Wikipedia

Chelation

(Redirected from Chelator)
This article is about sequestering agents in general. For chemicals used in food processing, see sequestrant. For the isopod genus, see Chelator (crustacean).

Chelation is a type of bonding of ions and their molecules to metal ions. It involves the formation or presence of two or more separate coordinate bonds between a polydentate (multiple bonded) ligand and a single central metal atom.[1][2] These ligands are called chelants, chelators, chelating agents, or sequestering agents. They are usually organic compounds, but this is not a necessity.

The word chelation is derived from Greek χηλή, chēlē, meaning "claw"; the ligands lie around the central atom like the claws of a crab. 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 crab 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."[3]

Chelation is useful in applications such as providing nutritional supplements, in chelation therapy to remove toxic metals from the body, as contrast agents in MRI scanning, in manufacturing using homogeneous catalysts, in chemical water treatment to assist in the removal of metals, and in fertilizers.

Chelate effect

edit
 
Ethylenediamine ligand chelating to a metal with two bonds
 
Cu2+ complexes with nonchelating methylamine (left) and chelating ethylenediamine (right) ligands

The chelate effect is the greater affinity of chelating ligands for a metal ion than that of similar nonchelating (monodentate) ligands for the same metal.

The thermodynamic principles underpinning the chelate effect are illustrated by the contrasting affinities of copper(II) for ethylenediamine (en) vs. methylamine.

Cu2+ + en ⇌ [Cu(en)]2+ (1)
Cu2+ + 2 MeNH2 ⇌ [Cu(MeNH2)2]2+ (2)

In (1) the ethylenediamine forms a chelate complex with the copper ion. Chelation results in the formation of a five-membered CuC2N2 ring. In (2) the bidentate ligand is replaced by two monodentate methylamine ligands of approximately the same donor power, indicating that the Cu–N bonds are approximately the same in the two reactions.

The thermodynamic approach to describing 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] (3)
[Cu(MeNH2)2] = β12[Cu][MeNH2]2 (4)

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, ⁠ ⁠ by

 

where R is the gas constant and T is the temperature in kelvins. ⁠ ⁠ is the standard enthalpy change of the reaction and ⁠ ⁠ is the standard entropy change.

Since the enthalpy should be approximately the same for the two reactions, the difference between the two stability constants is due to the effects of entropy. 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 difference means that less entropy of disorder is lost when the chelate complex is formed with bidentate ligand 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.[4]

Equilibrium log β ⁠ ⁠    
Cu2+ + 2 MeNH2 ⇌ Cu(MeNH2)22+ 6.55 −37.4 −57.3 19.9
Cu2+ + en ⇌ Cu(en)2+ 10.62 −60.67 −56.48 −4.19

These data confirm that the enthalpy changes are approximately equal for the two reactions and that the main reason for the greater stability of the chelate complex is the entropy term, which is much less unfavorable. 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,[5] are discussed in Greenwood and Earnshaw (loc.cit).

In nature

edit

Numerous biomolecules exhibit the ability to dissolve certain metal cations. Thus, proteins, polysaccharides, and polynucleic acids are excellent polydentate ligands for many metal ions. Organic compounds such as the amino acids glutamic acid and histidine, organic diacids such as malate, and polypeptides such as phytochelatin are also typical chelators. In addition to these adventitious chelators, several biomolecules are specifically produced to bind certain metals (see next section).[6][7][8][9]

Virtually all metalloenzymes feature metals that are chelated, usually to peptides or cofactors and prosthetic groups.[9] 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 pyochelin and pyoverdine that bind iron. Enterobactin, produced by E. coli, is the strongest chelating agent known. The marine mussels use metal chelation, especially Fe3+ chelation with the Dopa residues in mussel foot protein-1 to improve the strength of the threads that they use to secure themselves to surfaces.[10][11][12]

In earth science, chemical weathering is attributed to organic chelating agents (e.g., peptides and sugars) that extract metal ions from minerals and rocks.[13] 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 microorganisms. Selective chelation of heavy metals is relevant to bioremediation (e.g., removal of 137Cs from radioactive waste).[14]

