The dimethyl ester of 2,3:4,5-di-O-methylene-galactaric acid (Galx) was made to react in the melt with 1,n-alkanediols HO(CH 2 ) n OH containing even numbers of methylenes (n from 6 to 12) to produce linear polycyclic polyesters. Two sets of poly(alkylene 2,3:4,5-di-O-methylenegalactarate) polyesters (PE-nGalx) with weight-average molecular weights in the ∼5000À10000 and ∼35000À45000 ranges were obtained using TBT and DBTO catalysts, respectively. For comparative purposes a set of poly(alkylene adipate) polyesters (PE-nAd) was also synthesized with molecular weights in the higher range using a similar procedure. The thermal stability of PE-nGalx was greater than that of PE-nAd although it notably decayed as molecular weight decreased. The replacement of Ad by Galx in the polyesters caused increases in T g of up to 70 °C, and almost doubled the tensile mechanical parameters. All PE-nGalx were semicrystalline but only those made from 1,12-dodecanediol were able to crystallize from the melt with a crystallization rate that diminished as the molecular weight increased. In general, the galactarate containing polyesters displayed higher solubility and wettability than polyadipates, they hydrolyzed faster and exhibited comparable sensitivity to the action of lipases.
' NOTE ADDED AFTER ASAP PUBLICATIONThis article posted ASAP on May 25, 2011. It was discovered that the bicyclic acetal was not 2,4:3,5 as first formulated, but rather 2,3:4,5. This change affects the abstract, paragraph 3 in the Introduction, paragraphs 1, 3, 4, 5, 6, 7 in the Experimental Section, paragraphs 1, 5, 12 in the Results and Discussion, and the Conclusions paragraph. Other changes include the Table of Contents graphic, Figures 1, 2, 3, 11, 12, and the Supporting Information file. The corrected version posted on June 23, 2011.