화학공학소재연구정보센터
Journal of Polymer Science Part A: Polymer Chemistry, Vol.35, No.8, 1579-1591, 1997
Dicobalt Octacarbonyl-Catalyzed Cationic Polymerization of Allylic and Enolic Ethers
In the presence of silanes bearing Si-H groups, dicobalt octacarbonyl [Co-2(CO)(8)] efficiently catalyzes the cationic polymerization of a wide variety of enol ether and other related monomers including vinyl ethers, 1-propenyl ethers, 1-butenyl ethers, 2,3-dihydrofuran, 3,4-dihydro-2H-pyran, ketene acetals, and allene ethers. In addition, this catalyst system is also effective for the polymerization of complimentary allylic and propargylic ethers by a process involving tandem isomerization and cationic polymerization. This latter process occurs by a stepwise mechanism in which the allylic or propargylic ether is first isomerized, respectively, to the corresponding enol ether or allenic ether and then this latter compound is rapidly cationically polymerized in the presence of the catalyst. In accord with this mechanism, it has been shown that the structure of the polymers prepared from related enol and allyl ethers using the above catalyst system are identical.