0000000000011910
AUTHOR
Samia Benmansour
Alternating Ferro/Antiferromagnetic Copper(II) Chain Containing an Unprecedented Triple Formato/Hydroxido/Sulfato Bridge.
The first example of a triple formato/hydroxido/sulfato (FHS) bridge for any metal is reported in compound [Cu2(bpym)(OH)(HCO2)(SO4)(H2O)2]·3H2O (1). Its structure shows the presence of alternating triple FHS bridges and 2,2'-bipyrimidine (bpym) ones. Although in the initial synthesis the sulfate anions were introduced accidentally, here we report the rational synthesis and the magnetic properties of this compound. The magnetic properties show that 1 is an alternating ferro/antiferromagnetic (F/AF) chain compound with predominant antiferromagnetic interactions and were fit to an alternating F/AF S = (1)/2 chain with g = 2.103, JAF = -139 cm(-1), and JF = 116 cm(-1) (α = JF/|JAF| = 0.83). Th…
Delamination of 2D coordination polymers : the role of solvent and ultrasound
Two novel cadmium-based 2D coordination polymers have been synthesized and characterized. Experimental results evidence that the best delamination processes occurs when weak interactions dominate the cohesion between layers and solvent molecules are occluded within the crystalline network. In this case, the delamination of the crystals occurs spontaneously in water. On top of that, and thanks to the high stability of the resulting (flake) colloidal dispersions, we have completed a detailed study of the sonication assisted delamination impact by: I) comparison of two different sonication approaches (bath vs. tip sonication) and II) optimization of final flake morphology and yield by controll…
Solvent-tuned ultrasonic synthesis of 2D coordination polymer nanostructures and flakes
Highlights • Combined ultrasound and solvent assisted synthesis of 2D coordination polymers. • Role of interstitial solvent molecules in the delamination of 2D-CPs. • Influence of the sonication time in delamination and nanostructuration processes. • Morphological and supramolecular transformations in 2D-CPs.
Electrical conductivity and strong luminescence in copper Iodide double chains with isonicotinato derivatives
Direct reactions between CuI and isonicotinic acid (HIN) or the corresponding esters, ethyl isonicotinate (EtIN) or methyl isonicotinate (MeIN), give rise to the formation of the coordination polymers [CuI(L)] with L=EtIN (1), MeIN (2) and HIN (3). Polymers 1-3 show similar structures based on a CuI double chain in which ethyl-, methyl isonicotinate or isonicotinic acid are coordinated as terminal ligands. Albeit, their supramolecular architecture differs considerably, affecting the distances and angles of the central CuI double chains and thereby their physical properties. Hence, the photoluminescence shows remarkable differences; 1 and 2 show a strong yellow emission, whereas 3 displays a…
Magnetic Properties of End-to-End Azide-Bridged Tetranuclear Mixed-Valence Cobalt(III)/Cobalt(II) Complexes with Reduced Schiff Base Blocking Ligands and DFT Study.
Two tetranuclear mixed-valence cobalt(III/II) complexes having the general formula [(μ1,3-N3){CoII(Ln)(μ-O2CC6H4NO2)CoIII(N3)}2]PF6 (where H2L1 and H2L2 are two reduced Schiff base ligands) have been synthesized and characterized. The structures of both complexes show cobalt(II) and cobalt(III) centers with a distorted octahedral geometry with cobalt(III) and cobalt(II) centers located at the inner N2O2 and outer O4 cavities of the reduced Schiff base ligands, respectively. The oxidation states of both cobalt centers have been confirmed by bond valence sum (BVS) calculations. The magnetic properties show that both compounds behave as cobalt(II) dimers connected through an end-to-end azido b…
A Heterobimetallic Anionic 3,6-Connected 2D Coordination Polymer Based on Nitranilate as Ligand
In order to synthesize new coordination polymers with original architectures and interesting magnetic properties, we used the nitranilate ligand (C₆O₄(NO₂)₂2- = C₆N₂O₈2-), derived from the dianionic ligand dhbq2- (2,5-dihydroxy-1,4-benzoquinone = H₂C₆O₄2-). The use of this bis-bidentate bridging ligand led to [(DAMS)₂{FeNa(C₆N₂O₈)₃}·CH₃CN]n (1) (DAMS⁺ = C16H17N₂⁺ = 4-[4-(dimethylamino)-α-styryl]-1-methylpyridinium), a 2D heterometallic coordination polymer presenting an unprecedented structure for any anilato-based compound. This structural type is a 3,6-connected 2D coordination polymer derived from the well-known honeycomb hexagonal structure, where Fe(III) ions alternate with Na⁺ dimers …
Slow Relaxation of the Magnetization in Anilato-Based Dy(III) 2D Lattices.
The search for two- and three-dimensional materials with slow relaxation of the magnetization (single-ion magnets, SIM and single-molecule magnets, SMM) has become a very active area in recent years. Here we show how it is possible to prepare two-dimensional SIMs by combining Dy(III) with two different anilato-type ligands (dianions of the 3,6-disubstituted-2,5-dihydroxy-1,4-benzoquinone: C6O4X22−, with X = H and Cl) in dimethyl sulfoxide (dmso). The two compounds prepared, formulated as: [Dy2(C6O4H2)3(dmso)2(H2O)2]·2dmso·18H2O (1) and [Dy2(C6O4Cl2)3(dmso)4]·2dmso·2H2O (2) show distorted hexagonal honeycomb layers with the solvent molecules (dmso and H2O) located in the interlayer space and…
Influence of metal ions on the structures of Keggin polyoxometalate-based solids: Hydrothermal syntheses, crystal structures and magnetic properties
Abstract Three new Keggin polyoxometalate (POM)-based compounds linked to 3d metal complexes have been synthesized under hydrothermal conditions: [Cu(phen)2]2{[Cu(phen)]2 [SiMo12O40(VO)2]} (1), {[Zn(phen)2]2[GeMo12O40(VO)2]}{[Zn(phen)2(H2O)]2 [GeMo12O40(VO)2]}·3H2O (2) and {[Co(phen)2]2[PMo12O40(VO)2]}{[Co(phen)2(OH)]2 [PMo12O40(VO)2]}·2.5H2O (3) (phen=1,10-phenanthroline). These three compounds present, as building blocks, the bicapped Keggin anions [XMo12O40(VO)2] (X=Si, Ge and P). Compound 1 consists of a bicapped Keggin anion [SiMo12O40(VO)2]2− linked to two [Cu(phen)]+ complexes with two [Cu(phen)2]+ countercations. Compound 2 contains two bicapped Keggin anions [GeMo12O40(VO)2]4−, one…
Syntheses, structures and magnetic properties of cyano-bridged one-dimensional Ln3+–Fe3+ (Ln = La, Dy, Ho and Yb) coordination polymers
Four new heterometallic one-dimensional coordination polymers with formulae trans-[La(o-phen)3(H2O)(μ-CN)2Fe(CN)4]·7H2O (1) and trans-[Ln(H2O)2(phen)2(μ-CN)2Fe(CN)4]·nH2O [Ln/n = Dy/8 (2), Ho/7 (3) and Yb/7 (4), (o-phen = 1,10-phenanthroline)] have been synthesized by reacting Ln(NO3)3·xH2O with K3[Fe(CN)6] and 1,10-phenanthroline. The structures of 1–4 have been established by single crystal X-ray diffraction. Polymer 1 presents a chain structure with three o-phen ligands coordinated to La3+ and [Fe(CN)6]3− complexes connecting them through two trans CN− ligands to form a linear chain. Compounds 2–4 are solvates and contain Ln3+ ions coordinated to two o-phen ligands and also bridged by [F…
A trigonal prismatic anionic iron(iii) complex of a radical o-iminobenzosemiquinonate derivative: structural and spectral analyses
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…
Solvent-modulation of the structure and dimensionality in lanthanoid-anilato coordination polymers.
