GaussView

GaussView is an affordable, full-featured graphical user interface for Gaussian. With GaussView you can construct molecular systems of interest quickly and efficiently using its molecule building facility. You can also use it to set up and run Gaussian calculations and to visualize a variety of results.

GaussView incorporates an excellent molecule builder for rapidly building even very large molecules:

  • Build molecules by atom, ring, group and amino acid.
  • Import molecules from other sources by simply opening them.
  • You can also add hydrogens automatically to structures originating from PDB files with excellent reliability.
  • Rotate even very large molecules in three dimensions.

GaussView includes easy-to-use graphical interfaces for even the most complicated Gaussian input types: defining ONIOM layers, specifying unit cells for Periodic Boundary Conditions calculations, selecting orbitals for CASSCF calculations (see the lower left dialog in the illustration), and the like.

Gaussian jobs can be launched from within the user interface, and the calculation results can be examined when it finishes.

GaussView can visualize a variety of different Gaussian results, including:

  • Optimized structures.
  • Molecular orbitals.
  • Electron densities, electrostatic potentials and other surfaces.
  • IR and Raman spectra and the associated normal modes.
  • Animated geometry optimization, IRC and trajectory results.

Visualizing Molecules & Reactions with GaussView

The picture on the right side is a close up of a proton transfer IRC animation in nonheme iron enzyme isopenicillin N synthase (IPNS). This 5368-atom system was studied with the ONIOM method in Gaussian, and the results were visualized in GaussView. For illustration clarity, hydrogen atoms in the low layer are omitted from display in both the close up and full molecule views. The ONIOM high accuracy layer is visualized in ball-and-stick format; the low accuracy layer is visualized in wire frame format in the close up view and in tube format in the whole molecule view.
Reference: M. Lundberg, T. Kawatsu, T. Vreven, M. J. Frisch and K. Morokuma, JCTC 5 (2009) 222.

The second picture illustrtates a selected a molecular orbitals from a Gaussian calculation on U(II)2(COT)2. Each U(II)COT monomer has 4 U valence electrons available for metal-metal bonding: 2 electrons in f s-type MOs and 2 unpaired electrons in f d-type MOs. Beginning at the upper left and moving clockwise, the MOs visualized in GaussView are the LUMO, HOMO, and the second-lowest and next-lowest energy MOs below the HOMO; all have D8h symmetry.
Reference: J. Zhou, J. Sonnenberg and H. B. Schlegel, in preparation.

The last picture shows a Fe2S2 cluster with phenylthiolates—an open shell singlet system with charge -2—set up for a Gaussian fragment guess calculation to model antiferromagnetic coupling. Each iron atom and bridging sulfur atom is placed in its own fragment, and each phenylthiolate similarly defines a fragment, resulting in a total of eight fragments. The individual charge and spin multiplicity values for each fragment have been labeled in the illustration, and GaussView will place these values into the route section for the Gaussian job automatically.

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