Supramolecular Design Strategy of a Water-Soluble Diphenylguanidine-Cyclodextrin Polymer Inclusion Complex

Molecules. 2022 Oct 15;27(20):6919. doi: 10.3390/molecules27206919.

Abstract

Diphenylguanidine (DPG) is a widely used secondary accelerator for the vulcanization of natural rubber (NR) latex. However, its low water solubility and high toxicity limit its use in high-end NR products. In this study, a water-soluble inclusion complex of DPG and a β-cyclodextrin polymer (β-CDP), termed DPG-β-CDP, was prepared through supramolecular interactions and characterized using Fourier-transform infrared spectroscopy, 1H NMR, scanning electron microscopy, and UV-vis spectroscopy techniques. In comparison with that of DPG, the water solubility of DPG-β-CDP was greatly enhanced because of the water-soluble host molecule. The molar ratio of DPG to the CD unit in β-CDP was determined to be 1:1. At 25 °C, the binding constant of DPG-β-CDP was found to be 9.2 × 105 L/mol by UV-vis spectroscopy. The proposed method for forming inclusion complexes with high potential for use as water-soluble vulcanization accelerators is promising.

Keywords: characterization; cyclodextrin polymer; diphenylguanidine; inclusion complex; solubility.

MeSH terms

  • Calorimetry, Differential Scanning
  • Latex
  • Polymers / chemistry
  • Rubber*
  • Solubility
  • Spectroscopy, Fourier Transform Infrared
  • Water* / chemistry
  • X-Ray Diffraction

Substances

  • cyclodextrin polymer
  • diphenylguanidine
  • Latex
  • Polymers
  • Rubber
  • Water