0000000001310238

AUTHOR

Juan Manuel Herrera

showing 12 related works from this author

Minimally Invasive Sacroiliac Joint Arthrodesis: Experience in a Prospective Series with 24 Patients

2014

Background: Sacroiliac (SI) joint pain conservative treatments show poor outcomes. Hypothesis: surgical treatment will show better results. Patients and methods: Prospective series: 24 patients undergoing SI fusion after failure of medical treatment and showing temporary relief with SI infiltration. Period: Nov 2009-July 2013. Gender: 9/15. 11 cases bilaterally (all ). Age: 32-71 years (mean 47.4 years). Height: 161-178 cm (mean 168.2 cm). Weight: 56-84 kg (mean 68.4 kg). Etiology: 12 degenerative/spontaneous, 7 fall on buttocks, 3 coincident with lumbar disc and 2 with lumbar posterolateral fusion. Exclusion criteria: ankylosing spondylitis, osteitis condensans ilii, sacro-iliac joint arth…

Sacroiliac jointmedicine.medical_specialtyAnkylosing spondylitisCirurgiabusiness.industryVisual analogue scaleArthrodesismedicine.medical_treatmentOsteoarthritismedicine.diseaseArticulacions MalaltiesSurgeryOswestry Disability Indexmedicine.anatomical_structureSacroiliac joint dysfunctionJoint painMedicinemedicine.symptombusinessJournal of Spine
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Dilution-Triggered SMM Behavior under Zero Field in a Luminescent Zn2Dy2 Tetranuclear Complex Incorporating Carbonato-Bridging Ligands Derived from A…

2013

The synthesis, structure, magnetic, and luminescence properties of the Zn2Dy2 tetranuclear complex of formula {(mu(3)-CO3)2[Zn(mu-L)Dy(NO3)}(2)}center dot 4CH(3)OH (1), where H2L is the compartmental ligand N,N',N"-trimethyl-N,N"-bis(2-hydroxy-3-methoxy-5-methylbenzyl)diethylenetriamine, are reported. The carbonate anions that bridge two Zn(mu-L)Dy units come from the atmospheric CO2 fixation in a basic medium. Fast quantum tunneling relaxation of the magnetization (QTM) is very effective in this compound, so that single-molecule magnet (SMM) behavior is only observed in the presence of an applied dc field of 1000 Oe, which is able to partly suppress the QTM relaxation process. At variance,…

Models MolecularLuminescenceCarbonatesAnalytical chemistryRELAXATIONLigands010402 general chemistry7. Clean energy01 natural sciencesIonInorganic ChemistryMagnetizationOrganometallic CompoundsMoleculeSingle-molecule magnetIONPhysical and Theoretical ChemistryHYSTERESISANISOTROPYMolecular StructureSpintronics010405 organic chemistryChemistryIntermolecular forceMAGNETIZATIONCarbon Dioxide0104 chemical sciencesSINGLE-MOLECULE-MAGNETZincDipoleDYSPROSIUM(III)SPINSPINTRONICSMagnetsLuminescenceURANIUM(III) COMPLEXInorganic Chemistry
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[Mnii2(bpym)(H2O)8]4+ and [Miv(CN)8]4– (M = Mo and W) as building blocks in designing bpym- and cyanide-bridged bimetallic three-dimensional networks…

2002

One-pot reaction between the dinuclear [MnII2(bpym)(H2O)8]4+ complex and the mononuclear [MIV(CN)8]4− unit (M = Mo and W; bpym = 2,2′-bipyrimidine) in aqueous solution yields the novel heterobimetallic complexes of formula {(μ-bpym)[Mn(H2O)]2-(μ-NC)6M(CN)2} with M = Mo (1) and W (2). 1 and 2 are isostructural three-dimensional compounds where the manganese atoms are bridged by bisbidentate bpym and hexakismonodentate octacyanometalate units. Variable-temperature magnetic susceptibility data of 1 and 2 show the occurrence of a significant antiferromagnetic coupling between the high spin manganese(II) ions through bridging bpym (Jca. −1.1 cm−1, the exchange Hamiltonian being defined as H = −J…

Aqueous solutionCyanidechemistry.chemical_elementGeneral ChemistryManganeseMagnetic susceptibilityCatalysisAntiferromagnetic couplingchemistry.chemical_compoundCrystallographychemistryComputational chemistryMaterials ChemistryIsostructuralBimetallic stripNew Journal of Chemistry
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The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry

