A Self-locked β-Cyclodextrin-rhodamine B Spirolactam with Photoswitching Properties

Chem Asian J. 2022 Jan 17;17(2):e202101282. doi: 10.1002/asia.202101282. Epub 2021 Dec 8.

Abstract

Supramolecular organization and self-assembly are the pillars of functionality of many nanosystems. The covalent conjugate (6-spirolactam rhodamine B-6-monodeoxy)-β-cyclodextrin (Rho-βCD) is assembled as a self-included, rigid nanostructure, identical in the crystal and in aqueous solution, as revealed by detailed X-ray and NMR analyses. Rho-βCD self-assembly is the result of an interesting reaction pathway, which partially de-aggregates Rho and disturbs the zwitterion↔spirolactone equilibrium. Rho-βCD is stable at pH 4.6, but displays controllable photoswitching between the colored, fluorescent, zwitterionic and the colorless, non-fluorescent closed structures, during several iterative cycles. After an initial drop in absorbance, the on-off process continues without further changes under our irradiation conditions, a consequence of the specific self-locked arrangement of Rho in the cavity. Rho-βCD exemplifies a water soluble photoresponsive nanosystem with improved photostability suggesting promising applications in super resolution bioimaging.

Keywords: Host-guest systems; NMR; Rhodamine spirolactam; aggregation; crystal structure; cyclodextrins; photoswitching; self-assembly.

MeSH terms

  • Magnetic Resonance Spectroscopy
  • Rhodamines
  • Water
  • beta-Cyclodextrins*

Substances

  • Rhodamines
  • beta-Cyclodextrins
  • Water
  • rhodamine B