Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-10T06:46:49.679Z Has data issue: false hasContentIssue false

12 - Dissociation of van der Waals molecules

Published online by Cambridge University Press:  15 December 2009

Reinhard Schinke
Affiliation:
Max-Planck-Institut für Strömungsforschung, Göttingen, Germany
Get access

Summary

Van der Waals molecules are complexes held together by the weak longrange forces between closed-shell atoms and/or molecules, i.e., electrostatic forces, dispersive forces, hydrogen bonding, and charge transfer interactions (Van der Avoird, Wormer, Mulder, and Berns 1980; Buckingham, Fowler, and Hutson 1988). Typical examples are X … I2, X … IC1, X … Cl2, X … HF, HF … HF with X being He, Ne, Ar, etc. The dots indicate the weak physical bonding in contrast to a strong chemical bonding.

The main characteristics of van der Waals molecules are:

  1. 1) The small dissociation energy ranging from a few cm−1 to about 1000 cm−1.

  2. 2) The relatively large bond length, Re, of typically 4 Å.

  3. 3) The retention of the properties of the individual entities within the van der Waals complex.

  4. 4) Relatively weak coupling between the van der Waals mode and the internal coordinates of the molecular entity.

Owing to the small dissociation energy, van der Waals molecules exist mainly at very low temperatures as they prevail in the interstellar medium or in supersonic jets.

Van der Waals molecules are rather floppy complexes which can be best described by the usual Jacobi coordinates which we used throughout all previous chapters (see the inset of Figure 12.1): the van der Waals bond distance R, the intramolecular separation of the chemically bound molecule r, and the orientation angle γ. Figure 12.1 depicts the R dependence of a typical potential energy surface (PES) V(R, r, γ) for fixed values of r and γ. The long-range part of the potential is attractive and governed by the forces mentioned above.

Type
Chapter
Information
Photodissociation Dynamics
Spectroscopy and Fragmentation of Small Polyatomic Molecules
, pp. 293 - 313
Publisher: Cambridge University Press
Print publication year: 1993

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×