Related Experiment Video
Updated: Jun 6, 2025

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Unbuckling the 18-Crown-6 Ether Belt Around Metal Ions: Forging the Connection to the Condensed Phase
Ryu Sakuma1, Keisuke Hirata1, James M Lisy2,3
1Department of Chemistry, School of Science, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo 152-8550, Japan.
Abstract:
Crown ethers are central to supramolecular chemistry, recognizing and binding specific ions in solution. The most well-known, 18-Crown-6 (18C6), preferentially captures K+ in an aqueous solution, while gas phase binding of 18C6 with alkali metal ions decreases linearly with an increasing ionic radius. Why the high affinity for Li+ and Na+ in the gas phase is dramatically reduced with hydration remains an open question in understanding the K+ selectivity in the aqueous phase. A combined spectroscopic and computational study of M+18C6(H2O) (M = Li, Na, and K) in the CH stretch region has revealed how stepwise hydration unbuckles the crown ether belt from Li+ and Na+, substantially changing the backbone structure of 18C6. In contrast, the structure of the K+18C6 complex is unbuckled and is unaffected by hydration. Combined with new measurements of the OH stretch, a direct connection is provided between the stepwise hydration of M+18C6 and the selectivity for K+ in an aqueous solution. It demonstrates and validates at the molecular level the application of gas-phase measurements to condensed-phase studies.
Related Concept Videos
Crown Ethers
Physical Properties of Ethers
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
Autoxidation of Ethers to Peroxides and Hydroperoxides
Mass Spectrometry: Molecular Fragmentation Overview
One type of fragmentation pattern is the cleavage of a single bond in the molecular ion. The cleavage leads to a radical and a cation. The cleavage can...

