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Beilstein J. Org. Chem. 2013, 9, 1492–1500, doi:10.3762/bjoc.9.170
Graphical Abstract
Scheme 1: (a) Preparation of thiophene Grignard monomer and synthesis of P3HT by Kumada catalyst transfer pol...
Figure 1: Plot of number-average molecular weight, Mn, versus monomer–catalyst ratio [M]0/[I]0 for batch and ...
Figure 2: MALDI mass spectrum of low-molecular-weight preparation (GPC, Mn = 6.2 kg/mol) of P3HT in continuou...
Figure 3: Plot of number-average molecular weight, Mn, versus monomer–catalyst ratio [M]0/[I]0 for batch and ...
Scheme 2: Schematic representation of the telescoped preparation of P3HT in a flow reactor.
Figure 4: 1H NMR (CDCl3, 500 MHz) spectra of P3HT samples prepared in (a) flow and (b) batch show comparable ...
Figure 5: (a) Schematic diagram of the photovoltaic device geometry and (b) J–V curves of BHJ solar cells wit...
Beilstein J. Org. Chem. 2013, 9, 1102–1110, doi:10.3762/bjoc.9.122
Figure 1: N-ethylhexyl-substituted (1) [20] and target free N–H (2) cyanopyridone structures.
Scheme 1: Synthesis of the cyanopyridone 2, reagents and conditions: (i) Pd(PPh3)4, Cs2CO3, toluene, reflux, ...
Figure 2: (a) Chloroform (solid line) and thin-film (dashed line) UV–vis absorption and emission spectra and ...
Figure 3: The concentration dependence of (a) the NH 1H NMR chemical shift and (b) the vinyl proton chemical ...
Figure 4: AFM height image of observed nanostructures of films drop cast from (a) 10 mg/mL and (b) 1 mg/mL ch...
Figure 5: Dimeric structures of 2. (a) centrosymmetric dimer of 2; (b) bond-rotated centrosymmetric dimer of 2...
Figure 6: Schematic representation of self-complementary interactions leading to one-dimensional chains.