TY - JOUR
T1 - Metallocene-mediated synthesis of chain-end functionalized polypropylene and application in PP/clay nanocomposites
AU - Chung, T. C.
N1 - Funding Information:
The authors would like to thank the Office of Naval Research and the National Institute of Standards and Technology for their financial support.
PY - 2005/12/15
Y1 - 2005/12/15
N2 - This paper summarizes our research in the preparation of chain end functionalized isotactic polypropylene (PP) having a terminal functional group, such as Cl, OH, and NH2. The chemistry involves metallocene-mediated propylene polymerization using rac-Me2Si[2-Me-4-Ph(Ind)] 2ZrCl2/MAO complex in the presence of styrene derivatives (St-f) and hydrogen, which serve as the chain transfer agents. The molecular weight of the resulting PP polymers with a terminal Cl, OH and NH2 group (i.e., PP-t-Cl, PP-t-OH and PP-t-NH2) are inversely proportional to the molar ratio of [St-f]/[propylene]. Despite the extremely low concentration of functional group, the high molecular weight chain end functionalized PP-t-OH and PP-t-NH3+ exhibit a distinctive advantage over other functional PP polymers containing side chain functional groups or long functional blocks. The terminal hydrophilic OH and NH3+ cations, with good mobility and reactivity, effectively hydrogen bond and ion-exchange the cations (Li+, Na+, etc.) located between the clay interlayers, respectively. Such interactions anchor the PP chain to the clay surfaces. On the other hand, the remaining rest of the unperturbed end-tethered high molecular weight PP tail exfoliates the clay layers. This exfoliated structure is maintained even after further mixing of the PP-bearing platelets with pure neat PP polymers.
AB - This paper summarizes our research in the preparation of chain end functionalized isotactic polypropylene (PP) having a terminal functional group, such as Cl, OH, and NH2. The chemistry involves metallocene-mediated propylene polymerization using rac-Me2Si[2-Me-4-Ph(Ind)] 2ZrCl2/MAO complex in the presence of styrene derivatives (St-f) and hydrogen, which serve as the chain transfer agents. The molecular weight of the resulting PP polymers with a terminal Cl, OH and NH2 group (i.e., PP-t-Cl, PP-t-OH and PP-t-NH2) are inversely proportional to the molar ratio of [St-f]/[propylene]. Despite the extremely low concentration of functional group, the high molecular weight chain end functionalized PP-t-OH and PP-t-NH3+ exhibit a distinctive advantage over other functional PP polymers containing side chain functional groups or long functional blocks. The terminal hydrophilic OH and NH3+ cations, with good mobility and reactivity, effectively hydrogen bond and ion-exchange the cations (Li+, Na+, etc.) located between the clay interlayers, respectively. Such interactions anchor the PP chain to the clay surfaces. On the other hand, the remaining rest of the unperturbed end-tethered high molecular weight PP tail exfoliates the clay layers. This exfoliated structure is maintained even after further mixing of the PP-bearing platelets with pure neat PP polymers.
UR - http://www.scopus.com/inward/record.url?scp=28444442016&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=28444442016&partnerID=8YFLogxK
U2 - 10.1016/j.jorganchem.2005.04.031
DO - 10.1016/j.jorganchem.2005.04.031
M3 - Article
AN - SCOPUS:28444442016
SN - 0022-328X
VL - 690
SP - 6292
EP - 6299
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 26
ER -