We show the key role that the size and shape of the solvent molecules may play in the dimensionality and structure of a series of lanthanoid–chloranilato coordination polymers. We report the synthesis, structure and magnetic properties of six different coordination polymers prepared with Er(III) and chloranilato (C6O4Cl22− = 3,6-dichloro-2,5-dihydroxy-1,4-benzoquinone) and six different solvents: [Er2(C6O4Cl2)3(H2O)6]·10H2O (1), [Er2(C6O4Cl2)3(FMA)6]·4FMA·2H2O (2) (FMA = formamide = NH2CHO), [Er2(C6O4Cl2)3(DMSO)4]·2DMSO·2H2O (3) (DMSO = dimethy sulfoxide = Me2SO), [Er2(C6O4Cl2)3(DMF)6] (4) (DMF = dimethylformamide = Me2NCHO), [Er2(C6O4Cl2)3(DMA)4] (5) (DMA = dimethylacetamide = Me2NC(Me)O) …
High-dimensional mixed-valence copper cyanide complexes: Syntheses, structural characterizations and magnetism
International audience; Reactions of CuCl 2 with different CN complexes in presence of a neutral ancillary ligand lead to two novel mixed-valence Cu complexes [Cu II (bpy)Cu I (CN) 3 ] n , 1 (bpy=2,2′-bipyridine) and {[Cu II (tn) 2 ][Cu I 4 (CN) 6 ]} n 2 (tn=1,3-diaminopropane). For compound 1, the asymmetric unit involves two Cu ions Cu1 and Cu2 (Cu I and Cu II centres, respectively) which strongly differ in their environments. The Cu1 ion presents a CuC 4 pseudo-tetrahedral geometry, while the Cu2 ion presents a CuN 5 slightly distorted square-pyramidal geometry. The extended structure of 1 is generated by three cyano ligands which differ in their coordination modes. One CN group has a μ …
Slow Magnetic Relaxation in a Co 2 Dy Trimer and a Co 2 Dy 2 Tetramer
The combination of Co(III) and Dy(III) with a compartmental Schiff base ligand (H 3 L = 3-[(2-Hydroxy-3-methoxy-benzylidene)-amino]-propane-1,2-diol), presenting three different coordinating pockets, has allowed the synthesis of two novel Co(III)-Dy(III) complexes: [Co 2 Dy(HL) 4 ]NO 3 ·2CH 3 CN ( 1 ), a rare example of trinuclear linear Co III 2 Dy III complex (and the first with slow relaxation of magnetization in absence of a DC field) and [Co 2 Dy 2 (μ 3 -OH) 2 (HL) 2 (OAc) 6 ]·4.6H 2 O ( 2 ), the first tetranuclear Co III 2 Dy III 2 cluster with a rhomb-like structure where the Co(III) ions are connected along the short diagonal of the rhomb. 1 presents two different relaxation process…
Iron( ii ) and cobalt( ii ) complexes based on anionic phenanthroline-imidazolate ligands: reversible single-crystal-to-single-crystal transformations
A series of low-spin FeII and CoII complexes based on phenanthroline-imidazolate (PIMP) ligands are reported. The FeII complex (H9O4)[Fe(PIMP)3]·(C4H10O)2(H2O) (1a) shows reversible crystalline phase transformations to afford two new phases (H9O4)[Fe(PIMP)3]·(H2O) (1b) and (H9O4)[Fe(PIMP)3]·(C8H18O)(C4H10O)(H2O) (1c) by release of diethyl ether and absorption of diethyl/dibutyl ether, respectively. This reversible uptake/release of solvent molecules is a clear example of single-crystal-to-single-crystal transformation involving a discrete metal complex. On the other hand, the corresponding CoII complex (H9O4)[Co(PIMP)3]·(C4H10O)2(H2O)2 (2) does not exhibit similar phase transformations. In …
Back Cover: Electrical Conductivity and Strong Luminescence in Copper Iodide Double Chains with Isonicotinato Derivatives (Chem. Eur. J. 48/2015)
New Multidimensional Coordination Polymers with μ 2 ‐ and μ 3 ‐dcno Cyano Carbanion Ligand {dcno – = [(NC) 2 CC(O)O(CH 2 ) 2 OH] – }
New polymeric materials [M(dcno)2(H2O)2] [M = FeII (1), CoII (2)] and [M(dcno)2] [M = CuII (3), MnII (4)] with dcno– =[(NC)2CC(O)O(CH2)2OH]– = 2,2-dicyano-1-(2-hydroxyethoxy)ethenolate anion have been synthesised and characterised by IR spectroscopy, X-ray crystallography and magnetic measurements. In compounds 1 and 2, each organic ligand acts in a bridging mode with its two nitrogen atoms bound to two different metal ions, while in compounds 3 and 4, each organic anion acts as a μ3-bridging ligand through its two nitrogen atoms and the oxygen atom of the OH group. Each metal ion has a pseudo-octahedral trans-MN4O2 environment with four nitrogen atoms from four different organic ligands an…
Azido and thiocyanato bridged dinuclear Ni(II) complexes involving 8-aminoquinoline based Schiff base as blocking ligands: Crystal structures, ferromagnetic properties and magneto-structural correlations
Abstract The use of two 8-aminoquinoline-based tridentate N3-donor rigid Schiff base ligands (L1 and L2) with Ni(II) in the presence of the pseudohalides, NaN3 and NaSCN results in the crystallization of the two novel Ni(II) dimers: [Ni2(L1)2(µ1,1′-N3)2(N3)2] (1) and [Ni2(L2)2(µ1,3-NCS)2(NCS)2] (2). Both complexes are centrosymmetric Ni(II) dimers where the Schiff base ligands coordinate the octahedral Ni(II) centres in a mer configuration with one terminal and two bridging pseudohalide ligands in the remaining positions. Complex 1 shows Ni(II) ions connected by a double µ1,1′-N3− bridge whereas in complex 2 the Ni(II) ions are connected by a double µ1,3-NCS− bridge. The magnetic properties…
New planar polynitrile dianion and its first coordination polymer with unexpected short M⋯M contacts (tcno2−=[(NC)2CC(O)C(CN)2]2−)
International audience; A new planar polynitrile dianion ([tcno]2− = [(NC)2CC(O)C(CN)2]2−) has been synthesized as its potassium salt, K2[tcno] (1). The crystallization of 1 by the slow evaporation of an aqueous solution at room temperature gave two types of colourless crystals having two different shapes [1-A: fine plates and 1-B: needles] for which the crystal structure determinations showed similar geometries for the polynitrile anion in both the structures. The combination of this novel dianion with Cu(II) led to the coordination complex [Cu(tcno)2(H2O)2] (2), which constitutes the first coordination complex of this dianion. The structure of 2 can be described as a coordination polymer …
A novel oxovanadate structural type – Synthesis, single crystal structure and magnetic properties of a mixed-valence polyoxovanadate formed by {V17O40(Cl)} and {V15O36(Cl)} clusters
Abstract A novel polyoxovanadate structural type, with an average nuclearity of V16, formed by a mixture of two different polyoxovananadates: {V15O36(Cl)} and{V17O40(Cl)} has been synthesized and characterized. The title compound, formulated as [Ni(phen)3]2{[V15O36(Cl)]0.5[V17O40(Cl)]0.5} · H2O (1) (phen = 1,10′-phenanthroline), presents two different polyoxovanadate architectures: {V15O36(Cl)} and {V17O40(Cl)}, with the last one representing a new framework type in polyoxovanadate chemistry. Here, we present the synthesis of this novel polyoxovanadate under hydrothermal conditions and its characterization by IR and XPS spectroscopies, elemental and thermogravimetric analysis, redox titrati…
Nanosheets of Two-Dimensional Magnetic and Conducting Fe(II)/Fe(III) Mixed-Valence Metal-Organic Frameworks.
