TY - JOUR
T1 - Pseudo-living anionic telomerization of buta-1,3-diene
AU - Saito, Tomonori
AU - Harich, Kim C.
AU - Long, Timothy Edward
PY - 2008/10/7
Y1 - 2008/10/7
N2 - Low-molecular-weight liquid polybutadienes (1000-2000 g · mol -1) consisting of 60 mol-% poly(buta-1,2-diene) repeating units were synthesized via anionic telomerization. Maintaining theinitiation and reaction temperature at less than 70°C minimized chain transfer and enabled the polymerization to occur in a living fashion, which resulted in well-controlled molecular weights and narrow polydispersity indices. MALDI-TOF mass spectrometry confirmed that the end groups of liquid polybutadienes synthesized via anionic telomerization contained one benzyl end and one protonated end. In comparison, the end groups of liquid polybutadienes synthesized via living anionic polymerization contained one sec-butyl or butyl end and one protonated end.
AB - Low-molecular-weight liquid polybutadienes (1000-2000 g · mol -1) consisting of 60 mol-% poly(buta-1,2-diene) repeating units were synthesized via anionic telomerization. Maintaining theinitiation and reaction temperature at less than 70°C minimized chain transfer and enabled the polymerization to occur in a living fashion, which resulted in well-controlled molecular weights and narrow polydispersity indices. MALDI-TOF mass spectrometry confirmed that the end groups of liquid polybutadienes synthesized via anionic telomerization contained one benzyl end and one protonated end. In comparison, the end groups of liquid polybutadienes synthesized via living anionic polymerization contained one sec-butyl or butyl end and one protonated end.
KW - Anionic telomerization
KW - Liquid polybutadience
KW - Living polymerization
KW - MALDI-TOF mass sectrometry
KW - Microstructure
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U2 - 10.1002/macp.200800249
DO - 10.1002/macp.200800249
M3 - Article
AN - SCOPUS:55149121384
SN - 1022-1352
VL - 209
SP - 1983
EP - 1991
JO - Macromolecular Chemistry and Physics
JF - Macromolecular Chemistry and Physics
IS - 19
ER -