Lucas H. G. Kalinke

ORCID: 0000-0001-7765-1184
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Magnetism in coordination complexes
  • Metal complexes synthesis and properties
  • Lanthanide and Transition Metal Complexes
  • Metal-Organic Frameworks: Synthesis and Applications
  • Inorganic and Organometallic Chemistry
  • Thermal and Kinetic Analysis
  • Catalysis and Oxidation Reactions
  • Supramolecular Chemistry and Complexes
  • Nanomaterials for catalytic reactions
  • Crystallography and molecular interactions
  • Catalytic Processes in Materials Science
  • Metal-Catalyzed Oxygenation Mechanisms
  • Advanced NMR Techniques and Applications
  • Arsenic contamination and mitigation
  • Luminescence Properties of Advanced Materials
  • Adsorption and biosorption for pollutant removal
  • Nanocluster Synthesis and Applications

Instituto Federal de Goiás
2014-2025

Royal Society of Chemistry
2024

Centre National pour la Recherche Scientifique et Technique (CNRST)
2024

Universidade Federal de Goiás
2014-2022

Parc Científic de la Universitat de València
2019

Universitat de València
2019

We report a new water-stable multivariate (MTV) metal–organic framework (MOF) prepared by combining two different oxamide-based metalloligands derived from the natural amino acids l-serine and l-methionine. This unique material features hexagonal channels decorated with types of flexible functional "arms" (−CH2OH −CH2CH2SCH3) capable enabling, synergistically, simultaneous efficient removal both inorganic (heavy metals such as Hg2+, Pb2+, Tl+) organic (dyes Pyronin Y, Auramine O, Brilliant...

10.1021/jacs.9b06250 article EN Journal of the American Chemical Society 2019-08-08

Supramolecular coordination compounds (SCCs) represent the power of chemistry methodologies to self-assemble discrete architectures with targeted properties. SCCs are generally synthesized in solution, isolated fully coordinated metal atoms as structural nodes, thus severely limited metal-based catalysts. Metal–organic frameworks (MOFs) show unique features act chemical nanoreactors for situ synthesis and stabilization otherwise not accessible functional species. Here, we present...

10.1021/jacs.9b03914 article EN Journal of the American Chemical Society 2019-06-13

Herein, we present the synthesis and characterization of a series isostructural lanthanide(III) compounds with N-(4-carboxyphenyl)oxamic acid (H3pcpa) ligand general formula as {[Ln2(Hpcpa)3(H2O)5]}n [Ln = Dy(III) 1, Ho(III) 2, Er(III) 3]. The structure 3 consists neutral zig–zag chains ions, Hpcpa2– ligands acting bridges in bidentate/monodentate coordination mode five water molecules achieving eight-coordination around two ions within repeating bis(carboxylate)-bridged dinuclear units...

10.3390/magnetochemistry11040023 article EN cc-by Magnetochemistry 2025-03-24

Achieving fine control on the structure of metal–organic frameworks (MOFs) is mandatory to obtain target physical properties. Herein, we present how combination a metalloligand approach and postsynthetic method suitable highly useful synthetic strategy success this extremely difficult task. First, novel oxamato-based tetranuclear cobalt(III) compound with tetrahedron-shaped geometry used, for first time, as toward calcium(II) metal ions lead diamagnetic CaII–CoIII three-dimensional (3D) MOF...

10.1021/acs.inorgchem.9b02086 article EN Inorganic Chemistry 2019-10-17

Three heterobimetallic complexes of formula [Ca2Cu3(mpyba)2(2-apyma)(H2O)7]·8.3H2O (1), [Sr2Cu3(mpyba)2(2-apyma)(H2O)8]·11.6H2O (2) and [Sr4.5Cu4(mpyba)4(ox)(H2O)20]·8.5H2O (3) [H4mpyba = N,N'-2,6-pyridinebis(oxamic acid), 2-apyma 2-(6-aminopyridinyl)oxamate ox oxalate] have been synthesized structurally characterized. Complexes 1 2 are isostructural compounds, with tricopper(ii) units having mpyba its hydrolytic product (2-apyma) as ligands. They interlinked through strontium(ii) (1)...

10.1039/c8dt01686k article EN Dalton Transactions 2018-01-01

The cobalt(II)-mediated self-assembly of the potentially tris(chelating) N,N'-2,2'-(4,4'-bithiazole)bis(oxamate) (dabtzox) ligand gives a new metal-organic supramolecular nanomagnet formula K6Co3(dabtzox)3·8H2O·MeOH (1) featuring unique linear triple-stranded trinuclear structure helicate type.

10.1021/acs.inorgchem.2c00291 article EN Inorganic Chemistry 2022-04-06

Four new complexes of formula [Fe(H 2 pcpa) (H O) ] (1), {[Mn(Hpcpa)(Hoxamic acid; bipy = 2,2′-bipyridine] have been synthesized and their structures determined by X-ray diffraction.The structure 1 consists mononuclear iron(II) units where each ion is six-coordinate two trans-positioned water molecules bidentate H pcpa -ligands building a distorted octahedral environment.2 3 consist neutral zigzag chains Mn II Zn ions respectively, the Hpcpa 2-groups acting as linkers in...

10.21577/0103-5053.20190158 article EN cc-by Journal of the Brazilian Chemical Society 2019-01-01

Four heterobimetallic compounds of formula [Ni(Me 6 trans [14]dieneN 4 )][Co(NCS) ] ( 1 and 2 ), )] [Co(NCS) ](ClO ) · H O 3 ](PF (Me = 5,7,7,12,14,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradeca‐4,11‐diene) have been synthesised structurally characterised. Their structures are formed square‐planar 2+ cations tetrahedral 2– anions. The variable‐temperature magnetic properties – mainly obey the zero‐field splitting effects D A ground‐state term pseudo‐tetrahedral anionic complex (2 is energy...

10.1002/ejic.201701177 article EN European Journal of Inorganic Chemistry 2017-11-29

The efficient organization of discrete functional molecules into extended frameworks, while retaining their physical properties, is a mandatory requisite to move toward applications. Here we describe the validity metalloligand design strategy as versatile and powerful approach build up two-dimensional (2D) magnetic metal–organic framework (MOF) composed preformed antiferromagnetically coupled [3 × 3] Cu9II incomplete grids. In first stage, novel oxamato-based nonanuclear copper(II) complex...

10.1021/acs.cgd.9b00324 article EN Crystal Growth & Design 2019-05-29

New trinuclear Ni( ii ) complex exhibiting intratrimer both weak ferro- and antiferromagnetic interactions resulting from the strict orthogonality between magnetic orbitals, a combination of spin delocalisation polarisation mechanisms.

10.1039/d3nj04701f article EN New Journal of Chemistry 2024-01-01
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