Spectroscopic analysis reveals stronger hydrogen bonding in 1,8-cineole than other common ethers, indicating high solvent-solute interaction strength.
A study of the concentration dependence of the proton resonance signal of chloroform due to solvent-solute hydrogen bonding has indicated that 1,8-cineole is an appreciably stronger hydrogen bonding agent than is tetrahydrofuran, dioxane or diethyl ether. Comparisons were based on the magnitude of the difference between the positions of the chloroform resonance in the limits of dilute and concentrated solutions.
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Edwin Paul Swatek (2026) studied this question.
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