Analysis of Aromatic Delocalization: Individual Molecular Orbital Contributions to Nucleus-Independent Chemical Shifts

Individual MO (MO) contributions to the magnetic shielding of atoms as well as to the nucleus-independent chem. shifts (NICS) of arom. compds. can be computed by the widely used gauge-including AO (GIAO) method. Detailed analyses of magnetic shielding MO-NICS contributions provide interpretive insights that complement and extend those given by the localized MO ("dissected NICS", LMO-NICS) method. Applications to (4n + 2) pi-electron systems, ranging from [n] annulenes to Dnh S3, S5, and N6H62+ rings as well as to D2h cyclobutadiene, show the extent to which their diatropic character results from the sigma framework and from the pi orbitals. The diatropicity of both these contributions decreases with the no. of nodes of the wave function around the ring. The highest-energy orbitals can become paratropic. This is generally the case with the sigma orbitals, but is found only for "electron-rich" pi systems such as sulfur rings. MO-NICS contributions, which can be interpreted using London-H.ovrddot.uckel theory, correlate with inverse ring size. [on SciFinder (R)]

Published in:
Journal of Physical Chemistry A, 107, 33, 6470-6475
CAN 139:276486
Physical Organic Chemistry
Institute of Physical Chemistry and Electrochemistry,TU Dresden,Dresden,Germany.
written in English.
71-43-2 (Benzene); 293-96-9 (Cyclodecane); 1724-43-2 (Cyclopropyl cation); 12597-03-4 Role: CPS (Chemical process), PEP (Physical, engineering or chemical process), PRP (Properties), PROC (Process) (ab initio on aromaticity of individual MO contributions to nucleus-independent chem. shifts)

 Record created 2007-10-22, last modified 2018-03-17

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