TY - JOUR
T1 - Photoelectron spectroscopy of biologically active molecules 12 benzene‐containing amides
AU - Klasinc, L.
AU - Novak, I.
AU - SabljiĆ, A.
AU - Mcglynn, S. P.
AU - Klasinc, L.
PY - 1986
Y1 - 1986
N2 - The Hel photoelectron spectra of benzamide (1), 2‐hydroxybenzamide (salicylamide, 2), N‐phenylacetamide (acetanilide, 3), N‐(4‐hydroxyphenyl) acetamide (paracetamol, 4), and N‐(4‐ethoxyphenyl) acetamide (phenacetine, 5) have been recorded and analyzed. A tactical approach similar to the composite molecule analysis of benzoic acid derivatives (T. Meeks, A. Wahlborg and S. P. McGlynn, J. Electron Spectrosc. 22, 43 (1981) was used to determine the electronic structure of 1–5. The interaction of the benzene ring with the amidic group and the role of the benzenoid moiety in the biological activity of these compounds is emphasized.
AB - The Hel photoelectron spectra of benzamide (1), 2‐hydroxybenzamide (salicylamide, 2), N‐phenylacetamide (acetanilide, 3), N‐(4‐hydroxyphenyl) acetamide (paracetamol, 4), and N‐(4‐ethoxyphenyl) acetamide (phenacetine, 5) have been recorded and analyzed. A tactical approach similar to the composite molecule analysis of benzoic acid derivatives (T. Meeks, A. Wahlborg and S. P. McGlynn, J. Electron Spectrosc. 22, 43 (1981) was used to determine the electronic structure of 1–5. The interaction of the benzene ring with the amidic group and the role of the benzenoid moiety in the biological activity of these compounds is emphasized.
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U2 - 10.1002/qua.560300824
DO - 10.1002/qua.560300824
M3 - Article
AN - SCOPUS:84987159659
SN - 0020-7608
VL - 30
SP - 251
EP - 260
JO - International Journal of Quantum Chemistry
JF - International Journal of Quantum Chemistry
IS - 13 S
ER -