EDDHA
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EDDHA or ethylenediamine-N, -bis(2-hydroxyphenylacetic acid) is a chelating agent. Like EDTA, it binds metal ions as a hexadentate ligand, using two amines, two phenolate centers, and two carboxylates as the six binding sites. The complexes are typically anionic. The ligand itself is a white, water-soluble powder. Both the free ligand and its tetraanionic chelating agent are abbreviated EDDHA. In contrast to EDDHA, most related aminopolycarboxylic acid chelating agents feature tertiary amines and few have phenolate groups. :[[File:EFOREWdownC2.png|thumb|left|Structure of anion [Mn(EDDHA)] − , which is representative of related C 2 -symmetric complexes.
EDDHA or ethylenediamine-N, -bis(2-hydroxyphenylacetic acid) is a chelating agent. Like EDTA, it binds metal ions as a hexadentate ligand, using two amines, two phenolate centers, and two carboxylates as the six binding sites. The complexes are typically anionic. The ligand itself is a white, water-soluble powder. Both the free ligand and its tetraanionic chelating agent are abbreviated EDDHA. In contrast to EDDHA, most related aminopolycarboxylic acid chelating agents feature tertiary amines and few have phenolate groups. [[File:EFOREWdownC2.png|thumb|left|Structure of anion [Mn(EDDHA)] − , which is representative of related C 2 -symmetric complexes. ]]
Preparation
It is produced by the multicomponent reaction of phenol, glyoxalic acid, and ethylenediamine. In this process, the initial Schiff base condensate alkylates the phenol. Related ligands can be prepared more efficiently using para-cresol.
Uses
It is used to mobilize metal ions analogously to the use of EDTA. EDDHA has been used in phytoextraction of lead from contaminated soils. It degrades with release of salicylic acid.
References
Text derived from https://en.wikipedia.org/w/index.php?oldid=1293502253 under CC BY-SA 4.0; modifications have been made.