Applications

edit

Animal feed additives

edit

Synthetic chelates such as ethylenediaminetetraacetic acid (EDTA) proved too stable and not nutritionally viable. If the mineral was taken from the EDTA ligand, the ligand could not be used by the body and would be expelled. During the expulsion process, the EDTA ligand randomly chelated and stripped other minerals from the body.[15] According to the Association of American Feed Control Officials (AAFCO), a metal–amino acid chelate is defined as the product resulting from the reaction of metal ions from a soluble metal salt with amino acids, with a mole ratio in the range of 1–3 (preferably 2) moles of amino acids for one mole of metal.[citation needed] The average weight of the hydrolyzed amino acids must be approximately 150 and the resulting molecular weight of the chelate must not exceed 800 Da.[citation needed] Since the early development of these compounds, much more research has been conducted, and has been applied to human nutrition products in a similar manner to the animal nutrition experiments that pioneered the technology. Ferrous bis-glycinate is an example of one of these compounds that has been developed for human nutrition.[16]

Dental use

edit

Dentin adhesives were first designed and produced in the 1950s based on a co-monomer chelate with calcium on the surface of the tooth and generated very weak water-resistant chemical bonding (2–3 MPa).[17]

Chelation therapy

edit

Chelation therapy is an antidote for poisoning by mercury, arsenic, and lead. Chelating agents convert these metal ions into a chemically and biochemically inert form that can be excreted. Chelation using calcium disodium EDTA has been approved by the U.S. Food and Drug Administration (FDA) for serious cases of lead poisoning. It is not approved for treating "heavy metal toxicity".[18] Although beneficial in cases of serious lead poisoning, use of disodium EDTA (edetate disodium) instead of calcium disodium EDTA has resulted in fatalities due to hypocalcemia.[19] Disodium EDTA is not approved by the FDA for any use,[18] and all FDA-approved chelation therapy products require a prescription.[20]

Contrast agents

edit

Chelate complexes of gadolinium are often used as contrast agents in MRI scans, although iron particle and manganese chelate complexes have also been explored.[21][22] Bifunctional chelate complexes of zirconium, gallium, fluorine, copper, yttrium, bromine, or iodine are often used for conjugation to monoclonal antibodies for use in antibody-based PET imaging.[23] These chelate complexes often employ the usage of hexadentate ligands such as desferrioxamine B (DFO), according to Meijs et al.,[24] and the gadolinium complexes often employ the usage of octadentate ligands such as DTPA, according to Desreux et al.[25] Auranofin, a chelate complex of gold, is used in the treatment of rheumatoid arthritis, and penicillamine, which forms chelate complexes of copper, is used in the treatment of Wilson's disease and cystinuria, as well as refractory rheumatoid arthritis.[26][27]

Nutritional advantages and issues

edit

Chelation in the intestinal tract is a cause of numerous interactions between drugs and metal ions (also known as "minerals" in nutrition). As examples, antibiotic drugs of the tetracycline and quinolone families are chelators of Fe2+, Ca2+, and Mg2+ ions.[28][29]

EDTA, which binds to calcium, is used to alleviate the hypercalcemia that often results from band keratopathy. The calcium may then be removed from the cornea, allowing for some increase in clarity of vision for the patient.[citation needed]

Homogeneous catalysts are often chelated complexes. A representative example is the use of BINAP (a bidentate phosphine) in Noyori asymmetric hydrogenation and asymmetric isomerization. The latter has the practical use of manufacture of synthetic (–)-menthol.

Cleaning and water softening

edit

A chelating agent is the main component of some rust removal formulations. 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.[citation needed] Although the treatment is often referred to as "softening", chelation has little effect on the water's mineral content, other than to make it soluble and lower the water's pH level.

Fertilizers

edit

Metal chelate compounds are common components of fertilizers to provide micronutrients. These micronutrients (manganese, iron, zinc, copper) are required for the health of the plants. Most fertilizers contain phosphate salts that, in the absence of chelating agents, typically convert these metal ions into insoluble solids that are of no nutritional value to the plants. EDTA is the typical chelating agent that keeps these metal ions in a soluble form.[30]

Economic situation

edit

Because of their wide needs, the overall chelating agents growth was 4% annually during 2009–2014[31] and the trend is likely to increase. Aminopolycarboxylic acids chelators are the most widely consumed chelating agents; however, the percentage of the greener alternative chelators in this category continues to grow.[32] The consumption of traditional aminopolycarboxylates chelators, in particular the EDTA (ethylenediaminetetraacetic acid) and NTA (nitrilotriacetic acid), is declining (−6% annually), because of the persisting concerns over their toxicity and negative environmental impact.[31] In 2013, these greener alternative chelants represented approximately 15% of the total aminopolycarboxylic acids demand. This is expected to rise to around 21% by 2018, replacing and aminophosphonic acids used in cleaning applications.[33][32][31] Examples of some Greener alternative chelating agents include ethylenediamine disuccinic acid (EDDS), polyaspartic acid (PASA), methylglycinediacetic acid (MGDA), glutamic diacetic acid (L-GLDA), citrate, gluconic acid, amino acids, plant extracts etc.[32][34]

Reversal

edit
See also: Transmetalation

Dechelation (or de-chelation) is a reverse process of the chelation in which the chelating agent is recovered by acidifying solution with a mineral acid to form a precipitate.[35]: 7 

See also

edit
  • EDDS – chemical compound

References

edit

  This article incorporates text by Kaana Asemave available under the CC BY 4.0 license.

