Pregled bibliografske jedinice broj: 1258338
Crystallization and structural transformations of ternary copper(II) coordination compounds with 1,10-phenanthroline and glycine
Crystallization and structural transformations of ternary copper(II) coordination compounds with 1,10-phenanthroline and glycine // 28th Croatian-Slovenian Crystallographic Meeting
Poreč, Hrvatska, 2022. str. 34-34 (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1258338 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Crystallization and structural transformations of
ternary copper(II) coordination
compounds with 1,10-phenanthroline and glycine
Autori
Vušak, Darko ; Štriga, Silvija ; Prugovečki, Biserka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
28th Croatian-Slovenian Crystallographic Meeting
/ - , 2022, 34-34
Skup
28th Croatian-Slovenian Crystallographic Meeting
Mjesto i datum
Poreč, Hrvatska, 07.09.2022. - 11.09.2022
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
copper(II), 1, 10-phenanthroline, glycine structural transformations
Sažetak
Ternary coordination compounds of copper(II) with amino acids and chelating heterocyclic bases have been investigated for several decades due to their pronounced antitumor activity [1]. These compounds are interesting in crystal engineering since they have the ability to form predictive supramolecular motifs through non-covalent interactions, such as π-interactions and hydrogen bonds. However, systematic research of different solvatomorphs has been reported only in a few research articles [2–4]. Our group is also interested in exploring the properties of such compounds, i.e.stability of crystals in the solid state and their ability to absorb water molecules or other solvents [2, 3]. As a part of our research, we report the solution- based and mechanochemical syntheses and crystal structures of five ternary coordination compounds of copper(II), 1, 10- phenanthroline (phen) and glycine (HGly) with water and methanol as solvent. Different crystallization experiments with a very small difference in the amount of water (less than 1% of volume fraction) resulted in different solvatomorphs crystallizing. Water content in reactants was crucial for the formation of certain solvatomorphs in mechanochemical syntheses. All compounds contain crystallization solvent molecules forming pockets and/or infinite channels (1D or 2D). Stability and solid-state transformations in atmospheres of methanol vapors or different relative humidity were also investigated (Figure 1).
Izvorni jezik
Engleski
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb