4.8 Article

Heterolytic Bond Cleavage in a Scissile Triarylmethane Mechanophore

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 45, Pages 18859-18863

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c10004

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Funding

  1. Swiss National Science Foundation (SNSF) [20020_172619]
  2. Adolphe Merkle Foundation

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The study introduces a new mechanochromic triarylmethane mechanophore that dissociates through scissile heterolytic pathway and exhibits a pronounced mechanochromic response. This mechanophore can be incorporated as a cross-linker into polymer networks and undergo color change upon compression or tensile deformation.
Covalent mechanophores display the cleavage of a weak covalent bond when a sufficiently high mechanical force is applied. Three different covalent bond breaking mechanisms have been documented thus far, including concerted, homolytic, and heterolytic scission. Motifs that display heterolytic cleavage typically separate according to non-scissile reaction pathways that afford zwitterions. Here, we report a new mechanochromic triarylmethane mechanophore, which dissociates according to a scissile heterolytic pathway and displays a pronounced mechanochromic response. The mechanophore was equipped with two styrenylic handles that allowed its incorporation as a cross-linker into poly(N,N-dimethylacrylamide) and poly(methyl acrylate-co-2-hydroxyethyl acrylate) networks. These materials are originally colorless, but compression or tensile deformation renders the materials colored. By combining tensile testing and in situ transmittance measurements, we show that this effect is related to scissile cleavage leading to colored triarylmethane carbocations.

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