated with Hypocalcemia from Chelation Therapy" (March 3, 2006), http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5508a3.htm