4.8 Article

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

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 41, Pages 15609-15616

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja4081502

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Funding

  1. Dow-Resnick Bridge Award
  2. DoD, Air Force Office of Scientific Research, National Defense Science and Engineering Graduate (NDSEG) [32 CFR 168a]

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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.

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