Highly Ordered Dielectric Mirrors via the Self-Assembly of Dendronized Block Copolymers

被引:83
作者
Piunova, Victoria A. [1 ]
Miyake, Garret M. [1 ]
Daeffler, Christopher S. [1 ]
Weitekamp, Raymond A. [1 ]
Grubbs, Robert H. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Arnold & Mabel Beckman Labs Chem Synth, Pasadena, CA 91125 USA
关键词
OPENING METATHESIS POLYMERIZATION; POLYMERS; POLYDISPERSITY; DYNAMICS; BULK;
D O I
10.1021/ja4081502
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dendronized block copolymers were synthesized by ruthenium-mediated ring-opening methathesis polymerization of exo-norbomene functionalized dendrimer monomers, and their self-assembly to dielectric mirrors was investigated. The rigid-rod main-chain conformation of these polymers drastically lowers the energetic barrier for reorganization, enabling their rapid self-assembly to long-range, highly ordered nanostructures. The high fidelity of these dielectric mirrors is attributed to the uniform polymer architecture achieved from the construction of discrete dendritic repeat units. These materials exhibit light-reflecting properties due to the multilayer architecture, presenting an attractive bottom-up approach to efficient dielectric mirrors with narrow band gaps. The wavelength of reflectance scales linearly with block-copolymer molecular weight, ranging from the ultraviolet, through the visible, to the near-infrared. This allows for the modulation of photonic properties through synthetic control of the polymer molecular weight. This work represents a significant advancement in closing the gap between the precision obtained from top-down and bottom-up approaches.
引用
收藏
页码:15609 / 15616
页数:8
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