Polyamines. I. Spectroscopic properties of N,N-bis-(phthalimidopropyl)-N-propylamine and supramolecular interactions in its crystals
[ 1 ] Instytut Chemii i Elektrochemii Technicznej, Wydział Technologii Chemicznej, Politechnika Poznańska | [ P ] pracownik
2006
artykuł naukowy
angielski
- N.N-bis-(phthalimidopropyl)-N-propylamine
- X-ray diffraction
- B3LYP calculations
- FTIR
- Raman
- NMR spectra
EN A new derivative of polyamine, N,N-bis-(phthalimidopropyl)-N-propylamine (1) has been synthesized and its structure studied by X-ray diffraction, FTIR, Raman, 1H and 13C NMR spectroscopies. The B3LYP and DFT calculations have been carried out. The molecular structure of N,N-bis-(phthalimidopropyl)-N-propylamine (1) presents the first case of a folded conformation for this group of compounds which is stabilized by an intramolecular hydrogen bond C–H/O. Neither C–H/p, p/p or CaO/CaO interactions operate in this case. Also the supramolecular structure is stabilized by weak C–H/O and C–H/p hydrogen bonds. The optimized bond lengths as well as bond angles for 1 calculated by B3LYP/6-31G(d,p) approach are compared with the X-ray data. The screening constants for 13C and 1H atoms have been calculated by the GIAO/B3LYP/6-31G(d,p) approach and analyzed. Linear correlations between the experimental 1H and 13C chemical shifts and the computed screening constants have been obtained.
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