Pregled bibliografske jedinice broj: 102576
Molecular self-assembling of nitro derivatives of 2-oxo1-naphthaldimine via C-H'''O intermolecular hydrogen bonds
Molecular self-assembling of nitro derivatives of 2-oxo1-naphthaldimine via C-H'''O intermolecular hydrogen bonds // Abstracts, Volume II / Larsen, S (ur.).
Ženeva: IUCr, 2002. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 102576 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Molecular self-assembling of nitro derivatives of 2-oxo1-naphthaldimine via C-H'''O intermolecular hydrogen bonds
Autori
Pavlović, Gordana ; Popović, Zora ; Roje, Vibor ; Leban, Ivan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts, Volume II
/ Larsen, S - Ženeva : IUCr, 2002
Skup
XIX Congress and General Assembly of the International Union of Crystallography
Mjesto i datum
Ženeva, Švicarska, 06.08.2002. - 15.08.2002
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
ketoamino/enolimino tautomers; C-H'''O intermolecular hydrogen bonds; polymorphism
Sažetak
Schiff bases of type Ar-CH=N-Ar derivated from 2-hydroxy-1-naphthaldehyde and m-nitro (1) and p-nitro aniline (2) are prepare by template condensation. Compounds 1 and 2 exist in the solid state as the cis-quinoid (or ketoamino) tautomers characterized by strong, resonance assisted hydrogen bond of the N-H'''O type.
Izvorni jezik
Engleski
Znanstvena područja
Kemija