Lipid-Inspired Low Melting Ionic Liquids via Synergistic Cyclopropanation and Branching of Terpenoids
Muhammadiqboli Musozoda1, Richard A O'Brien2, Zachary J Metott1
1Department of Chemistry, State University of New York at Oswego, Oswego, New York 13126, United States.
Abstract:
Bacteria employ cyclopropane motifs as bioisosteres for unsaturations to modulate lipid bilayer fluidity and protect cellular membranes under environmental stress. Drawing inspiration from this biological strategy, we investigated how cyclopropanation impacts the thermophysical properties of lipid-inspired ionic liquids. We synthesized a series of imidazolium-based ionic liquids incorporating cyclopropanated derivatives of three renewable terpenoids: phytol, farnesol, and geraniol. Through an integrated approach combining property-driven design, thermophysical analysis, X-ray crystallography, and computational modeling, we systematically examined how these structural modifications influence quantitative structure-property relationships. Our findings demonstrate that ionic liquids with long alkyl appendages respond to side-chain modificationsparticularly the synergistic combination of cyclopropanation and branchingin a manner that mimics homeoviscous adaptation in living organisms. The strategic incorporation of cyclopropyl moieties combined with chiral methyl branching produced dramatic melting point depressions, with phytol-derived ionic liquids achieving the lowest melting points reported to date for these bioinspired materials. This effectiveness results from positioning these structural elements within the symmetry-breaking region of alkyl chains, where they maximally disrupt molecular packing and enhance fluidity. X-ray crystallographic analysis of a cyclopropanated citronellyl-based ionic liquid revealed that the cyclopropyl ring induces significant conformational distortions that prevent efficient molecular organization. The use of terpenoids from the chiral pool as starting materials imparts inherent sustainability to these ILs. Enantiopure ILs can be synthesized from renewable feedstocks like phytol and citronellol while exploiting bioinspired structural design principles. This work provides new insights into IL structure-property relationships that both complement and extend previous discoveries, establishing a framework for the rational design of lipidic ionic liquid systems with enhanced fluidity and chemical stability from renewable resources.
More Related Videos
06:44From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Thermal Activation
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: Overview
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Biosynthesis of Lipids
