Interception and characterization of a hydridoalkylrhodium intermediate in a homogeneous catalytic hydrogenation reaction

1980 ◽  
Vol 102 (2) ◽  
pp. 838-840 ◽  
Author(s):  
A. S. C. Chan ◽  
Jack Halpern
Keyword(s):  
Catalytic Hydrogenation ◽  
Hydrogenation Reaction

Nanometer Scale Spectroscopic Visualization of Catalytic Sites During a Hydrogenation Reaction on a Pd/Au Bimetallic Catalyst

2020 ◽  
Author(s):  
hao yin ◽  
Liqing Zheng ◽  
Wei Fang ◽  
Yin-Hung Lai ◽  
Nikolaus Porenta ◽  
...  
Keyword(s):  
Catalytic Hydrogenation ◽  
Density Functional ◽  
Hydrogen Transfer ◽  
Bimetallic Catalyst ◽  
Local Environment ◽  
Hydrogenation Reaction ◽  
Boundary Density ◽  
Catalytic Sites ◽  
Powerful Analytical Tool ◽  
Tip Enhanced Raman Spectroscopy

<p>Understanding the mechanism of catalytic hydrogenation at the local environment requires chemical and topographic information involving catalytic sites, active hydrogen species and their spatial distribution. Here, tip-enhanced Raman spectroscopy (TERS) was employed to study the catalytic hydrogenation of chloro-nitrobenzenethiol on a well-defined Pd(sub-monolayer)/Au(111) bimetallic catalyst (<i>p</i><sub>H2</sub>=1.5 bar, 298 K), where the surface topography and chemical fingerprint information were simultaneously mapped with nanoscale resolution (≈10 nm). TERS imaging of the surface after catalytic hydrogenation confirms that the reaction occurs beyond the location of Pd sites. The results demonstrate that hydrogen spillover accelerates hydrogenation at the Au sites within 20 nm from the bimetallic Pd/Au boundary. Density functional theory was used to elucidate the thermodynamics of interfacial hydrogen transfer. We demonstrate that TERS as a powerful analytical tool provides a unique approach to spatially investigate the local structure-reactivity relationship in catalysis.</p>

Nanometer Scale Spectroscopic Visualization of Catalytic Sites During a Hydrogenation Reaction on a Pd/Au Bimetallic Catalyst

2020 ◽  
Author(s):  
Hao Yin ◽  
Liqing Zheng ◽  
Wei Fang ◽  
Yin-Hung Lai ◽  
Nikolaus Porenta ◽  
...  
Keyword(s):  
Catalytic Hydrogenation ◽  
Density Functional ◽  
Hydrogen Transfer ◽  
Bimetallic Catalyst ◽  
Local Environment ◽  
Hydrogenation Reaction ◽  
Boundary Density ◽  
Catalytic Sites ◽  
Powerful Analytical Tool ◽  
Tip Enhanced Raman Spectroscopy

<p>Understanding the mechanism of catalytic hydrogenation at the local environment requires chemical and topographic information involving catalytic sites, active hydrogen species and their spatial distribution. Here, tip-enhanced Raman spectroscopy (TERS) was employed to study the catalytic hydrogenation of chloro-nitrobenzenethiol on a well-defined Pd(sub-monolayer)/Au(111) bimetallic catalyst (<i>p</i><sub>H2</sub>=1.5 bar, 298 K), where the surface topography and chemical fingerprint information were simultaneously mapped with nanoscale resolution (≈10 nm). TERS imaging of the surface after catalytic hydrogenation confirms that the reaction occurs beyond the location of Pd sites. The results demonstrate that hydrogen spillover accelerates hydrogenation at the Au sites within 20 nm from the bimetallic Pd/Au boundary. Density functional theory was used to elucidate the thermodynamics of interfacial hydrogen transfer. We demonstrate that TERS as a powerful analytical tool provides a unique approach to spatially investigate the local structure-reactivity relationship in catalysis.</p>

Catalytic asymmetric hydrogenation reaction by in situ formed ultra-fine metal nanoparticles in live thermophilic hydrogen-producing bacteria

Nanoscale ◽  
2021 ◽  
Author(s):  
Wei Bing ◽  
Faming Wang ◽  
Yuhuan Sun ◽  
Jinsong Ren ◽  
Xiaogang Qu
Keyword(s):  
Metal Nanoparticles ◽  
Catalytic Hydrogenation ◽  
Asymmetric Hydrogenation ◽  
Environmentally Friendly ◽  
Hydrogenation Reaction ◽  
Highly Efficient ◽  
Hydrogenation Reactions ◽  
Live Bacteria ◽  
Catalytic Asymmetric Hydrogenation

