0000000000007878
AUTHOR
Sacramento Ferrer
showing 54 related works from this author
Copper(II) and nickel(II) chelates with dihydrogen Trans-1,2-diaminocyclohexane-N,N,N′,N′-tetraacetate(2−) ion (H2CDTA2−). Synthesis, XRD structure a…
1996
Abstract Stoichiometric reactions of metal hydroxycarbonates with the acid trans -1,2-cyclohexanediaminotetraacetic acid (H 4 CDTA) in water under reduced pressure yielded [Cu(H 2 CDTA)]·H 2 O ( I ) and [Ni(H 2 CDTA) (H 2 O)]·4H 2 O ( II ). Both compounds were characterized by TG-DTA analysis, spectral properties (IR, reflectance and RSE) and X-ray diffraction. In I the copper(II) atom exhibits a distorted square-base coordination (type 4+1) by chelation of one H 2 CDTA 2− ligand through two N and two O (carboxylate) at the square base and one O (carboxylic) at the apex of the coordination polyhedron; a second carboxymethyl group of H 2 CDTA 2− remains free. In II the H 2 CDTA 2− chelating …
Functional superoxide dismutase mimics. Structural characterization and magnetic exchange interactions of copper(II)-N-substituted sulfonamide dimer …
2004
Dinuclear copper(II) complexes with N-substituted sulfonamide ligands as superoxide dismutase (SOD) mimics have been investigated. The new N-(thiazol-2-yl)toluenesulfonamide (Htz-tol) and N-(thiazol-2-yl)naphthalenesulfonamide (Htz-naf) ligands have been prepared and structurally characterized. The complexes derived from these ligands, [Cu(2)(tz-tol)(4)] (1) and [Cu(2)(tz-naf)(4)] (2), have been synthesized, and their crystal structure, magnetic properties, and EPR spectra were studied in detail. In both compounds the metal centers are bridged by four nonlinear triatomic NCN groups. The coordination geometry of the coppers in the dinuclear entity of 1 and 2 is distorted square planar with t…
Synthesis, crystal structure and properties of two acetazolamide (5-acetamido-1,3,4-thiadiazole-2-sulfonamide) complexes: bis(5-acetamidato- 1,3,4-th…
1992
Abstract The diverse coordination chemistry exhibited by acetazolamide (H2acm), a potent inhibitor of the carbonic anhydrase metalloenzyme, is highlighted in two new copper(II) complexes of this ligand: [Cu(Hacm)2(en)2] (I) and [Cu(Hacm)2(tn)2] (II). The synthesis, crystal structure and spectroscopic properties of both compounds are reported in this paper. The structures of both compounds consist of discrete units of [Cu(Hacm)2(en)2] (I) and [Cu(Hacm)2(tn)2] (II), respectively, interacting through van der Waals contacts and hydrogen bonds only. Hacm, however, binds differently in each compound. In both cases, the Cu(II) ions, lying on the symmetry centers, show an elongated octahedral geome…
Two copper complexes from two novel naphthalene-sulfonyl-triazole ligands: different nuclearity and different DNA binding and cleavage capabilities.
