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Some transition and non-transition metal complexes of the hexadentate N₄O₂ donor Schiff base ligand 1,8-N-bis(3-carboxy)disalicylidene-3,6-diazaoctane-1,8-diamine, abbreviated to H₄fsatrien, have been synthesized. All the 14 metal complexes have been fully characterized with the help of elemental analyses, molecular weights, molar conductance values, magnetic moments and spectroscopic (UV-Vis, IR, NMR, ESR) data. The analytical data helped to elucidate the structures of the metal complexes. The Schiff base, H₄fsatrien, is found to act as a dibasic hexadentate ligand using N₂N₂O₂ donor set of atoms (leaving the COOH group uncoordinated) leading to an octahedral geometry for the complexes around all the metal ions except VO²(+) and UO₂²(+). However, surprisingly the same ligand functions as a neutral hexadentate and neutral tetradentate one towards UO₂²(+) and VO²(+), respectively. In case of divalent metal complexes they have the general formula [M(H₂fsatrien)] (where M stands for Cu, Co, Hg and Zn); for trivalent metal complexes it is [M(H₂fsatrien)]X·nH₂O (where M stands for Cr, Mn, Fe, Co and X stands for CH₃COO, Cl, NO₃, ClO₄) and for the complexes of VO²(+) and UO₂²(+), [M(H₄fsatrien)]Y (where M=VO and Y=SO₄); M=UO₂ and Y=2 NO₃). The Schiff base ligand and most of the complexes have been screened in vitro to judge their antibacterial (Escherichia coli and Staphylococcus aureus) and antifungal (Aspergillus niger and Pencillium chrysogenum) activities.
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http://dx.doi.org/10.1016/j.saa.2010.06.041 | DOI Listing |
RSC Adv
September 2025
Department of Chemistry, University of Guelph Guelph ON N1G 2W1 Canada
In the context of the importance of manganese β-diketonates as precursors for the preparation of manganese oxide thin films and nanostructured materials, we report synthetic protocols and pitfalls encountered in the preparation of a family of Mn(ii) complexes of two fluorinated β-diketonates, 1,1,1-trifluoroacetylacetonato- (tfac) and 1,1,1,5,5,5-hexafluoroacetylacetonato- (hfac). The synthetic conditions and crystal structures of six new complexes are reported, including a coordination polymer {K[Mn(tfac)]}, an unusual trinuclear complex Mn(tfac)(OH), and a series of mononuclear complexes with coordinated solvents tetrahydrofuran, 1,2-dimethoxyethane, water, and acetonitrile. The crystal structures of two known Mn(ii) complexes are also reported for completeness.
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September 2025
Department of Chemistry, Istanbul Technical University, Maslak, Istanbul, 34469, Türkiye.
A novel phthalonitrile derivative (a) containing three functional groups (hexyl, aminated ester, phenoxy) was synthesized and subsequently cyclotetramerized in the presence of the corresponding metal chloride salts to obtain hexadeca-substituted metal {M = Cu(II) and Co(II)} phthalocyanines (b and c). The water-soluble phthalocyanines (d and e) were prepared by treating the newly synthesized complexes (b and c) with methyl iodide. Moreover, gold nanoparticles (1) and silver nanoparticles (2) were prepared, and their surfaces were modified with quaternary phthalocyanines (d and e).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Key Laboratory of Organic Synthesis of Jiangsu Province & State Key Laboratory of Bioinspired Interfacial Materials Science, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, P.R. China.
Reaction of LZnI [L = BuC(N-DIPP), DIPP = 2,6-Pr-CH] with KC in the presence of cyclic (alkyl)(amino)carbene (cAAC) affords a stable radical complex [LZn(cAAC)] (3). Single-crystal structural analysis of 3 shows a short Zn─C bond and concomitant elongation of C─N bond within the cAAC ligand, indicating a significant π-backbonding from the metal to the cAAC ligand. EPR spectroscopy and DFT calculations reveal that the spin density is mainly localized on the carbenic carbon atom, with a small portion on the zinc center.
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September 2025
Department of Chemistry, Indian Institute of Technology Guwahati, Assam 781039, India.
Motivated by copper's essential role in biology and its wide range of applications in catalytic and synthetic chemistry, this work aims to understand the effect of heteroatom substitution on the overall stability and reactivity of biomimetic Cu(II)-alkylperoxo complexes. In particular, we designed a series of tetracoordinated ligand frameworks based on iso-BPMEN = (,-bis(2-pyridylmethyl)-','-dimethylethane-1,2-diamine) with varying the primary coordination sphere using different donor atoms (N, O, or S) bound to Cu(II). The copper(II) complexes bearing iso-BPMEN and their modified heteroatom-substituted ligands were synthesized and structurally characterized.
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September 2025
College of Emergency Management, Chongqing Vocational Institute of Safety Technology, Wanzhou, Chongqing, 404020, P. R. China.
Allyl sulfones are common motifs in many drugs and natural products, exhibiting a wide range of biological activities such as anticancer and antibacterial properties, etc. An overview is provided on the synthesis of allylic sulfones via generation of metal π-allyl complexes in metal-catalyzed sulfonylation over the period from 2020 to the present. The generation process of metal π-allyl complexes is introduced from the perspective of reaction mechanism and the reaction processes such as nucleophilic substitution, insertion of SO, and reductive elimination involving metal π-allyl complexes is discussed.
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