Metal complexes of a novel heterocyclic benzimidazole ligand formed by rearrangement-cyclization of the corresponding Schiff base. Electrosynthesis, structural characterization and antimicrobial activity. Issue 12 (28th February 2018)
- Record Type:
- Journal Article
- Title:
- Metal complexes of a novel heterocyclic benzimidazole ligand formed by rearrangement-cyclization of the corresponding Schiff base. Electrosynthesis, structural characterization and antimicrobial activity. Issue 12 (28th February 2018)
- Main Title:
- Metal complexes of a novel heterocyclic benzimidazole ligand formed by rearrangement-cyclization of the corresponding Schiff base. Electrosynthesis, structural characterization and antimicrobial activity
- Authors:
- Casanova, I.
Durán, M. L.
Viqueira, J.
Sousa-Pedrares, A.
Zani, F.
Real, J. A.
García-Vázquez, J. A. - Abstract:
- Abstract : One-pot electrochemical synthesis of metal complexes containing a novel heterocyclic benzimidazole ligand is reported and characterized. Abstract : The electrochemical oxidation of anodic metals (M = cobalt, nickel, copper, zinc and cadmium) in a solution of the ligand 1 H -anthra[1, 2- d ]imidazol-6, 11-dione-2-[2-hydroxyphenyl] [H2 L] afforded homoleptic [ML] compounds. The addition to the electrochemical cell of coligands (L′) such as 2, 2′-bipyridine (bpy) or 1, 10-phenanthroline (phen) allowed the synthesis, in one step, of heteroleptic [MLL′] compounds. The crystal structures of H2 L (1 ), [CoL(MeOH)]2 (2 ), [CoL(phen)]2 (3 ), [NiL(bpy)]2 (4 ), [CuL(bpy)] (5 ), [CuL(phen)] (6 ) and [CdL(bpy)]2 (7 ) have been determined by X-ray diffraction techniques. The crystal structures of2, 3, 4 and7 consist of dimeric species in which both metallic atoms are connected through two phenolate bridges in a penta-coordinated (2 ) or hexa-coordinated (3, 4 and7 ) environment. Copper compounds5 and6 are monomeric species with the metal in a pentacoordinated [N4 O] environment. In all the compounds, the main interactions responsible for the crystal packing are classic (N–H⋯O, O–H⋯N and O–H⋯O) and non-classic (C–H⋯O and C–H⋯N) hydrogen bond interactions, and π interactions (π–π-stacking and C–H⋯π). All compounds were also characterized by microanalysis, IR spectroscopy, FAB mass spectrometry and 1 H NMR spectroscopy. Magnetic susceptibility data were measured for2–4 over theAbstract : One-pot electrochemical synthesis of metal complexes containing a novel heterocyclic benzimidazole ligand is reported and characterized. Abstract : The electrochemical oxidation of anodic metals (M = cobalt, nickel, copper, zinc and cadmium) in a solution of the ligand 1 H -anthra[1, 2- d ]imidazol-6, 11-dione-2-[2-hydroxyphenyl] [H2 L] afforded homoleptic [ML] compounds. The addition to the electrochemical cell of coligands (L′) such as 2, 2′-bipyridine (bpy) or 1, 10-phenanthroline (phen) allowed the synthesis, in one step, of heteroleptic [MLL′] compounds. The crystal structures of H2 L (1 ), [CoL(MeOH)]2 (2 ), [CoL(phen)]2 (3 ), [NiL(bpy)]2 (4 ), [CuL(bpy)] (5 ), [CuL(phen)] (6 ) and [CdL(bpy)]2 (7 ) have been determined by X-ray diffraction techniques. The crystal structures of2, 3, 4 and7 consist of dimeric species in which both metallic atoms are connected through two phenolate bridges in a penta-coordinated (2 ) or hexa-coordinated (3, 4 and7 ) environment. Copper compounds5 and6 are monomeric species with the metal in a pentacoordinated [N4 O] environment. In all the compounds, the main interactions responsible for the crystal packing are classic (N–H⋯O, O–H⋯N and O–H⋯O) and non-classic (C–H⋯O and C–H⋯N) hydrogen bond interactions, and π interactions (π–π-stacking and C–H⋯π). All compounds were also characterized by microanalysis, IR spectroscopy, FAB mass spectrometry and 1 H NMR spectroscopy. Magnetic susceptibility data were measured for2–4 over the temperature range 2–300 K, and their analysis has revealed the occurrence of intramolecular antiferromagnetic coupling for2 ( J = −2 cm −1 ) and ferromagnetic coupling for3 ( J = 7.8 cm −1 ) and4 ( J = 2.8 cm −1 ) [J being the isotropic magnetic coupling parameter]. The nature of the magnetic coupling in2–4 is correlated with the magnitude of the M–Ophenolate –M angle between the phenolate bridge and the metallic centers [M(ii ) = Co, Ni]. The in vitro antimicrobial properties of the novel ligand and its metal complexes were detected against Gram positive and Gram negative bacteria and fungi. [NiL(bpy)]2 and all tested Cd(ii ) complexes were the most active compounds, showing the highest inhibitory effect against bacilli (MIC 1.5–3 μg mL −1 ) and Sarcina, Streptococci and Haemophilus influenzae bacterial strains (MIC 12–50 μg mL −1 ), while almost no antifungal properties were observed. … (more)
- Is Part Of:
- Dalton transactions. Volume 47:Issue 12(2018)
- Journal:
- Dalton transactions
- Issue:
- Volume 47:Issue 12(2018)
- Issue Display:
- Volume 47, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 47
- Issue:
- 12
- Issue Sort Value:
- 2018-0047-0012-0000
- Page Start:
- 4325
- Page End:
- 4340
- Publication Date:
- 2018-02-28
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8dt00532j ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6149.xml