We report the synthesis, magnetic properties, electrical conductivity, and delamination into thin nanosheets of two anilato-based Fe(II)/Fe(III) mixed-valence two-dimensional metal–organic frameworks (MOFs). Compounds [(H3O)(H2O)(phenazine)3][FeIIFeIII(C6O4X2)3]·12H2O [X = Cl (1) and Br (2)] present a honeycomb layered structure with an eclipsed packing that generates hexagonal channels containing the water molecules. Both compounds show ferrimagnetic ordering at ca. 2 K coexisting with electrical conductivity (with room temperature conductivities of 0.03 and 0.003 S/cm). Changing the X group from Cl to Br leads to a decrease in the ordering temperature and room temperature conductivity tha…
A fluorescent layered oxalato-based canted antiferromagnet
We report the synthesis and characterization of the first fluorescent oxalato-based canted antiferromagnet. Compound [DOC][MnFe(C2O4)3] (1) (DOC = 3,3'-diethyloxacarbocyanine) combines the well-known canted antiferromagnetic [MnFe(C2O4)3]- honeycomb layers with a fluorescent cationic cyanine-type fluorescent dye. Besides the expected spin canted antiferromagnetic order in the oxalato layer at ca. 29 K, we show the key role played by the anionic oxalato lattice in the optical properties of the cation since it provides isolation of dye cations in the hexagonal cavities of the oxalato-based matrix. The emission of the DOC+ dye shows a redshift and a broadening of the emission as well as an inc…
Solvent-modulated structures in anilato-based 2D coordination polymers
Abstract This work highlights the key role of the solvents in the structures of the series of 2D compounds [Ln2(C6O4Br2)3·(Solvent)n]·G (G = Guest). This study is based on the affinity and ability of these solvents to coordinate to lanthanides and on their possibility to act as solvation molecules. For this purpose here we focus on the Er(III) ion and on the bromanilato bridging ligand ([C6O4Br2]2− = dianion of 3,6-dibromo-2,5-dihydroxy-1,4-benzoquinone) and we play with three solvents: H2O, DMSO (dimethylsulfoxide) and DMF (dimethylformamide). Here we report the synthesis, crystal structure and magnetic characterization of compounds [Er2(C6O4Br2)3(H2O)6]·12H2O (1), [Er2(C6O4Br2)3(DMSO)4]·2…
Homo and heterometallic rhomb-like Ni4 and Mn2Ni2 complexes
Abstract Two new polynuclear complexes with hydroxyl-rich Schiff base ligand 3-[(2-Hydroxy-benzylidene)-amino]-propane-1,2-diol (H3L), namely [NiII2(HL)(H2L)(SCN)]2·DMF (1) and [MnIII2NiII2(HL)2(L)2] (2) have been synthesized and characterized by single crystal X-ray diffraction, elemental analyses, FTIR, UV–Vis spectroscopy and variable temperature magnetic susceptibility measurements. The X-ray refinements reveal that both compounds present defective rhomb-like dicubane central cores (Ni4 in 1 and Mn2Ni2 in 2). Magnetic susceptibility measurements indicate the presence of overall antiferromagnetic exchange interactions in 1 along the side connected by a N and O atoms (J1 = −43.6 cm−1) and…
Solvent Modulated Assembly of Two Ni(II) Complexes: Syntheses, Structures and Magnetic Properties
A dinuclear [Ni2(L)2(DMSO)2(MeOH)2] (1) and a tetra-nuclear [Ni4(L)4(DMF)2(H2O)2].DMF (2) Ni(II) complexes have been prepared by treating nickel nitrate hexahydrate with the Schiff base ligand H2L (H2L=(E)-2-(2-hydroxybenzyliden)amino-4-nitrophenol) in a one-pot reaction. Complex 1 was obtained after recrystallization of the precipitate from the reaction with a 1:1:1 mixture of DMSO/CH2Cl2/MeOH. In contrast, the tetrameric complex 2 was obtained after slow evaporation of the filtrate. Both complexes were characterized by analytical, thermogravimetric, optical and magnetic techniques. The solid state molecular structures of 1 and 2 were determined by single crystal X-ray crystallography. Com…
Hepta- and tetra-nuclear copper(II) clusters self-assembled by cyano- and azacyano-carbanions
International audience; Two polynuclear copper(II) complexes with hydroxido-bridging ligands and polycyanide units, [Cu{Cu(tn)}6(μ2-OH)2(μ3-OH)4Cl2](tcm)4Cl2·2H2O (1) and [{Cu(bpy)}4(OH)4(dca)2](dca)2·bpy·2H2O (2) (tn = NH2(CH2)3NH2; tcm− = [C(CN)3]−, bpy = 2,2′-bipyridyl, dca− = [N(CN)2]−) have been prepared by one-pot reactions. The structure of 1 consists of a centrosymmetric heptanuclear ion [Cu{Cu(tn)}6(μ2-OH)2(μ3-OH)4Cl2]6+. The tcm− and the halide anions which appear as counter-ions in the formula unit, play an important role in the stabilization of the complex since the hydrogen bonding between nitrogen atoms of the tcm− anion and halide anions, and hydrogen atoms of the terminal wa…
Polynitrile anions as ligands: From magnetic polymeric architectures to spin crossover materials
International audience; The use of polynitrile anions as ligands (L) either alone or in combination with neutral co-ligands (L′) is a very promising and appealing strategy to get molecular architectures with different topologies and dimensionalities thanks to their ability to coordinate and bridge metal ions in many different ways. The presence of several potentially coordinating nitrile groups (or even other donor groups as –OH, –SH or –NH2), their rigidity and their electronic delocalization allow the synthesis of original magnetic high dimensional coordination polymers with transition metals ions. Furthermore, these ligands have shown coordinating and bridging capabilities in novel discr…
Reversible stimulus-responsive Cu(i) iodide pyridine coordination polymer
We present a structurally flexible copper–iodide–pyridine-based coordination polymer showing drastic variations in its electrical conductivity driven by temperature and sorption of acetic acid molecules. The dramatic effect on the electrical conductivity enables the fabrication of a simple and robust device for gas detection. X-ray diffraction studies and DFT calculations allow the rationalisation of these observations.
Field-induced single molecule magnet behavior of a dinuclear cobalt(II) complex: a combined experimental and theoretical study.
