Abstract

Novel dual-functionalized ammonium-based hydrophobic ionic liquids (ILs) have been synthesized by mimicking the water structure to carry both ether group (hydrogen-bond acceptor) and tert-alcohol group (hydrogen-bond donor). These ammonium-type ionic solvents exhibit the advantage of lower viscosities (as low as 129 mPa s at 30 °C) than the imidazolium analogue (∼300 mPa s at 30 °C); more importantly, these “water-like” media are highly compatible with immobilized Candida antarctica lipase B (Novozym 435) in terms of producing high transesterification activities (1.5-fold higher than that in tert-butanol, and slightly higher than that in diisopropyl ether) and higher thermal stability than that in tert-butanol. To demonstrate the utilization of this new solvent system, enzymatic ring-opening polymerization (ROP) of ε-caprolactone using these “water-like” ILs as co-solvents was carried out to synthesize polyesters, achieving high molecular mass Mw (up to 18,000 Da) and high yields (up to 74 %).

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call