Anisotropy of chemical shift and J coupling for P-31 and Se-77 in trimethyl and triphenyl phosphine selenides

被引:22
作者
Grossmann, G
Potrzebowski, MJ
Fleischer, U
Krüger, K
Malkina, OL
Ciesielski, W
机构
[1] Tech Univ Dresden, Inst Analyt Chem, D-01062 Dresden, Germany
[2] Polish Acad Sci, Ctr Mol & Macromol Studies, PL-90362 Lodz, Poland
[3] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
[4] Univ Arkansas, Dept Chem, Fayetteville, AR 72701 USA
[5] Slovak Acad Sci, Ctr Comp, SK-84235 Bratislava, Slovakia
[6] Slovak Acad Sci, Inst Inorgan Chem, SK-84235 Bratislava, Slovakia
基金
美国国家科学基金会;
关键词
chemical shift tensors; J coupling tensor; phosphorus-31; selenium-77; trimethylphosphine selenide; triphenylphosphine selenide;
D O I
10.1016/S0926-2040(98)00077-0
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
The (31)P and (77)Se magic angle spinning (MAS) nuclear magnetic resonance (NMR) experiments for selenium-77 enriched (70%) trimethylphosphine selenide 1 and triphenylphosphine selenide 2 were carried out in order to determine the nuclear magnetic shielding tensors of both nuclei and to establish values of the phosphorus-selenium indirect spin-spin coupling anisotropy Delta J. The m = +1/2 and m = - 1/2 subspectra were analysed by the dipolar-splitting-ratio method of Eichele and Wasylischen. For the C(s) molecule 1, Delta J was obtained to be +640 +/- 260 Hz from the (31)P spectrum and + 550 +/- 140 Hz from the (77)Se spectrum. Density functional theory (DFT) calculations give a Delta J value of about + 705 Hz. The value of Delta J could not be determined unambiguously by analysis of the (31)P spectra for the C(1) molecules 2; nevertheless, an estimation of Delta J was possible. The principal axis 3 of the phosphorus shielding tensor was determined to be nearly parallel to the PSe bond in 1 and 2. For the selenium shielding of 1, the same orientation was found, whereas in 2, the principal axis 2 of the selenium shielding was found to be oriented nearly along the PSe bond. The experimentally determined phosphorus nuclear magnetic shielding tensors agree well with those calculated by the IGLO method. For those two principal values of the selenium-shielding tensors corresponding to directions nearly perpendicular to the SeP bend, the agreement between calculated and experimental values is satisfactory. For the third one, corresponding to the principal axis close to the SeP bond, the calculated deshielding contributions are distinctly too small for both compounds investigated. Trends observed for the calculated molecular orbital (MO) contributions to the shielding as well as possible reasons for the underestimation of the deshielding contributions along the SeP bond are discussed. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:71 / 85
页数:15
相关论文
共 45 条
[1]   Se-77 shielding tensors of diphenyl diselenide, comparison of the results from CP/MAS NMR spectroscopy and IGLO calculations [J].
Balzar, G ;
Duddeck, H ;
Fleischer, U ;
Rohr, F .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1997, 357 (05) :473-476
[2]   ACCURATE COMPUTATIONS OF SE-77 NMR CHEMICAL-SHIFTS WITH THE GIAO-CCSD METHOD [J].
BUHL, M ;
GAUSS, J ;
STANTON, JF .
CHEMICAL PHYSICS LETTERS, 1995, 241 (03) :248-252
[3]  
BUHL M, 1995, J PHYS CHEM-US, V99, P4000
[4]   A comparison of models for calculating nuclear magnetic resonance shielding tensors [J].
Cheeseman, JR ;
Trucks, GW ;
Keith, TA ;
Frisch, MJ .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (14) :5497-5509
[5]   CRYSTAL-STRUCTURE STUDIES OF GROUP-V CHALCOGENIDE COMPOUNDS .3. TRIPHENYLPHOSPHINE SELENIDE [J].
CODDING, PW ;
KERR, KA .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1979, 35 (MAY) :1261-1263
[6]   ANISOTROPY OF THE 1J(PSE) SPIN-SPIN COUPLING - X-RAY AND LIQUID-CRYSTAL NMR-STUDY OF SE=P(CH3)3 [J].
COGNE, A ;
GRAND, A ;
LAUGIER, J ;
ROBERT, JB ;
WIESENFELD, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (07) :2238-2242
[7]   SOLID-STATE P-31 NMR AND X-RAY CRYSTALLOGRAPHIC STUDIES OF TERTIARY PHOSPHINES AND THEIR DERIVATIVES [J].
DAVIES, JA ;
DUTREMEZ, S ;
PINKERTON, AA .
INORGANIC CHEMISTRY, 1991, 30 (10) :2380-2387
[8]   THE DIPOLAR-SPLITTING-RATIO METHOD - A CONVENIENT APPROACH TO THE ANALYSIS OF DIPOLAR-CHEMICAL-SHIFT NMR-SPECTRA OF STATIC POWDER SAMPLES [J].
EICHELE, K ;
WASYLISHEN, RE .
JOURNAL OF MAGNETIC RESONANCE SERIES A, 1994, 106 (01) :46-56
[9]  
EICHELE K, 1993, COMPUTER PROGRAM DIP
[10]  
ELLIS PD, 1993, NATO ADV SCI INST SE, V386, P539