Two dinuclear cobalt(ii) complexes, [(dmso)CoIIL1(μ-(m-NO2)C6H4COO)CoII(NCS)] (1) and [(dmso)CoIIL2(μ-(m-NO2)C6H4COO)CoII(NCS)] (2) [dmso = dimethylsulfoxide, H2L1 = (2,2-dimethyl-1,3-propanediyl)bis(iminomethylene)bis(6-methoxyphenol) and H2L2 = (2,2-dimethyl-1,3-propanediyl)bis(iminomethylene)bis(6-ethoxyphenol)] have been synthesized and structurally characterized by single-crystal X-ray diffraction, magnetic-susceptibility measurements and various spectroscopic techniques. Each complex contains a cobalt(ii) center with a slightly distorted octahedral geometry and a second cobalt(ii) center with a distorted trigonal prismatic one. To obtain insight into the physical nature of weak non-co…
Slow relaxation in doped coordination polymers and dimers based on lanthanoids and anilato ligands
Abstract In this work we report the synthesis, structure and magnetic properties of two lanthanoid based coordination polymers (CP) and two dimers prepared with two derivatives of the 2,5-dihydroxy-1,4-benzoquinone (C6O4X2)2− as ligands. Using the bromanilato ligand: (C6O4Br2)2− we have prepared the CP [Eu1.96Dy0.04(C6O4Br2)3(DMSO)6]·2DMSO (1) (DMSO = dimethylsulfoxide) and with the chlorocyananilato ligand: (C6O4(CN)Cl)2−) we have prepared one CP formulated as [Eu1.96Dy0.04(C6O4(CN)Cl)3(DMSO)6] (2) and two isostructural dimers: [Eu1.96Dy0.04(C6O4(CN)Cl)3(H2O)10]·6H2O (3) and [Eu2(C6O4(CN)Cl)3(H2O)10]·6H2O (4). Compounds 1, 2 and 3 are Eu(III) compounds doped with 2.0 % of Dy(III), whereas …
Metallic Charge‐Transfer Salts of Bis(ethylenedithio)tetrathiafulvalene with Paramagnetic Tetrachloro(oxalato)rhenate(IV) and Tris(chloranilato)ferrate(III) Anions
The synthesis, crystal structure and physical characterization of three radical salts of the donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF or ET) and tetrachloro(oxalato)rhenate(IV) {[ReCl4(C2O4)]2–} or tris(chloranilato)ferrate(III) {[Fe(C6O4Cl2)3]3–} anions are reported. The isolated salts with ReIV are (ET)[ReCl4(C2O4)] [1, monoclinic, space group C2/c with a = 18.3409(3) A, b = 10.8414(2) A, c = 11.1285(3) A, β = 99.9714(7)°, V = 2179.38(8) A3, Z = 4] and (ET)4[ReCl4(C2O4)]·C6H5CN [2, monoclinic, space group P21/c with a = 11.8549(2) A, b = 32.9079(5) A, c = 36.4154(5) A, β = 96.742(2)°, V = 14108.1(4) A3, Z = 8]. The salt with FeIII is (ET)6[Fe(C6O4Cl2)3]·(H2O)1.5·(CH2Cl2)0.5 […
Effects of water removal on the structure and spin-crossover in an anilato-based compound
The crucial role played by a crystallization water molecule in the spin crossover (SCO) temperature and its hysteresis is described and discussed in compound [NBu4][Fe(bpp)2][Cr(C6O4Br2)3]⋅2.5H2O (1), where bpp = 2,6-bis(pyrazol-3-yl)pyridine and (C6O4Br2)2− = dianion of the 3,6-dibromo-2,5-dihydroxy-1,4-benzoquinone. The compound has isolated [Fe(bpp)2]2+ cations surrounded by chiral [Cr(C6O4Br2)3]3− anions, NBu4+ cations, and a water molecule H-bonded to one of the non-coordinated N–H groups of one bpp ligand. This complex shows a gradual almost complete two-step spin transition centered at ca. 180 and 100 K with no hysteresis. The loss of the water molecules results in a phase transition…
Linkage isomerism in coordination polymers.
The use of the recently prepared polynitrile ligand tcnopr3OH(-) ([(NC)(2)CC(OCH(2)CH(2)CH(2)OH)C(CN)(2)](-)) with different salts of Fe(II), Co(II), and Ni(II) has led to a very rare example of linkage isomerism in a coordination chain. These pairs of linkage isomers can be formulated as [M(tcnopr3OH-κN,κO)(2)(H(2)O)(2)]; M = Fe (1), Co (3), and Ni(5) and [M(tcnopr3OH-κN,κN')(2)(H(2)O)(2)]; M = Fe (2), Co (4), and Ni (6). Compounds 1-2, 3-4, and 5-6 are three pairs of linkage isomers since they present the same formula and chain structure and they only differ in the connectivity of the polynitrile ligand bridging the metal ions in the chain: through a N and an O atom (1κN:2κO-isomer) or th…
Syntheses, structures and physical characterization of two new three-dimensional mixed-valence hexadecavanadate derivatives
Abstract Two new hexadecavanadate derivatives, (bpy)[Zn(4,4′-bpy)2]2[H4ClV16O38]·6H2O 1 and (bpy)[Co(4,4′-bpy)2]2[H4ClV16O38]·6H2O 2 (bpy = 4,4′-bipyridine), were synthesized under the hydrothermal conditions and structurally characterized by IR, XPS and EPR spectroscopy, redox titration and single-crystal X-ray diffraction. The two compounds are isostructural and crystallize in the tetragonal non-centrosymmetric space group P-4n2 (No. 118) with a = 17.124(2), b = 17.124(2), c = 14.724(3) A, V = 4317.5(12) A3 and Z = 1 for the compound 1, and a = 17.038(2), b = 17.038(2), c = 14.754(3) A, V = 4282.9(12) A3 and Z = 1 for the compound 2. Compounds 1 and 2 were constructed from 4-connected {H4…
Key Role of the Cation in the Crystallization of Chiral Tris(Anilato)Metalate Magnetic Anions
A complete study of the role played by the usually considered “innocent” cation in the synthesis of chiral tris(anilato)metalate magnetic complexes is presented. This study is based on the rational synthesis of the family of compounds formulated as A3[MIII(C6O4X2)3] with A+ = [PPh3Et]+, [PPh3Pr]+, [PBu4]+, [NHep4]+, and [PPh4]+; MIII = CrIII, FeIII, and GaIII; and [C6O4X2]2– (X = Cl, Br, and NO2; [C6O4X2]2– = dianion of the 3,6-disubstituted derivatives of 2,5-dihydroxy-1,4-benzoquinone, H4C6O4). We show and explain the unexpected key role played by the cations in isolating chiral or achiral crystals of these [MIII(C6O4X2)3]3– anions with D3 point group symmetry. Thus, among the 18 new comp…
Supramolecular 2D/3D isomerism in a compound containing heterometallic Cu(II)2Co(II) nodes and dicyanamide bridges.
