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One-electron Properties (one-electron + property)

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Chemistry100%

Selected Abstracts

Ab initio quality one-electron properties of large molecules: Development and testing of molecular tailoring approach

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 4 2003
K. Babu
Abstract The development of a linear-scaling method, viz. "molecular tailoring approach" with an emphasis on accurate computation of one-electron properties of large molecules is reported. This method is based on fragmenting the reference macromolecule into a number of small, overlapping molecules of similar size. The density matrix (DM) of the parent molecule is synthesized from the individual fragment DMs, computed separately at the Hartree,Fock (HF) level, and is used for property evaluation. In effect, this method reduces the O(N3) scaling order within HF theory to an n·O(N,3) one, where n is the number of fragments and N,, the average number of basis functions in the fragment molecules. An algorithm and a program in FORTRAN 90 have been developed for an automated fragmentation of large molecular systems. One-electron properties such as the molecular electrostatic potential, molecular electron density along with their topography, as well as the dipole moment are computed using this approach for medium and large test chemical systems of varying nature (tocopherol, a model polypeptide and a silicious zeolite). The results are compared qualitatively and quantitatively with the corresponding actual ones for some cases. This method is also extended to obtain MP2 level DMs and electronic properties of large systems and found to be equally successful. © 2003 Wiley Periodicals, Inc. J Comput Chem 24: 484,495, 2003 [source]

Molecular one-electron properties using the multireference Hartree,Fock CI method

INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 13 2008
A. M. C. Sobrinho
Abstract The recently introduced multireference Hartree,Fock configuration interaction (MRHFCI) method has been applied to the calculation of the dipole moment of the LiH, BH, FH, CO, and H2O molecules. The results obtained indicate that MRHFCI wave functions, much more compact but of the same quality of the orthogonal full CI ones, can provide better dipole moments than the corresponding full CI wave functions. The value of the dipole moments obtained with the MRHFCI wave functions is quite insensitive to the choice of the HF references but the same is not true for the electronic energy. Therefore, further studies are necessary to develop a criterion for selecting a set of HF references which could provide the best values of energy and dipole moment. Also, it would be important to verify if other one-electron properties can be computed with the same degree of accuracy obtained for the dipole moments. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2008 [source]

Ab initio quality one-electron properties of large molecules: Development and testing of molecular tailoring approach

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 4 2003
K. Babu
Abstract The development of a linear-scaling method, viz. "molecular tailoring approach" with an emphasis on accurate computation of one-electron properties of large molecules is reported. This method is based on fragmenting the reference macromolecule into a number of small, overlapping molecules of similar size. The density matrix (DM) of the parent molecule is synthesized from the individual fragment DMs, computed separately at the Hartree,Fock (HF) level, and is used for property evaluation. In effect, this method reduces the O(N3) scaling order within HF theory to an n·O(N,3) one, where n is the number of fragments and N,, the average number of basis functions in the fragment molecules. An algorithm and a program in FORTRAN 90 have been developed for an automated fragmentation of large molecular systems. One-electron properties such as the molecular electrostatic potential, molecular electron density along with their topography, as well as the dipole moment are computed using this approach for medium and large test chemical systems of varying nature (tocopherol, a model polypeptide and a silicious zeolite). The results are compared qualitatively and quantitatively with the corresponding actual ones for some cases. This method is also extended to obtain MP2 level DMs and electronic properties of large systems and found to be equally successful. © 2003 Wiley Periodicals, Inc. J Comput Chem 24: 484,495, 2003 [source]