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Title

Beryllium bonds, do they exist?

AuthorsYáñez, M.; Sanz, P.; Mó, O.; Alkorta, Ibon ; Elguero, José
Issue Date2009
PublisherAmerican Chemical Society
CitationJournal of Chemical Theory and Computation 5: 2763- 2771 (2009)
AbstractThe complexes between BeX2 (X = H, F, Cl, OH) with different Lewis bases have been investigated through the use of B3LYP, MP2, and CCSD(T) approaches. This theoretical survey showed that these complexes are stabilized through the interaction between the Be atom and the basic center of the base, which are characterized by electron densities at the corresponding bond critical points larger than those found in conventional hydrogen bonds (HBs). Actually, all bonding indices indicate that, although these interactions that we named >beryllium bonds> are in general significantly stronger than HBs, they share many common features. Both interactions have a dominant electrostatic character but also some covalent contributions associated with a non-negligible electron transfer between the interacting subunits. This electron transfer, which in HBs takes place from the HB acceptor lone-pairs toward the σYH* antibonding orbital of the HB donor, in beryllium bonds goes from the lone pairs of the Lewis base toward the empty p orbital of Be and the σBeX* antibonding orbital. Accordingly, a significant distortion of the BeX2 subunit, which in the complex becomes nonlinear, takes place. Concomitantly, a significant red-shifting of the X-Be-X antisymmetric stretching frequencies and a significant lengthening of the X-Be bonds occur. The presence of the beryllium bond results in a significant blue-shifting of the X-Be-X symmetric stretch. © 2009 American Chemical Society.
URIhttp://hdl.handle.net/10261/65545
DOI10.1021/ct900364y
Identifiersdoi: 10.1021/ct900364y
issn: 1549-9618
e-issn: 1549-9626
Appears in Collections:(IQM) Artículos
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