1989
DOI: 10.1021/ja00195a029
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Affinities of racemic and meso forms of N,N'-ethylenebis[2-(o-hydroxyphenyl)glycine] for divalent and trivalent metal ions

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Cited by 65 publications
(64 citation statements)
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“…These species present a similar structure to the Fe 3+ species defined for these ligands and described by Yunta et al (2003a,b) with an octahedral coordination around the metals. However, the close values for the Mn stability constants obtained for o,o-EDDHA and o,p-EDDHA supports the fact that the axial donor groups may be only weakly interacting with the metallic ion in agreement with the Bannochie and Martell (1989) data for Zn (Figure 1). Although Mn can present different oxidation numbers due to its variable electronic configuration (4s 2 3d 5 ) (Wallace and Wallace, 1983b,c), probably the most stable ion in the chelates is Mn 2+ , this accords with other reports that have described a stability complex with Mn 3+ and EDTA but with faster kinetics to form the Mn 2+ complex (Klewicki and Morgan, 1998 Mn 2+ = pe − 25.55 ) than those defined for the same cations with similar chelating agents to EDDHA (Bannochie, and Martell, 1989;L'Eplattenier et al, 1966).…”
Section: Theoretical Speciation Of Fe Mn and Zn Chelates In Hydroponsupporting
confidence: 81%
“…These species present a similar structure to the Fe 3+ species defined for these ligands and described by Yunta et al (2003a,b) with an octahedral coordination around the metals. However, the close values for the Mn stability constants obtained for o,o-EDDHA and o,p-EDDHA supports the fact that the axial donor groups may be only weakly interacting with the metallic ion in agreement with the Bannochie and Martell (1989) data for Zn (Figure 1). Although Mn can present different oxidation numbers due to its variable electronic configuration (4s 2 3d 5 ) (Wallace and Wallace, 1983b,c), probably the most stable ion in the chelates is Mn 2+ , this accords with other reports that have described a stability complex with Mn 3+ and EDTA but with faster kinetics to form the Mn 2+ complex (Klewicki and Morgan, 1998 Mn 2+ = pe − 25.55 ) than those defined for the same cations with similar chelating agents to EDDHA (Bannochie, and Martell, 1989;L'Eplattenier et al, 1966).…”
Section: Theoretical Speciation Of Fe Mn and Zn Chelates In Hydroponsupporting
confidence: 81%
“…a Ma and Martell (1993) b Bannochie and Martell (1989) c Smith and Martell (1989) Fig (Fig. 2), is used, Fe precipitation in the growth media or at root surfaces were not expected and the Si effect on internal plant mechanisms could be studied.…”
Section: Iron Deficiencymentioning
confidence: 99%
“…HBED is a relative of EDDHA; both have higher specificity for Fe 3 + than the EDT A family of chelators because HBED and EDDHA contain phenolic ligands. HBED was used in this modelling because of the complexity of chelation by EDDHA; modelling of EDDHA is no longer considered valid since Bannochie and Martell (1989) showed that EDDHA is comprised of several optical isomers with different metal chelate fonnation constants. HBED is simpler, and the fonnation constant database is more complete for HBED than for EDDHA (see Parker et al, 1993).…”
Section: Physiological Aspects Of Zn Phytoxicitymentioning
confidence: 99%