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Beilstein J. Org. Chem. 2016, 12, 2378–2389, doi:10.3762/bjoc.12.232
Graphical Abstract
Figure 1: Structures of used monomers and the time-conversion plot of the corresponding free-radical polymeri...
Scheme 1: Stereospecific propagation of chiral MLA illustrating the triade formation [15].
Figure 2: Plot of log Pn versus log [In] of the polymerization of MLA with different mol % AIBN.
Scheme 2: Postulated mechanism of the self-initiation of MLA.
Figure 3: DFT-calculated C–C binding length (yellow) of (A) MLA and (B) the corresponding radical.
Figure 4: IR spectra of (A) MLA and of (B) poly(MLA) prepared by the self-initiated polymerization at 70 °C.
Figure 5: Conversion plot of the polymerization of MLA in 1,4-dioxane and DMF (cMLA = 1.8 mol L−1, cAIBN = 1....
Figure 6: UV–vis spectra of the reaction mixture with DPPH radical at the beginning (violet line, 0.23 mM) of...
Figure 7: Copolymer composition curves for the systems MLA with styrene and MMA.
Figure 8: 1H NMR spectrum of MLA with 1 equiv of thioacetic acid and 0.15 equivalents of an inhibitor 4-metho...
Scheme 3: Mechanism of RAFT polymerization [24].
Figure 9: Structures of used RAFT agents examined in the polymerization of MLA.
Figure 10: A) Kinetic plot for the RAFT copolymerization of MLA and DMA for the ratio 90/10 employing EMP. B) ...