Magnitude of Finite-Nucleus-Size Effects in Relativistic Density Functional Computations of Indirect NMR Nuclear Spin-Spin Coupling Constants

被引:68
作者
Autschbach, Jochen [1 ]
机构
[1] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
基金
美国国家科学基金会;
关键词
density functional calculations; finite nuclei; NMR spectroscopy; nuclear spin-spin coupling; spin-orbit coupling; ORDER REGULAR APPROXIMATION; HYPERFINE-STRUCTURE; SHIELDING CONSTANTS; PERTURBATION-THEORY; COMPLEXES; TENSORS; MODEL; PARAMETERS; DEPENDENCE; CHEMISTRY;
D O I
10.1002/cphc.200900271
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A spherical Gaussian nuclear charge distribution model has been implemented for spin-free (scalar) and two-component (spin-orbit) relativistic density functional calculations of indirect NMR nuclear spin-spin coupling (J-coupling) constants. The finite nuclear volume effects on the hyperfine integrals are quite pronounced and as a consequence they noticeably alter coupling constants involving heavy NMR nuclei such as W, Pt, Hg, Tl, and Pb. Typically, the isotropic J-couplings are reduced in magnitude by about 10 to 15% for couplings between one of the heaviest NMR nuclei and a light atomic ligand, and even more so for couplings between two heavy atoms. For a subset of the systems studied, viz. the Hg atom, Hg(2)(2+), and Tl-X where X = Br, I, the basis set convergence of the hyperfine integrals and the coupling constants was monitored. For the Hg atom, numerical and basis set calculations of the electron density and the 1s and 6s orbital hyperfine integrals are directly compared. The coupling anisotropies of TlBr and TII increase by about 2% due to finite-nucleus effects.
引用
收藏
页码:2274 / 2283
页数:10
相关论文
共 58 条
[1]   Toward reliable density functional methods without adjustable parameters: The PBE0 model [J].
Adamo, C ;
Barone, V .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (13) :6158-6170
[2]  
AKAI H, 1990, PROG THEOR PHYS SUPP, P11, DOI 10.1143/PTPS.101.11
[3]   Finite nuclear charge density distributions in electronic structure calculations for atoms and molecules [J].
Andrae, D .
PHYSICS REPORTS-REVIEW SECTION OF PHYSICS LETTERS, 2000, 336 (06) :413-525
[4]   The accuracy of hyperfine integrals in relativistic NMR computations based on the zeroth-order regular approximation [J].
Autschbach, J .
THEORETICAL CHEMISTRY ACCOUNTS, 2004, 112 (01) :52-57
[5]   Double perturbation theory: a powerful tool in computational coordination chemistry [J].
Autschbach, J ;
Ziegler, T .
COORDINATION CHEMISTRY REVIEWS, 2003, 238 :83-126
[6]   A theoretical study of the large Hg-Hg spin-spin coupling constants in Hg22+, Hg32+, and Hg22+-crown ether complexes [J].
Autschbach, J ;
Igna, CD ;
Ziegler, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (16) :4937-4942
[7]   Nuclear spin-spin coupling constants from regular approximate relativistic density functional calculations. I. Formalism and scalar relativistic results for heavy metal compounds [J].
Autschbach, J ;
Ziegler, T .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (03) :936-947
[8]   Nuclear spin-spin coupling constants from regular approximate relativistic density functional calculations. II. Spin-orbit coupling effects and anisotropies [J].
Autschbach, J ;
Ziegler, T .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (21) :9410-9418
[9]  
Autschbach J., 2002, ENCY NUCL MAGNETIC R, V9, P306
[10]  
Autschbach J., 2004, Calculation of NMR and EPR Parameters