Sequence of rubbing-induced molecular segmental reorientations in the nanoscale film surface of a brush polymer rod

被引:34
作者
Chae, B
Lee, SW
Lee, B
Choi, W
Kim, SB
Jung, YM
Jung, JC
Lee, KH
Ree, M
机构
[1] Pohang Univ Sci & Technol, Polymer Res Inst, Ctr Integrated Mol Syst, Div Mol & Life Sci,Dept Chem,BK21 Program, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol, Ctr Adv Funct Polymers, Pohang 790784, South Korea
[3] Pohang Univ Sci & Technol, Dept Mat Sci & Engn, Pohang 790784, South Korea
关键词
D O I
10.1021/jp034955q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly(p-phenylene-3,6-bis(4-(n-butoxy)phenyloxy)pyromellitimide) (C4-PMDA-PDA PI), a well-defined model brush polymer composed of a rodlike polymer backbone with two bristles per repeat unit, was the first reported polyimide to align liquid crystals perpendicular to the rubbing direction at the rubbed film surface. In the present study, we used polarized infrared (IR) spectroscopy and 2D correlation analyses of the resulting IR spectra to study nanoscale films of C4-PMDA-PDA PI rubbed at various rubbing densities. The results of these studies allowed us to establish the nature and sequence of the rubbing-induced segmental reorientations that occur in the polymer molecules at the film surface. The rubbing process was found to reorient the fully rodlike polymer backbones and the n-butyl bristle end groups such that they lay parallel to the rubbing direction. In contrast, rubbing caused the phenyloxy bristle units to reorient to a direction perpendicular to the rubbing direction. These reorientations of the polymer's main chain and bristles became more pronounced with increasing rubbing density, and the rubbing process had a greater effect on the polymer's main chains than on the bristles. The rubbing-induced reorientations of the polymer segments were found to follow the sequence PDA (phenyl ring), imide ring, phenyloxy unit, imide C-N bond, and n-butyl group. It was additionally evident that the rubbing process reorients the imide rings biaxially, that is, both along the rubbing direction and out of the plane. This biaxial reorientation was found to be accompanied by a biaxial reorientation of the bristles chemically bonded to the PMDA unit that includes the imide rings. In particular, increasing the rubbing density enhanced the out-of-plane reorientation of the imide rings. In contrast, no rubbing-induced inclination of the reoriented imide rings (i.e., the polymer's main chains) was detected.
引用
收藏
页码:11911 / 11916
页数:6
相关论文
共 41 条
[1]  
[Anonymous], LIQUID CRYSTALS
[2]  
[Anonymous], 1997, Handbook of Liquid Crystal Research
[3]   ALIGNMENT PROPERTIES OF RUBBED POLYMER SURFACES [J].
BECKER, ME ;
KILIAN, RA ;
KOSMOWSKI, BB ;
MLYNSKI, DA .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 1986, 132 (1-2) :167-180
[4]   SOLID SURFACE SHAPE AND ALIGNMENT OF AN ADJACENT NEMATIC LIQUID-CRYSTAL [J].
BERREMAN, DW .
PHYSICAL REVIEW LETTERS, 1972, 28 (26) :1683-&
[5]   ALIGNMENT OF LIQUID-CRYSTALS BY GROOVED SURFACES [J].
BERREMAN, DW .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 1973, 23 (3-4) :215-231
[6]   Photoinduced orientation in azopolymers studied by infrared spectroscopy: Cooperative and biaxial orientation in semicrystalline polymers [J].
Buffeteau, T ;
Pezolet, M .
MACROMOLECULES, 1998, 31 (08) :2631-2635
[7]   SURFACE ANCHORING OF LIQUID-CRYSTAL MOLECULES ON VARIOUS SUBSTRATES [J].
CASTELLANO, JA .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 1983, 94 (1-2) :33-41
[8]   Photoreaction and molecular reorientation in a nanoscaled film of poly(methyl 4-(methacryloyloxy)cinnamate) studied by two-dimensional FTIR and UV correlation spectroscopy [J].
Chae, B ;
Lee, SW ;
Ree, M ;
Jung, YM ;
Kim, SB .
LANGMUIR, 2003, 19 (03) :687-695
[9]   Surface morphology, molecular reorientation, and liquid crystal alignment properties of rubbed nanofilms of a well-defined brush polyimide with a fully rodlike backbone [J].
Chae, B ;
Kim, SB ;
Lee, SW ;
Kim, SI ;
Choi, W ;
Lee, B ;
Ree, M ;
Lee, KH ;
Jung, JC .
MACROMOLECULES, 2002, 35 (27) :10119-10130
[10]   ORDER ELECTRICITY IN LIQUID-CRYSTALS [J].
DURAND, G .
PHYSICA A, 1990, 163 (01) :94-100