2013
[EN] Two novel naphthalene-sulfonyl-triazole ligands, 5-amino-N1-(naphthalen-3-ylsulfony1)-1,2,4-triazole (anstrz) and 3,5-diamino-N1-(naphthalen-3-ylsulfony1)-1,2,4-triazole (danstrz), purposely designed to interact with DNA, have been prepared for the first time and then fully characterized by H-1, C-13 NMR and IR spectroscopy, mass spectrometry and elemental analysis. The crystal structures of two copper complexes of these derivatives, i.e. [Cu(anstrz)(4)(NO3)(2)]center dot 4CH(3)OH (1), mononuclear, and [Cu(danstrz)(mu-OAc)(2)](2)center dot 2(danstrz) (OAc = acetato) (2), dinuclear, have been determined by single-crystal X-ray diffraction. In both cases the ligand coordinates in a monod…
Syntheses, crystal structures, and oxidative DNA cleavage of some Cu(II) complexes of 5-amino-3-pyridin-2-yl-1,2,4-triazole
2004
Three new monomeric Cu(II) complexes of 5-amino-3-pyridin-2-yl-1,2,4-triazole (Hapt), [Cu(Hapt)(H(2)O)(2)(SO(4))] (1), [Cu(Hapt)(2)(H(2)O)(NO(3))](NO(3)) (2), and [Cu(Hapt)(2)(NCS-N)](NCS).H(2)O (3), have been prepared and characterized by single crystal X-ray diffraction. One distorted [CuN(2)O(2)+O(')] square-pyramidal (1), one distorted [CuN(3)O+N(')+O(')] octahedral (2), and one distorted [CuN(4)+N(')] intermediate between square-pyramidal and trigonal-bipyramidal (3) coordination configuration were found and are suggested to be due to the chelating nature of the ligand, which interacts with Cu(II) through the N4(triazole) and N(pyridine) atoms. Spectral properties of these chelates are…
A Co(III) complex of carbonic anhydrase inhibitor methazolamide and the amino-imino ‘aib’ ligand formed by reaction of acetone and ammonia
1993
Abstract Reaction of Co(NO 3 ) 2 ·6H 2 O with methazolamide {[ N -(3-methyl-5-sulfamoyl-1,3,4-thiadiazol-2(3 H )-ylidene)acetamide] (Hmacm)} and ammonia in acetone to produce [Co(methazolamidate)(2-methyl-2-amino-4-iminopentane) 2 (NH 3 )](NO 3 ) 2 ·2H 2 O is described. The ligand 2-methyl-2-amino-4-iminopentane (aib) is the product obtained from the condensation of two ammonia and two acetone molecules. The complex crystallizes in the monoclinic space group P 2 1 / c with a =16.713(5), b =9.180(1), c =20.273(1) A, β=97.44(4)° for Z =4. The R value is 0.081 for 2150 significant reflections. The Co(III) ion exhibits a nearly regular octahedral arrangement with the CoN bond distances in the …
Synthesis and characterization of mononuclear complexes containing 3-acetylamino-1,2,4-triazole (aat). X-ray structure of [Co(aat)2(H2O)2]Br2
1993
Abstract The spectroscopic characteristics of the isostructural compounds [M(aat) 2 (H 2 O) 2 ]X 2 (aat = 3-acetylamino-1,2,4-triazole; M = Co, Cu, X = Br, CI; M = Ni, X = Cl) are described. The structure of [Co(aat) 2 (H 2 O) 2 ]Br 2 has been determined by X-ray diffraction methods. Crystals are monoclinic, space group P 2 1 / a with a = 9.686(3), b = 14.433(4), c = 6.169(2) A, β = 92.84(2)° and Z = 2. The structure was refined to final R and R ′ values of 0.033 and 0.039 for 1066 observed reflections. In the mononuclear cationic complex, having an imposed crystallographic C i symmetry, the cobalt atom is surrounded in a slightly distorted octahedral arrangement by two axial water molecule…
Acetazolamide-M(II) [M(II) = Co(II), Ni(II), Cu(II)] complexes with ethylamine, diethylamine, triethylamine, and potassium hidroxide
1991
Abstract Complexes of Co(II), Ni(II), and Cu(II) with dideprotonated Acm are synthesized and characterized. Acm acts as bidentate ligand through the N-sulfonamido atom and the N-thiadiazole atom except for K6CoAcm4·6H2O in which Acm behaves as monodentate through the N-sulfonamido atom.
Hexanuclear Cu3O–3Cu triazole-based units as novel core motifs for high nuclearity copper(ii) frameworks
2019
The asymmetric 3,5-disubstituted 1,2,4-triazole ligand H2V (5-amino-3-picolinamido-1,2,4-triazole) by reaction with an excess of Cu(II) perchlorate (Cu : H2V being 12 : 1) has produced a novel hexanuclear {Cu6(m3-O/H)(HV/V)3} fragment, with one triangular Cu3(m3-O/H) group connected to three peripheral single Cu(II) ions through a cis–cis–trans bridging mode of the ligand, which is the building block of the three structures described here: one hexanuclear, [Cu6(m3-O)(HV)3(ClO4)7(H2O)9]$8H2O (1), one dodecanuclear, [Cu12(m3-O)2(V)6(ClO4)5(H2O)18](ClO4)3$6H2O (2), and one tetradecanuclear 1D-polymer, {[Cu14(m3-OH)2(V)6(HV)(ClO4)11(H2O)20](ClO4)2$14H2O}n (3), the last two containing hexanuclea…
Coordination behaviour of methazolamide [N(-4-methyl-2-sulfamoyl-Δ2-1,3,4-thiadiazolin-5-ylidene)] acetamide, an inhibitor of carbonic anhydrase enzy…
1993
Abstract The interaction of methazolamide (Hmacm) with Ni(II) ion and ammonia molecules gives rise to the complex of formula [Ni(macm)2(NH3)4]. The complex crystallizes in the monoclinic P21/n space group with a = 14.255(4), b = 7.126(2), c = 12.444(3) A, β = 113.12(3)° and Z = 2. The structure was refined to R = 0.065 (Rw = 0.065). The complex consists of monomeric units which interact through hydrogen bonds and van der Waals contacts. The Ni(II) ion is coordinated with the deprotonated sulfonamido nitrogen of the macm− ligand in axial sites and the ammonia molecules in equatorial positions. IR, electronic spectra and 1H NMR results are also reported.
