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dc.contributor.authorCalabrese, Camilla
dc.contributor.authorLi, Weixing
dc.contributor.authorPrampolini, Giacomo
dc.contributor.authorEvangelisti, Luca
dc.contributor.authorUriarte, Iciar
dc.contributor.authorCacelli, Ivo
dc.contributor.authorMelandri, Sonia
dc.contributor.authorCocinero, Emilio José
dc.date.accessioned2025-01-29T14:21:21Z
dc.date.available2025-01-29T14:21:21Z
dc.date.issued2019
dc.identifier.citationAngew.Chem. Int.Ed. 2019, 58, 8437 – 8442es
dc.identifier.issn1433-7851es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/74588
dc.description.abstractRotational spectra of several difluoromethane–water adducts have been observed using two broadband chirpedpulse Fourier-transform microwave (CP-FTMW) spectrometers. The experimental structures of (CH2F2)···(H2O)2, (CH2F2)2···(H2O), (CH2F2)···(H2O)3, and (CH2F2)2···(H2O)2 were unambiguously identified with the aid of 18 isotopic substituted species. A subtle competition between hydrogen, halogen, and carbon bonds is observed and a detailed analysis was performed on the complex network of non-covalent interactions which stabilize each cluster. The study shows that the combination of stabilizing contact networks is able to reinforce the interaction strength through a cooperative effect, which can lead to large stable oligomers.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleA General Treatment to Study Molecular Complexes Stabilized by Hydrogen‐, Halogen‐, and Carbon‐Bond Networks: Experiment and Theory of (CH2F2)n⋅⋅⋅(H2O)mes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1002/anie.201902753es
dc.identifier.publicationfirstpage8437es
dc.identifier.publicationissue25es
dc.identifier.publicationlastpage8442es
dc.identifier.publicationtitleAngewandte Chemie International Editiones
dc.identifier.publicationvolume58es
dc.peerreviewedSIes
dc.identifier.essn1521-3773es
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones


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