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Oligomerization of 10,16-Dihydroxyhexadecanoic Acid and Methyl 10,16-Dihydroxyhexadecanoate catalyzed by lipases
MAYRA BEATRIZ GOMEZ PATIÑO
JULIA CASSANI HERNANDEZ
María Eugenia Jaramillo Flores
LUIS GERARDO ZEPEDA VALLEJO
Georgina Coral Sandoval Fabián
Manuel Jiménez Estrada
DANIEL ARRIETA BAEZ
Acceso Abierto
Atribución-NoComercial-SinDerivadas
https://doi.org/10.3390/molecules18089317
"The main monomer of tomato cuticle, 10,16-dihydroxyhexadecanoic acid (10,16-DHPA) and its methyl ester derivative (methyl-10,16-dihydroxyhexadecanote; methyl-10,16-DHHD), were used to study their oligomerization reactions catalyzed by five lipases: Candida antarctica lipase B (CAL-B), Rhizomucor miehei lipase (RM), Thermomyces lanuginosus lipase (TL), Pseudomonas cepacia lipase (PCL) and porcine pancreatic lipase (PPL). For 10,16-DHPA, optimum yields were obtained at 60 °C using toluene and 2-methyl-2-butanol (2M2B) as solvent, while for methyl-10,16-DHHD the bests yields were obtained in toluene and acetonitrile. Both reactions leaded to linear polyesters according to the NMR and FT-IR analysis, and there was no data indicating the presence of branched polymers. Using optimized conditions, poly(10,16-DHPA) and poly(methyl-10,16-DHHD) with Mw = 814 and Mn = 1,206 Da, and Mw = 982 and Mn = 860 Da, respectively, were formed according to their MALDI-TOF MS and ESI-MS data. The self-assembly of the polyesters obtained were analyzed by AFM."
05-08-2013
Artículo
Molecules 2013, 18(8), 9317-9333
Inglés
BIOLOGÍA Y QUÍMICA
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