Two Novel Ternary Dicopper(II) μ-Guanazole Complexes with Aromatic Amines Strongly Activated by Quantum Dots for DNA Cleavage
2013
Two novel (μ-guanazole)-bridged binuclear copper(II) complexes with 1,10-phenanthroline (phen) or 2,2'-bipyridine (bipy), [Cu2(μ-N2,N4-Hdatrz)(phen)2(H2O)(NO3)4] (1) and [Cu2(μ-N1,N2-datrz)2(μ-OH2)(bipy)2](ClO4)2 (2) (Hdatrz = 3,5-diamino-1,2,4-triazole = guanazole), have been prepared and characterized by X-ray diffraction, spectroscopy, and susceptibility measurements. Compounds 1 and 2 differ in the aromatic amine, which acts as a coligand, and in the Cu···Cu'-bridging system. Compound 1, which contains two mono-bridged copper ions, represents the first example of a discrete Cu-(NCN-trz)-Cu' complex. Compound 2, with two triply bridged copper ions, is one of the few compounds featuring a…
Coordination compounds of methazolamide. Synthesis, spectroscopic studies and crystal structures of [M(Methazolamidato)2(py)2(OH2)2] (M CoII, NiII …
1992
Abstract The synthesis and X-ray crystallographic characterization of three monomeric transition-metal coordination compounds with the ligand methazolamide {[N(4-methyl-2- sulphamoyl-Δ21,3,4-thiodiazolin-5-ylidene)],acetamide} (abbreviated as Hmacm) are described, via [M(macm)2(py)2(OH2)2] [M Co(1), Ni(2) and Cu(3)]. In all the compounds the metal ion, lying on the centre of symmetry, is surrounded by two sulphonamidato nitrogen atoms and two pyridine nitrogen atoms in equatorial sites and two oxygen water molecules in axial positions. The coordination geometry of the metal is an almost regular octahedron around the cobalt(II) and nickel(II) ions. In contrast, the copper(II) ion has a sig…
Novel Hexanuclear Copper(II) Complex Built from a Simple Tetrachelating Triazole Ligand: Synthesis, Structure, and Magnetism
2013
A new easy symmetric 3,5-disubstituted 1,2,4-triazole ligand (H3diV) by reaction with an excess of copper(II) salt has afforded a novel hexanuclear compound (Cu/HdiV ratio of 6:2) through a bis(trans-cis-cis-trans) binding mode, exhibiting two types of Cu(II) centers and two clearly distinguishable antiferromagnetic J1 (-234 cm(-1)) and J2 (-35 cm(-1)) coupling constants.
One-dimensional metal-organic framework with unprecedented heptanuclear copper units.
2007
The reaction of copper(II) sulfate, copper(II) chloride, 3,5-diacetylamino-1,2,4-triazole, and 3-acetylamino-5-amino-1,2,4-triazole in water yields green, plate-shaped crystals of [[{Cu3(mu3-OH(1/2))L(H2O)2Cl}2{mu-Cu(H2O)2Cl2}].12H2O]n (1), where L is a new triazole-derived macrocyclic ligand. The structure of 1 consists of heptanuclear (H)OCuII(3)-CuII-CuII(3)O(H) entities linked in pairs through symmetric mu3-O...H...O-mu3 hydrogen bonds to form a double-stranded one-dimensional network. A significant overall antiferromagnetic behavior has been observed for 1.