2016

The development of catalysts able to assist industrially important chemical processes is a topic of high importance. In view of the catalytic capabilities of small metal clusters, research efforts are being focused on the synthesis of novel catalysts bearing such active sites. Here we report a heterogeneous catalyst consisting of Pd4 clusters with mixed-valence 0/+1 oxidation states, stabilized and homogeneously organized within the walls of a metal-organic framework (MOF). The resulting solid catalyst outperforms state-of-the-art metal catalysts in carbene-mediated reactions of diazoacetates, with high yields (>90%) and turnover numbers (up to 100,000). In addition, the MOF-supported Pd4 c…

Chemical processMechanical Engineeringchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsHeterogeneous catalysis01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMechanics of MaterialsOrganic chemistryGeneral Materials ScienceMetal catalyst0210 nano-technologyCarbenePalladiumMetal clustersNature Materials
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Two-step spin crossover behaviour in the chiral one-dimensional coordination polymer [Fe(HAT)(NCS)2]∞

2015

Solvated and unsolvated forms of the complex [Fe(HAT)(NCS)2]∞·(nMeOH) (1) (n = 1.5, 0; HAT = 1,4,5,8,9,12-hexaazatriphenylene) were prepared. The structure of 1·(1.5MeOH), measured at 120 K, showed that this system crystallizes in the homochiral P43 tetragonal space group. The solid is constituted of stacks of one-dimensional coordination polymers running along c-axis. All the FeII centres have the same Λ or Δ conformation and are in the LS state at 120 K. In the range of temperatures 10–300 K the magnetic properties of 1·(1.5MeOH) shows the occurrence of reversible spin crossover behaviour. However, above ca. 310 K complete desolvation of 1·(1.5MeOH) to give 1 was observed from crystal str…

chemistry.chemical_classificationChemistryCoordination polymerGeneral Chemical EngineeringTwo stepEnthalpyGeneral ChemistryCrystal structurePolymerTetragonal crystal systemchemistry.chemical_compoundCrystallographySpin crossoverThermal analysisRSC Advances
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High frequency of lumbar fusion in patients denied surgical treatment of the sacroiliac joint.

2019

Purpose: Effective treatment of medical conditions relies on proper diagnosis. Clinical trials show the safety and effectiveness of sacroiliac joint (SIJ) fusion in patients with chronic SI joint dysfunction. To what extent is the condition under recognised? Objective: To determine whether under recognition of SIJ pain affects healthcare trajectories in Spanish patients with low back pain. Methods: Retrospective study of characteristics and consequences of 189 patients with persistent SIJ pain seen in an outpatient neurosurgery clinic. Results: Patients with SIJ pain who were denied surgical treatment had a longer pain duration, higher likelihood of prior lumbar fusion, and a high rate (63%…

musculoskeletal diseasesMalemedicine.medical_specialtyTime FactorsSacroiliac joint pain03 medical and health sciences0302 clinical medicineLumbarCirurgia operatòriamedicineEffective treatmentHumansIn patientSurgical treatmentRetrospective StudiesSacroiliac jointbusiness.industryLumbosacral RegionSacroiliac JointGeneral MedicineMiddle AgedLow back painArthralgiaSurgeryClinical trialmedicine.anatomical_structureSpinal FusionTreatment Outcome030220 oncology & carcinogenesisSurgeryFemaleNeurology (clinical)Lumbàlgiamedicine.symptomChronic PainbusinessLow Back Pain030217 neurology & neurosurgeryBritish journal of neurosurgery
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Three-dimensional bimetallic octacyanidometalates $[M^{IV}{(\mu-CN)_{4}Mn^{II}(H_{2}O)_2}_2 \cdot 4H_{2}O]_{n}$ (M=Nb,Mo,W) : synthesis, single-cryst…

