0000000001304274
AUTHOR
Eugenio Garribba
showing 29 related works from this author
Structural Variation and Magneto-Structural Correlation in Two New Dinuclear Bis(µ2-Phenoxo)-Bridged CuII Schiff-Base Complexes: Catalytic Potential …
2010
Two new dinuclear bis(μ2-phenoxo)-bridged copper(ii) complexes [Cu(NCS)L1]2 (1) and [Cu(NCS)L2]2 (2) have been synthesized using two tridentate NNO-donor Schiff-base ligands, L1H (Me2N(CH2)3N=CHC6H3(OMe)(OH)) and L2H (Me2N(CH2)3N=C(CH3)C6H4(OH)), respectively. They have been characterized by elemental analyses, IR, UV-visible, and electron paramagnetic resonance (EPR) spectroscopy, cyclic voltammetry, and magnetic susceptibility measurements. X-Ray single-crystal structures reveal a central Cu2O2 core in each complex with an isothiocyanate ligand coordinated terminally to each metal centre. The coordination environments around the CuII ions in 1 and 2 are a distorted trigonal bipyramid and…
Effect of temperature and ligand protonation on the electronic ground state in Cu( ii ) polymers having unusual secondary interactions: a magnetic an…
2018
International audience; Two new copper(II) polymeric complexes, {[Cu(HPymat)(H2O)](NO3)}n (1) and [Cu2(Pymat)2(H2O)3]n (2), have been synthesized using the Schiff base ligand H2Pymat [H2Pymat = (E)-2-(1-(pyridin-2-yl)-methyleneamino)terephthalic acid]. Complex 1 is a cationic 1D polymer, whereas complex 2 is a two dimensional polymer. Both complexes were crystallographically, spectroscopically and magnetically characterized. Theoretical studies were performed and the catecholase activity of the complexes was also examined. Complex 1 is a ferromagnetically coupled complex with J = 2.8 cm−1 and 2 shows antiferromagnetic coupling with J = −1.6 cm−1. Both complexes show notable features in the …
A novel mixed valent Cu(II)-Cu(I) 2D framework made of a hydrazone and μ-SCN bridged metallacyclic loops cross-linked by μ3-SCN chains.
2012
A mixed valent copper complex [Cu(II)Cu(I)(L)(μ-SCN)(μ(3)-SCN)](n) (LH = N'-((pyridin-2-yl)methylene)acetohydrazide) has been synthesized and characterized. It is a unique example of a 2D mixed valent Cu(II)-Cu(I) interlinked molecular assembly with a very unusual bridging property of the hydrazone ligand. An extraordinary in situ partial Cu(II)→ Cu(I) reduction is observed in this system at room temperature.
Synthesis, structural aspects and magnetic properties of an unusual 2D thiocyanato-bridged cobalt(II)–Schiff base network
2010
Abstract A new two-dimensional (2D) thiocyanato-bridged cobalt(II) network formulated as [LCo2(NCS)2]n (1), has been synthesized with the Schiff base ligand N,N′-bis(3-methoxysalicylidenimino)-1,3-diaminopropane (H2L) and thiocyanate anions. This novel layered compound has been completely characterized by elemental analysis, FT-IR, UV–Vis spectroscopy and the structure has been established by single crystal X-ray diffraction studies. The structure of 1 consists of a doubly phenoxo-bridged dimer comprising two different cobalt(II) centers with different coordination geometries (octahedral and tetrahedral). The 2D network is accomplished by bridging thiocyanate ligands, connecting the dimeric…
Synthesis, structure, physicochemical characterization and theoretical evaluation of non-covalent interaction energy of a polymeric copper(II)-hydraz…
2019
Abstract One dimensional polymeric copper-hydrazone complex {[Cu(H0.5L)(µ1,3-SCN)]0.5ClO4·0.5MeOH}n (1) has been synthesized with Cu(ClO4)2·xH2O and N'-(1-(pyridin-2-yl)ethylidene)acetohydrazide (HL) in presence of NaSCN. The ligand and the complex have been characterized by several spectroscopic techniques (IR, UV–Vis and EPR), cyclic voltammetry and the structure of 1 has been determined by single crystal X-ray diffraction. The complex is an infinite one dimensional polymer bridged by thiocyanate. The magneto-structural correlation has been determined and the non-covalent interactions present in the molecule have been energetically evaluated by means of DFT calculations.
