scholarly journals Solid-state supramolecular architectures of a series of Hg(ii) halide coordination compounds based on hydroxyl-substituted Schiff base ligands

CrystEngComm ◽  
2019 ◽  
Vol 21 (41) ◽  
pp. 6301-6312 ◽  
Author(s):  
Taraneh Hajiashrafi ◽  
Shiva Salehi ◽  
Maciej Kubicki ◽  
Antonio Bauzá ◽  
Antonio Frontera ◽  
...  
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Coordination Compounds ◽  
Theoretical Calculations ◽  
Schiff Base Ligands ◽  
Supramolecular Architectures

Herein, six Hg(ii) coordination compounds containing Schiff base ligands were synthesized, characterized and studied using geometrical and Hirshfeld analyses as well as theoretical calculations.

New Copper Compounds with Antiplatelet Aggregation Activity

2019 ◽  
Vol 15 (8) ◽  
pp. 850-862
Author(s):  
Mirthala Flores-García ◽  
Juan Manuel Fernández-G. ◽  
Cristina Busqueta-Griera ◽  
Elizabeth Gómez ◽  
Simón Hernández-Ortega ◽  
...  
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Thrombotic Event ◽  
X Ray Diffraction ◽  
Nmr Studies ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Antiplatelet Aggregation ◽  
Aggregation Activity ◽  
L1 And L2

Background: Ischemic heart disease, cerebrovascular accident, and venous thromboembolism have the presence of a thrombotic event in common and represent the most common causes of death within the population. Objective: Since Schiff base copper(II) complexes are able to interact with polyphosphates (PolyP), a procoagulant and potentially prothrombotic platelet agent, we investigated the antiplatelet aggregating properties of two novel tridentate Schiff base ligands and their corresponding copper( II) complexes. Methods: The Schiff base ligands (L1) and (L2), as well as their corresponding copper(II) complexes (C1) and (C2), were synthesized and characterized by chemical analysis, X-ray diffraction, mass spectrometry, and UV-Visible, IR and far IR spectroscopy. In addition, EPR studies were carried out for (C1) and (C2), while (L1) and (L2) were further analyzed by 1H and 13C NMR. Tests for antiplatelet aggregation activities of all of the four compounds were conducted. Results: X-ray diffraction studies show that (L1) and (L2) exist in the enol-imine tautomeric form with a strong intramolecular hydrogen bond. NMR studies show that both ligands are found as enol-imine tautomers in CDCl3 solution. In the solid state, the geometry around the copper(II) ion in both (C1) and (C2) is square planar. EPR spectra suggest that the geometry of the complexes is similar to that observed in the solid state by X-ray crystallography. Compound (C2) exhibited the strongest antiplatelet aggregation activity. Conclusion: Schiff base copper(II) complexes, which are attracting increasing interest, could represent a new approach to treat thrombosis by blocking the activity of PolyP with a potential anticoagulant activity and, most importantly, demonstrating no adverse bleeding events.

scholarly journals Thermal and long period stability of series of V(V), V(IV) and V(III) complex with Schiff base ligands in solid state

2019 ◽  
Vol 4 (1) ◽  
pp. 30-36 ◽  
Author(s):  
Janusz Szklarzewicz ◽  
Anna Jurowska ◽  
Maciej Hodorowicz ◽  
Ryszard Gryboś
Keyword(s):  
Thermal Stability ◽  
Schiff Base ◽  
Solid State ◽  
Physicochemical Properties ◽  
General Formula ◽  
Oxidation State ◽  
Magnetic Moment ◽  
Tridentate Ligand ◽  
Schiff Base Ligands ◽  
Long Period

The synthesis and physicochemical properties of three new complexes of vanadium at +5, +4 and +3 oxidation state are described and discussed. The octahedral surrounding of vanadium for V(III) complexes of [V(L1)(HL1)] general formula is filled with two ONO tridentate ligand L, for V(IV) one ONO ligand L, oxido ligand and 1,10-phenanthroline (phen) as a co-ligand are presented in complexes of [VO(L2)(phen)]. For V(V) the complexes of [VO2(L1)(solv)] type were formed. As ligands, the H2L Schiff bases were formed in reaction between 5-hydroxysalcylaldehyde and phenylacetic hydrazide (H2L1) and 3,5-dichlorosalicyaldehyde and 4-hydroxybenzhydrazide (L2). The magnetic moment measurements, in 8 year period, show, that V(III) complexes slowly oxidise to V(IV) with preservation of the nonoxido character of the complexes, while V(IV) complexes were found to be stable. The TG and SDTA measurements indicate, that thermal stability depends mainly on the oxidation state of vanadium. The less thermally stable are the V(V) complexes, while V(IV) and V(III) are stable up to ca. 200oC. In solution, at pH 2 (similar to that in human digestion system), again the V(IV) are the most stable, only at pH 7.0 V(III) complexes had higher stability. The most stable, thus best for pharmaceutical use, are V(IV) complexes.

From solid state to in vitro anticancer activity of copper(ii) compounds with electronically-modulated NNO Schiff base ligands

2020 ◽  
Vol 49 (41) ◽  
pp. 14626-14639
Author(s):  
Luca Rigamonti ◽  
Francesco Reginato ◽  
Erika Ferrari ◽  
Laura Pigani ◽  
Lara Gigli ◽  
...  
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Anticancer Activity ◽  
Nitro Group ◽  
Schiff Base Ligands

The electron withdrawing nitro group enhances the in vitro cytotoxicity of copper(ii) complexes bearing tridentate NNO Schiff base ligands.

