PREPARATION OF HETEROTACTIC-RICH POLY(METHYL METHACRYLATE) WITH NARROW MOLECULAR-WEIGHT DISTRIBUTION BY TERT-BUTYLLITHIUM BIS(2,6-DI-TERT-BUTYLPHENOXY)METHYLALUMINUM/
T. Kitayama et al., PREPARATION OF HETEROTACTIC-RICH POLY(METHYL METHACRYLATE) WITH NARROW MOLECULAR-WEIGHT DISTRIBUTION BY TERT-BUTYLLITHIUM BIS(2,6-DI-TERT-BUTYLPHENOXY)METHYLALUMINUM/, Polymer bulletin, 32(4), 1994, pp. 439-446
Polymerization of methyl methacrylate (MMA) with tert-butyllithium (t-
C4H9Li) in toluene in the presence of aluminum alkoxides such as ethox
ide, tert-butoxide and 2,6-di-tert-butylphenoxide, were examined at va
rious Al/Li ratios. In the cases of ethoxide and tert-butoxide, predom
inantly isotactic polymers with broad molecular weight distribution we
re obtained. CombinationS Of t-C4H9Li and bis(2,6-di-tert-butylphenoxy
)methylaluminum [MeAl(ODBP)2] were found to be an efficient initiating
system for heterotactic polymerization of MMA, which gives PMMA rich
in heterotactic triads up to 68% with narrow molecular weight distribu
tion (MwBAR/MnBAR =1.09-1.17). End group analysis by H-1 NMR indicated
that t-C4H9Li initiates the polymerization and MeAl(ODBP)2 works as a
stereospecific modifier. From stereosequence analysis of the heterota
ctic PMMA by C-13 NMR, it was found that the calculated pentad fractio
ns from the first-order Markovian statistics (Pm/r=0.742, Pr/m=0.627)
fitted the observed ones better than those from Bernoullian statistics
. The glass transition temperature of the heterotactic PMMA was 13-deg
rees-C lower than that of syndiotactic PMMA, and the intrinsic viscosi
ty in tetrahydrofuran was close to that of isotactic PMMA with a simil
ar molecular weight but higher than that of syndiotactic PMMA.