Jordi Puiggalí-Jou

ORCID: 0000-0003-4862-0973
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About
Contact & Profiles
Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Polyoxometalates: Synthesis and Applications
  • Organometallic Complex Synthesis and Catalysis
  • Catalytic Processes in Materials Science
  • Metal-Organic Frameworks: Synthesis and Applications
  • Chemical Synthesis and Analysis
  • Chemical Synthesis and Characterization
  • Catalysis and Oxidation Reactions
  • Peptidase Inhibition and Analysis
  • Asymmetric Hydrogenation and Catalysis
  • Synthesis and characterization of novel inorganic/organometallic compounds

Universitat Rovira i Virgili
2023-2024

The decomposition of hydrogen peroxide (H2O2) is the main undesired side reaction in catalytic oxidation processes industrial interest that make use H2O2 as a terminal oxidant, such epoxidation alkenes. However, mechanism responsible for this still poorly understood, thus hindering development design rules to maximize efficiency oxidations terms product selectivity and oxidant utilization efficiency. Here, we thoroughly investigated using Zr-monosubstituted dimeric Lindqvist tungstate,...

10.1021/acscatal.3c02416 article EN cc-by ACS Catalysis 2023-07-24

Effective degradation of non-natural phosphate triesters (PTs) widely used in pesticides and warfare agents is paramount relevance for human environmental safety, particularly under acidic conditions where they are highly stable. Here, we present a detailed reactivity mechanistic study pioneering discrete {Zr

10.1039/d4sc03946g article EN cc-by-nc Chemical Science 2024-01-01

Hydrogenolysis of a series alkyl sulfido-bridged tantalum(IV) dinuclear complexes [Ta(η5-C5Me5)R(μ-S)]2 [R = Me, nBu (1), Et, CH2SiMe3, C3H5, Ph, CH2Ph (2), p-MeC6H4CH2 (3)] has led quantitatively to the Ta(III) tetrametallic sulfide cluster [Ta(η5-C5Me5)(μ3-S)]4 (4) along with corresponding alkane. Mechanistic information for formation unique low-valent compound 4 was gathered by hydrogenation phenyl-substituted precursor [Ta(η5-C5Me5)Ph(μ-S)]2, which proceeds through stepwise process,...

10.1021/acs.inorgchem.3c00043 article EN cc-by Inorganic Chemistry 2023-06-15

The capricious reactivity and speciation of earth-abundant metals (EAM) hinder the mechanistic understanding essential to boost their efficiency versatility in catalysis. Moreover, metal's solution chemistry are conventionally controlled using organic ligands, while fundamental operando conditions is often overlooked. However, this study, we showcase how a better may result improved catalytic reactions. By assessing composition structure active species for Zr-catalyzed direct amide bond...

10.1021/acs.inorgchem.4c02526 article EN cc-by Inorganic Chemistry 2024-10-18
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