Near neutral pH, the principal complex is [Fe(EDTA)(H2O)]−, although most sources ignore the aquo ligand. The [Fe(EDTA)(H2O)]− anion has been crystallized with many cations, e.g., the trihydrate Na[Fe(EDTA)(H2O)].2H2O.[3] The salts as well as the solutions are yellow-brown. Provided the nutrient solution in which the [Fe(EDTA)(H2O)]− complex will be used has a pH of at least 5.5, all the uncomplexed iron, as a result of incomplete synthesis reaction, will still change into the chelated ferric form.[4]
Uses
EDTA is used to solubilize iron(III) in water. In the absence of EDTA or similar chelating agents, ferric ions form insoluble solids and are thus not bioavailable.[1]
Together with pentetic acid (DTPA), EDTA is widely used for sequestering metal ions. Otherwise these metal ions catalyze the decomposition of hydrogen peroxide, which is used to bleach pulp in papermaking. Several million kilograms EDTA are produced for this purpose annually.[5]
Iron chelate is commonly used for agricultural purposes to treat chlorosis, a condition in which leaves produce insufficient chlorophyll. Iron and ligand are absorbed separately by the plantroots whereby the highly stable ferric chelate is first reduced to the less stable ferrous chelate.[6] In horticulture, iron chelate is often referred to as 'sequestered iron' and is used as a plant tonic, often mixed with other nutrients and plant foods (e.g. seaweed). It is recommended in ornamental horticulture for feeding ericaceous plants like Rhododendrons if they are growing in calcareoussoils. The sequestered iron is available to the ericaceous plants, without adjusting the soil's pH, and thus, lime-induced chlorosis is prevented.
Ferric EDTA can be used as a component for the Hoagland solution or the Long Ashton Nutrient Solution.[7] According to Jacobson (1951),[2] the stability of ferric EDTA was tested by adding 5 ppm iron, as the complex, to Hoagland's solution at various pH values. No loss of iron occurred below pH 6. In addition to Jacobson's original recipe and a modified protocol by Steiner and van Winden (1970),[4] an updated version for producing the ferric EDTA complex by Nagel et al. (2020)[8] is presented in Table (1).
Aside from EDTA, the chelating agent EDDHA is used to solubilize iron in water. It also can be used for the purposes of agriculture, accessible to plants.[10]
^ abXue, Hanbin; Sigg, Laura; Kari, Franz Guenter (1995). "Speciation of EDTA in Natural Waters: Exchange Kinetics of Fe-EDTA in River Water". Environmental Science and Technology. 29 (1): 59–68. doi:10.1021/es00001a007. PMID22200201.
^Solans, X.; Font Altaba, M.; Garcia-Oricain, J. (1984). "Crystal Structures of Ethylenediaminetetraacetato Metal Complexes. V. Structures Containing the [Fe(C10H12N2O8)(H2O)]− Anion". Acta Crystallographica Section C. 40 (4): 635–638. doi:10.1107/S0108270184005151.
^J. Roger Hart "Ethylenediaminetetraacetic Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.doi:10.1002/14356007.a10_095
^Van Driel, W. (1964). "The effect of iron ethylenediaminetetraacetic acid on the growth and metabolism of tomato plants in water culture". Plant and Soil. 20: 85–104. doi:10.1007/BF01378101. S2CID28252630.
^Hewitt E. J. (1966). Sand and Water Culture Methods Used in the Study of Plant Nutrition. Farnham Royal, England: Commonwealth Agricultural Bureaux, pp. 547. Technical Communication No. 22 (Revised 2nd Edition) of the Commonwealth Bureau of Horticulture and Plantation Crops.
^Batra, P.P.; Maier, R.H. (1964). "Isolation and determination of the ferric iron chelate of ethylenediamine di(o-hydroxyphenylacetic acid) in plant tissues". Plant and Soil. 20: 105–115. doi:10.1007/BF01378102. S2CID9873911.