A trigonal prismatic anionic iron(iii) complex of a radical o-iminobenzosemiquinonate derivative: structural and spectral analyses
2017
A new iron(III) complex, [Et3NH][FeIII(L2−˙)2] (1) with a substituted o-aminophenol based ligand is reported. Complex 1 is an anionic complex with a triethylammonium cation in the lattice. It contains two O,O,N-coordinated o-iminobenzosemiquinonate(2−) radical anions with an Fe(III) centre in a high-spin configuration. The crystal structure of 1 was determined by X-ray diffraction, which revealed a trigonal prismatic coordination environment whose electronic structure was established by various physical methods including EPR, Mossbauer spectroscopy and variable-temperature (2–300 K) magnetic susceptibility measurements. Electrochemical analysis indicated primarily ligand-centred redox proce…
Two new supramolecular architectures of singly phenoxo-bridged copper(II) and doubly phenoxo-bridged manganese(II) complexes derived from an unusual …
2009
International audience; Two new coordination complexes {[(L)Cu2('-L)(NO3)(CH3OH)0.3(H2O)0.7]·NO3}[Cu(L)(NO3)(CH3OH)] (1) and [Mn2(-L)2(H2O)(1-N3)2(CH3OH)] (2) derived from (E)-N-(2-hydroxy-3-methoxybenzylidene)acetohydrazide [LH] have been synthesized. The new potentially tetradentate ONOO donor hydrazone ligand [LH] has shown considerable metal ion selective phenoxo bridging in 1 and 2. It has coordinated copper(II) ions in its tridentate as well as in tetradentate fashion whereas for manganese(II) ions it solely showed its tetradentate character. In 1 the two adjacent pentacoordinate copper(II) centers are connected by a rare single phenoxo linkage of the hydrazone ligand whereas 2 is a d…
Reversible switching of the electronic ground state in a pentacoordinated Cu(ii) complex.
2013
International audience; An easy reversible switching of the electronic ground state in a pentacoordinated copper(ii) complex is reported for the first time. The simple protonation of a carboxylic group in a Cu(ii) complex with a {dx(2)-y(2)}(1) electronic configuration leads to a flip of the ground electronic configuration from {dx(2)-y(2)}(1) to {dz(2)}(1) in the metal ion.
Switching and redox isomerism in first-row transition metal complexes containing redox active Schiff base ligands.
2014
International audience; The reversible redox isomerisms in first row transition metal complexes of the type ML2 were studied. The six ML2 complexes (M = Mn(III) (), Fe(II) (), Co(III) (), Ni(II) (), Cu(II) () and Zn(II) ()) were synthesized with a redox active Schiff base ligand [2-(3,5-di-tert-butyl-2-hydroxyphenylamino)-4-chlorophenol] (H3L) presenting different oxidation states from -2 to 0 (L(2-), L(-) and L(0)). EPR spectra and magnetic susceptibility measurements indicate the presence of complexes of the type [Mn(III)(L(2-))(L(-))] () with S = 1/2, [Fe(II)(L(-))2] () with S = 2, [Co(III)(L(2-))(L(-))] () with S = 1/2, [Ni(II)(L(-))2] () with S = 1, [Cu(II)(L(-))2] () with S = 1/2 and …
Double azido/cyanato bridged copper(II) dimers incorporating tridentate nitrogen donors Schiff base: Structure, EPR and magnetic studies
2015
Abstract A neutral tridentate nitrogen donor Schiff base ligand L (L = (E)-N-(phenyl(pyridin-2-yl)methylene)-2-(pyridin-2-yl)ethanamine) has been synthesized and characterized by spectroscopic techniques, and employed to synthesize two new μ1,1-azido/cyanato bridged dinuclear copper(II) complexes, [Cu(L)(μ1,1-N3)(ClO4)]2 (1) and [Cu(L)(μ1,1-NCO)(ClO4)]2 (2). Both compounds have been spectroscopically and structurally characterized. Structural investigation reveals centro-symmetric nature of the complexes in which the center of inversion lies at the midpoint of the two copper(II) ions. The metal ions display distorted octahedral geometry. The tridentate neutral ligand L coordinates the metal…