Dimetallic complexes derived from a novel dinucleating chelating symmetric triazole ligand; crystal structure, magnetic properties and ESR study of b…
1999
Reaction of 3,5-diacetylamino-1,2,4-triazole (Hdaat) with copper(II), nickel(II) and cobalt(II) salts yields dinuclear co-ordination compounds, which were spectroscopically characterized. The crystal and molecular structure of one of the compounds, bis[µ-3,5-diacetylamino-1,2,4-triazolato-O′,N 1,N 2,O″]bis[(nitrato)(aqua)copper(II)] 1, was determined by single-crystal X-ray diffraction. Complex 1 consists of dinuclear units with an inversion center at the midpoint of the Cu–Cu vector. The most remarkable feature of this structure is that the daat ligand forms a six-membered chelate ring [Cu–N3–C3–N1–C2–O1; Cua–N4–C4–N5–C5–O2], in contrast with the five-membered chelate rings always found in…
Complex formation equilibria between the acetazolamide ((5-acetamido-1,3,4-thiadiazole)-2-sulphonamide), a potent inhibitor of carbonicanhydrase, and…
1990
Abstract The stability constants for the equilibrium of complexation between acetazolamide and the divalent metal ions copper(II), nickel(II), zinc(II), and cobalt(II) have been determined by potentiometry both in water and in water-ethanol 50 vol. % solutions in 0.15 mol dm −3 NaNO 3 at 25°C. This mixed solvent has been used in order to obtain higher concentrations of acetazolamide in solution. For copper(II) and nickel(II), the binuclear species [Cu 2 (Acm) 2 ] and [Ni 2 (Acm) 3 ] 2− are detected in both solvents together with hydroxo species. The values of the stability constants are always higher in the mixed solvent than in water. For cobalt(II) and zinc(II), while in aqueous solution …
ChemInform Abstract: Synthesis and Characterization of the Acetazolamide Complexes of Co(II) and Zn(II).
1987
Abstract The preparation and characterization of the complexes of Acetazolamide (Acm) with Co(II) and Zn(II) are described. The complexes are of the type M(Acm) 2 (NH 3 ) 2 . Monodentate or bidentate behaviour of Acm from the electronic properties and the IR spectral data is discussed. The probable structures of the complexes are proposed.
Thermal studies of sulphonamide derivative complexes
1991
Abstract A thermal study of a new series of acetazolamidate complexes of Co(II), Ni(II) and Cu(II) using the TG, DTG and DTA techniques in flowing air, static air and N 2 atmospheres is described. From the TG-DTG and DTA curves, different thermal behaviours can be observed. Although in all the complexes the processes of dehydration, deammination and pyrolysis can be clearly observed, in some cases they appear as several well-separated steps and, in others, as continuous stages which take place simultaneously. The differences observed between the pyrolytic decomposition in flowing air and in nitrogen are described. In flowing air, metal sulphate is formed from the thiadiazole ring, except fo…
A dinucleating ligand which promotes DNA cleavage with one and without a transition metal ion.
2013
The dinucleating ligand L (1,3-bis[bis(pyridin-2-ylmethyl)amino]propan-2-ol) combined with metal ions efficiently cleaves DNA when M : L is 1 : 1 (M = Co(II) or Fe(III)) at pH 5.5–7.0, with free L being more active at acidic pH than when bound to Zn(II), Cu(II) or Ni(II) at neutral pH.
N-(5-Amino-1H-1,2,4-triazol-3-yl)pyridine-2-carboxamide
2013
The title compound, C8H8N6O, was obtained by the reaction of 3,5-diamino-1,2,4-triazole with ethyl 2-picolinate in a glass oven. The dihedral angles formed between the plane of the amide group and the pyridine and triazole rings are 11.8 (3) and 5.8 (3)°, respectively. In the crystal, an extensive system of classical N—H...N and N—H...O hydrogen bonds generate an infinite three-dimensional network.
