Wavefunctions derived from experiment. I. Motivation and theory

被引:189
作者
Jayatilaka, D [1 ]
Grimwood, DJ [1 ]
机构
[1] Univ Western Australia, Dept Chem, Nedlands, WA 6907, Australia
来源
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES | 2001年 / 57卷
关键词
D O I
10.1107/S0108767300013155
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An experimental wavefunction is one that has an assumed form and that is also fitted to experimental measurements according to some well defined procedure. In this paper, the concept of extracting wavefunctions from experimental data is critically examined and past efforts are reviewed. In particular, the importance of scattering experiments for wavefunction fitting schemes is highlighted in relation to the more familiar model, the Hamiltonian paradigm. A general and systematically improvable method for fitting a wavefunction to experimental data is proposed. In this method, the parameters in a model wavefunction are determined according to the variational theorem but subject to an imposed constraint that an agreement statistic between the calculated and observed experimental data has a certain acceptable value. Advantages of the method include the fact that any amount of experimental data can be used in the fitting procedure irrespective of the number of parameters in the model wavefunction, the fact that a unique answer is obtained for a given choice of the model wavefunction, and the fact that the method can be used to model different experiments simultaneously. The wavefunction fitting method is illustrated by developing the theory for extracting a single-determinant wavefunction for a fragment of a molecular crystal, using data obtained from elastic X-ray scattering data. Effects due to thermal motion of the nuclei, secondary extinction of the X-ray scattering and different choices for the crystal fragment are treated.
引用
收藏
页码:76 / 86
页数:11
相关论文
共 89 条
[1]   On the possibility of kinetic energy density evaluation from the experimental electron-density distribution [J].
Abramov, YA .
ACTA CRYSTALLOGRAPHICA SECTION A, 1997, 53 :264-272
[2]   Application of DFT and EMS to the study of strained organic molecules [J].
Adcock, W ;
Brunger, MJ ;
Michalewicz, MT ;
Winkler, DA .
AUSTRALIAN JOURNAL OF PHYSICS, 1998, 51 (04) :707-728
[3]   THE CRYSTAL ELECTRON-ENERGY AND COMPTON PROFILE CALCULATIONS FROM X-RAY-DIFFRACTION DATA [J].
ALEKSANDROV, YV ;
TSIRELSON, VG ;
REZNIK, IM ;
OZEROV, RP .
PHYSICA STATUS SOLIDI B-BASIC SOLID STATE PHYSICS, 1989, 155 (01) :201-207
[4]  
[Anonymous], 1982, Molecular vibrational-rotational spectra
[5]   EMPIRICAL MOLECULAR-HYDROGEN WAVE-FUNCTION MODELED FROM THEORETICALLY DERIVED X-RAY-DIFFRACTION DATA [J].
BOEHME, RF ;
LAPLACA, SJ .
PHYSICAL REVIEW LETTERS, 1987, 59 (09) :985-987
[6]   CRYSTALLOGRAPHIC R-FACTOR REFINEMENT BY MOLECULAR-DYNAMICS [J].
BRUNGER, AT ;
KURIYAN, J ;
KARPLUS, M .
SCIENCE, 1987, 235 (4787) :458-460
[7]  
CassamChenai P, 1996, INT J QUANTUM CHEM, V60, P667, DOI 10.1002/(SICI)1097-461X(1996)60:2<667::AID-QUA5>3.0.CO
[8]  
2-V
[9]   ENSEMBLE REPRESENTABLE DENSITIES FOR ATOMS AND MOLECULES .1. GENERAL-THEORY [J].
CASSAMCHENAI, P .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 1995, 54 (04) :201-210
[10]  
CLINTON WL, 1973, INT J QUANTUM CHEM, P505