Three new heterometallic copper(II)-cobalt(II) complexes [(CuL(2))2Co{dca}2]·H2O(1), [(CuL(1))2Co{dca}2]n (2a), and [(CuL(1))2Co{dca}2]n (2b) [dca(-) = dicyanamide = N(CN)2(-)] have been synthesized by reacting the "metallo-ligand" [CuL(1)] or [CuL(2)] with cobalt(II) perchlorate and sodium dicyanamide in methanol-water medium (where H2L(1) = N,N'-bis(salicylidene)-1,3-propanediamine and H2L(2) = N,N'-bis(α-methylsalicylidene)-1,3-propanediamine). The three complexes have been structurally and magnetically characterized. Complex 1 is a discrete trinuclear species in which two metallo-ligands coordinate to a cobalt(II) ion through the phenoxido oxygen atoms along with two terminally coordina…
2D and 3D Anilato-Based Heterometallic M(I)M(III) Lattices: The Missing Link
The similar bis-bidentate coordination mode of oxalato and anilato-based ligands is exploited here to create the first examples of 2D and 3D heterometallic lattices based on anilato ligands combining M(I) and a M(III) ions, phases already observed with oxalato but unknown with anilato-type ligands. These lattices are prepared with alkaline metal ions and magnetic chiral tris(anilato)metalate molecular building blocks: [M(III)(C6O4X2)3](3-) (M(III) = Fe and Cr; X = Cl and Br; (C6O4X2)(2-) = dianion of the 3,6-disubstituted derivatives of 2,5-dihydroxy-1,4-benzoquinone, H4C6O4). The new compounds include two very similar 2D lattices formulated as (PBu3Me)2[NaCr(C6O4Br2)3] (1) and (PPh3Et)2[KF…
New coordination polymers based on a novel polynitrile ligand: Synthesis, structure and magnetic properties of the series [M(tcnoetOH)2(4,4′-bpy)(H2O)2] (tcnoetOH−=[(NC)2CC(OCH2CH2OH)C(CN)2]−; M=Fe, Co and Ni)
International audience; A novel polynitrile anionic ligand, tcnoetOH−(=[(NC)2CC(OCH2CH2OH)C(CN)2]−), has been synthesized by a one-pot reaction from a cyclic acetal and malononitrile. This ligand has been successfully used to prepare, with 4,4′-bpy as co-ligand, a novel series of coordination polymers formulated as [M(tcnoetOH)2(4,4′-bpy)(H2O)2] with M(II) = Fe (1), Co (2) and Ni (3). These isostructural compounds present a linear chain structure consisting of octahedrally coordinated metal ions bridged by trans 4,4′-bpy ligands. The coordination sphere of the metal ions is completed with two terminal tcnoetOH− ligand and two water molecules. The magnetic properties indicate that the three …
Effect of the lanthanoid-size on the structure of a series of lanthanoid-anilato 2-D lattices
AbstractWe report the synthesis and characterization of a series of Ln-based bromoanilato 2-D lattices with dimethyl sulfoxide (DMSO): [Ln2(C6O4Br2)3(DMSO)n]·2DMSO·mH2O with n = 6 and m = 0 for Ln = La (1), Ce (2), Pr (3), Nd (4), Sm (5), Eu (6) and Gd (7); n = 4 and m = 2 for Ln = Tb (8), Dy (9), Ho (10), Er (11), Tm (12) and Yb (13) (C6O4Br22− = 3,6-dibromo-2,5-dihydroxy-1,4-benzoquinone = bromoanilato). The X-ray analysis shows that the largest Ln(III) ions (La-Gd, 1-7) crystallize in the monoclinic P21/n space group (phase I), whereas the smaller Ln(III) ions (Tb–Yb, 8–13) crystallize in the triclinic P-1 space group (phase II). Both phases present a (6,3)-2-D topology but show importan…
Trinuclear Lanthanide Coordination Clusters: Single-Molecule-Magnet Behavior and Catalytic Activity in the Friedel-Crafts Alkylation Reaction.
A new multidentate ligand (H3 L) was synthesized by the condensation reaction of 4-tert-butyl-2,6-diformylphenol and 2-amino-4-nitrophenol. The reaction of the ligand with hydrated lanthanide nitrate produced two isostructural trinuclear coordination clusters: [DyLn3 L3 (DMF)3 (H2 O)2 ] ⋅ 3.8DMFLn=Dy (1) and Nd (2) (DMF=N, N-dimethylformamide). Single-crystal X-ray diffraction analysis revealed that there are three lanthanide ions arranged in an almost perfect linear fashion in both complexes. Magnetic studies show single-molecule-magnet (SMM) behavior in the Dy derivative with τ0 =1.7×10-6 s and a thermal energy barrier of 7.0 cm-1 . Both complexes were used as catalysts towards the Fried…
Synthesis and characterization of a novel dicyanamide-bridged Co(II) 1-D coordination polymer with a N 4 -donor Schiff base ligand
The synthesis, structure and magnetic properties of a novel Co(II) 1D coordination polymer, [Co(L)(µ1,5-dca)(ClO4)2·MeOH]n (1) are described. Compound 1 contains two independent cationic Co(II) chains (CoA and CoB) which are parallel to the c direction and present short π-π and C-H⋯π interactions with two neighbouring chains along the b direction, giving rise to alternating layers of chains A and B in the bc plane. Variable-temperature magnetic susceptibility measurements shows a weak antiferromagnetic coupling among the adjacent cobalt(II) centres mediated through μ1,5-dca− bridge.
Slow relaxation of the magnetization, reversible solvent exchange and luminescence in 2D anilato-based frameworks.
A series of multifunctional 2D frameworks prepared with Dy(iii) and the bromanilato ligand, formulated as: [Dy2(C6O4Br2)3(G)n]·nG with G = H2O, dimethylformamide (dmf) and dimethylsulfoxide (dmso), can exchange the coordinated and non-coordinated solvent molecules (G) in a reversible way. These multifunctional frameworks show field induced slow relaxation of the magnetization and luminescence that can be easily and reversibly modified by solvent exchange.
New coordination polymer based on a triply bridged dicarboxylate ligand: Synthesis, structure, and magnetic properties of the adipato complex [Cu4(bpy)4(adip)3](tcnoet)2·2H2O {bpy=C10H8N2; adip2−=[O2C(CH2)4CO2]2−; tcnoet−=[(NC)2CC(OEt)C(CN)2]−}
International audience; One-pot reaction of copper(II) chloride dihydrate CuCl2 · 2H2O with 2,2′-bipyridyl (bpy = C10H8N2) in the presence of sodium adipate Na2adip (adip2− = [O2C(CH2)4CO2]2−) and potassium 1,1,3,3-tetracyano-2-ethoxypropenide (tcnoet− = [(NC)2CC(OEt)C(CN)2]−) gives the new compound [Cu4(bpy)4(adip)3](tcnoet)2 · 2H2O (1), which was characterized by single crystal X-ray diffraction analysis. The Cu(II) metal ion presents an elongated square pyramidal CuN2O3 environment, with an oxygen atom in apical position and a base plane involving almost equivalent bond lengths. The structure can be described as a pseudo dinuclear species in which two Cu(bpy) units are triply bridged by …
Guidelines to design new spin crossover materials
International audience; This review focuses on new families of spin crossover (SCO) complexes based on polynitrile anions as new anionic ligands or on polyazamacrocycles as neutral macrocyclic ligands. We have shown that the structural and electronic characteristics (original coordination modes and high electronic delocalization) of the polynitrile anions can be tuned by slight chemical modifications such as substitution of functional groups or variation of the negative charge to design new discrete or polymeric SCO systems.In our ongoing work on the design of new molecular systems based on new ligands that can be fine-tuned via chemical modifications, another promising way which has been r…
Guest-dependent single-ion magnet behaviour in a cobalt(ii) metal-organic framework.