Switchable Spin-Crossover Hofmann-Type 3D Coordination Polymers Based on Tri- and Tetratopic Ligands
2018
[EN] Fe-II spin-crossover (SCO) coordination polymers of the Hofmann type have become an archetypal class of responsive materials. Almost invariably, the construction of their architectures has been based on the use of monotopic and linear ditopic pyridine like ligands. In the search for new Hofmann-type architectures with SCO properties, here we analyze the possibilities of bridging ligands with higher connectivity degree. More precisely, the synthesis and structure of {Fe-II(L-N3)[M-I(CN)(2)](2)}center dot(Guest) (Guest = nitro-benzene, benzonitrile, o-dichlorobenzene; M-I = Ag, Au) and {Fe-II(L-N4)[Ag-2(CN)(3)][Ag(CN)(2)]}center dot H2O are described, where L-N3 and L-N4 are the tritopic…
Synthesis and characterization of acetazolamide complexes of Ni(II), Cd(II), Hg(II), and Ag(I)
1989
The preparation and characterization of K2Ni2(Acm)3·5H2O, Cd(Acm)·32 H2O, Hg(Acm)·12H2O, Ag2(Acm), and Ag2(Acm)(NH3) complexes are described. The spectral properties suggest that Acm interacts with the metal ions through the doubly deprotonated form as observed in the [Cu(Acm)(NH3)2(OH2)]2·2H2O complex, whose crystalline structure has been previously reported. The crystal field parameters of the Ni(II) complex indicate an octahedral environment for the metal ion in the solid and its aqueous, DMSO, and DMF solutions. UV spectra of all the Acm complexes until now synthesized are discussed.
A Unique Discrete Tetranuclear Cu′–Cu(N-N)2Cu–Cu′ Copper(II) Complex, Built from a μ3-1,2,4-Triazolato-μ-carboxylato Ligand, as an Effective DNA Clea…
2012
The title compound, characterized by means of an X-ray structure analysis, represents an easy example of a noncatena "1 + 2 + 1" tetranuclear copper(II) μ(3)-triazolate compound. [Cu(4)(atc)(2)(dien)(4)(ClO(4))(2)](ClO(4))(2)·2H(2)O (1), where H(2)atc = 5-amino-l,2,4-triazole-3-carboxylic acid and dien = diethylenetriamine = 1,4,7-triazaheptane, contains two copper atoms linked by a double diazinic bridge, each of which is further connected to a third and fourth copper atom (Cu') through the triply bridging triazolato ring and the bidentate carboxylato group of the atc(2-) ligands. The copper-copper distances within the tetranuclear unit are Cu-Cu = 4.059 Å, Cu-Cu' = 5.686 and 6.370 Å, and …
Trinuclear N,N-Bridged Copper(II) Complexes Involving a Cu3OH Core: [Cu3(μ3-OH)L3A(H2O)2]A·(H2O)x {L = 3-Acetylamino-1,2,4-triazolate; A = CF3SO3, N…
2000
The reaction of Haat [Haat = (3-acetylamino-1,2,4-triazole)] with aquated Cu(CF3SO3)2, Cu(NO3)2, and Cu(ClO4)2, respectively, in water results in the trinuclear complexes [Cu3(OH)(aat)3(CF3SO3)(H2O)2](CF3SO3) (1), [Cu3(OH)(aat)3(NO3)(H2O)2](NO3).(H2O)2 (2), and [Cu3(OH)(aat)3(ClO4)(H2O)2](ClO4) (3). The synthesis, X-ray structure, and magnetic and spectroscopic properties of the three title complexes are described. The cation of the three complexes is trinuclear with a Cu3OH skeleton which has the N-N diazine grouping of a triazole ring as bridge between each pair of copper atoms. The Cu3OH units have an average Cu-O distance of 1.991(6) (1), 2.000(6) (2), and 2.007(6) (3) A, an average Cu-…
From six-coordinate to eight-coordinate iron(ii) complexes with pyridyltriazolo-pyridine frameworks
2016
A new octacoordinated Fe(II) compound, [FeII(LN4)2](BPh4)2·3CH2Cl2, as an example of the scarce FeN8 systems, has been isolated with a tetradentate triazolopyridine-based ligand from a solution containing the related hexacoordinated [FeII(LN3)2]2+ complex, with LN3 = pyridyltriazolo-pyridyl-bromopyrimidine and LN4 = bis(pyridyltriazolo-pyridine).
Spectroscopic behavior of metal–drug complexes. Infrared spectra of Cu(II) dimer complexes with acetazolamide (H2acm) and an analogue sulfonamide (B-…
1999
Abstract The infrared spectra of the drugs H2acm and B-H2ats, and their copper(II) dimer complexes with stoichiometries [Cu(acm)(NH3)2(OH2)]2·H2O and [Cu(B-ats)(NH3)2]2 are reported and discussed. The Raman spectra of H2acm and B-H2ats are also reported. An assignment of H2acm and B-H2ats modes in the complexes is proposed in comparison with the modes of the free ligands. The spectral modifications due to the deprotonation and coordination effects are analyzed. The ν(N–H) modes of the sulfonamido, carbonamido and Nring–H of the imine tautomer have been accurately assigned. Important information about the S–O and S–N vibrations has been obtained.
