Pregled bibliografske jedinice broj: 576657
Three routes to nickel(II) salicylaldehyde 4-phenyl and 4-methylthiosemicarbazonato complexes: mechanochemical, electrochemical and conventional approach
Three routes to nickel(II) salicylaldehyde 4-phenyl and 4-methylthiosemicarbazonato complexes: mechanochemical, electrochemical and conventional approach // Crystengcomm, 14 (2012), 3039-3045 doi:10.1039/c2ce06611d (međunarodna recenzija, članak, znanstveni)
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Naslov
Three routes to nickel(II) salicylaldehyde 4-phenyl and 4-methylthiosemicarbazonato complexes: mechanochemical, electrochemical and conventional approach
Autori
Cindrić, Marina ; Uzelac, Marina ; Cinčić, Dominik ; Halasz, Ivan ; Pavlović, Gordana ; Hrenar, Tomica ; Ćurić, Manda ; Kovačević, Davor
Izvornik
Crystengcomm (1466-8033) 14
(2012);
3039-3045
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Ni(II) salicylaldehyde 4-phenyl and 4-methyl-thiosemicarbazonato complexes; conventional; electrochemical and mechanochemical synthesis
Sažetak
In the synthesis of Ni(II) salicylaldehyde 4-phenyl and 4-methyl-thiosemicarbazonato complexes conventional, electrochemical and mechanochemical routes were applied and compared. Polynuclear tetrahedral [Ni(sal 4-Metsc)]n (1) and mononuclear square planar [Ni(sal 4-Phtsc)(H2sal 4-Phtsc)]$ CH3OH (2) were obtained by the conventional method. The electrochemical synthesis proved to be a simple and efficient route for the synthesis of brownish-red single crystals of square planar (2) and polycrystalline green octahedral [Ni(Hsal 4-Metsc)2]$(3) complexes, while the liquid-assisted mechanochemical synthesis was a fast route for the synthesis of green octahedral [Ni(Hsal 4- Metsc)2]$(3) and [Ni(Hsal 4-Phtsc)2]$(4). The advantages and disadvantages of all used synthetic methods were discussed. The characterization of square planar (2) and two octahedral complexes (3) and (4) was performed by X-ray diffraction methods, infrared and NMR spectroscopy. In addition quantum chemical calculations were performed for CS (conformer which enables O–H/S intramolecular hydrogen bond formation in 2-hydroxyaryl Schiff base thiosemicarbazones) and SC (conformer with the thiocarbonyl group turned away from O–H/N intramolecular hydrogen bond) forms of both ligands and in each case the CS conformer was lower in energy.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982915-2950 - Dizajn, sinteza i svojstva organskih liganada i njihovih metalnih kompleksa (Ćurić, Manda, MZOS ) ( CroRIS)
098-1191344-2943 - Protein-ligand međudjelovanja na atomnoj razini (Luić, Marija, MZOS ) ( CroRIS)
119-1191342-1334 - Reakcije organskih spojeva u čvrstom stanju: mehanizmi i supramolekulski inženje (Vančik, Hrvoj, MZOS ) ( CroRIS)
119-1193079-3069 - Novi organski i koordinacijski spojevi - sinteza i suodnos struktura-svojstvo (Kaitner, Branko, MZOS ) ( CroRIS)
119-1191342-1082 - Novi kompleksni spojevi i materijali-kemijski i biološki katalizatori (Cindrić, Marina, MZOS ) ( CroRIS)
119-1191342-2961 - Fizikalna kemija koloida i međupovršina (Kallay, Nikola, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Dominik Cinčić
(autor)
Marina Cindrić
(autor)
Manda Ćurić
(autor)
Tomica Hrenar
(autor)
Davor Kovačević
(autor)
Gordana Pavlović
(autor)
Ivan Halasz
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus