ALTERNATING COPOLYMERIZATION OF CYCLOHEXENE OXIDE AND CARBON DIOXIDE UNDER COBALT PORPHYRIN CATALYST

Cobalt porphyrin complexes (TPPConIX) (TPP = 5,10,15,20-tetraphenyl-porphyrin; X = halide) in combination with bis(triphenylphosphine) iminium chloride (PPNC1) were used for the eopolymerization of cyelohexene oxide and CO2. The highest turnover frequency of 67.2 h^-1 was achieved after 13 h at 20℃,...

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Published inChinese journal of polymer science Vol. 29; no. 5; pp. 602 - 608
Main Authors Qin, Yu-sheng, Chen, Li-jie, Wang, Xian-hong, Zhao, Xiao-jiang, Wang, Fo-song
Format Journal Article
LanguageEnglish
Published Heidelberg Chinese Chemical Society and Institute of Chemistry, CAS 01.09.2011
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Summary:Cobalt porphyrin complexes (TPPConIX) (TPP = 5,10,15,20-tetraphenyl-porphyrin; X = halide) in combination with bis(triphenylphosphine) iminium chloride (PPNC1) were used for the eopolymerization of cyelohexene oxide and CO2. The highest turnover frequency of 67.2 h^-1 was achieved after 13 h at 20℃, and the obtained poly(1,2-cyclohexylene carbonate) (PCHC) showed number average molecular weight (Mn) of 10 × 10^3. Though the obtained PCHC showed atactie structure, the m-centered tetrads content reached 58.1% at CO2 pressure of 1.0 MPa, and decreased to 51.9% at CO2 pressure of 6.0 MPa, indicating that it was inclined to form atactic polymer at high CO2 pressure.
Bibliography:Carbon dioxide; Cobalt porphyrin; Cyclohexene oxide; Poly(1,2-cyclohexylene carbonate); Sstereochemistry;Copolymerization.
Cobalt porphyrin complexes (TPPConIX) (TPP = 5,10,15,20-tetraphenyl-porphyrin; X = halide) in combination with bis(triphenylphosphine) iminium chloride (PPNC1) were used for the eopolymerization of cyelohexene oxide and CO2. The highest turnover frequency of 67.2 h^-1 was achieved after 13 h at 20℃, and the obtained poly(1,2-cyclohexylene carbonate) (PCHC) showed number average molecular weight (Mn) of 10 × 10^3. Though the obtained PCHC showed atactie structure, the m-centered tetrads content reached 58.1% at CO2 pressure of 1.0 MPa, and decreased to 51.9% at CO2 pressure of 6.0 MPa, indicating that it was inclined to form atactic polymer at high CO2 pressure.
11-2015/O6
ISSN:0256-7679
1439-6203
DOI:10.1007/s10118-011-1073-3