Abstract
A variety of multisubstituted cyclooctenes were prepared and employed as monomers for ring-opening metathesis polymerization using the Grubbs second or third generation catalysts. The resulting polymers were characterized by NMR spectroscopy, size exclusion chromatography, and differential scanning calorimetry. Monomers possessing a substituent at the 3-position afforded highly regio- and stereoregular polyalkenamers, from which the corresponding sequence-specific vinyl quaterpolymers were obtained upon hydrogenation. Simultaneous control of tacticity was also demonstrated by employing monomers with defined stereochemistry.
Original language | English (US) |
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Pages (from-to) | 1383-1387 |
Number of pages | 5 |
Journal | ACS Macro Letters |
Volume | 1 |
Issue number | 12 |
DOIs | |
State | Published - Dec 18 2012 |