  1. ^ IUPAC definition of chelation.
  2. ^ Latin chela, from Greek, denotes a claw.
  3. ^ Morgan GT, Drew HD (1920). "CLXII.—Researches on residual affinity and co-ordination. Part II. Acetylacetones of selenium and tellurium". Journal of the Chemical Society, Transactions. 117: 1456–65. doi:10.1039/ct9201701456.
  4. ^ Greenwood NN, Earnshaw A (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 910. ISBN 978-0-08-037941-8.
  5. ^ Schwarzenbach G (1952). "Der Chelateffekt" [The Chelation Effect]. Helvetica Chimica Acta (in German). 35 (7): 2344–59. doi:10.1002/hlca.19520350721.
  6. ^ Krämer U, Cotter-Howells JD, Charnock JM, Baker AJ, Smith JA (1996). "Free histidine as a metal chelator in plants that accumulate nickel". Nature. 379 (6566): 635–8. Bibcode:1996Natur.379..635K. doi:10.1038/379635a0. S2CID 4318712.
  7. ^ Magalhaes JV (June 2006). "Aluminum tolerance genes are conserved between monocots and dicots". Proceedings of the National Academy of Sciences of the United States of America. 103 (26): 9749–50. Bibcode:2006PNAS..103.9749M. doi:10.1073/pnas.0603957103. PMC 1502523. PMID 16785425.
  8. ^ Ha SB, Smith AP, Howden R, Dietrich WM, Bugg S, O'Connell MJ, Goldsbrough PB, Cobbett CS (June 1999). "Phytochelatin synthase genes from Arabidopsis and the yeast Schizosaccharomyces pombe". The Plant Cell. 11 (6): 1153–64. doi:10.1105/tpc.11.6.1153. PMC 144235. PMID 10368185.
  9. ^ a b Lippard SJ, Berg JM (1994). Principles of Bioinorganic Chemistry. Mill Valley, CA: University Science Books. ISBN 978-0-935702-73-6..[page needed]
  10. ^ Das S, Miller DR, Kaufman Y, Martinez Rodriguez NR, Pallaoro A, Harrington MJ, Gylys M, Israelachvili JN, Waite JH (March 2015). "Tough coating proteins: subtle sequence variation modulates cohesion". Biomacromolecules. 16 (3): 1002–8. doi:10.1021/bm501893y. PMC 4514026. PMID 25692318.
  11. ^ Harrington MJ, Masic A, Holten-Andersen N, Waite JH, Fratzl P (April 2010). "Iron-clad fibers: a metal-based biological strategy for hard flexible coatings". Science. 328 (5975): 216–20. Bibcode:2010Sci...328..216H. doi:10.1126/science.1181044. PMC 3087814. PMID 20203014.
  12. ^ Das S, Martinez Rodriguez NR, Wei W, Waite JH, Israelachvili JN (September 2015). "Peptide Length and Dopa Determine Iron-Mediated Cohesion of Mussel Foot Proteins". Advanced Functional Materials. 25 (36): 5840–5847. doi:10.1002/adfm.201502256. PMC 5488267. PMID 28670243.
  13. ^ Pidwirny M. "Introduction to the Lithosphere: Weathering". University of British Columbia Okanagan.
  14. ^ Prasad M (2001). Metals in the Environment: Analysis by Biodiversity. New York, NY: Marcel Dekker. ISBN 978-0-8247-0523-7.[page needed]
  15. ^ Ashmead HD (1993). The Roles of Amino Acid Chelates in Animal Nutrition. Westwood: Noyes Publications. ISBN 0815513127.[page needed]
  16. ^ "Albion Ferrochel Website". Albion Laboratories, Inc. Archived from the original on September 3, 2011. Retrieved July 12, 2011.
  17. ^ Anusavice KJ (2012-09-27). "Chapter 12: Bonding and Bonding Agents". Phillips' Science of Dental Materials (12th ed.). Elsevier Health. pp. 257–268. ISBN 978-1-4377-2418-9. OCLC 785080357.
  18. ^ a b "FDA Issues Chelation Therapy Warning". September 26, 2008. Retrieved May 14, 2016.
  19. ^ Centers for Disease Control Prevention (CDC) (March 2006). "Deaths associated with hypocalcemia from chelation therapy--Texas, Pennsylvania, and Oregon, 2003–2005". MMWR. Morbidity and Mortality Weekly Report. 55 (8): 204–7. PMID 16511441.
