Pregled bibliografske jedinice broj: 1257298
Ligand-modulated nuclearity and geometry in nickel(II) hydrazone complexes: from mononuclear complexes to acetato- and/or phenoxido-bridged clusters
Ligand-modulated nuclearity and geometry in nickel(II) hydrazone complexes: from mononuclear complexes to acetato- and/or phenoxido-bridged clusters // International journal of molecular sciences, 24 (2023), 3; 1909, 19 doi:10.3390/ijms24031909 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1257298 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Ligand-modulated nuclearity and geometry in
nickel(II) hydrazone complexes: from mononuclear
complexes to acetato- and/or phenoxido-bridged
clusters
Autori
Vrdoljak, Višnja ; Hrenar, Tomica ; Rubčić, Mirta ; Pavlović, Gordana ; Friganović, Tomislav ; Cindrić, Marina
Izvornik
International journal of molecular sciences (1422-0067) 24
(2023), 3;
1909, 19
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
4-hydroxybenzhydrazone ; Ni(II) complexes ; clusters ; hybrid organic–inorganic ; polyoxometalate ; acetato ; phenoxido ; bridged complexes ; nuclearity
Sažetak
The propensity of 4-hydroxybenzhydrazone-related ligands derived from 3-methoxysalicylaldehyde (H2L3OMe), 4-methoxysalicylaldehyde (H2L4OMe), and salicylaldehyde (H2LH) to act as chelating and/or bridging ligands in Ni(II) complexes was investigated. Three clusters of different nuclearities, [Ni3(L3OMe)2(OAc)2(MeOH)2]∙2MeOH∙MeCN (1∙2MeOH∙MeCN), [Ni2(HL4OMe)(L4OMe)(OAc) (MeOH)2]∙4.7MeOH (2∙4.7MeOH), and [Ni4(HLH)2(LH)2(OAc)2]∙4MeOH·0.63H2O·0.5MeCN·HOAc (3∙4MeOH·0.63H2O·0.5MeCN·HOAc), were prepared from Ni(OAc)2∙4H2O and the corresponding ligand in the presence of Et3N. The hydrazones in these acetato- and phenoxido-bridged clusters acted as singly or doubly deprotonated ligands. When pyridine was used, mononuclear complexes with the square-planar geometry seemed to be favoured, as found for complexes [Ni(L3OMe)(py)] (4), [Ni(L4Ome)(py)] (5) and [Ni(LH)(py)] (6). Ligand substituent effects and the stability of square-planar complexes were investigated and quantified by extensive quantum chemical analysis. Obtained results showed that standard Gibbs energies of binding were lower for square-planar than for octahedral complexes. Starting from [MoO2(L)(EtOH)] complexes as precursors and applying the metal-exchange procedure, the mononuclear complexes [Ni(HL3OMe)2]∙MeOH (7∙MeOH) and [Ni(HLH)]∙2MeOH (9∙2MeOH) and hybrid organic–inorganic compound [Ni2(HL4OMe)2(CH3OH)4][Mo4O10(OCH3)6] (10) were achieved. The octahedral complexes [Ni(HL)2] (7–9) can also be obtained by the direct synthesis from Ni(Oac)2∙4H2O and the appropriate ligand under specific reaction conditions. Crystal and molecular structures of 1∙2MeOH∙MeCN, 2∙4.7MeOH, 3∙4MeOH∙0.63H2O∙0.5MeCN∙HOAc, 4, 5, 9∙2MeOH, and 10 were determined by the single-crystal X-ray diffraction method.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Marina Cindrić (autor)
Mirta Rubčić (autor)
Tomica Hrenar (autor)
Gordana Pavlović (autor)
Višnja Vrdoljak (autor)
Tomislav Friganović (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
- MEDLINE