We have described a new route for the preparation of partially methylated polygalacturonic acid containing hydrolyzed (acidic) and unhydrolyzed (methyl esterified) carboxylate groups in a ratio of 1:1 (PGA, compound ), and one of its basic Fe-salts (compound ) with a ~1:2 Fe:GA stoichiometry (GA means galacturonic acid and methylated galacturonic acid units). The partially hydrolyzed pectin was transformed into compound with the use of double ion exchange with a strongly acidic macroreticular sulfonated styrene-divinylbenzene copolymer as a hydrogen ion source. The reaction of compound with FeCl resulted in compound . Compound has a polymeric nature and contains binuclear Fe(µ-O)(µ-OH)Fe core units with two kinds of distorted octahedral iron geometries. The salt-forming acidic and methylated GA units of compound are coordinated to Fe centers in asymmetric bidentate-chelating and -bridging (via C=O group and glycosidic oxygen) modes, respectively. Two kinds of outer-sphere chloride anions were also detected by XPS in various chemical environments fixed by different sets of hydrogen bonds. We also observed a partial reduction of Fe into Fe due to the ring-opening of the chain-end GA units of compound . This reaction provides a new route to determine the number of chain-ends in compound , and with the use of the number of GA units calculated from charge neutrality, the average length of these chains and the average molecular weight were also determined. The average molecular weight of the partially methylated polygalacturonic acid used in the industrial-scale production of commercial anti-anemic iron-polygalacturonate agents was ~50,000 g/mol. Compound was also characterized by IR, Mössbauer, and X-ray photoelectron spectroscopy, and magnetic susceptibility measurements. These results on the structure and average molecular weight of basic iron(III) polygalacturonate provide a tool to design Fe-PGA complexes with tuned iron-releasing properties.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10893460PMC
http://dx.doi.org/10.3390/molecules29040890DOI Listing

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