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Carbon-carbon (CC) backbone polymers are a class of polymer materials widely used in daily life.
The research group of Prof.
Figure 1.
1.
The research team first optimized the polymerization conditions and tried a series of catalytic systems composed of different Ni compounds (R'–Ni–X) and different ligands (L1–L6) to induce benzyl diazoacetate (1a) The polymerization reaction was studied, as shown in Figure 2
Figure 2.
Figure 3.
2.
Next, the research team studied the polymerization kinetics of BT–Ni(dppp)Cl-initiated polymerization of diazo monomer 1a (internal standard is polystyrene; Mn = 41.
Figure 4.
3.
Since BT-Ni(dppp)Cl showed excellent performance during the polymerization of diazotate, the team tried to study the functional polymer with similar Ni(II)-complex ends to initiate the living polymerization of diazoacetic acid, thereby obtaining Functional block copolymers
Figure 5.
Using the above-mentioned functional polymer P3HT-initiated diazotate polymerization strategy, a series of π-conjugated copolymers with controllable molecular weight and structure, such as amphiphilic block copolymers, can be prepared
The significance of this study is to establish a method for the controllable polymerization of diazotes with non-noble metal Ni(II) catalysts, and to easily synthesize CC backbone polymers and π-conjugated interpolymers with substituents on each backbone carbon atom.
The above related research results were published in Nature Communications (Nat.
Commun.
13, 811 (2022))
.
The co-first authors of the paper are Zhou Li, a teacher from the School of Chemistry and Chemical Engineering, Hefei University of Technology, and Xu Lei, a postdoctoral fellow, and the corresponding author is Professor Wu Zongquan.
Currently, they have joined the State Key Laboratory of Supramolecular Structure and Materials, Jilin University
.