TY - JOUR
T1 - Synthesis of star-shaped polystyrenes via nitroxide-mediated stable free-radical polymerization
AU - Pasquale, Anthony J.
AU - Long, Timothy Edward
PY - 2001/1/1
Y1 - 2001/1/1
N2 - High molecular weight star-shaped polystyrenes were prepared via the coupling of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) terminated polystyrene oligomers with divinylbenzene (DVB) in m-xylene at 138°C. The optimum ratio of the coupling solvent (m-xylene) to divinylbenzene was determined to be 9 to 1 based on volume. Linear polystyrene oligomers (Mn = 19,300 g/mol, Mw/Mn = 1.10) were prepared in bulk styrene using benzoyl peroxide in the presence of TEMPO at approximately 130°C under an inert atmosphere. Coupling of the TEMPO-terminated oligomers under optimum conditions resulted in a product with a number average oligomers under optimum conditions resulted in a product with a number average molecular weight exceeding 300,000 g/mol (Mw/Mn = 3.03) after 24 h, suggesting the formation of relatively well-defined star-shaped polymers. Additionally, the intrinsic viscosities of the star-shaped products were lower than calculated values for linear analogs of equivalent molecular weight, which further supported the formation of a star-shaped architecture.
AB - High molecular weight star-shaped polystyrenes were prepared via the coupling of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) terminated polystyrene oligomers with divinylbenzene (DVB) in m-xylene at 138°C. The optimum ratio of the coupling solvent (m-xylene) to divinylbenzene was determined to be 9 to 1 based on volume. Linear polystyrene oligomers (Mn = 19,300 g/mol, Mw/Mn = 1.10) were prepared in bulk styrene using benzoyl peroxide in the presence of TEMPO at approximately 130°C under an inert atmosphere. Coupling of the TEMPO-terminated oligomers under optimum conditions resulted in a product with a number average oligomers under optimum conditions resulted in a product with a number average molecular weight exceeding 300,000 g/mol (Mw/Mn = 3.03) after 24 h, suggesting the formation of relatively well-defined star-shaped polymers. Additionally, the intrinsic viscosities of the star-shaped products were lower than calculated values for linear analogs of equivalent molecular weight, which further supported the formation of a star-shaped architecture.
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U2 - 10.1002/1099-0518(20010101)39:1<216::AID-POLA240>3.0.CO;2-Z
DO - 10.1002/1099-0518(20010101)39:1<216::AID-POLA240>3.0.CO;2-Z
M3 - Article
AN - SCOPUS:0035151959
SN - 0887-624X
VL - 39
SP - 216
EP - 223
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 1
ER -