A conformational study of aromatic imide compounds. Part 2. Compounds containing diphenyl sulfide, Diphenyl sulfone (cas 127-63-9), and diphenylmethane moieties☆

Add time:09/27/2019    Source:sciencedirect.com

An attempt was made to estimate the dihedral angles, φ, ψ, ω1, and ω2, of bis(4-hydroxyphthalimide)s (BHPI) and bis(phenylphthalimide)s (BPI) having diphenyl sulfide, diphenyl sulfone, or diphenylmethane linkages at the center of molecules using solid–state 13C CP/MAS NMR and ab initio nuclear shielding calculations. The TOSS and TOSS & DD pulse sequences were performed in the NMR measurements to obtain exact chemical shifts of each carbon. Total energies were calculated using the B3LYP/6-31G(d) level of theory, and shielding constants were calculated using the RHF/6-31G(d) level of theory for diphenyl sulfide, diphenyl sulfone, diphenylmethane with varying angles of φ, ψ from 0 to 180° at intervals of 10°. It was clarified that the –S– and –SO2– linkages lead asymmetrical conformations with different ω1 and ω2 or with different φ and ψ for BHPIs and BPIs. In contrast, the compounds having –CH2– linkages have symmetrical conformations. The dihedral angle of imide ring and phenylene ring (ω) are in the range of 40–90°, and the dihedral angles (φ,ψ) distribute in the stable regions of the energy surfaces ranging from 40 to 90°.

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