2014
DOI: 10.1080/00958972.2014.905686
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Spectroscopy and theoretical studies of natural melanin (eumelanin) and its complexation by iron(III)

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Cited by 9 publications
(3 citation statements)
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“…A basic possible reason for the high radical scavenging and metal chelating efficiency of EAM is the specific polymeric melanic structure in which the phenolic net can act as a one-dimensional semiconductor and electron acceptor [ 88 ]. The movable balance between the catechol, semiquinone, and quinine forms of melanoidin provides high-speed redox processes and a neutralizing effect on the free radicals and reactive oxygen forms [ 90 ]. Although this has not been discussed previously, the surface functional groups of melanoidins could act as metal chelators and electron conductors.…”
Section: Resultsmentioning
confidence: 99%
“…A basic possible reason for the high radical scavenging and metal chelating efficiency of EAM is the specific polymeric melanic structure in which the phenolic net can act as a one-dimensional semiconductor and electron acceptor [ 88 ]. The movable balance between the catechol, semiquinone, and quinine forms of melanoidin provides high-speed redox processes and a neutralizing effect on the free radicals and reactive oxygen forms [ 90 ]. Although this has not been discussed previously, the surface functional groups of melanoidins could act as metal chelators and electron conductors.…”
Section: Resultsmentioning
confidence: 99%
“…Compared with BSM, the partial absorption peak of BM-Fe was weak, indicating that COOH, OH and NH may participate in the chelation of metal ions. 46 After chelation, the absorption at 3365 cm −1 corresponding to N–H and O–H stretching vibration peaks decreased and moved to 3169 cm −1 , which indicated that N–H and O–H are involved in chelation, indicating that the Fe–N bond might replace N-OH. 47 The band corresponding to the carboxyl group (1425 cm −1 ) in BM-Fe has a low intensity compared to that in BSM.…”
Section: Resultsmentioning
confidence: 96%
“…A distinctive feature that distinguishes eumelanin from pheomelanin is the absence of a sulfur group. 82 Pheomelanin or dopamine melanin chemically modified by amino acids ( e.g. cys-DOPA melanin) is known to have a sulfur content of about 6–16%.…”
Section: Structure Analysis and Physicochemical Properties Of Melaninmentioning
confidence: 99%