Pregled bibliografske jedinice broj: 1084004
Multiple crystalline forms of 1,5- bis(salicylidebne)carbohydrazide
Multiple crystalline forms of 1,5- bis(salicylidebne)carbohydrazide // 24. Congress of Chemists and Technologists of Macedonia : Book of Abstracts
Skopje: Society of Chemists and Technologists of Macedonia, 2016. str. 302-302 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Multiple crystalline forms of 1,5-
bis(salicylidebne)carbohydrazide
Autori
Rubčić, Mirta ; Galić, Nives ; Halasy, Ivan ; Jednačak, Tomislav ; Judaš, Nenad ; Plavec, Janez ; Šket, Primož ; Novak, Predrag
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
24. Congress of Chemists and Technologists of Macedonia : Book of Abstracts
/ - Skopje : Society of Chemists and Technologists of Macedonia, 2016, 302-302
Skup
24. Congress of Chemists and Technologists of Macedonia
Mjesto i datum
Ohrid, Sjeverna Makedonija, 11.09.2016. - 14.09.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Carbohydrazide ; Schiff base ; polymorphism ; thermal reactivity
Sažetak
Carbohydrazide, as a higher urea homologue, offers a versatile platform for tailoring Schiff bases, either mono- or bis-substituted ones. Over the years, such systems have been recognized as supreme multitopic ligands for the construction of extended metal-organic architectures, but also as functional molecules for e.g. selective anion binding. Reactions of salicylaldehyde and carbohydrazide afforded, depending on the synthetic procedure and crystallization conditions, mono(salicylidene)carbohydrazide and a diver¬sity of crystalline forms of 1, 5- bis(salicylidene)carbohydrazide: three polymorphs and two solvates. All crystalline forms of 1, 5-bis(salicylidene)carbohydrazide comprise the same tautomer of the title compound. As established via X-ray crystallography, IR spectroscopy, and CP MAS NMR its salicylidene residues adopt the enol- imino form while the carbamide fragment is in all cases found in the keto form. Conformations of 1, 5-bis(salicylidene)carbohydrazide molecules and their hydrogen-bonding patterns are similar for two polymorphs while the third one in this context significantly differs. All solid phases of 1, 5- bis(salicylidene)carbohydrazide undergo complicated degradation upon heating, yielding salicylideneazine, CO2, and N2 either directly or via intermediates as established by thermal analyses. In addition, relative phase stability was inspected mechanochemically and by solvent- mediated experiments.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Tomislav Jednačak
(autor)
Nenad Judaš
(autor)
Mirta Rubčić
(autor)
Predrag Novak
(autor)
Nives Galić
(autor)