Single-ion magnets (SIMs) are the smallest possible magnetic devices for potential applications in quantum computing and high-density information storage. Both, their addressing in surfaces and their organization in metal-organic frameworks (MOFs) are thus current challenges in molecular chemistry. Here we report a two-dimensional 2D MOF with a square grid topology built from cobalt(ii) SIMs as nodes and long rod-like aromatic bipyridine ligands as linkers, and exhibiting large square channels capable to host a large number of different guest molecules. The organization of the cobalt(ii) nodes in the square layers improves the magnetic properties by minimizing the intermolecular interaction…
A novel polynitrile ligand with different coordination modes: Synthesis, structure and magnetic properties of the series [M(tcnoprOH)2(H2O)2] (M=Mn, Co and Cu) (tcnoprOH−=[(NC)2CC(OCH2CH2CH2OH)C(CN)2]−)
International audience; A novel polynitrile ligand (tcnoprOH− = [(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) with up to five potentially coordinating groups has been synthesized in a one-pot reaction from a cyclic acetal and malononitrile. The combination of this novel ligand with different transition metal ions has led to the synthesis of two different structural types with the same formula but with different coordination modes in the ligand. Mn(II) and Cu(II) lead to a μ2-N,O-coordinating mode in the series of compounds formulated as [M(N,O-tcnoprOH)2(H2O)2] (M = MnII (1) and CuII (2)), whereas Co(II) and, most probably Ni(II), lead to a μ2-N,N′-coordinating mode in [Co(N,N′-tcnoprOH)2(H2O)2] (3). Bot…
A family of layered chiral porous magnets exhibiting tunable ordering temperatures.
A simple change of the substituents in the bridging ligand allows tuning of the ordering temperatures, Tc, in the new family of layered chiral magnets A[M(II)M(III)(X2An)3]·G (A = [(H3O)(phz)3](+) (phz = phenazine) or NBu4(+); X2An(2-) = C6O4X2(2-) = 2,5-dihydroxy-1,4-benzoquinone derivative dianion, with M(III) = Cr, Fe; M(II) = Mn, Fe, Co, etc.; X = Cl, Br, I, H; G = water or acetone). Depending on the nature of X, an increase in Tc from ca. 5.5 to 6.3, 8.2, and 11.0 K (for X = Cl, Br, I, and H, respectively) is observed in the MnCr derivative. Furthermore, the presence of the chiral cation [(H3O)(phz)3](+), formed by the association of a hydronium ion with three phenazine molecules, lead…
Modulation of the ordering temperature in anilato-based magnets
Abstract Four new 2D honeycomb anilato-based ferrimagnets with Mn(II) and Cr(III) have been prepared and characterized. These compounds, formulated as (NBu4)[MnCr(C6O4X2)3(PhCHO)]·PhY (X/Y = Cl/H (1), Br/H (2), Cl/CHO (3) and Br/CHO (4) show that it is possible to include benzaldehyde as a co-ligand coordinated to the Mn(II) metal atom in these 2D ferrimagnets. This inclusion increases the coordination number of Mn(II) to seven resulting in a change in the ordering temperatures of these 2D ferrimagnets (from ca. 10–11 K to ca. 7 K). Here we show the role played by the additional benzaldehyde ligand and by the crystallization solvent molecules (benzene in 1 and 2 and benzaldehyde in 3 and 4)…
Coordination polymers based on diiron tetrakis(dithiolato) bridged by alkali metals, electrical bistability around room temperature, and strong antiferromagnetic coupling.
Coordination polymer chains have been formed by the direct reaction between HSC6H2Cl2SH and FeCl3·6H2O in the presence of an aqueous solution of the corresponding alkali-metal hydroxide (M = Li, Na, and K) or carbonate (M = Rb and Cs). The structures consist of dimeric [Fe2(SC6H2Cl2S)4](2-) entities bridged by [M2(THF)4] [M = K (1), Rb (2), and Cs (3); THF = tetrahydrofuran] or {[Na2(μ-H2O)2(THF)2] (5 and 5') units. The smaller size of the lithium atom yields an anion/cation ion-pair molecule, [Li(THF)4]2[Fe2(SC6H2Cl2S)4] (4), in which the dianionic moieties are held together by Cl···Cl interactions. Electrical characterization of these compounds shows a general semiconductor behavior in wh…
Multifunctional Ni(II)-Based Metamagnetic Coordination Polymers for Electronic Device Fabrication
The combination of two 8-aminoquinoline-based Schiff base ligands (L1 and L2) with SCN– and Ni(II) has led to the synthesis of two new one-dimensional thiocyanato-bridged coordination polymers: [Ni...
Synthesis and characterization of a new Organic – Inorganic sulfate (C5H6N2O)2[Co(H2O)6]3(SO4)4.2H2O
crystals of a new hybrid compound, (C 5 H 6 N 2 O) 2 [Co(H 2 O) 6 ] 3 (SO 4 ) 4 .2H 2 O, were synthesized in aqueous solution and characterized. This compound crystallizes in the triclinic system with the space group P-1, the unit cell :a=6.632(3) A, b=11.769(5) A, c=14.210(6) A, α=67.86(4)°, β=81.32(4)°, γ=85.18(4)° and V=1015.14(8) A 3 . Its crystal structure can be described as a packing of alternated inorganic and organic layers. The different components are connected by a three-dimensional network of O-H…O and N-H…O hydrogen bonds.
Polymorphism and Metallic Behavior in BEDT-TTF Radical Salts with Polycyano Anions
Up to five different crystalline radical salts have been prepared with the organic donor BEDT-TTF and three different polynitrile anions. With the polynitrile dianion tcpd2− (=C[C(CN)2]32−), two closely related radical salts: α'-(ET)4tcpd·THF (1) (THF = tetrahydrofurane) and α'-(ET)4tcpd·H2O (2) have been prepared, depending on the solvent used in the synthesis. With the mono-anion tcnoetOH− (=[(NC)2CC(OCH2CH2OH)C(CN)2]−) two polymorphs with similar physical properties but different crystal packings have been synthesized: θ-(ET)2(tcnoetOH) (3) and β''-(ET)2(tcnoetOH) (4). Finally, with the mono-anion tcnoprOH− (=[(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) we have prepared a metallic…
Pre- and post-synthetic modulation of the ordering temperatures in a family of anilato-based magnets
We report the synthesis and characterization of six novel heterometallic molecule-based 2D magnets with the bromanilato ligand (C6O4Br22− = 1,3-dibromo-2,5-dihydroxy-1,4-benzoquinone dianion) and six different benzene derivative molecules. The compounds, formulated as (NBu4)[MnCr(C6O4Br2)3]·1.75C6H5Br (1), (NBu4)[MnCr(C6O4Br2)3]·C6H5X with X = Cl (2), I (3) and CH3 (4) and (NBu4)[MnCr(C6O4Br2)3]·2C6H5X with X = CN (5) and NO2 (6), present the classical hexagonal honeycomb-(6,3) lattice with alternating Mn(II) and Cr(III) ions. The layers are packed in an eclipsed way along the a direction giving rise to hexagonal channels where the benzene derivative molecules are located with π–π interacti…
CCDC 2054147: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hern��ndez-Paredes, Mar��a Bayona-Andr��s, Carlos J. G��mez-Garc��a|2021|Molecules|26|1190|doi:10.3390/molecules26041190
CCDC 1415637: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Patricia Gómez-Claramunt, Cristina Vallés-García, Guillermo Mínguez Espallargas, Carlos J. Gómez García|2016|Cryst.Growth Des.|16|518|doi:10.1021/acs.cgd.5b01573
CCDC 1054137: Experimental Crystal Structure Determination
Related Article: Souvik Pal, Kartick Dey, Samia Benmansour, Carlos J. Gómez-García, Hari Pada Nayek|2019|New J.Chem.|43|6228|doi:10.1039/C8NJ05173A
CCDC 1054136: Experimental Crystal Structure Determination
Related Article: Souvik Pal, Kartick Dey, Samia Benmansour, Carlos J. Gómez-García, Hari Pada Nayek|2019|New J.Chem.|43|6228|doi:10.1039/C8NJ05173A
CCDC 982641: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Eugenio Coronado, Carlos Giménez-Saiz, Carlos J. Gómez-García, Carola Rößer|2014|Eur.J.Inorg.Chem.||3949|doi:10.1002/ejic.201402023
CCDC 1415919: Experimental Crystal Structure Determination
Related Article: Julia Vallejo, Francisco R. Fortea-Pérez, Emilio Pardo, Samia Benmansour, Isabel Castro, J. Krzystek, Donatella Armentano, Joan Cano|2016|Chemical Science|7|2286|doi:10.1039/C5SC04461H
