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Implicit Solvation Models

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Title: Implicit Solvation Models


1
Implicit Solvation Models
Computational Chemistry 5510 Spring 2006 Hai Lin
2
Solvent Effects
  • Many reactions take place in solution
  • Short-range effects
  • Typically concentrated in the first solvation
    sphere
  • Examples H-bonds, preferential orientation near
    an ion
  • Long-range effects
  • Polarization (charge screening)

3
Two Kinds of Solvatin Models
4
Self-Consistent Reaction Field
  • Solvent A uniform polarizable medium with a
    dielectric constant e
  • Solute A molecule in a suitably shaped cavity in
    the medium
  • Solvation free energy

DGsolv DGcav DGdisp DGelec
M
e
  • Create a cavity in the medium costs energy
    (destabilization).
  • Dispersion (mainly Van der Waals) interactions
    between solute and solvent lower the energy
    (stabilization).
  • Polarization between solute and solvent induces
    charge redistribution until self-consistent and
    lowers the energy (stabilization).

5
We need to know ...
  • How to define the size and shape of the cavity?
  • How to claculate the cavity and dispersion
    contributions?
  • How to represent the charge distribution of the
    solute?
  • How to describe the solute (e.g., classically or
    quantum mechanically)?
  • How the dielectic medium is described?

6
The Cavity
  • Simple models

Ellipsoid
Sphere
  • Molecular shaped models

Not accessible to solvent
Van der Waals surface
Solvent accessible surface
Determined by QM wave function and/or electron
density
7
Cavity Dispersion Contributions
  • Create a cavity
  • Change in entropy
  • Loss of slovent-solvent VDW interactions.
  • Add the solute into the cavity
  • Gain of solute-solvent VDW interactions
  • The energy change is often empirically given as

DGcav DGdisp Si xiSi
xi is a parameter for the i-th atom and depends
on the atom type, and Si is the surface of the
i-th atom as defined in the previous slide.
8
Describe the Solute Solvent
  • Represent the solute
  • Classical description (force field)
  • Quantum description (semi-empirical, DFT, ab
    initio)
  • Charge distribution of the solute
  • Force field point charges
  • QM calculation derived point charges
  • Multipole expansions
  • Represent the solvent
  • Uniform medium with dielectric constant e
  • Sometimes e is made distance-dependent or
    frequency-dependent

e
9
Charge Density on Surface
  • Determined by the dielectric constant e and the
    electric field F generated by charges in the
    cavity

F
s
4pe s(rs) (e 1) F(rs)
rs
  • Born Model
  • A point charge q in a spheric cavity
  • Generalized Born Model
  • A set of point charges in a spheric cavity
  • Onsager Model
  • A dipole m in a spheric cavity
  • Kirkwood Model
  • A general multipole expansion in a spheric cavity
  • Kirkwood-Westheimer Model
  • A general multipole expansion in a ellipsoidal
    cavity

10
Models with Molecular Shaped Cavity
  • Charge distribution on the cavity surface must be
    solved numerically.
  • Polarizable continuum model (PCM)
  • Conductor-like screening model (COSMO)
  • Solvation model (SMx, x 1, 2, ..., 5)
  • Generalized Born/Surface Area (GB/SA) model
  • Generally found that the molecular shape is
    important
  • Accuracy is difficult to systematically improve.
  • In favorable cases, accuracy can reach a few
    kcal/mol.

11
Mixed Solvation Model
  • The first solvation sphere is explicitly
    described by a number of solvent molecules.
  • The remaining solvent molecules are described by
    an uniform continuum medium with a dielectric
    constant.
  • Advantage
  • Account for specific short-range effects (e.g.,
    H-bonding).
  • Disadvantage
  • Increase computational cost.
  • Generally give substantial better results than
    pure continuum models.

e
12
Which Model should I Use?
  • A compromise between accuracy and cost.
  • Start with gas-phase model (without solvent)
    before you go for solvation models. Gas-phase
    calculations usually help to understand the
    quantum nature of the problem under study. Yet
    sometimes gas-phase models can be qualitatively
    wrong.
  • Try continuum models before you go for explicit
    models. Continuum model calculations are unlikely
    to give you very accurate results, but they are
    informative in suggesting whether or not
    long-range solvation effects are important.
  • Try mixed models before you go for explicit
    models. Mixed models are relatively easy to
    handle and much less expensive, with possibly
    reasonably good results.

Continuum
Mixed
Explicit
Gas-phase
Realisitic description computational cost
13
Summary
  • Solvation Effects
  • Short-range effects
  • Long-range effects
  • Self-consistent reaction field
  • Cavity
  • Dispersion
  • Polarization
  • Solvation models
  • Explicit models
  • Implicit (continuum) models
  • Mixed models

14
Your Homework
  • Read the slides.
  • Read textbook (Take notes when you read.)
  • 16.3
  • Questions
  • What are the short-range and long-range solvation
    effects?
  • How to calculate the free energy change for
    solvation?
  • What is a solvent accessible surface?
  • What is the difference between the Born model and
    the Onsage model?
  • What are the differences between explicit,
    continuum, and mixed solvation models? Which
    model do you like?
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