TY - JOUR
T1 - Preparation and characterization of polyisoprenes and polybutadienes having 1,2- and 3,4-linkages preferentially
AU - Takano, Atsushi
AU - Horaiya, Takeshi
AU - Odamaki, Fumitake
AU - Akazawa, Yoshihiko
AU - Ohta, Yutaka
AU - Kawaguchi, Daisuke
AU - Takahashi, Yoshiaki
AU - Matsushita, Yushu
N1 - Funding Information:
This work was partly performed under the Cooperative Research Program of “Network Joint Research Center for Materials and Devices (Institute for Materials Chemistry and Engineering, Kyushu University)”.
PY - 2012/7/6
Y1 - 2012/7/6
N2 - Polyisoprenes (PI) and polybutadienes (PB) both having vinyl-type side chains preferentially were prepared and characterized. Both polymers were anionically polymerized with cumyl potassium or pottassium naphthalenide as initiators in a polar solvent, tetrahydrofuran, at low temperature. From the 1H NMR measurement, the PI contains 3,4- and 1,2-microstructures and PB does 1,2-microstructure preferentially. All the samples covering the molecular weight range of 37 k ≤ Mw ≤ 724 k for PI and 35 k ≤ Mw ≤ 197 k for PB were confirmed to have narrow molecular weight distribution. Measured glass transition temperatures, i.e., 11.0 °C for PI and -0.7 °C for PB are both considerably high compared with those of 1,4-microstructure-rich analogues. Intrinsic viscosity measurements in 1,3-dioxane for PI and 2-octanol for PB were carried out, and the segment lengths of the 3,4-/1,2-rich PI and 1,2-rich PB were estimated to be 0.60 nm and 0.59 nm, which are both considerably shorter than the values for two polydienes having 1,4-microstructures preferentially, i.e., 0.66 nm for both 1,4-rich PI and PB. Furthermore plateau moduli of both polymers are determined by dynamic viscoelastic measurements.
AB - Polyisoprenes (PI) and polybutadienes (PB) both having vinyl-type side chains preferentially were prepared and characterized. Both polymers were anionically polymerized with cumyl potassium or pottassium naphthalenide as initiators in a polar solvent, tetrahydrofuran, at low temperature. From the 1H NMR measurement, the PI contains 3,4- and 1,2-microstructures and PB does 1,2-microstructure preferentially. All the samples covering the molecular weight range of 37 k ≤ Mw ≤ 724 k for PI and 35 k ≤ Mw ≤ 197 k for PB were confirmed to have narrow molecular weight distribution. Measured glass transition temperatures, i.e., 11.0 °C for PI and -0.7 °C for PB are both considerably high compared with those of 1,4-microstructure-rich analogues. Intrinsic viscosity measurements in 1,3-dioxane for PI and 2-octanol for PB were carried out, and the segment lengths of the 3,4-/1,2-rich PI and 1,2-rich PB were estimated to be 0.60 nm and 0.59 nm, which are both considerably shorter than the values for two polydienes having 1,4-microstructures preferentially, i.e., 0.66 nm for both 1,4-rich PI and PB. Furthermore plateau moduli of both polymers are determined by dynamic viscoelastic measurements.
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U2 - 10.1016/j.polymer.2012.05.038
DO - 10.1016/j.polymer.2012.05.038
M3 - Article
AN - SCOPUS:84862774783
SN - 0032-3861
VL - 53
SP - 3354
EP - 3359
JO - Polymer
JF - Polymer
IS - 15
ER -