Table 1.
Monomer | Solvent | T 1 (°C) | Time (min) | Wavelength (nm) | Light Intensity (mW/cm2) | Reference |
---|---|---|---|---|---|---|
MPC | H2O | 60 | 5–90 | 350 ± 50 | 5 | [10,20,21,22] 2 |
MPC | 1-butanol | NIA 3 | NIA | 350 ± 50 | 1 | [23] |
MPC | H2O | 25–60 | 90 | 350 ± 50 | 1.5–9 | [24] |
MPC | H2O | 60 | 90 | NIA | 2.5–10 | [25] |
MPC | H2O | 60 | 5–90 | 350 ± 50 | 20 | [26] |
St | NIA | rt 4 | 270 | 315–400 | NIA | [27] |
AA | NIA | rt | 270 | 315–400 | NIA | [27] |
MeOEGMA | NIA | rt | 270 | 315–400 | NIA | [27] |
VPA | NIA | rt | 270 | 315–400 | NIA | [27] |
BA | NIA | rt | 270 | 315–400 | NIA | [27] |
MTAC | H2O | rt | 5–90 | 365 | 5 | [28] |
SPMK | H2O | rt | 5–90 | 365 | 5 | [28] |
AA | H2O | NIA | 30, 45, 60, 90 | 350 ± 50 | NIA | [29] |
MeHA | NIA | NIA | 0.5, 1, 1.5, 2, 4 | NIA | 5 | [30] |
VSA | H2O | rt | 40 | 365 | NIA | [31] |
VPA | H2O | rt | 20, 50, 90 | 365 | NIA | [32] |
VPA | H2O | rt | 40 | 365 | NIA | [33] |
1 Temperature; 2 all cited papers were based on the same synthetic procedure; 3 no information available; 4 synthesis was carried out at room temperature.