Optically Active Precision Aliphatic Polyesters via Cross‐Metathesis Polymerization

May 22, 2018

Title

Optically Active Precision Aliphatic Polyesters via Cross‐Metathesis Polymerization

Author

Fu‐Rong Zeng, Ji‐Mei Ma, Lin‐Hao Sun, Zhen Zeng, Hong Jiang, Zi‐Long Li

Year

2018

Journal

Macromolecular Chemistry and Physics

Abstract

Precision synthesis of optically active poly(lactic‐alt‐caprolactic acid) is realized using cross‐metathesis polymerization (CMP) and hydrogenation. Enantiopure monomers MLand MD are generated through two consecutive esterification reactions. CMP of these two monomers in different feed ratios, followed by hydrogenation, afford saturated polymers HPL, HPD, and HPDL comprising L‐lactic and/or D‐lactic acid and ε‐caprolactone‐derived motifs with alternating sequences. CMP kinetic analysis by nuclear magnetic resonance (NMR) is performed by employing a racemic monomer Mrac. Enantiomeric polyesters HPL and HPD display opposite rotation values and mirror‐imaged cotton effects in circular dichroism (CD) spectra, whereas HPDL derived from equimolar ML and MD shows inactive optical rotation and no CD response. Stereocomplex HPD+HPL is obtained by equimolar mixing of HPL and HPD, since this specimen is the only one to exhibit a sharp melting peak on differential scanning calorimetry (DSC) curve at 45.7 °C. Hence, an amorphous, enantiomerically pure polyester becomes crystalline via stereocomplexation with its complementary enantiomer.

Instrument

J-1500

Keywords

Circular dichroism, Stereochemistry, Cotton effect, Polymers