Nanoporosity, Inclusion Chemistry, and Spin Crossover in Orthogonally Interlocked Two-Dimensional Metal-Organic Frameworks
2015
[Fe(tvp)(2)(NCS)(2)] (1) (tvp=trans-(4,4-vinylenedipyridine)) consists of two independent perpendicular stacks of mutually interpenetrated two-dimensional grids. This uncommon supramolecular conformation defines square-sectional nanochannels (diagonal approximate to 2.2nm) in which inclusion molecules are located. The guest-loaded framework 1@guest displays complete thermal spin-crossover (SCO) behavior with the characteristic temperature T-1/2 dependent on the guest molecule, whereas the guest-free species 1 is paramagnetic whatever the temperature. For the benzene-guest derivatives, the characteristic SCO temperature T-1/2 decreases as the Hammet sigma(p) parameter increases. In general, …
Synthesis and characterization of the acetazolamide complexes of Co(II) and Zn(II)
1987
Abstract The preparation and characterization of the complexes of Acetazolamide (Acm) with Co(II) and Zn(II) are described. The complexes are of the type M(Acm) 2 (NH 3 ) 2 . Monodentate or bidentate behaviour of Acm from the electronic properties and the IR spectral data is discussed. The probable structures of the complexes are proposed.
Superoxide dismutase activity of ternary copper complexes of sulfathiazole and imidazole derivatives. Synthesis and properties of [CuL2(R-Him)2] [HL=…
2000
Abstract New ternary copper(II) complexes of sulfathiazole (4-amino-N-(thiazol-2-yl)benzenesulfonamide)(HL) and methyl imidazole derivatives have been synthesised and characterised. The crystal structure of the complex [CuL2(4,4-dmHim)2] (1) [4,4-dmHim=4,4-dimethylimidazoline] has been determined. The copper centre has a quasi regular square planar environment with Cu-nitrogen bond lengths ranging from 1.952 to 2.010 A. From the spectroscopic properties of the complexes [CuL2(1,2-dmHim)2] (2) [1,2-dmHim=1,2-dimethylimidazole] and [CuL2(4-mHim)2] (3) [4-mHim=4-methylimidazole] a distorted tetragonal octahedral geometry is deduced. The compounds showed SOD mimetic activity in fact, a low conc…
Antisymmetric exchange in triangular tricopper(II) complexes: correlation among structural, magnetic, and electron paramagnetic resonance parameters.
2011
Two new trinuclear copper(II) complexes, [Cu(3)(μ(3)-OH)(daat)(Hdat)(2)(ClO(4))(2)(H(2)O)(3)](ClO(4))(2)·2H(2)O (1) and [Cu(3)(μ(3)-OH)(aaat)(3)(H(2)O)(3)](ClO(4))(2)·3H(2)O (2) (daat = 3,5-diacetylamino-1,2,4-triazolate, Hdat = 3,5-diamino-1,2,4-triazole, and aaat = 3-acetylamino-5-amino-1,2,4-triazolate), have been prepared from 1,2,4-triazole derivatives and structurally characterized by X-ray crystallography. The structures of 1 and 2 consist of cationic trinuclear copper(II) complexes with a Cu(3)OH core held by three N,N-triazole bridges between each pair of copper(II) atoms. The copper atoms are five-coordinate with distorted square-pyramidal geometries. The magnetic properties of 1 …
Metal complexes of sulfanilamide derivatives. Crystal structure of [Zn(sulfathiazole)2]·H2O
1993
Abstract The crystal structure of the Zn(sulfathiazole) 2 ·H 2 O complex is reported. The complex crystallizes in the monoclinic space group C 2/ c . The cell dimensions are a = 9.098(3) A, b = 17.871(5) A, c = 14.61(1) A, β = 99.44(6)°, V = 2343(2) A 3 , Z = 4, and D x = 1.68 g/cm 3 . The final conventional R-factor = 0.027 for 2669 “observed” reflections and 191 variables. The Zn ion is surrounded in a regular tetrahedral arrangement by two N amino and two N thiazole atoms pertaining to four sulfathiazole (Hstz) ligands. Each stz anion, acting as a bidentate ligand, chelates to two Zn ions as a bridge through the N thiazole and the N amino atoms. The IR, 13 C NMR in solid state, 1 H NMR, …
Coordinative Versatility of Guanazole [3,5‐Diamino‐1,2,4‐triazole]: Synthesis, Crystal Structure, EPR, and Magnetic Properties of a Dinuclear and a L…