  20. ^ "Questions and Answers on Unapproved Chelation Products". FDA. February 2, 2016. Retrieved May 14, 2016.
  21. ^ Caravan P, Ellison JJ, McMurry TJ, Lauffer RB (September 1999). "Gadolinium(III) Chelates as MRI Contrast Agents: Structure, Dynamics, and Applications". Chemical Reviews. 99 (9): 2293–352. doi:10.1021/cr980440x. PMID 11749483.
  22. ^ Pan D, Schmieder AH, Wickline SA, Lanza GM (November 2011). "Manganese-based MRI contrast agents: past, present and future". Tetrahedron. 67 (44): 8431–8444. doi:10.1016/j.tet.2011.07.076. PMC 3203535. PMID 22043109.
  23. ^ Vosjan MJ, Perk LR, Visser GW, Budde M, Jurek P, Kiefer GE, van Dongen GA (April 2010). "Conjugation and radiolabeling of monoclonal antibodies with zirconium-89 for PET imaging using the bifunctional chelate p-isothiocyanatobenzyl-desferrioxamine". Nature Protocols. 5 (4): 739–43. doi:10.1038/nprot.2010.13. PMID 20360768. S2CID 5087493.
  24. ^ Price, Eric W.; Orvig, Chris (2014-01-07). "Matching chelators to radiometals for radiopharmaceuticals". Chemical Society Reviews. 43 (1): 260–290. doi:10.1039/c3cs60304k. ISSN 1460-4744. PMID 24173525.
  25. ^ Parac-Vogt, Tatjana N.; Kimpe, Kristof; Laurent, Sophie; Vander Elst, Luce; Burtea, Carmen; Chen, Feng; Muller, Robert N.; Ni, Yicheng; Verbruggen, Alfons (2005-05-06). "Synthesis, characterization, and pharmacokinetic evaluation of a potential MRI contrast agent containing two paramagnetic centers with albumin binding affinity". Chemistry: A European Journal. 11 (10): 3077–3086. doi:10.1002/chem.200401207. ISSN 0947-6539. PMID 15776492.
  26. ^ Kean WF, Hart L, Buchanan WW (May 1997). "Auranofin". British Journal of Rheumatology. 36 (5): 560–72. doi:10.1093/rheumatology/36.5.560. PMID 9189058.
  27. ^ Wax PM (December 2013). "Current use of chelation in American health care". Journal of Medical Toxicology. 9 (4): 303–307. doi:10.1007/s13181-013-0347-2. PMC 3846961. PMID 24113860.
  28. ^ Campbell NR, Hasinoff BB (March 1991). "Iron supplements: a common cause of drug interactions". British Journal of Clinical Pharmacology. 31 (3): 251–5. doi:10.1111/j.1365-2125.1991.tb05525.x. PMC 1368348. PMID 2054263.
  29. ^ Lomaestro BM, Bailie GR (May 1995). "Absorption interactions with fluoroquinolones. 1995 update". Drug Safety. 12 (5): 314–33. doi:10.2165/00002018-199512050-00004. PMID 7669261. S2CID 2006138.
  30. ^ Hart JR (2011). "Ethylenediaminetetraacetic Acid and Related Chelating Agents". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a10_095.pub2. ISBN 978-3527306732.
  31. ^ a b c (2013) IHS Chemical, Chemical Insight and Forecasting: Chelating Agents.
  32. ^ a b c Dixon NJ (2012) Greener chelating agents, In Handbook of green chemistry: Designing safer chemicals. Wiley 9: 281-307.
  33. ^ Kołodyńska D (2011) Chelating agents of a new generation as an alternative to conventional chelators for heavy metal ions removal from different waste waters. In Expanding Issues in Desalination pp. 339-370.
  34. ^ Kolodynska D (2013) Application of a new generation of complexing agents inremoval of heavy metal ions from different wastes. Env Sci Pollut Res 20: 5939-5949.
  35. ^ Ryczkowski, Janusz (2019). "EDTA – synthesis and selected applications". Annales Universitatis Mariae Curie-Sklodowska. 74. ISSN 2083-358X.
edit
  •   The dictionary definition of chelate at Wiktionary
Retrieved from "https://en.wikipedia.org/w/index.php?title=Chelation&oldid=1258430542"