TY - JOUR
T1 - The marriage of metallacycle transfer chemistry with suzuki-miyaura cross-coupling to give main group element-containing conjugated polymers
AU - He, Gang
AU - Kang, Le
AU - Torres Delgado, William
AU - Shynkaruk, Olena
AU - Ferguson, Michael J.
AU - McDonald, Robert
AU - Rivard, Eric
PY - 2013/4/10
Y1 - 2013/4/10
N2 - A versatile and general synthetic route for the synthesis of conjugated main group element-based polymers, previously inaccessible by conventional means, is reported. These polymers contain five-membered chalcogenophene rings based on S, Se, and Te, and we demonstrate that optoelectronic properties can be readily tuned via controlled atom substitution chemistry. In addition, regioregular hybrid thiophene-selenophene-tellurophene and selenophene-fluorene copolymers were synthesized to provide a further illustration of the scope of the presented metallacycle transfer/cross-coupling polymerization method.
AB - A versatile and general synthetic route for the synthesis of conjugated main group element-based polymers, previously inaccessible by conventional means, is reported. These polymers contain five-membered chalcogenophene rings based on S, Se, and Te, and we demonstrate that optoelectronic properties can be readily tuned via controlled atom substitution chemistry. In addition, regioregular hybrid thiophene-selenophene-tellurophene and selenophene-fluorene copolymers were synthesized to provide a further illustration of the scope of the presented metallacycle transfer/cross-coupling polymerization method.
UR - https://www.scopus.com/pages/publications/84876045193
U2 - 10.1021/ja402242z
DO - 10.1021/ja402242z
M3 - 文章
C2 - 23517048
AN - SCOPUS:84876045193
SN - 0002-7863
VL - 135
SP - 5360
EP - 5363
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 14
ER -