Magneto-structural and theoretical study of the weak interactions in a Mn(II) complex with a very unusual N,O-chelating coordination mode of 2-aminot…
2017
International audience; The Mn(II) complex {[Mn(atpa)(H2O)2]·H2O}n (1),with the dicarboxylate ligand 2-aminoterephthalic acid (H2atpa), has been synthesized and crystallographically, spectroscopically and magnetically characterized. Complex 1 shows a very unusual 1κ2N,O coordination mode of the aminoterephthalate dianion with the Mn(II) ion. One of the carboxylate groups shows a syn-anti-μ2-η1:η1 binding mode to form a 2D square grid. The magnetic properties of this compound can be very well reproduced with a regular S = 5/2 chain model with a very weak antiferromagnetic coupling constant of J = −0.2 cm−1 through the single syn-anti carboxylate bridges. EPR measurement also supports the exp…
Magneto-structural correlations and DFT calculations in two rare tetranuclear copper(II)-clusters with doubly phenoxo and end-on azido bridges: Synth…
2010
International audience; By slightly changing the synthetic conditions, we have prepared two closely related linear tetranuclear CuII complexes with the symmetrical ONNO donor tetradentate Schiff-base ligand [H2L = (OH)C6H4(CH3)Cdouble bond; length as m-dashN(CH2)3Ndouble bond; length as m-dashC(CH3)C6H4(OH)] and with azide ions. These two distinctly coloured crystalline products were characterized by elemental analysis, IR and UV–Vis spectroscopy, CV, EPR spectra and variable temperature magnetic measurements. Single crystal X-ray diffraction studies of the green [Cu4(μ-L)2(μ1,1-N3)2(N3)2] (1) and the red [Cu4(μ-L)2(μ1,1-N3)2(N3)2(H2O)2] (2) crystals show that the coordination environment o…
A new linear double phenoxide-bridged trinuclear Cu(II) Schiff base complex: Synthesis, crystallographic elucidation, magneto-structural correlation …
2014
Abstract The tetradentate (ONNO) donor Schiff base ligand LH2, derived from the condensation of salicylaldehyde and 1,3-diaminopropane, has been synthesized and reacted with CuBr2 to yield a trinuclear complex with the molecular formula [Cu3L2Br2]. Single crystal X-ray diffraction study reveals that the two terminal copper atoms adopt a square pyramidal geometry, whereas the central copper atom, situated at the inversion centre, is surrounded by four phenoxide oxygen atoms in a square planar fashion. Variable temperature magnetic susceptibility measurement study shows strong antiferromagnetic intra-trimer interactions between the copper centers with a J value of −302 cm−1. EPR study of the …
Sterically-controlled nuclearity in new copper(II) complexes with di-compartmental ligands: Formation of antiferromagnetically coupled angular trimer…
2010
Abstract Two new copper(II) complexes, [Cu3(L1)2(H2O)2](ClO4)2 (1) and [CuL2 ⊂ (H2O)] (2) have been derived from two di-compartmental Schiff base ligands H2L1 and H2L2, respectively. Depending on slight modification of the substituent group of the potentially N2O4 donor ligands, tri- and mononuclear structures are obtained, which have been confirmed by single-crystal X-ray diffraction studies. Both complexes have been characterized by elemental analysis, IR, UV–vis and EPR spectroscopy. Complex 1 consists of an angular trinuclear array of copper ions, while complex 2 consists of a mononuclear copper center. Variable temperature magnetic susceptibility measurements have been performed to inv…
Ferromagnetic exchange coupling in a new bis(μ-chloro)-bridged copper(II) Schiff base complex: Synthesis, structure, magnetic properties and catalyti…
2009
