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TEMPO Containing Radical Polymonothiocarbonate Polymers with Regio‐ and Stereo‐Regularities: Synthesis, Characterization, and Electrical Conductivity Studies
Author(s) -
Bhat Gulzar A.,
Rashad Ahmed Z.,
Ji Xiaozhou,
Quiroz Manuel,
Fang Lei,
Darensbourg Donald J.
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202108041
Subject(s) - tacticity , polymer , monomer , copolymer , polymer chemistry , conductivity , annealing (glass) , materials science , cyclic voltammetry , electrical resistivity and conductivity , radical , chemistry , polymerization , organic chemistry , electrochemistry , composite material , electrode , electrical engineering , engineering
We report the synthesis of a (2,2,6,6‐tetramethylpiperidin‐1‐yl)oxidanyl) (TEMPO) appended polymonothiocarbonates through the ring‐opening copolymerization of (4‐glycidyloxy‐2,2,6,6‐tetramethylpiperidine‐1‐oxyl) (GTEMPO) in the presence of carbonyl sulfide under ambient conditions. We have prepared the atactic and isotactic versions of this polymer, using enantiopure R or S forms of the GTEMPO monomer in the latter instances. Cyclic voltammetry studies revealed both oxidation and reduction events that were characteristic of TEMPO radicals. Electrical conductivity of these polymers was measured as solid‐state films after annealing the samples above their glass transition temperatures. At room temperature the isotactic polymer shows much greater conductivity (ca. 10 −4 S cm −1 ) than the atactic (ca. 10 −7 S cm −1 ), attributed to the well‐defined stereochemistry and regulated charge transport pathway of isotactic polymer chains in contrast to the irregular structure of the atactic counterpart.