2008

Abstract We report the synthesis, the single-crystal X-ray crystallographic structures and the magnetic properties of three new isostructural cyanido-bridged networks: [M IV {(μ-CN) 4 Mn II (H 2 O) 2 } 2 ·4H 2 O] n [M IV  = Nb IV ( 1 ), Mo IV ( 2 ), W IV ( 3 )]. For compound 1 , the magnetic properties reveal a ferrimagnetic phase below 50 K. In contrast, compounds 2 and 3 show a paramagnetic behaviour with no magnetic ordering down to 2 K. The only electronic difference between the two kinds of compounds is the presence of two paired electrons on Mo IV ( 2 ) and W IV ( 3 ) (d 2 electronic configuration, S  = 0) with no possible exchange interactions with Mn II ions (d 5 electronic configur…

magnetic exchange interactionMagnetismGeneral Chemical Engineering010402 general chemistry01 natural sciencesMagnetizationParamagnetismcrystal structuresunpaired electronsstructure cristallineAntiferromagnetismIsostructural010405 organic chemistryChemistrymolecule-based magnetsGeneral Chemistrypont cyanure3. Good health0104 chemical sciencesCrystallographycyanido bridgeUnpaired electronoctacyanométallatesoctacyanidometalatesCurie temperatureinteraction d'échange magnétiqueelectronscélibatairesaimants à précurseurs moléculairesMolecule-based magnets
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CCDC 1060123: Experimental Crystal Structure Determination

2015

Related Article: Tania Romero-Morcillo, Francisco J. Valverde-Muñoz, M. Carmen Muñoz, Juan Manuel Herrera, Enrique Colacio, José A. Real|2015|RSC Advances|5|69782|doi:10.1039/C5RA13491A

catena-[(mu-dipyrazino[23-f:2'3'-h]quinoxaline)-bis(isothiocyanato)-iron methanol solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 968170: Experimental Crystal Structure Determination

2013

Related Article: Silvia Titos-Padilla, José Ruiz, Juan Manuel Herrera, Euan K. Brechin, Wolfgang Wersndorfer, Francesc Lloret, and Enrique Colacio|2013|Inorg.Chem.|52|9620|doi:10.1021/ic401378k

Space GroupCrystallographyCrystal Systembis(mu~3~-Carbonato)-bis(mu~2~-22'-((methylimino)bis(ethane-21-diyl(methylimino)methylene))bis(6-methoxy-4-methylphenolato))-bis(nitrato-OO')-di-dysprosium-di-zinc methanol solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 968171: Experimental Crystal Structure Determination

2013

Related Article: Silvia Titos-Padilla, José Ruiz, Juan Manuel Herrera, Euan K. Brechin, Wolfgang Wersndorfer, Francesc Lloret, and Enrique Colacio|2013|Inorg.Chem.|52|9620|doi:10.1021/ic401378k

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatesbis(mu~3~-Carbonato)-bis(mu~2~-22'-((methylimino)bis(ethane-21-diyl(methylimino)methylene))bis(6-methoxy-4-methylphenolato))-bis(nitrato-OO')-di-yttrium-di-zinc methanol solvate
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CCDC 1517224: Experimental Crystal Structure Determination

2017

Related Article: Francisco R. Fortea-Pérez, Marta Mon, Jesús Ferrando-Soria, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan Manuel Herrera, Dmitrii Osadchii, Jorge Gascon, Donatella Armentano and Emilio Pardo|2017|Nat.Mater|16|760|doi:10.1038/nmat4910

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-[(mu-oxido)-hexa-ammine-di-palladium(ii) tetra-ammine-palladium(ii) bis(tris(mu-22'-((246-trimethyl-13-phenylene)diazanedi-idyl)bis(oxoacetato))-tetra-aqua-tri-copper(ii)-di-nickel(ii)) unknown solvate hydrate]Cell ParametersExperimental 3D Coordinates
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CCDC 1517225: Experimental Crystal Structure Determination

2017

Related Article: Francisco R. Fortea-Pérez, Marta Mon, Jesús Ferrando-Soria, Mercedes Boronat, Antonio Leyva-Pérez, Avelino Corma, Juan Manuel Herrera, Dmitrii Osadchii, Jorge Gascon, Donatella Armentano and Emilio Pardo|2017|Nat.Mater|16|760|doi:10.1038/nmat4910

catena-[tri-sodium hemikis(di-palladium(i)-di-palladium(0)) bis(tris(mu-22'-[(246-trimethyl-13-phenylene)diazanedi-idyl]bis(oxoacetato))-tetra-aqua-tri-copper(ii)-di-nickel(ii)) unknown solvate hexapentacontahydrate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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