Evoking Photothermy by Capturing Intramolecular Bond Stretching Vibration-Induced Dark-State Energy

ACS Nano. 2020 Apr 28;14(4):4265-4275. doi: 10.1021/acsnano.9b09625. Epub 2020 Mar 17.

Abstract

Development of highly effective approaches to desirable photothermal conversion agents is particularly valuable. Herein, we report a concept, namely, bond stretching vibration-induced photothermy, that serves as a mechanism to construct advanced photothermal conversion agents. As a proof-of-concept, two compounds (DCP-TPA and DCP-PTPA) with donor-acceptor (D-A) structures were synthesized. The bond stretching vibration of the pyrazine-containing unit in these molecules is vigorous and insensitive to the external environmental restraint, which efficiently transforms the absorbed photons to dark-state heat energy. The nanoparticles (NPs) of DCP-TPA and DCP-PTPA show rather high photothermal conversion efficiency (52% and 59%) and stronger photoacoustic (PA) signal than commercial methylene blue and reported high-performance semiconducting polymer nanoparticles. The DCP-PTPA NPs perform better than DCP-TPA NPs in terms of photothermal conversion, PA signal production, and in vivo PA tumor imaging because of the increased bond stretching vibration in the former molecule.

Keywords: intramolecular bond stretching vibration; near-infrared absorption; photoacoustic tumor imaging; photothermal conversion; pyrazine-containing electron acceptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Nanoparticles*
  • Photoacoustic Techniques*
  • Phototherapy
  • Polymers
  • Vibration

Substances

  • Polymers