Essentials of Computational Chemistry provides a balanced introduction to this dynamic subject. Suitable for both experimentalists and theorists, a wide range of samples and applications are included drawn from all key areas. The book carefully leads the reader thorough the necessary equations providing information explanations and reasoning where necessary and firmly placing each equation in context.
Since publication of the first edition I have become increasingly, painfully aware of just
how short the half-life of certain ‘Essentials’ can be in a field growing as quickly as is
computational chemistry. While I utterly disavow any hubris on my part and indeed blithely
assign all blame for this text’s title to my editor, that does not detract from my satisfaction at
having brought the text up from the ancient history of 2001 to the present of 2004. Hopefully,
readers too will be satisfied with what’s new and improved.
So, what is new and improved? In a nutshell, new material includes discussion of docking,
principal components analysis, force field validation in dynamics simulations, first-order
perturbation theory for relativistic effects, tight-binding density functional theory, electronegativity
equalization charge models, standard-state equilibrium constants, computation of pKa
values and redox potentials, molecular dynamics with implicit solvent, and direct dynamics.
With respect to improved material, the menagerie of modern force fields has been restocked
to account for the latest in new and ongoing developments and a new menagerie of density
functionals has been assembled to help the computational innocent navigate the forest of
acronyms (in this last regard, the acronym glossary of Appendix A has also been expanded
with an additional 64 entries). In addition, newly developed basis sets for electronic structure
calculations are discussed, as are methods to scale various theories to infinite-basis-set limits,
and new thermochemical methods. The performances of various more recent methods for the
prediction of nuclear magnetic resonance chemical shifts are summarized, and discussion of
the generation of condensed-phase potentials of mean force from simulation is expanded.
