Controlling Chain Conformation in Conjugated Polymers Using Defect Inclusion Strategies

被引:55
作者
Bounos, Giannis [1 ,2 ]
Ghosh, Subhadip [1 ,2 ]
Lee, Albert K. [1 ,2 ]
Plunkett, Kyle N. [3 ]
DuBay, Kateri H. [3 ]
Bolinger, Joshua C. [1 ,2 ]
Zhang, Rui [1 ,2 ]
Friesner, Richard A. [3 ]
Nuckolls, Colin [3 ]
Reichman, David R. [3 ]
Barbara, Paul F. [1 ,2 ]
机构
[1] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[2] Univ Texas Austin, Ctr Nano & Mol Sci & Technol, Austin, TX 78712 USA
[3] Columbia Univ, Dept Chem, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
ENERGY-TRANSFER; SOLAR-CELLS; DYNAMICS;
D O I
10.1021/ja2006687
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Horner method was used to synthesize random copolymers of poly(2-methoxy-5-(2'-ethylhexyloxy)-p-phenylene vinylene) (MEH-PPV) that incorporated different backbone-directing monomers. Single-molecule polarization absorption studies of these new polymers demonstrate that defects that preserve the linear backbone of PPV-type polymers assume the highly anisotropic configurations found in defect-free MEH-PPV. Rigid defects that are bent lower the anisotropy of the single chain, and saturated defects that provide rotational freedom for the chain backbone allow for a wide variety of possible configurations. Molecular dynamics simulations of model defect PPV oligomers in solution demonstrate that defect-free and linearly defected oligomers remain extended while the bent and saturated defects tend toward more folded, compact structures.
引用
收藏
页码:10155 / 10160
页数:6
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