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Esters are key components in CO 2 -based solvents and reactions, yet their microscopic interactions with CO 2 remain poorly defined. Using high-resolution rotational spectroscopy combined with quantum-chemical analysis, we directly observed how CO 2 binds and organizes around methyl formate, the simplest ester. Three dimer isomers were detected, revealing competing carbonyl- and ether-based binding motifs with population ratios of 87:10:3. As more CO 2 molecules attach, they form a cage-like network that progressively encapsulates the carbonyl site. Remarkably, a single water molecule can replace CO 2, forming cooperative H 2 O ··· CO 2 interactions and redirecting the aggregation pathway. By bridging binary and ternary clusters, this work establishes the first direct insights for ester–CO 2 recognition and demonstrates how the delicate balance between dispersion-biased encapsulation and hydrogen bonding competition by water dictates molecular organization, offering a molecular-level framework for understanding solvation, selectivity, and reactivity in CO 2 -rich environments.
Tian et al. (Tue,) studied this question.