Abstract A new (μ-chloro)-bridged complex [Cu(HL)Cl]2 · H2O (1) with the Schiff base ligand H2L, [2-((E)-(2-hydroxyethylimino)methyl)-4-bromophenol], has been synthesized and characterized by elemental analysis, IR, UV–Vis and EPR spectroscopic studies. X-ray diffraction studies show that 1 is a binuclear CuII complex with a pair of chlorine atoms bridging the copper atoms in a central Cu2Cl2 core. Each copper atom in 1 adopts a distorted square-pyramidal geometry with the imine nitrogen atom, alkoxy and phenoxy oxygen atoms from the Schiff base ligand and a bridging chlorine atom constructing the basal plane, while the apical position of the pyramid is occupied by the other bridging chlori…
CCDC 921248: Experimental Crystal Structure Determination
2014
Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H
CCDC 921246: Experimental Crystal Structure Determination
2014
Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H
CCDC 1018391: Experimental Crystal Structure Determination
2015
Related Article: Madhusudan Nandy, Shyamapada Shit, Eugenio Garribba, Carlos J. Gómez-García, Samiran Mitra|2015|Polyhedron|102|137|doi:10.1016/j.poly.2015.07.034
CCDC 881999: Experimental Crystal Structure Determination
2013
Related Article: Ashok Sasmal,Sandeepta Saha,Carlos J. Gomez-Garcia,Cedric Desplanches,Eugenio Garribba,Antonio Bauza,Antonio Frontera,Reum Scott,Ray J. Butcher,Samiran Mitra|2013|Chem.Commun.|49|7806|doi:10.1039/C3CC44276D
CCDC 1544334: Experimental Crystal Structure Determination
2018
Related Article: Dipali Sadhukhan, Monami Maiti, Antonio Bauzá, Antonio Frontera, Eugenio Garribba, Carlos J. Gomez-García|2019|Inorg.Chim.Acta|484|95|doi:10.1016/j.ica.2018.09.031
CCDC 1051564: Experimental Crystal Structure Determination
2015
Related Article: Sandeepta Saha, Chirantan Roy Choudhury, Carlos J. Gómez-García, Eugenio Garribba, Antonio Bauzá, Antonio Frontera, Guillaume Pilet, Samiran Mitra|2017|Inorg.Chim.Acta|461|183|doi:10.1016/j.ica.2017.02.016
CCDC 882000: Experimental Crystal Structure Determination
2014
Related Article: Sandeepta Saha, Ashok Sasmal, Chirantan Roy Choudhury, Carlos J. Gomez-Garcia, Eugenio Garribba, Samiran Mitra|2014|Polyhedron|69|262|doi:10.1016/j.poly.2013.12.006
CCDC 1560984: Experimental Crystal Structure Determination
2018
Related Article: Sandeepta Saha, Niladri Biswas, Ashok Sasmal, Carlos J. Gómez-García, Eugenio Garribba, Antonio Bauza, Antonio Frontera, Guillaume Pilet, Georgina M. Rosair, Samiran Mitra, Chirantan Roy Choudhury|2018|Dalton Trans.|47|16102|doi:10.1039/C8DT02417K
CCDC 984617: Experimental Crystal Structure Determination
2014
Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H
CCDC 1055476: Experimental Crystal Structure Determination
2017
Related Article: Sandeepta Saha, Chirantan Roy Choudhury, Carlos J. Gómez-García, Samia Benmansour, Eugenio Garribba, Antonio Frontera, Corrado Rizzoli, Samiran Mitra|2017|New J.Chem.|41|7283|doi:10.1039/C7NJ01212H
CCDC 1018392: Experimental Crystal Structure Determination
2015
Related Article: Madhusudan Nandy, Shyamapada Shit, Eugenio Garribba, Carlos J. Gómez-García, Samiran Mitra|2015|Polyhedron|102|137|doi:10.1016/j.poly.2015.07.034
CCDC 921249: Experimental Crystal Structure Determination
2014
Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H
CCDC 1560985: Experimental Crystal Structure Determination
2018
Related Article: Sandeepta Saha, Niladri Biswas, Ashok Sasmal, Carlos J. Gómez-García, Eugenio Garribba, Antonio Bauza, Antonio Frontera, Guillaume Pilet, Georgina M. Rosair, Samiran Mitra, Chirantan Roy Choudhury|2018|Dalton Trans.|47|16102|doi:10.1039/C8DT02417K
CCDC 921247: Experimental Crystal Structure Determination
2014
Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H