CCDC 1835925: Experimental Crystal Structure Determination
Related Article: Alexandre Abhervé, Samia Benmansour, Carlos José Gómez-García, Narcis Avarvari|2018|CrystEngComm|20|4141|doi:10.1039/C8CE00561C
CCDC 1415635: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Patricia Gómez-Claramunt, Cristina Vallés-García, Guillermo Mínguez Espallargas, Carlos J. Gómez García|2016|Cryst.Growth Des.|16|518|doi:10.1021/acs.cgd.5b01573
CCDC 1579865: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hernández Paredes, Carlos J. Gómez García|2018|J.Coord.Chem.|71|845|doi:10.1080/00958972.2017.1420182
CCDC 1470626: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Alexandre Abhervé, Patricia Gómez-Claramunt, Cristina Vallés-García, Carlos J. Gómez-García|2017|ACS Applied Materials and Interfaces|9|26210|doi:10.1021/acsami.7b08322
CCDC 990028: Experimental Crystal Structure Determination
Related Article: Saptarshi Biswas, Carlos J. Gómez-García, Juan M. Clemente-Juan, Samia Benmansour, Ashutosh Ghosh|2014|Inorg.Chem.|53|2441|doi:10.1021/ic4023536
CCDC 953847: Experimental Crystal Structure Determination
Related Article: Matteo Atzori, Samia Benmansour, Guillermo Mínguez Espallargas, Miguel Clemente-León, Alexandre Abhervé, Patricia Gómez-Claramunt, Eugenio Coronado, Flavia Artizzu, Elisa Sessini, Paola Deplano, Angela Serpe, Maria Laura Mercuri, and Carlos J. Gómez García|2013|Inorg.Chem.|52|10031|doi:10.1021/ic4013284
CCDC 1499648: Experimental Crystal Structure Determination
Related Article: Richa Vinayak, A. Harinath, Carlos J. Gomez-Garcıa, Tarun K. Panda, Samia Benmansour, and Hari Pada Nayek|2016|Chem. Sel.|1|6532|doi:10.1002/slct.201601385
CCDC 1415917: Experimental Crystal Structure Determination
Related Article: Julia Vallejo, Francisco R. Fortea-Pérez, Emilio Pardo, Samia Benmansour, Isabel Castro, J. Krzystek, Donatella Armentano, Joan Cano|2016|Chemical Science|7|2286|doi:10.1039/C5SC04461H
CCDC 1907204: Experimental Crystal Structure Determination
Related Article: Antonio Hernández-Paredes, Christian Cerezo-Navarrete, Carlos J. Gómez García, Samia Benmansour|2019|Polyhedron|170|476|doi:10.1016/j.poly.2019.06.004
CCDC 1981327: Experimental Crystal Structure Determination
Related Article: Ritwik Modak, Yeasin Sikdar, Carlos J. Gómez‐García, Samia Benmansour, Sudipta Chatterjee, Sanchita Goswami|2021|Chem.Asian J.|16|666|doi:10.1002/asia.202001468
CCDC 1047310: Experimental Crystal Structure Determination
Related Article: Khaled Hassanein, Javier Conesa-Egea, Salome Delgado, Oscar Castillo, Samia Benmansour, José I. Martínez, Gonzalo Abellán, Carlos J. Gómez-García, Félix Zamora, Pilar Amo-Ochoa|2015|Chem.-Eur.J.|21|17282|doi:10.1002/chem.201502131
CCDC 2054148: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hernández-Paredes, María Bayona-Andrés, Carlos J. Gómez-García|2021|Molecules|26|1190|doi:10.3390/molecules26041190
CCDC 1579871: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hernández Paredes, Carlos J. Gómez García|2018|J.Coord.Chem.|71|845|doi:10.1080/00958972.2017.1420182
CCDC 1909315: Experimental Crystal Structure Determination
Related Article: Cristian Martínez-Hernández, Samia Benmansour, Carlos J. Gómez García|2019|Polyhedron|170|122|doi:10.1016/j.poly.2019.05.034
CCDC 1054832: Experimental Crystal Structure Determination
Related Article: Samia Benmansour , Esther Delgado , Carlos J. Gómez-García , Diego Hernández , Elisa Hernández , Avelino Martin , Josefina Perles , and Félix Zamora|2015|Inorg.Chem.|54|2243|doi:10.1021/ic502789v
CCDC 1415636: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Patricia Gómez-Claramunt, Cristina Vallés-García, Guillermo Mínguez Espallargas, Carlos J. Gómez García|2016|Cryst.Growth Des.|16|518|doi:10.1021/acs.cgd.5b01573
CCDC 1579872: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hernández Paredes, Carlos J. Gómez García|2018|J.Coord.Chem.|71|845|doi:10.1080/00958972.2017.1420182
CCDC 1532867: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Irene Pérez-Herráez, Gustavo López-Martínez, Carlos J. Gómez García|2017|Polyhedron|135|17|doi:10.1016/j.poly.2017.06.052
CCDC 917971: Experimental Crystal Structure Determination
Related Article: Ritwik Modak, Yeasin Sikdar, Senjuti Mandal, Carlos J. Gómez-García, Samia Benmansour, Sudipta Chatterjee, Sanchita Goswami|2014|Polyhedron|70|155|doi:10.1016/j.poly.2013.12.031
CCDC 1415638: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Patricia Gómez-Claramunt, Cristina Vallés-García, Guillermo Mínguez Espallargas, Carlos J. Gómez García|2016|Cryst.Growth Des.|16|518|doi:10.1021/acs.cgd.5b01573
CCDC 1054830: Experimental Crystal Structure Determination
Related Article: Samia Benmansour , Esther Delgado , Carlos J. Gómez-García , Diego Hernández , Elisa Hernández , Avelino Martin , Josefina Perles , and Félix Zamora|2015|Inorg.Chem.|54|2243|doi:10.1021/ic502789v
CCDC 1457366: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Carlos J. Gómez-García|2016|Polymers|8|89|doi:10.3390/polym8030089
CCDC 1586538: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Irene Pérez-Herráez, Christian Cerezo-Navarrete, Gustavo López-Martínez, Cristian Martínez Hernández, Carlos J. Gómez-García|2018|Dalton Trans.|47|6729|doi:10.1039/C8DT00143J
CCDC 1401258: Experimental Crystal Structure Determination
Related Article: Khaled Hassanein, Javier Conesa-Egea, Salome Delgado, Oscar Castillo, Samia Benmansour, José I. Martínez, Gonzalo Abellán, Carlos J. Gómez-García, Félix Zamora, Pilar Amo-Ochoa|2015|Chem.-Eur.J.|21|17282|doi:10.1002/chem.201502131
CCDC 990027: Experimental Crystal Structure Determination
Related Article: Saptarshi Biswas, Carlos J. Gómez-García, Juan M. Clemente-Juan, Samia Benmansour, Ashutosh Ghosh|2014|Inorg.Chem.|53|2441|doi:10.1021/ic4023536
CCDC 1835922: Experimental Crystal Structure Determination
Related Article: Alexandre Abhervé, Samia Benmansour, Carlos José Gómez-García, Narcis Avarvari|2018|CrystEngComm|20|4141|doi:10.1039/C8CE00561C
CCDC 1032220: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Cristina Vallés-García, Patricia Gómez-Claramunt, Guillermo Mínguez Espallargas, Carlos J. Gómez-García|2015|Inorg.Chem.|54|5410|doi:10.1021/acs.inorgchem.5b00451
CCDC 1469282: Experimental Crystal Structure Determination
Related Article: Carlos J. Gómez-García, Emilio Escrivà, Samia Benmansour, Juan J. Borràs-Almenar, José-Vicente Folgado, and Carmen Ramírez de Arellano|2016|Inorg.Chem.|55|2664|doi:10.1021/acs.inorgchem.6b00105
CCDC 1054827: Experimental Crystal Structure Determination
Related Article: Samia Benmansour , Esther Delgado , Carlos J. Gómez-García , Diego Hernández , Elisa Hernández , Avelino Martin , Josefina Perles , and Félix Zamora|2015|Inorg.Chem.|54|2243|doi:10.1021/ic502789v
CCDC 1478367: Experimental Crystal Structure Determination
Related Article: Saikat Banerjee, Sattwick Halder, Paula Brandão, Carlos J. Gómez García, Samia Benmansour, Amrita Saha|2017|Inorg.Chim.Acta|464|65|doi:10.1016/j.ica.2017.04.056
CCDC 1586535: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Irene Pérez-Herráez, Christian Cerezo-Navarrete, Gustavo López-Martínez, Cristian Martínez Hernández, Carlos J. Gómez-García|2018|Dalton Trans.|47|6729|doi:10.1039/C8DT00143J
CCDC 1936484: Experimental Crystal Structure Determination
Related Article: Pravat Ghorai, Arka Dey, Paula Brandão, Samia Benmansour, Carlos J. Gómez García, Partha Pratim Ray, Amrita Saha|2020|Inorg.Chem.|59|8749|doi:10.1021/acs.inorgchem.0c00389
CCDC 1579869: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Antonio Hernández Paredes, Carlos J. Gómez García|2018|J.Coord.Chem.|71|845|doi:10.1080/00958972.2017.1420182
