2 article(s) from Balan, Mihaela
Graphical Abstract
Scheme 1: Ring opening of L-LA in the presence of cyclodextrins.
Figure 1: (a) ELSD chromatogram of crude β-CD-LA reaction mixture and (b) MALDI–MS spectrum of fraction f5.
Figure 2: MALDI–MS spectra of the fractionated α-, β- and γ-CD-LA products – fractions precipitated in THF: (...
Figure 3: MALDI–MS spectra of the fractionated α-, β- and γ-CD-LA products – fractions soluble in THF: (a) α-...
Figure 4: 1H NMR spectrum of fractions precipitated in THF of (A) α-CD-LA, (B) β-CD-LA and (C) γ-CD-LA.
Figure 5: 13C NMR spectra of (A) β-CD-LA F2 fraction and (B) β-CD-LA F1 fraction.
Figure 6: DEPT135-NMR experiment of (A) β-CD-LA F2 fraction and (B) β-CD-LA F1 fraction.
Graphical Abstract
Scheme 1: Synthesis of PDOF-BT and PDOF-BTc copolymers.
Figure 1: 1H NMR spectrum (CDCl3) of the BTc inclusion complex.
Figure 2: FTIR spectra (KBr pellet) of PDOF-BT (A) and PDOF-BTc (B) copolymers.
Figure 3: 1H NMR spectrum of PDOF-BT copolymer (CDCl3).
Figure 4: 1H NMR spectrum of PDOF-BTc copolymer (CDCl3).
Figure 5: DSC curves of BTc and PDOF-BTc from second-heating DSC measurements.
Figure 6: Thermogravimetric curves (TG) for BTc, PDOF-BT, and PDOF-BTc compounds.
Figure 7: High-resolution tapping-mode AFM images and cross-section plots (along the solid line in the images...