DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS
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DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS
DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS
高分子科学(英文版)2006年第1期 页码:87-93
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中图分类号:O631.3
纸质出版:2006
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[1].DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS[J].Chinese Journal of Polymer Science,2006(01):87-93.
Hai-zhu Ma and Gao-xiang Ye a Department of Physics, Zhejiang University, Hangzhou 310027, et al. DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS[J]. 2006, (1): 87-93.
[1].DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS[J].Chinese Journal of Polymer Science,2006(01):87-93.DOI:
Hai-zhu Ma and Gao-xiang Ye a Department of Physics, Zhejiang University, Hangzhou 310027, et al. DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS[J]. 2006, (1): 87-93.DOI:
DIMENSIONS OF ATACTIC POLY(α-METHYLSTYRENE)CHAINS WITH SIDE GROUPS
An improved configurational-confomational statistical method is developed and the mean-square radius of gyration for atactic poly(α-methylstyrene)(PαMS)chains is studied
in which the effect of large side groups is considered. The deduced formulas
based on the rotational isomer state theory
are used to investigate the configuration-dependent properties of the atactic polymer chain
and the statistical correlation of the unperturbed polymer chain dimension and structure parameters are calculated.For the fraction of meso dyads w
m
=0.4
the dependence of the radius of gyration R
g
and the intrinsic viscosity[η]on the molecule mass M are R
g
=2.63×10
-2
M
0.50
nm and[η]=7.36×10
-2
M
0.497
respectively
which are in agreement with the previous experimental data for the PαMS samples.A small hump is detected in the curve of the characteristic ratio of the unperturbed mean-square radius of gyration versus the chain length for short PαMS chains.The R
g
increases linearly with the temperature T
and the effects of the chain length and the tacticity on the temperature coefficient are remarkable.These are quite different from the results for PαMS chains not considering side groups or for the monosubstituted polystyrene chain.
Abstract
An improved configurational-confomational statistical method is developed and the mean-square radius of gyration for atactic poly(α-methylstyrene)(PαMS)chains is studied
in which the effect of large side groups is considered. The deduced formulas
based on the rotational isomer state theory
are used to investigate the configuration-dependent properties of the atactic polymer chain
and the statistical correlation of the unperturbed polymer chain dimension and structure parameters are calculated.For the fraction of meso dyads w
m
=0.4
the dependence of the radius of gyration R
g
and the intrinsic viscosity[η]on the molecule mass M are R
g
=2.63×10
-2
M
0.50
nm and[η]=7.36×10
-2
M
0.497
respectively
which are in agreement with the previous experimental data for the PαMS samples.A small hump is detected in the curve of the characteristic ratio of the unperturbed mean-square radius of gyration versus the chain length for short PαMS chains.The R
g
increases linearly with the temperature T
and the effects of the chain length and the tacticity on the temperature coefficient are remarkable.These are quite different from the results for PαMS chains not considering side groups or for the monosubstituted polystyrene chain.
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