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• W2061738230 abstract "We have optimized the geometry and calculated interaction energies for over 100 different complexes of CO(2) with various combinations of electron accepting (Lewis acid) and electron donating (Lewis base) molecules. We have used the recently developed explicitly correlated coupled cluster singles doubles and perturbative triples [CCSD(T)-F12] methods and the associated VXZ-F12 (where X = D,T,Q) basis sets. We observe only modest changes in the geometric parameters of CO(2) upon complexation, which suggests that the geometry of CO(2) adsorbed in a nanoporous material should be similar to that of CO(2) in gas phase. When CO(2) forms a complex with two Lewis acids via the two electron rich terminal oxygen atoms, the interaction energy is less than twice what would be expected for the same complex involving a single Lewis acid. We consider a series of complexes that exhibit simultaneous CO(2)-Lewis acid and CO(2)-Lewis base intermolecular interactions, with total interaction energies spanning 14.1-105.9 kJ mol(-1). For these cooperative complexes, we find that the total interaction energy is greater than the sum of the interaction energies of the constituent complexes. Furthermore, the intermolecular distances of the cooperative complexes are contracted as compared to the constituent complexes. We suggest that metal-organic-framework or similar nanoporous materials could be designed with adsorption sites specifically tailored for CO(2) to allow cooperative intermolecular interactions, facilitating enhanced CO(2) adsorption." @default.
• W2061738230 created "2016-06-24" @default.
• W2061738230 creator A5018764358 @default.
• W2061738230 creator A5054034571 @default.
• W2061738230 date "2011-08-11" @default.
• W2061738230 modified "2023-09-27" @default.
• W2061738230 title "Quantifying cooperative intermolecular interactions for improved carbon dioxide capture materials" @default.
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• W2061738230 doi "https://doi.org/10.1063/1.3624363" @default.
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