Synthesis, Crystallographic and Spectral Studies of 3-(4-(Phenylamino) Phenylamino)Cyclohex-2-Enone

[ X ]

Tarih

2010

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Springer/Plenum Publishers

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

The title compound, 3-(4-(phenylamino)phenylamino)cyclohex-2-enone, beta- enaminone of 1,3-cyclohexanedione and p-amino diphenylamine (C18H18N2O) was prepared and characterized by H-1-NMR, C-13-NMR, Elemental analysis and IR spectroscopy as well as single crystal X-ray diffraction. These results indicate the predominance of the keto-enol tautomerism. Molecular conformation around the central disubstituted benzene ring is affected by the tautomerism and two steric effects between side molecular groups and mono substituted benzene ring. Electron delocalizations due to these effects have been observed in the molecular structure, the structure being stabilized by some intermolecular hydrogen bonds.

Açıklama

Anahtar Kelimeler

Schiff Base, Beta-Enaminone, Cyclohexanedione, Crystal Structure, Spectroscopic Studies, Tautomerism

Kaynak

Journal of Chemical Crystallography

WoS Q Değeri

Q4

Scopus Q Değeri

Q3

Cilt

40

Sayı

4

Künye