0000000000001659

AUTHOR

Gregorio López

showing 7 related works from this author

Solid state conformational and theoretical study of complexes containing the (CxN)Pd moiety (CxN = 2-(phenylazo)phenyl-C,N and its derivatives)

2003

Palladium complexes having the 2-(phenylazo)phenyl-C,N ligand exhibit a planar chelating ring with NN and N–C distances longer and shorter respectively than those found in trans-azobenzene. The ligand is not planar upon complexation, the mean angle between the phenyl ring and the chelating one found in the Cambridge Structural Database being of 45.6°. We have quantified and characterised the kind of distortion from planar coordination around metallic centers. The method employed makes use of two improper torsion angles, tetrahedral distortion being most frequently found in phenylazophenyl palladium complexes. Crystal structures of three succinimidate complexes having the title moiety are re…

StereochemistryAb initiochemistry.chemical_elementGeneral ChemistryCrystal structureCatalysisMetalCrystallographychemistryvisual_artMaterials ChemistryTetrahedronvisual_art.visual_art_mediumMoietyDensity functional theoryChelationPalladiumNew J. Chem.
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Reactivity of the di-μ-hydroxo-complexes [{Pd(NN)}2(μ-OH)2][ClO4]2 (NN=bis(pyrazol-1-yl)alkanes) towards protic electrophiles. Hydration of coordin…

2000

Abstract The hydroxo-complexes [{Pd(μ-OH)(NN)}2][ClO4]2 (NN=bpzm:bis(pyrazol-1-yl) methane: a-compounds, bpzm*:bis(3,5-dimethylpyrazol-1-yl)methane; b-compounds) react with a wide variety of weak protic electrophiles H(LL) in a 1:2 molar ratio to give the mononuclear cationic palladium(II) derivatives of general formula [Pd(LL)(NN)][ClO4] [LL=2-pyridine-methoxo (OCH2-py) (1a,b); picolinate (pic) (2a,b); 8-hydroxiquinolinate (oxin) (3a,b)] or the dinuclear complexes [{Pd(NN)}2(μ-ox)][ClO4]2 [ox=oxalate: (4a,b)] and [{Pd(μ-LL)(NN)}2][ClO4]2 [LL=pyrazolate (pz) (5a,b); p-thiocresolate (SC6H4Me-p) (6a,b); triazolate (tz) (7b); thiophenolate (SPh) (8b)] when reacting with oxalic acid, azole…

chemistry.chemical_classificationNucleophilic additionStereochemistrychemistry.chemical_elementCrystal structureMedicinal chemistryOxalateInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryElectrophileMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryDithiocarbamatePalladiumPolyhedron
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New Di- and Trinuclear Complexes with Pyrazolato Bridges. Crystal Structures of [{(C6F5)2Pd(μ-pz)(μ-Cl)}2Pd]2– and [(C6F5)2Pd(μ-pz)2Pd(η3-C4H7)] (pz …

2000

Inorganic ChemistryCrystallographychemistryInorganic chemistrychemistry.chemical_elementCrystal structurePlatinumPalladiumEuropean Journal of Inorganic Chemistry
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Reactivity Towards Acidic Protic Ligands of Cyclopalladated Di‐μ‐hydroxo Complexes

2008

The dinuclear hydroxo complexes [{Pd(μ-OH)(C∧N)}2] [C∧N = 2-(2-pyridyl)phenyl (Phpy) (I), 7,8-benzoquinolyl (Bzq) (II) and 2-(2-oxazolinyl)phenyl (Phox) (III)] react in a 1:2 molar ratio with a wide variety of protic electrophiles H(L∧L) bearing different sets of donor atoms (L∧L = O∧O or O∧N) to give the mononuclear neutral palladium(II) derivatives with the general formula [Pd(L∧L)(C∧N)] [O∧O = salicylaldehydate (sal) (1), acetylacetonate (acac) (2) and benzoylacetonate (bzac) (3); O∧N = N-phenylsalicylaldiminate (N-Phsal) (4), N-p-chlorophenylsalicylaldiminate (N-pClPhsal) (5), 2-pyrrolecarbaldeydate (2-pcal) (6), 8-hydroxyquinolinate (oxin) (7)]. Structural characterisation of complexes…

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementMedicinal chemistryInorganic ChemistryDeprotonationchemistryMolar ratioElectrophileProton NMRAmine gas treatingReactivity (chemistry)DithiocarbamatePalladiumEuropean Journal of Inorganic Chemistry
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Organometallic Nickel(II) Complexes Containing Thiolate and Dithiocarbamate Ligands

2000

Inorganic Chemistrychemistry.chemical_classificationNickelChemistryOrganic chemistrychemistry.chemical_elementBioinorganic chemistryDithiocarbamateEuropean Journal of Inorganic Chemistry
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Synthesis and characterization of monomeric siloxo palladium(II) complexes: crystal structure of [Pd(tmeda)(C6F5)(OSiPh3)]

2004

Abstract Mononuclear palladium-hydroxo complexes of the type [Pd(N–N)(C6F5)(OH)] [(N–N)=2,2′-bipyridine (bipy), 4,4′-dimethyl-2,2′-bipyridine (Me2bipy), or N,N,N′,N′-tetramethylethylenediamine (tmeda)] react with silanols HOSiR3 in toluene giving the corresponding siloxo complexes [Pd(N–N)(C6F5)(OSiR3)]. The X-ray crystal structure of [Pd(tmeda)(C6F5)(OSiPh3)] has been determined. In one of the two molecules in the asymmetric unit there is an intramolecular interaction by phenyl–pentafluorophenyl π-stacking.

Organic Chemistrychemistry.chemical_elementCrystal structureBiochemistryTolueneInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryIntramolecular forceMaterials ChemistryMoleculePhysical and Theoretical ChemistryPalladiumJournal of Organometallic Chemistry
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Synthesis and characterization of new oxazoline-based palladacycles with bridging or terminal imidate ligands. Crystal structures of [{Pd(μ-dibromoma…

2008

Abstract The dinuclear hydroxo complex [{Pd(μ-OH)(Phox)}2] (I) (Phox = 2-(2-oxazolinyl)phenyl) reacts in a 1:2 molar ratio with several imidate ligands to yield new cyclometallated palladium complexes [{Pd(μ-NCO)(Phox)}2] containing asymmetric imidate –NCO– bridging units. [–NCO– = succinimidate (succ) (1), phtalimidate (phtal) (2), maleimidate (mal) (3), 2,3-dibromomaleimidate (2,3-diBrmal) (4) and glutarimidate (glut) (5)]. The reaction of these complexes with tertiary phosphines provides novel mononuclear N-bonded imidate derivatives of the general formula [Pd(imidate)(Phox)(PR3)] [R = Ph (a), 4-F–C6H4 (b) or CH2CH2CN (c)]. The new complexes were characterized by partial elemental analys…

Inorganic Chemistrychemistry.chemical_compoundChemistryMolar ratioStereochemistryMaterials Chemistrychemistry.chemical_elementCrystal structureOxazolinePhysical and Theoretical Chemistry2-phenyl-2-oxazolinePalladiumPolyhedron
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