Noncovalent interactions strength

Noncovalent interactions such as van der Waals, hydrogen bonding, n-n stacking and electrostatic interactions have been widely used to hybridize pristine nanocarbons via ex situ approaches. The major advantage of this route is that the nanocarbons do not require modification prior to hybridization and their structure remains undisturbed, an important factor in many electronic applications. The strength of hybridization is weaker compared to covalent interactions but the synthetic process is generally simpler. Noncovalent attachment of small molecules to nanocarbons is often used to change the surface chemistry for subsequent ex situ or in situ hybridization. 

The term bioadhesion ean be defined as the ability of a material (synthetic or natural) to stick (adhere) to a biological tissue for extended periods of time [27]. The phenomenon of bioadhesion can be visualized as a two-step process. The first step involves the initial contaet between polymer and the biological tissue. The second step is the formation of seeondary bonds due to noncovalent interactions. The strength of bioadhesion (expressed as the foree of detachment) for a novel oligosaccharide gum Hakea Gibbosa) contained in a buccal tablet developed by Alur et al. [28,29]... 

Analysis of supramolecular structures in ionic liquids Supramolecular assemblies are the molecular base for some of the unique properties of ILs. Therefore, the knowledge of the nature, type, and strength of these structures [23] is a prerequisite for a deeper understanding of ILs as well as for the tailor-made design of new compounds. The most important noncovalent interactions responsible for the formation of such a structure are C-H hydrogen bonds [25]. Other interactions encompass the formation of clusters by ion pairing, which can be found, for example, in chloroaluminates [12]. 

Noncovalent interactions between the two separate molecules define, in the gas phase analogue of this reactive system, the preferential channels of approach (in the simpler cases there is just one channel leading to the reaction) with shape and strength determined only by these interactions. As a general rule, these channels carry the reactants to a stationary point on the potential energy surface called the initial reaction complex. 

The use of biomacromolecules and artificial variants thereof as hosts for homogeneous catalysts, linked by noncovalent bonds, was first implemented in the 1970s recently, this field has attracted enormous attention. The biomacromolecules are used specifically to induce chirality into catalysts for well-known reactions. Linking by noncovalent interactions is more easily achieved than linking by covalent bonding—and these interactions need not imply that the link is weak the strengths of the bonds vary enormously. For example, the avidin-biotin bond is much stronger than most supramolecular bonds considered in this context. As yet, the interest in this field is merely scientific, and applications are not anticipated in the near future. 

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