Christian Wittee Lopes

Dr. Christian Wittee Lopes

Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 July 2019 in Nature Materials
Verified
Journal Article
Closed access
PDF file
LLLichen Liu
Lichen Liu
MLMiguel Lopez-Haro
Miguel Lopez-Haro
CLChristian Wittee Lopes
Christian Wittee Lopes
CLChengeng Li
Chengeng Li
Patricia ConcepcionPatricia Concepcion
Patricia Concepcion
ACAvelino Corma
Avelino Corma

22 June 2020 in Nature Catalysis
Verified
Journal Article
Closed access
PDF file
LLLichen Liu
Lichen Liu
MLMiguel Lopez-Haro
Miguel Lopez-Haro
CLChristian Wittee Lopes
Christian Wittee Lopes
SRSergio Rojas-Buzo
Sergio Rojas-Buzo
Patricia ConcepcionPatricia Concepcion
Patricia Concepcion
ACAvelino Corma
Avelino Corma

5 July 2021 in Chemical Science
Verified
Journal Article
Open access
PDF file
SRSergio Rojas-Buzo
Sergio Rojas-Buzo
BBBenjamin Bohigues
Benjamin Bohigues
CLChristian Wittee Lopes
Christian Wittee Lopes
DMDébora M. Meira
Débora M. Meira
MBMercedes Boronat
Mercedes Boronat
ACAvelino Corma
Avelino Corma
The Lewis/Brønsted catalytic properties of the Metal–Organic Framework (MOF) nodes can be tuned by simply controlling the solvent employed in the synthetic procedure. In this work, we demonstrate that Hf-MOF-808 can be prepared from a material with a higher amount of Brønsted acid sites, via modulated hydrothermal synthesis, to a material with a higher proportion of unsaturated Hf Lewis acid sites, via modulated solvothermal synthesis. The Lewis/Brønsted acid properties of the resultant metallic clusters have been studied by different characterization techniques, including XAS, FTIR and NMR spectroscopies, combined with a DFT study. The different nature of the Hf-MOF-808 materials allows their application as selective catalysts in different target reactions requiring Lewis, Brønsted or Lewis–Brønsted acid pairs.

1 May 2020 in ACS Catalysis
Verified
Journal Article
Closed access
Francine BertellaFrancine Bertella
Francine Bertella
CLChristian Wittee Lopes
Christian Wittee Lopes
ESEli Stavitski
Eli Stavitski
GAGiovanni Agostini
Giovanni Agostini
Patricia ConcepcionPatricia Concepcion
Patricia Concepcion
AMAgustín Martínez
Agustín Martínez

6 November 2018 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
MRMiguel A. Rivero‐Crespo
Miguel A. Rivero‐Crespo
MMMarta Mon
Marta Mon
JSJesus Ferrando Soria
Jesus Ferrando Soria
CLChristian Wittee Lopes
Christian Wittee Lopes
MBMercedes Boronat
Mercedes Boronat
Emilio PardoEmilio Pardo
Emilio Pardo

11 May 2021 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
SGSilvia Gutiérrez
Silvia Gutiérrez
SRSergio Rojas-Buzo
Sergio Rojas-Buzo
CLChristian Wittee Lopes
Christian Wittee Lopes
GAGiovanni Agostini
Giovanni Agostini
JCJosé J. Calvino
José J. Calvino
POPascual Oña-Burgos
Pascual Oña-Burgos
The development of active and selective non-noble metal-based catalysts for the chemoselective reduction of nitro compounds in aquo media under mild conditions is an attractive research area. Herein, the synthesis of subnanometric and stable cobalt nanoclusters, covered by N-doped carbon layers as core–shell (Co@NC-800), for the chemoselective reduction of nitroarenes is reported. The Co@NC-800 catalyst was prepared by the pyrolysis of the Co(tpy)2 complex impregnated on Vulcan carbon. In fact, the use of a molecular complex based on six N–Co bonds drives the formation of a well-defined and distributed cobalt core–shell nanocluster covered by N-doped carbon layers. In order to elucidate its nature, it has been fully characterized by using several advanced techniques. In addition, this as-prepared catalyst showed high activity, chemoselectivity and stability toward the reduction of nitro compounds with H2 and under mild reaction conditions; water was used as a green solvent, improving the previous results based on cobalt catalysts. Moreover, the Co@NC-800 catalyst is also active and selective for the one-pot synthesis of secondary aryl amines and isoindolinones through the reductive amination of nitroarenes. Finally, based on diffraction and spectroscopic studies, metallic cobalt nanoclusters with surface CoNx patches have been proposed as the active phase in the Co@NC-800 material.