Issue 8, 2015

Insight into the role of intermolecular interactions on the enhanced solubility of fluorinated epoxide oligomers in supercritical CO2

Abstract

A prominent enhancement in solubility of epoxide oligomers in supercritical CO2 (scCO2) was definitively accomplished via fluorination. The fluorinated epoxide oligomers (FEO) exhibited incredibly low transition pressure (PT) as compared with a library of other epoxide oligomers. For determining the nature of the observed special affinity of the FEO to CO2, the detailed solvation behaviors of 14 epoxide oligomers in gaseous and supercritical CO2 were investigated using a high-pressure in situ ATR FTIR system as the pressure increased from 0.1 to 40.0 MPa. The key role of the intermolecular interactions on the enhanced solubility of the FEO in scCO2 was established and the major factors impacting the molecular interplay between the epoxide oligomers and CO2 were systematically evaluated. We attribute the uniquely enhanced solubility of the FEO in scCO2 to the synergistic effects of the increased special attraction between the FEO and CO2, the decreased self-interaction among the FEO and the excellent accessibility of the FEO to CO2. Since the FEO are suggested to be the most soluble species in scCO2, we optimistically believe that the FEO may act as the ideal solubilizing chain after being transplanted or grafted into other targeted molecules and thus can be employed in developing a series of novel fluorinated monomers, ligands/complexes/catalysts and surfactants in a scCO2 system.

Graphical abstract: Insight into the role of intermolecular interactions on the enhanced solubility of fluorinated epoxide oligomers in supercritical CO2

Supplementary files

Article information

Article type
Paper
Submitted
19 May 2015
Accepted
14 Jul 2015
First published
15 Jul 2015

Green Chem., 2015,17, 4489-4498

Author version available

Insight into the role of intermolecular interactions on the enhanced solubility of fluorinated epoxide oligomers in supercritical CO2

G. Zhou, J. Chen, M. Wang, M. Zhang, J. Guo, S. Shen, Z. Liu, Z. Liu, J. Jiang and J. Lu, Green Chem., 2015, 17, 4489 DOI: 10.1039/C5GC01069A

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