An environmentally friendly biomimetic strategy has been presented and validated for the catalytic hydrogenation reaction in live bacteria. In situ formed ultra-fine metal nanoparticles can realize highly efficient asymmetric hydrogenation reactions.

scholarly journals Fractionation of Birch Wood by Integrating Alkaline-Acid Treatments and Hydrogenation in Ethanol over a Bifunctional Ruthenium Catalyst

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1362
Author(s):  
Boris N. Kuznetsov ◽  
Sergey V. Baryshnikov ◽  
Angelina V. Miroshnikova ◽  
Aleksandr S. Kazachenko ◽  
Yuriy N. Malyar ◽  
...  
Keyword(s):  
Microcrystalline Cellulose ◽  
Catalytic Hydrogenation ◽  
Liquid Product ◽  
Gel Permeation Chromatography ◽  
Ruthenium Catalyst ◽  
Birch Wood ◽  
Gaseous Products ◽  
Liquid Products ◽  
First Time

For the first time, the fractionation of birch wood into microcrystalline cellulose, xylose and methoxyphenols is suggested based on the integration of alkali-acid pretreatments and hydrogenation in ethanol over a bifunctional Ru/C catalyst. It is established that removal of hemicelluloses during pretreatments of birch wood influences the yields of the liquid, gaseous and solid products of the non-catalytic and catalytic hydrogenation of pretreated samples in ethanol at 225 °C. The bifunctional Ru/carbon catalyst affects in different ways the conversion and yields of products of hydrogenation of the initial and acid- and alkali-pretreated birch wood. The most noticeable influence is characteristic of the hydrogenation of the acid-pretreated wood, where in contrast to the non-catalytic hydrogenation, the wood conversion and the yields of liquid products increase but the yields of the solid and gaseous products decrease. GC-MS, gel permeation chromatography and elemental analysis were used for characterization of the liquid product composition. The molecular mass distribution of the liquid products of hydrogenation of the initial and pretreated wood shifts towards the low-molecular range in the presence of the catalyst. From the GC-MS data, the contents of monomer compounds, predominantly 4-propylsyringol and 4-propanolsyringol, increase in the presence of the ruthenium catalyst. The solid products of catalytic hydrogenation of the pretreated wood contain up to 95 wt% of cellulose with the structure, similar to that of microcrystalline cellulose.

Gas-liquid catalytic hydrogenation reaction in small catalyst channel

AIChE Journal ◽  
2005 ◽  
Vol 51 (8) ◽  
pp. 2285-2297 ◽  
Author(s):  
Wei Liu ◽  
Shantanu Roy ◽  
Xiaodong Fu
Keyword(s):  
Catalytic Hydrogenation ◽  
Hydrogenation Reaction

Studien zum Vorgang der Wasserstoffübertragung, 78 [1]. Untersuchungen zur Charakterisierung des im Raney-Nickel (Ra-Ni) gebundenen Wasserstoffs / Studies on the Occurrence of Hydrogentransfer, 78 [1]. Investigations for the Characterization of the Hydrogen Present in Raney-Nickel (Ra-Ni)

1985 ◽  
Vol 40 (10) ◽  
pp. 1398-1400
Author(s):  
L. Horner ◽  
U. Kaps
Keyword(s):  
Raney Nickel ◽  
Catalytic Hydrogenation ◽  
Sulfur Compounds

Hydride supported alloys Mg2Ni (A), CaNi5 (B) and FeTi (C) are in contrast to Ra-Ni unable for the catalytic hydrogenation and the hydrogenolysis of sulfur compounds. The origin and quality of the “structure bonded hydrogen” in Ra-Ni is still speculative.

Recyclable catalyst for catalytic hydrogenation of phenylacetylene by coupling Pd nanoparticles with highly compressible graphene aerogels

RSC Advances ◽  
2014 ◽  
Vol 4 (104) ◽  
pp. 59977-59980 ◽  
Author(s):  
Xu Zhang ◽  
Zhiyu Wang ◽  
Shuang Li ◽  
Chunlei Wang ◽  
Jieshan Qiu
Keyword(s):  
Graphene Oxide ◽  
Catalytic Hydrogenation ◽  
Chemical Reduction ◽  
Pd Nanoparticles ◽  
Catalytic Performance ◽  
Hydrogenation Reaction ◽  
Recyclable Catalyst ◽  
Graphene Aerogels ◽  
Excellent Catalytic Performance

Highly compressible graphene aerogels were made by chemical reduction of graphene oxide with HI, which act as recyclable catalyst to exhibit excellent catalytic performance towards selective semi-hydrogenation reaction after loading Pd nanoparticles.

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