4.7 Article

Strategies to Stabilize the Photoinduced Supramolecular Chirality in Azobenzene Liquid Crystalline Polymers

Journal

POLYMERS
Volume 11, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/polym11050885

Keywords

liquid crystallinity; light induced chirality; photoactive polymers; azobenzene; cinnamate ester

Funding

  1. Ministerio de Economia y Competitividad of Spain [MAT2017-84838-P]
  2. Fondo Europeo de Desarrollo Regional (FEDER)
  3. Gobierno de Aragon of Spain

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This paper describes the synthesis, thermal characterization and optical properties of liquid crystalline homopolymers and block copolymers with a repeating unit consisting of two functional units, with at least one of them being an azobenzene. Films of these polymers have been irradiated with circularly polarized light at room temperature, evaluating the intensity of the photoinduced chiral signal and its temporal stability upon storage. The paper also explores two different strategies to restrict the relaxation of the photoinduced order. Firstly, block copolymers have been prepared to confine the photoaddressable segments into nanoscopic domains where relaxation should be restricted. Secondly, an alternative homopolymer has been synthesized where the repeating unit combines two chromophores that can be separately photoaddressed, an azobenzene unit to efficiently photoinduce chirality and a cinnamate to fix the chiral signal by photocrosslinking.

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