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Chemical Compounds
Chemical Compounds

... S Think of your molecular structure diagrams. Can you draw ...
Organometallic Chemistry at the Magnesium− Tris (8
Organometallic Chemistry at the Magnesium− Tris (8

... which is inconsistent with relative first ionization energies for the two metals (7.64 and 4.34 eV, respectively), upon which the ion pair model is based.3 It is also contrary to prediction.4 We propose that the trend in core level binding energy changes for N(1s) and the opposite one for O(1s) and ...
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... (c) (4 marks) Explain the difference between hydrolysis and hydration of a metal ion. Illustrate your answer with an appropriate example. 1 (a) Answer In group 13-17, in 4th 5th and 6th periods – ns2 electroms are much harder to remove than expected (i.e. they are “inert”). (these elements are less ...
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... In the present work thermochemistry of intermolecular interactions of organic compounds in solutions of imidazolium based ionic liquids (ILs) has been studied using solution calorimetry method. Enthalpies of solution at infinite dilution of non-polar (alkanes, aromatic hydrocarbons) and polar (alcoho ...
Intermolecular Forces
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... hydrogen bonded to one another, and these strong interactions account for the unusually high boiling point of water compared to other simple liquids and many of the other anomalous features of water. The strengths of most hydrogen bonds are ~2-10kcal/mol. However, in most of the applications we will ...
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... hydrogen bonded to one another, and these strong interactions account for the unusually high boiling point of water compared to other simple liquids and many of the other anomalous features of water. The strengths of most hydrogen bonds are ~2-10kcal/mol. However, in most of the applications we will ...
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... molecular recognition properties of molecules. Bringing two or more molecules together results in preferences for particular orientations that can lead to particular reactivity or expressed properties. These resultant structures are highly dependent on amongst other factors: - solvent - temperature ...
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... as donor-acceptor molecular pairs, since the introduction of the supramolecular interaction may have an influence on the molecule-substrate interaction. The accurate understanding of the intermolecular and molecule-substrate interactions, as well as of the interplay among them, is therefore a fundam ...
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... A hydrogen bond is an attractive interaction between two species that arises from a link of the form A–H · · B , where A and B are highly electronegative elements and B possesses a lone pair of electrons. It is conventionally regarded as being limited to N, O, and F, but if B is an ionic species (su ...
Fundamental Interactions: 6 Forces
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... - the electromagnetic interaction: binds electrons to nucleus, binds atoms to molecules, responsible for all chemistry and biology, acts in electron-positron annihilation, time scale lies between strong and weak interaction, interaction is mediated by the photon, acts primarily between charged parti ...
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... van der Waals Forces Between Macroscopic Objects The van der Waals forces between two macroscopic bodies can be calculated (as approximation) by integrating over the molecular / atom-atom vdW pair potential ( w(r) = -C / r6) of all molecules / atoms in one body with all molecules / atoms in the oth ...
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< 1 ... 4 5 6 7 8

Cation–pi interaction



Cation–π interaction is a noncovalent molecular interaction between the face of an electron-rich π system (e.g. benzene, ethylene, acetylene) and an adjacent cation (e.g. Li+, Na+). This interaction is an example of noncovalent bonding between a monopole (cation) and a quadrupole (π system). Bonding energies are significant, with solution-phase values falling within the same order of magnitude as hydrogen bonds and salt bridges. Similar to these other non-covalent bonds, cation–π interactions play an important role in nature, particularly in protein structure, molecular recognition and enzyme catalysis. The effect has also been observed and put to use in synthetic systems.
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