The vibrational and NMR spectra, conformations and ab initio calculations of aminomethylene, propanedinitrile and itsN-methyl derivatives

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The IR and Raman spectra of aminomethylene propanedinitrile (AM) [H2N-CH=C(CN)2], (methylamino)methylene propanedinitrile (MAM) [CH3NH-CH=C(CN)2] and (dimethylamino)methylene propanedinitrile (DMAM) [(CH3)2N-CH=C(CN)2] as solids and solutes in various solvents have been recorded in the region 4000-50 cm−1. AM and DMAM can exist only as one conformer. From the vibrational and NMR spectra of MAM in solutions, the existence of two conformers with the methyl group orientedanti andsyn toward the double C=C bond were confirmed. The enthalpy difference δH 0 between the conformers was measured to be 3.7±1.4 kJ mol−1 from the IR spectra in acetonitrile solution and 3.4±1.1 kJ mol−1 from the NMR spectra in DMSO solution. Semiempirical (AM1, PM3, MNDO, MINDO3) and ab initio SCF calculations using a DZP basis set were carried out for all three compounds. The calculations support the existence of two conformersanti andsyn for MAM, withanti being 7.8 kJ mol−1 more stable thansyn from ab initio and 8.6, 13.4, 11.6, and 10.8 kJ mor−1 from AM1, PM3, MNDO, and MINDO3 calculations, respectively. Finally, complete assignments of the vibrational spectra for all three compounds were made with the aid of normal coordinate calculations employing scaled ab initio force constants. The same scale factors were optimized on the experimental frequencies of all three compounds, and a very good agreement between calculated and experimental frequencies was achieved.