Zhou, Liuyang; Xia, Xinxin; Meng, Lei; Zhang, Jinyuan; Lu, Xinhui; Li, Yongfang published their research in Chemistry of Materials in 2021. The article was titled 《Introducing Electron-Withdrawing Linking Units and Thiophene π-Bridges into Polymerized Small Molecule Acceptors for High-Efficiency All-Polymer Solar Cells》.HPLC of Formula: 51364-51-3 The article contains the following contents:
A series of narrow bandgap polymer acceptors (PY5-BTZ, PY5-2TZ, PY5-PZ, and PY5-BT) were synthesized by copolymerizing a Y5-like small mol. acceptor (SMA) and different electron-withdrawing (A) units with thiophene π-bridges. Among the polymerized SMAs (PSMAs), the A-unit is bifluoro-benzotriazole for PY5-BTZ, thiazolo[5,4-d]thiazole for PY5-2TZ, pyrazine for PY5-PZ, and benzothiadiazole for PY5-BT. The four PSMA films possess narrower bandgaps of 1.43-1.45 eV. Interestingly, PY5-BTZ shows a higher-lying LUMO energy level of -3.72 eV (-3.76 eV for PY5-2TZ, -3.75 eV for PY5-PZ, and -3.78 eV for PY5-BT) and a stronger absorbance of 1.5 x 105 cm-1 (1.4 x 105 cm-1 for the other three PSMAs). The all-polymer solar cells (all-PSCs) with PY5-BTZ as the polymer acceptor and PBDB-T as the polymer donor exhibit a peak power conversion efficiency of 14.82% with a high open circuit voltage of 0.92 V, which benefits from the higher-lying LUMO level and stronger absorbance of the PY5-BTZ polymer acceptor. The results indicate that introducing weak electron-withdrawing A-units and thiophene π-bridges could be an effective approach in designing and synthesizing high-performance PSMA polymer acceptors for high-efficiency all-PSCs in the future. The results came from multiple reactions, including the reaction of Tris(dibenzylideneacetone)dipalladium(0)(cas: 51364-51-3HPLC of Formula: 51364-51-3)
Tris(dibenzylideneacetone)dipalladium(0)(cas: 51364-51-3) is the most widely used PdO precursor complex in synthesis and catalysis, in particular as a catalyst for various coupling reactions. HPLC of Formula: 51364-51-3 It is used as a catalyst precursor for palladium-catalyzed carbon-nitrogen bond formation, conversion of aryl chlorides, triflates and nonaflates to nitroaromatics.
Referemce:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI