Back to chapter

11.3:

Intermoleculaire Krachten

JoVE Core
Química
É necessária uma assinatura da JoVE para visualizar este conteúdo.  Faça login ou comece sua avaliação gratuita.
JoVE Core Química
Intermolecular Forces

Idiomas

COMPARTILHAR

Intermoleculaire krachten, die tussen moleculen bestaan, zijn afkomstig van elektrostatische interacties tussen ladingen, gedeeltelijke ladingen en tijdelijke ladingen. Alle moleculen produceren tijdelijke ladingen. Vanwege de variërende verdeling van elektronen, resulteert een hogere elektronendichtheid in een gebied van de elektronenwolk in een instantane dipool of een tijdelijke dipool.Dit induceert vervolgens een andere instantane dipool in het naburige molecuul. Het domino-effect van dipolen veroorzaakt zwakke intermoleculaire aantrekkingskrachten, dispersiekrachten genaamd, die tussen alle moleculen bestaan, of ze nu polair of niet-polair zijn. Sommige covalente verbindingen, zoals water, vertonen bijvoorbeeld elektronenrijke en elektronenarme gebieden die worden veroorzaakt door de verschillen in elektronegativiteit van de atomen.De ongelijke verdeling van gedeelde elektronen en de moleculaire vorm van de verbinding creëren permanente partiële ladingen, wat resulteert in een permanente dipool in de verder neutrale verbinding, waardoor deze polair wordt. Moleculen met permanente dipolen ook wel polaire verbindingen genoemd richten zich op elkaar via dipool-dipoolkrachten, waarbij het positieve uiteinde van één molecuul elektrostatisch in wisselwerking staat met het negatieve uiteinde van het naburige molecuul. Als een polaire verbinding een waterstofatoom bevat dat covalent is gebonden aan een klein, sterk elektronegatief atoom zoals fluor, zuurstof of stikstof, hebben de atomen de neiging grotere partiële ladingen te vertonen.Bijgevolg werkt het waterstofatoom in F-H-O-H-of N-H-bindingen sterk samen met het elektronegatieve atoom op zijn buur door een speciaal type dipool-dipoolkracht, een waterstofbrug genaamd. Met name waterstofbruggen zijn sterker dan dipool-dipoolkrachten, en verbindingen die waterstofbruggen kunnen vormen, vertonen hogere smelt-en kookpunten. De drie intermoleculaire krachten dispersie, dipool dipool en waterstofbruggen zijn, in vergelijking met intramoleculaire krachten, relatief zwak, met verschillende sterktes.Ze worden gezamenlijk geclassificeerd als Vanderwaalskrachten. Hoewel er verspreidingskrachten aanwezig zijn tussen alle moleculen, polair of niet-polair, bestaan dipool-dipoolkrachten en waterstofbruggen alleen rond polaire moleculen. Exclusief voor oplossingen is de ion-dipoolkracht, de sterkste intermoleculaire kracht.Wanneer een ionische verbinding zoals natriumchloride wordt opgelost in een polair oplosmiddel zoals water, interageren de gedissocieerde ionen met de dipolen van het oplosmiddel via sterke ion-dipoolkrachten. Hier associëren de kationen zich met de negatieve uiteinden van de watermoleculen, terwijl de anionen een interactie aangaan met de positieve uiteinden.

11.3:

Intermoleculaire Krachten

Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are iondipole, dipoledipole, hydrogen bonds, and dispersion; among these, dipoledipole, hydrogen bonds, and dispersion forces exist between neutral atoms and molecules and are collectively known as van der Waals forces.

Dipole–dipole forces

Polar molecules have a partial positive charge on one end and a partial negative charge on the other end of the molecule—a separation of charge called a dipole. In a polar molecule like HCl, the more electronegative Cl atom bears the partial negative charge, whereas the less electronegative H atom bears the partial positive charge. An attractive force between HCl molecules results from the attraction between the positive end of one HCl molecule and the negative end of another. This attractive force is called a dipoledipole attraction—the electrostatic force between the partially positive end of one polar molecule and the partially negative end of another.

Dispersion Forces

One of the three van der Waals forces is present in all condensed phases, regardless of the nature of the atoms or molecules composing the substance. This attractive force is called the London dispersion force in honor of German-born American physicist Fritz London who, in 1928, first explained it. This force is often referred to as simply the dispersion force. Because the electrons of an atom or molecule are in constant motion (or, alternatively, their location is subject to quantum-mechanical variability), at any moment in time, an atom or molecule can develop a temporary, instantaneous dipole if its electrons are distributed asymmetrically. The presence of this dipole can, in turn, distort the electrons of a neighboring atom or molecule, producing an induced dipole. These two rapidly fluctuating, temporary dipoles thus result in a relatively weak electrostatic attraction between the species—a so-called dispersion force.

Dispersion forces that develop between atoms in different molecules can attract the two molecules to each other. The forces are relatively weak, however, and become significant only when the molecules are very close. Larger and heavier atoms and molecules exhibit stronger dispersion forces than do smaller and lighter atoms and molecules. F2 and Cl2 are gases at room temperature (reflecting weaker attractive forces); Br2 is a liquid, and I2 is a solid (reflecting stronger attractive forces).

Hydrogen Bonding

Nitrosyl fluoride (ONF, molecular mass 49 amu) is a gas at room temperature, whereas water (H2O, molecular mass 18 amu) is a liquid, even though it has a lower molecular mass. Both molecules have about the same shape, and ONF is the heavier and larger molecule. It is, therefore, expected to experience more significant dispersion forces. Additionally, this difference in boiling points cannot be the result of differences in the dipole moments of the molecules. Both molecules are polar and exhibit comparable dipole moments. The large difference between the boiling points is due to a particularly strong dipoledipole attraction that may occur when a molecule contains a hydrogen atom bonded to a fluorine, oxygen, or nitrogen atom (the three most electronegative elements). The very large difference in electronegativity between the H atom (2.1) and the atom to which it is bonded (4.0 for a F atom, 3.5 for an O atom, or 3.0 for a N atom), combined with the very small size of a H atom and the relatively small sizes of F, O, or N atoms, leads to highly concentrated partial charges with these atoms. Molecules with F-H, O-H, or N-H moieties are very strongly attracted to similar moieties in nearby molecules, a particularly strong type of dipoledipole attraction called hydrogen bonding. Examples of hydrogen bonds include HF⋯HF, H2O⋯HOH, and H3N⋯HNH2, in which the hydrogen bonds are denoted by dots.

 Ion–dipole forces

An iondipole force is the electrostatic attraction between an ion and a dipole. These forces are common in solutions and play an important role in the dissolution of ionic compounds in water.

When an ionic compound like KCl is added to a polar solvent like water, the ions in the solid separate and disperse uniformly. Iondipole forces attract the positive (hydrogen) end of the polar water molecules to the negative chloride ions at the surface of the solid, and they attract the negative (oxygen) ends to the positive potassium ions. The water molecules surround individual K+ and Cl ions, reducing the strong interionic forces that bind the ions together (in a solid) and letting them move off into solution as solvated ions. Overcoming the electrostatic attraction permits the independent motion of each hydrated ion in a dilute solution as the ions transition from fixed positions in the undissolved compound to widely dispersed, solvated ions in solution.

The strength of iondipole interactions is directly proportional to i) the charge on the ion and ii) the magnitude of the dipole of polar molecules.

This text is adapted from Openstax, Chemistry 2e, Chapter 10: Liquids and Solids.