CCDC 1586536: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Irene Pérez-Herráez, Christian Cerezo-Navarrete, Gustavo López-Martínez, Cristian Martínez Hernández, Carlos J. Gómez-García|2018|Dalton Trans.|47|6729|doi:10.1039/C8DT00143J
CCDC 1936483: Experimental Crystal Structure Determination
Related Article: Pravat Ghorai, Arka Dey, Paula Brandão, Samia Benmansour, Carlos J. Gómez García, Partha Pratim Ray, Amrita Saha|2020|Inorg.Chem.|59|8749|doi:10.1021/acs.inorgchem.0c00389
CCDC 1415920: Experimental Crystal Structure Determination
Related Article: Julia Vallejo, Francisco R. Fortea-Pérez, Emilio Pardo, Samia Benmansour, Isabel Castro, J. Krzystek, Donatella Armentano, Joan Cano|2016|Chemical Science|7|2286|doi:10.1039/C5SC04461H
CCDC 1470627: Experimental Crystal Structure Determination
Related Article: Samia Benmansour, Alexandre Abhervé, Patricia Gómez-Claramunt, Cristina Vallés-García, Carlos J. Gómez-García|2017|ACS Applied Materials and Interfaces|9|26210|doi:10.1021/acsami.7b08322
CCDC 929633: Experimental Crystal Structure Determination
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CCDC 1060081: Experimental Crystal Structure Determination
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CCDC 1047311: Experimental Crystal Structure Determination
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CCDC 1909314: Experimental Crystal Structure Determination
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CCDC 1032219: Experimental Crystal Structure Determination
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CCDC 1579867: Experimental Crystal Structure Determination
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CCDC 1403318: Experimental Crystal Structure Determination
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CCDC 1579866: Experimental Crystal Structure Determination
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CCDC 1579874: Experimental Crystal Structure Determination
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CCDC 990029: Experimental Crystal Structure Determination
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CCDC 1032218: Experimental Crystal Structure Determination
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CCDC 1835924: Experimental Crystal Structure Determination
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CCDC 1835923: Experimental Crystal Structure Determination
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CCDC 2005220: Experimental Crystal Structure Determination
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CCDC 1415918: Experimental Crystal Structure Determination
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CCDC 1565283: Experimental Crystal Structure Determination
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CCDC 1415921: Experimental Crystal Structure Determination
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CCDC 1579873: Experimental Crystal Structure Determination
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CCDC 982640: Experimental Crystal Structure Determination
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CCDC 1047309: Experimental Crystal Structure Determination
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CCDC 1469281: Experimental Crystal Structure Determination
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CCDC 1532866: Experimental Crystal Structure Determination
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CCDC 953846: Experimental Crystal Structure Determination
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CCDC 1054831: Experimental Crystal Structure Determination
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CCDC 1579868: Experimental Crystal Structure Determination
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CCDC 1909316: Experimental Crystal Structure Determination
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CCDC 1415915: Experimental Crystal Structure Determination
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CCDC 1579870: Experimental Crystal Structure Determination
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CCDC 1835927: Experimental Crystal Structure Determination
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CCDC 1532868: Experimental Crystal Structure Determination
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CCDC 1923203: Experimental Crystal Structure Determination
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CCDC 1415639: Experimental Crystal Structure Determination
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CCDC 1055476: Experimental Crystal Structure Determination
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CCDC 1586540: Experimental Crystal Structure Determination
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CCDC 1828981: Experimental Crystal Structure Determination
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CCDC 1415916: Experimental Crystal Structure Determination
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CCDC 1910770: Experimental Crystal Structure Determination
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CCDC 1054829: Experimental Crystal Structure Determination
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CCDC 984545: Experimental Crystal Structure Determination
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CCDC 1909317: Experimental Crystal Structure Determination
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CCDC 1985127: Experimental Crystal Structure Determination
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CCDC 1944125: Experimental Crystal Structure Determination
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CCDC 1586539: Experimental Crystal Structure Determination
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CCDC 1907203: Experimental Crystal Structure Determination
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CCDC 1054139: Experimental Crystal Structure Determination
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CCDC 1923202: Experimental Crystal Structure Determination
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CCDC 1499647: Experimental Crystal Structure Determination
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CCDC 1918388: Experimental Crystal Structure Determination
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CCDC 1415634: Experimental Crystal Structure Determination
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CCDC 1907202: Experimental Crystal Structure Determination
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CCDC 953848: Experimental Crystal Structure Determination
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CCDC 1835926: Experimental Crystal Structure Determination
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CCDC 1032217: Experimental Crystal Structure Determination
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CCDC 1054138: Experimental Crystal Structure Determination
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CCDC 1579875: Experimental Crystal Structure Determination
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CCDC 1918387: Experimental Crystal Structure Determination
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CCDC 953849: Experimental Crystal Structure Determination
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CCDC 1907205: Experimental Crystal Structure Determination
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CCDC 1586537: Experimental Crystal Structure Determination
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CCDC 1054828: Experimental Crystal Structure Determination
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CCDC 2043543: Experimental Crystal Structure Determination
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