In:
Israel Journal of Chemistry, Wiley, Vol. 33, No. 4 ( 1993-01), p. 369-385
Kurzfassung:
NMR chemical shift calculations provide the basis for an intensive collaboration between quantum chemists and experimentalists. Calculated shift data can be used to describe the magnetic properties of a molecule, to identify unknown compounds by comparison of experimental and theoretical shift values, to determine equilibrium geometries, to investigate conformational changes, to elucidate the mechanism of molecular rearrangements, to determine solvent effects on NMR data, to identify complexation or coordination of soluted molecules by solvent molecules, to detect electronic structure changes caused by the medium, and to describe chemical bonding. This is demonstrated by three examples, namely the determination of the equilibrium structure of the homotropylium cation, the description of BH 3 NH 3 in solution or condensed phases, and the investigation of stannyl cation complexes in solution. IGLO calculations of 13 C, 11 B, 15 N, and 119 Sn chemical shifts with DZ+P or TZ+P basis sets lead to the following results: (1) The homotropylium cation possesses an equilibrium 1,7 distance of 2 Å that is indicative of strong through‐space interactions and, as a consequence, homoaromatic character. (2) In solution, the charge transfer from NH 3 to BH 3 is increased, which leads to a decrease of the BN bond length, an increase of the dipole moment, and a shielding of both the B and the N nucleus. The experimental δ( 11 B) and δ( 15 N) values can be reproduced when the geometry effect and the direct solvent effect are included in the shift calculations. (3) Stannyl cations form strongly‐bounded coordination complexes with solvent molecules (binding energy: ≥ 50 kcal/mol) that make the cation properties, in particular δ( 119 Sn) values, similar to those of covalently‐bounded stannyl compounds. An experimental detection of stannyl cations in solution by NMR spectroscopy should only be possible by extensive solvent variations.
Materialart:
Online-Ressource
ISSN:
0021-2148
,
1869-5868
DOI:
10.1002/ijch.199300045
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
1993
ZDB Id:
2066481-3
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