Efekt kooperatywności oddziaływań iekowalencyjnych w wybranych układach molekularnych stabilizowanych wiązaniami wodorowymi i halogenowymi Cooperativity effect in noncovalent interactions of selected molecular complexes stabilised by hydrogen and halogen bonds
Among various so-called weak interactions, a halogen bond [8 and references
therein] is currently probably one of more explored by researchers. This is due to the
fact that it has several properties in common with the hydrogen bonding, and thus,
similarly as already well characterised H-bond, it may have a crucial role in different
physical, chemical, and biological processes. This bond is formed due to stabilising
interactions between a region of positive charge located on a surface of the halogen
atom and the other atomic center possessing the electron charge surplus (e.g. a lone
pair) [8]. The region of positive charge appears on the halogen atom surface due
to deformation of its electron cloud resulting in its ellipsoidal shape with the short
axis opposite the covalent bond and the long axis in the perpendicular direction
[11]. This results in a particular distribution of local charges on the atomic surface,
as shown in Figure 1. As a consequence the halogen atom may exhibit a dual character,
acting as either electron charge donor or acceptor, depending on the type of
interaction and the direction of the appearing interactomic contact. A good example
of such situation is shown in Figure 2. Thus, one may consider the situation when
two interactions are formed simultaneously and the halogen atom acts as an electron
charge donor and acceptor at the same time. For such situation the synergism
of both interactions may strengthen complexation. In order to analyze that case,
various representative complexes were investigated [13, 17, 18, 20, 21] by means
of many-body interaction approach [5, 6]. In general, it appears that as distinct to
hydrogen bond [2–4], the synergism is rather weak, with some exceptions for iodine
atom due to stronger halogen bonds formed by that atomic centre [13, 17, 18]. In the
case of halo-amine tetramers [21] the additional stabilising effect derived from back
bonding of π type was found – for the first time for a halogen bond.
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