2006
New complexes with guanazole (3,5-diamino-1,2,4-triazole = Hdatrz), [Cu 2 (Hdatrz) 2 (μ-OH 2 )(H 2 O) 4 (SO 4 )](SO 4 )·3.5H 2 O (1) and [Cu 3 (Hdatrz) 4 (μ-Cl) 2 (H 2 O) 4 (SO 4 ) 2 ]·11.4H 2 O (2), have been prepared and structurally characterized. Complex 1 is a noncentrosymmetric dinuclear compound in which the cop-per(II) ions are bridged by two triazole ligands and one μ-OH 2 molecule, with a Cu(1)···Cu(2) distance of 3.4945(8) A. The chromophores are Cu(1)N 2 O 2 O' (square pyramidal), and Cu(2)N 2 O 2 O'O" (octahedral). Complex 2 has a linear trinuclear copper(II) structure, with two crystallographically independent copper(II) atoms. Neighboring copper(II) ions are linked by two tri…
CCDC 1042612: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1852557: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842
CCDC 1042617: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1042613: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1852556: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842
CCDC 907781: Experimental Crystal Structure Determination
2013
Related Article: Javier Hernández-Gil, Sacramento Ferrer, Nuria Cabedo, María Pilar López-Gresa, Alfonso Castiñeiras, Francesc Lloret|2013|J.Inorg.Biochem.|125|50|doi:10.1016/j.jinorgbio.2013.04.007
CCDC 1852560: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842
CCDC 1935980: Experimental Crystal Structure Determination
2019
Related Article: Sacramento Ferrer, Javier Hernández-Gil, Francisco Javier Valverde-Muñoz, Francisco Lloret, Alfonso Castiñeiras|2019|RSC Advances|9|29357|doi:10.1039/C9RA05922A
CCDC 1935981: Experimental Crystal Structure Determination
2019
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CCDC 1852559: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842
CCDC 1042615: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1042614: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 907780: Experimental Crystal Structure Determination
2013
Related Article: Javier Hernández-Gil, Sacramento Ferrer, Nuria Cabedo, María Pilar López-Gresa, Alfonso Castiñeiras, Francesc Lloret|2013|J.Inorg.Biochem.|125|50|doi:10.1016/j.jinorgbio.2013.04.007
CCDC 1852562: Experimental Crystal Structure Determination
2018
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CCDC 1439487: Experimental Crystal Structure Determination
2016
Related Article: Rosa Adam, Rafael Ballesteros-Garrido, Sacramento Ferrer, Belén Abarca, Rafael Ballesteros, José Antonio Real, M. Carmen Muñoz|2016|CrystEngComm|18|7950|doi:10.1039/C6CE01540A
CCDC 1042616: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1852558: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842
CCDC 1935979: Experimental Crystal Structure Determination
2019
Related Article: Sacramento Ferrer, Javier Hernández-Gil, Francisco Javier Valverde-Muñoz, Francisco Lloret, Alfonso Castiñeiras|2019|RSC Advances|9|29357|doi:10.1039/C9RA05922A
CCDC 1042611: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1439488: Experimental Crystal Structure Determination
2016
Related Article: Rosa Adam, Rafael Ballesteros-Garrido, Sacramento Ferrer, Belén Abarca, Rafael Ballesteros, José Antonio Real, M. Carmen Muñoz|2016|CrystEngComm|18|7950|doi:10.1039/C6CE01540A
CCDC 1042610: Experimental Crystal Structure Determination
2015
Related Article: Tania Romero-Morcillo, Noelia De la Pinta, Lorena M. Callejo, Lucía Piñeiro-López, M. Carmen Muñoz, Gotzon Madariaga, Sacramento Ferrer, Tomasz Breczewski, Roberto Cortés, José A. Real|2015|Chem.-Eur.J.|21|12112|doi:10.1002/chem.201500310
CCDC 1852561: Experimental Crystal Structure Determination
2018
Related Article: Francisco Javier Valverde-Muñoz, M. Carmen Muñoz, Sacramento Ferrer, Carlos Bartual-Murgui, José A. Real|2018|Inorg.Chem.|57|12195|doi:10.1021/acs.inorgchem.8b01842