Highly cytotoxic DNA-interacting copper(ii) coordination compounds

Metallomics ◽  
2014 ◽  
Vol 6 (10) ◽  
pp. 1853-1868 ◽  
Author(s):  
Rosa F. Brissos ◽  
Ester Torrents ◽  
Francyelli Mariana dos Santos Mello ◽  
Wanessa Carvalho Pires ◽  
Elisângela de Paula Silveira-Lacerda ◽  
...  
Keyword(s):  
Schiff Base ◽  
Cell Lines ◽  
Cancer Cell ◽  
Coordination Compounds ◽  
Copper Complexes ◽  
Cancer Cell Lines ◽  
Schiff Base Ligands ◽  
High Cytotoxicity

Copper complexes from Schiff-base ligands show high cytotoxicity against diverse cancer cell lines, with IC50 values down to 0.23 μM.

The Copper(II) Complex with Two Didentate Schiff Base Ligands. The Unique Rearrangment that Proceeds under Alcohol Vapor in the Solid State to Construct Noninclusion Structure

2008 ◽  
Vol 37 (1) ◽  
pp. 78-79 ◽  
Author(s):  
Yuhki Shibuya ◽  
Keiko Nabari ◽  
Mitsuru Kondo ◽  
Sachie Yasue ◽  
Kenji Maeda ◽  
...  
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Schiff Base Ligands ◽  
Alcohol Vapor

scholarly journals Self-Assembly of Antiferromagnetically-Coupled Copper(II) Supramolecular Architectures with Diverse Structural Complexities

Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5549 ◽  
Author(s):  
Santokh S. Tandon ◽  
Scott D. Bunge ◽  
Neil Patel ◽  
Esther C. Wang ◽  
Laurence K. Thompson
Keyword(s):  
Schiff Base ◽  
Self Assembly ◽  
Three Dimensional ◽  
The Self ◽  
Basic Building Block ◽  
Schiff Base Ligands ◽  
X Ray ◽  
Supramolecular Architectures ◽  
Hydroxy Groups ◽  
New Discovery

The self-assembly of 2,6-diformyl-4-methylphenol (DFMP) and 1-amino-2-propanol (AP)/2-amino-1,3-propanediol (APD) in the presence of copper(II) ions results in the formation of six new supramolecular architectures containing two versatile double Schiff base ligands (H3L and H5L1) with one-, two-, or three-dimensional structures involving diverse nuclearities: tetranuclear [Cu4(HL2−)2(N3)4]·4CH3OH·56H2O (1) and [Cu4(L3−)2(OH)2(H2O)2] (2), dinuclear [Cu2(H3L12−)(N3)(H2O)(NO3)] (3), polynuclear {[Cu2(H3L12−)(H2O)(BF4)(N3)]·H2O}n (4), heptanuclear [Cu7(H3L12−)2(O)2(C6H5CO2)6]·6CH3OH·44H2O (5), and decanuclear [Cu10(H3L12−)4(O)2(OH)2(C6H5CO2)4] (C6H5CO2)2·20H2O (6). X-ray studies have revealed that the basic building block in 1, 3, and 4 is comprised of two copper centers bridged through one μ-phenolate oxygen atom from HL2− or H3L12−, and one μ-1,1-azido (N3−) ion and in 2, 5, and 6 by μ-phenoxide oxygen of L3− or H3L12− and μ-O2− or μ3-O2− ions. H-bonding involving coordinated/uncoordinated hydroxy groups of the ligands generates fascinating supramolecular architectures with 1D-single chains (1 and 6), 2D-sheets (3), and 3D-structures (4). In 5, benzoate ions display four different coordination modes, which, in our opinion, is unprecedented and constitutes a new discovery. In 1, 3, and 5, Cu(II) ions in [Cu2] units are antiferromagnetically coupled, with J ranging from −177 to −278 cm−1.

scholarly journals Synthesis, crystal structures and spectroscopic investigation of new Cu/Schiff-base complexes

2014 ◽  
Vol 10 (8) ◽  
pp. 3068-3079
Author(s):  
Ahmed Toumi ◽  
Mohamed Rzaigui ◽  
Hichem Ben Jannet
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Copper Complexes ◽  
Spectroscopic Properties ◽  
Schiff Base Complexes ◽  
X Ray Diffraction ◽  
Neutral Complex ◽  
Schiff Base Ligands ◽  
1H And 13C Nmr ◽  
Solid State Structures

Three novel Copper complexes, [Cu(L1)2][CuCl2] (1),  [Cu(L2)Cl] (2) and [Cu2(L3)3Cl2] (3), have been prepared by reaction of CuCl with the Schiff-base ligands L1: N,N’-bis(thiophen-2-ylmethylene)-ethane-1,2-diamine, L2: N,N’-bis(1H-pyrrol-2-ylmethylene)ethane-1,2-diamine and L3: N,N’-bis(2-nitrobenzylidene)-ethane-1,2-diamine in acetonitrile. The solid-state structures of these complexes were determined by X-ray diffraction from single crystal data and characterized by 1H and 13C NMR, IR and UV/Vis spectroscopies. This study shows that (1) is an ionic complex with a Cu(I)-centered cation and an isolated linear dichlorocuprate(I) anion, (3) is a dinuclear neutral complex of Cu(I) while (2)  is a mononuclear neutral complex of Cu(II). In the three complexes, Cu is tetracordinated in different geometrical environments. The atomic arrangements and spectroscopic properties of the three complexes are reported. Complexes 1-3 exhibit, in the solid state at room temperature, photoluminescence between 320 and 550 nm.

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