Method of making a pyrrolo bisthiazole homopolymer
AssigneeQatar Foundation for Education, Science and Community Development
InventorsMohammed Al-Hashimi, Hugo Bronstein
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AssigneeQatar Foundation for Education, Science and Community Development
InventorsMohammed Al-Hashimi, Hugo Bronstein
Estimating the term…
The method of making a pyrrolo bisthiazole homopolymer starts with dissolving a dibrominated pyrrolo[3,2-d:4,5-d′]bisthiazole monomer having the formula: where R is an alkyl group, in anhydrous tetrahydrofuran (THF). Then, the solvated monomer is treated with 1 equivalent of a Turbo-Grignard reagent complex having the formula iPrMgCl.LiCl at 0° C. to form a reaction mixture. The reaction mixture is stirred for 1 hour at room temperature, and after stirring, the reaction mixture is refluxed for 24 hours. A conjugated homopolymer product having the formula: where n is the number of repeating units of pyrrolo[3,2-d:4,5-d′]bisthiazole, is recovered from the reaction mixture. The PBTz-based homopolymers showed broad absorption from 450 to 850 nm in thin film and excellent photochemical and thermal stability, making the polymers suitable for lightweight, low cost plastic electronic devices.
A method of making a pyrrolo bisthiazole homopolymer, comprising the step of polymerizing a fused pyrrolo[3,2-d:4,5-d′]bisthiazole monomer using a turbo-Grignard reagent (iPrMgCl.LiCl) complex to obtain a conjugated homopolymer.
A method of making a pyrrolo bisthiazole homopolymer, comprising the steps of:
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