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The entropy of mixing provides information about constitutive differences of intermolecular forces or specific molecular effects in the materials.

The HF molecules, with a short H–F bond of 95"nbsp;pm, are linked to neighboring molecules by intermolecular H–F distances of 155 pm.

Additional strong intermolecular bonding occurs between these phenyllithium dimers and the π-electrons of the phenyl groups in the adjacent dimers, resulting in an infinite polymeric ladder structure.

In ideal materials, intermolecular forces are the same between every pair of molecular kinds, so that a molecule feels no difference between other molecules of its own kind and of those of the other kind.

Specifically, the process through which intermolecular reactions forward and amplify extracellular signals across the cell surface has developed to occur by two mechanisms.

Macroscopic hardness is generally characterized by strong intermolecular bonds, but the behavior of solid materials under force is complex; therefore, there are different measurements of hardness: scratch hardness, indentation hardness, and rebound hardness.

Kutzelnigg has published papers on various topics in quantum chemistry: methods of treating electron correlation, magnetic properties of molecules (especially chemical shift), relativistic quantum chemistry, theory of chemical bonding and theory of intermolecular forces.

This molecule has been detected in the interstellar medium, where molecules are so dilute that intermolecular collisions are unimportant.

This quadruple bond is also confirmed by the low magnetic moment and short intermolecular distance between the two atoms of 236.

Although a diatomic molecule, HF forms relatively strong intermolecular [bond]s.

Alternatively, the reaction begins with an intermolecular condensation and subsequent formation of the imine intermediate.

In non-ideal materials, there may be differences of intermolecular forces or specific molecular effects between different species, even though they are chemically non-reacting.

By orienting the molecule in such a way that the two reactive alkenes are in close proximity, the risk of intermolecular cross-metathesis is minimized.

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