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<dc:creator>Calabrese ., Camilla</dc:creator>
<dc:creator>Li, Weixing</dc:creator>
<dc:creator>Prampolini, Giacomo</dc:creator>
<dc:creator>Evangelisti, Luca</dc:creator>
<dc:creator>Uriarte, Iciar</dc:creator>
<dc:creator>Cacelli, Ivo</dc:creator>
<dc:creator>Melandri, Sonia</dc:creator>
<dc:creator>Cocinero, Emilio José</dc:creator>
<dc:date>2019</dc:date>
<dc:description>Rotational spectra of several difluoromethane–water&#xd;
adducts have been observed using two broadband chirpedpulse&#xd;
Fourier-transform microwave (CP-FTMW) spectrometers.&#xd;
The experimental structures of (CH2F2)···(H2O)2,&#xd;
(CH2F2)2···(H2O), (CH2F2)···(H2O)3, and (CH2F2)2···(H2O)2&#xd;
were unambiguously identified with the aid of 18 isotopic&#xd;
substituted species. A subtle competition between hydrogen,&#xd;
halogen, and carbon bonds is observed and a detailed analysis&#xd;
was performed on the complex network of non-covalent&#xd;
interactions which stabilize each cluster. The study shows that&#xd;
the combination of stabilizing contact networks is able to&#xd;
reinforce the interaction strength through a cooperative effect,&#xd;
which can lead to large stable oligomers.</dc:description>
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<dc:identifier>https://uvadoc.uva.es/handle/10324/74588</dc:identifier>
<dc:language>eng</dc:language>
<dc:title>A General Treatment to Study Molecular Complexes Stabilized by Hydrogen‐, Halogen‐, and Carbon‐Bond Networks: Experiment and Theory of (CH2F2)n⋅⋅⋅(H2O)m</dc:title>
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