Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 22, Issue 28, Pages 16421-16430Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cp02697b
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Funding
- University of Bristol
- Ministerio de Ciencia, Innovacion y Universidades of Spain [PGC2018-094644-B-C22]
- Comunidad de Madrid [P2018/EMT-4329 AIRTEC-CM]
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The alkali-metal bonds formed by simple molecules LiR and NaR (R = F, H or CH3) with each of the six Lewis bases B = OC, HCN, H2O, H3N, H2S and H3P were investigated byab initiocalculations at the CCSD(T)/AVTZ and CCSD(T)/awCVTZ levels of theory with the aim of characterising this type of non-covalent interaction. In some complexes, two minima were discovered, especially for those involving the NaR. The higher-energy minimum (referred to as Type I) for a given B was found to have geometry that is isomorphous with that of the corresponding hydrogen-bonded analogue BMIDLINE HORIZONTAL ELLIPSISHF. The lower-energy minimum (when two were present) showed evidence of a significant secondary interaction of R with the main electrophilic region of B (Type II complexes). EnergiesDCBSe for dissociation of the complexes into separate components were found to be directly proportional to the intermolecular stretching force constantksigmaThe value ofDCBSe could be partitioned into a nucleophilicity of B and an electrophilicity of LiR or NaR, with the orderELiHgreater than or similar to ELiF=ELiCH3for the LiR andENaF>ENaHapproximate to ENaCH3for the NaR. For a given B, the order of the electrophilicities isELiR>ENaR, which presumably reflects the fact that Li+is smaller than Na+and can approach the Lewis base more closely. A SAPT analysis revealed that the complexes BMIDLINE HORIZONTAL ELLIPSISLiR and BMIDLINE HORIZONTAL ELLIPSISNaR have larger electrostatic contributions toDethan do the hydrogen- and halogen-bonded counterparts BMIDLINE HORIZONTAL ELLIPSISHCl and BMIDLINE HORIZONTAL ELLIPSISClF.
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