<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(17)</volume><submitter>Rosetto G</submitter><pubmed_abstract>Lignin-derived aromatic carboxylic acids can be produced from oxidative catalytic processes and are promising building blocks for performance-advantaged bioproducts that leverage their inherent heteroatom functionalities. Here, we synthesize 2-methoxyterephthalate and 2,6-dimethoxyterephthalate derivatives by electrochemical carboxylation of guaiacyl- and syringyl-derived lignin monomers obtained from the oxidative deconstruction of lignin. These methoxylated terephthalates are evaluated as co-monomers in poly(ethylene terephthalate) (PET) and as plasticizers that could replace petrochemically-derived isophthalate and phthalate, respectively. Specifically, we co-polymerize 2-methoxy- and 2,6-dimethoxyterephthalate with dimethyl terephthalate to form several PET co-polymers, both of which e</pubmed_abstract><journal>ACS sustainable chemistry &amp; engineering</journal><pagination>6342-6354</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12376922</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lignin-Derived Methoxyterephthalates for Performance-Advantaged Polymers and Plasticizers.</pubmed_title><pmcid>PMC12376922</pmcid><pubmed_authors>Konev MO</pubmed_authors><pubmed_authors>Rorrer NA</pubmed_authors><pubmed_authors>Rosetto G</pubmed_authors><pubmed_authors>Haugen SJ</pubmed_authors><pubmed_authors>Lazarenko D</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Ramirez KJ</pubmed_authors><pubmed_authors>Chism KA</pubmed_authors><pubmed_authors>Knott BC</pubmed_authors><pubmed_authors>Curley JB</pubmed_authors><pubmed_authors>Wernke KM</pubmed_authors><pubmed_authors>Stahl SS</pubmed_authors><pubmed_authors>Lincoln C</pubmed_authors><pubmed_authors>Cardinale L</pubmed_authors><pubmed_authors>Hamernik LJ</pubmed_authors><pubmed_authors>Beckham GT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lignin-Derived Methoxyterephthalates for Performance-Advantaged Polymers and Plasticizers.</name><description>Lignin-derived aromatic carboxylic acids can be produced from oxidative catalytic processes and are promising building blocks for performance-advantaged bioproducts that leverage their inherent heteroatom functionalities. Here, we synthesize 2-methoxyterephthalate and 2,6-dimethoxyterephthalate derivatives by electrochemical carboxylation of guaiacyl- and syringyl-derived lignin monomers obtained from the oxidative deconstruction of lignin. These methoxylated terephthalates are evaluated as co-monomers in poly(ethylene terephthalate) (PET) and as plasticizers that could replace petrochemically-derived isophthalate and phthalate, respectively. Specifically, we co-polymerize 2-methoxy- and 2,6-dimethoxyterephthalate with dimethyl terephthalate to form several PET co-polymers, both of which e</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-05-09T19:10:00.028Z</modification><creation>2026-04-08T01:10:36.202Z</creation></dates><accession>S-EPMC12376922</accession><cross_references><pubmed>40855899</pubmed><doi>10.1021/acssuschemeng.5c01330</doi></cross_references></HashMap>