A fully relativistic Dirac–Hartree–Fock and second-order Mo” ller–Plesset study of the lanthanide and actinide contraction

نویسنده

  • J. K. Laerdahl
چکیده

Fully relativistic four-component self-consistent field and correlated calculations at the Mo”ller– Plesset second-order perturbation theory level ~MP2! have been performed for the monofluorides and monoand trihydrides of lanthanum, lutetium, actinium, and lawrencium. The calculated spectroscopic constants are in good agreement with available experimental data. The calculated bond lengths have been compared with values from nonrelativistic calculations to give an estimate of the effect of relativity on the molecular lanthanide and actinide contraction. The calculated lanthanide contraction at the relativistic MP2 level is 0.12, 0.12, and 0.19 Å for the monohydrides, monofluorides, and trihydrides, respectively. The corresponding results for the actinides are 0.20, 0.15, and 0.28 Å, and we demonstrate that the larger size of the actinide contraction is a consequence of relativistic effects. Between 10% and 30% of the lanthanide contraction and between 40% and 50% of the actinide contraction is caused by relativity in these compounds. © 1998 American Institute of Physics. @S0021-9606~98!30348-7#

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Mo” ller–Plesset convergence issues in computational quantum chemistry

The Hartree–Fock self-consistent-field approximation has provided an invaluable conceptual framework and a standard computational procedure for atomic and molecular quantum theory. Its shortcomings are significant however, and require remediation. Mo”ller–Plesset perturbation theory offers a popular correction strategy: it formally expands eigenfunctions and eigenvalues as power series in a cou...

متن کامل

Relativistic and correlation effects on molecular properties . I

The additivity of relativistic and electron correlation effects has long been questioned. Until recently few methods were available to quantitatively assess the interplay of both deviations of the nonrelativistic mean-field theory in molecular calculations. The so-called scalar relativistic methods usually assume that corrections of higher order than c can be neglected for chemical accuracy. Fu...

متن کامل

Noncollinear and collinear relativistic density-functional program for electric and magnetic properties of molecules

The quick development of computational methods in Physics and Chemistry nowadays allows us to calculate energies and other properties of atoms, molecules, and small clusters with ab initio methods. In the first place these are ‘‘classical’’ but still very popular methods in quantum chemistry such as the Hartree-~Dirac-!Fock methods @1–3#, configuration interaction, multiconfiguration Dirac-Fock...

متن کامل

Some reasons not to use spin projected density functional theory

Spin unrestricted calculations using density functional theory can yield wave functions with spin contamination. In conventional post Hartree–Fock calculations ~such as Mo”ller–Plesset perturbation theory!, spin projection can ameliorate some of the problems caused by spin contamination. However, spin projection can seriously degrade the quality of potential energy surfaces calculated by densit...

متن کامل

electric-field-induced second harmonic generation ~ESHG! vibrational second hyperpolarizability of CF4. With the exception of the small ESHG vibrational second hyperpolarizability the infinite optical frequency method

The frequency-dependent vibrational second hyperpolarizability of CH42nFn molecules with n 50 – 4 has been computed for the most common nonlinear optical ~NLO! processes by adopting the perturbation approach due to Bishop and Kirtman @J. Chem. Phys. 95, 2646 ~1991!#. These calculations have been performed by using the Sadlej atomic basis set with the Hartree-Fock technique as well as with the M...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 1998