Archive for August, 2013

MOF-artificial enzyme enters the field of glucose detection

A study published in the journal Diabetes Care estimated that in 2000, 171 million people worldwide had diabetes. People with diabetes have high blood sugar levels so biosensors that detect glucose are crucial in the diagnosis and treatment of this disease. Many diagnostic glucose sensors have been developed with widespread use in clinical and biotechnology applications.

In this Catalysis Science & Technology advance article, Liu and co-workers developed a colorimetric method for the detection of H2O2. Hydrogen peroxide is a by-product formed when glucose is oxidized by glucose oxidase (GOx), so coupling these events is a common strategy for glucose detection. The resultant H2O2 in the presence of an oxidation catalyst oxidizes 3,3,5,5-tetramethylbenzidine (TMB) to the diimine (oxTMB) producing a deep blue color. The researchers synthesized a composite material (H@M)to catalyse the oxidation by anchoring Hemin, to an amino-containing MOF (MIL-101(Al)-NH2).

This represents the first use of a MOF-artificial enzyme in glucose detection. Immobilizing Hemin on a metal-organic framework prevents problematic oxidative degradation and molecular aggregation. Also, the pore structure of the MOF mimics protein structure, which is important for activity and selectivity. The catalytic activity of this enzyme mimic is dependent on pH, temperature and H2O2 concentration. However, glucose oxidation is optimal at a pH of 7.0 and TMB oxidation by H@M is optimal at a pH of 5.0. The glucose detection is finally realized by first reacting glucose with GOx then adding a TMB and H@M solution and adjusting the acidity of the solution.

To read more, follow the link below:

Hemin@metal-organic framework with peroxidase-like activity and its application to glucose detection

Feng-Xiang Qin, Shao-Yi Jia, Fei-Fei Wang, Song-Hai Wu, Jia Song and Yong Liu

Catal. Sci. Technol. 2013, Advance Article, DOI: 10.1039/c3cy00268c

Tien Nguyen is a web contributor working towards her PhD in David Nicewicz’s research  group at the University of North Carolina at Chapel Hill, USA. Her current area of research  focuses on anti-Markovnikov hydroamination of alkenes using photoredox catalysis.

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Art in action: Novel Sulfated Zirconia as bifunctional catalysts

With context to the ever increasing problem of dwindling energy resources, sugars like 5-Hydroxymethylfurfural (5-HMF) and furfural are considered to be the key for next-generation energy demands. These sugars have been recently identified to have potential applications in the petrochemicals and plastic industry. While efforts are ongoing to find a cheaper and greener way for the production of 5-HMF, it has eluded most of the researchers till now.

In their quest for a total green 5-HMF synthesis, the authors moved towards sulfated zirconia as a bifunctional catalyst for the one-pot conversion of glucose to 5-HMF in aqueous phase. It has been observed that isomerisation of glucose to fructose is possible with zirconia, and the subsequent dehydration of fructose to 5-HMF with sulfated zirconia (SZ). The authors tried to capitalize on their previous experience of employing SZ in aqueous media and went on to create the first ever bifunctional catalyst for 5-HMF production in water. The key towards the holy grail was tuning the acid strength in SO2/ZrO2 to achieve both the isomerisation and dehydration through a single bi-functional catalyst.

Sulfated Zirconia as bifunctional catalysts

The amphoteric nature of  zirconia was explored and tuned by adjusting the sulfate loading onto the metal, as the surface sulfate density directly relates to the acidity of the catalyst. The extensive investigations by the researchers showed that zirconia exists in a monoclinic state with large lewis base sites, which converts to a more stable tetragonal structure on sulfate addition with abundance of bronsted acid sites. The lewis base sites catalysed the glucose –> fructose isomerisation and the bronsted acid sites accelerated the fructose –> 5-HMF dehydration. This knowledge helped them in optimising the sulfate loading to 0.3 ml which gives a perfect platform for Glucose –> Fructose –> 5-HMF conversion.

To read more about the art of synthesizing such novel bifunctional catalysts, follow the link below:

Bifunctional SO4/ZrO2 catalysts for 5-hydroxymethylfurfural (5-HMF) production from glucose

Catal. Sci. Technol., 2013, Accepted Manuscript
Shreesha Bhat, Web Writer Shreesha Bhat is a M.S.(Pharm.) in Medicinal Chemistry from National Institute  of Pharmaceutical        Education and Research, India. His area of interests  include chemical synthesis of biologically important  molecules and developing  newer methods for organic synthesis using novel catalysts.
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Make it a single – Hydrogenation of acrylonitrile-butadiene rubber with water soluble catalysts

Hydrogenated acrylonitrile butadiene rubber (HNBR) is an important elastomer heavily relied on by the automotive and petroleum industry. Identified for its tensile strength and ability to resist oxidative degradation, HNBR is used to make seals, hoses and belts. On an industrial scale, HNBR is synthesized by the hydrogenation of unsaturated acrylonitrile butadiene rubber (NBR). This process involves an organic solvent, hydrogen gas and a transition metal catalyst.

In this advance article, Rempel, Pan and co-workers have developed a green method to hydrogenate NBR that employs water-soluble Rhodium catalysts in purely aqueous media. Rhodium chloride monosulfonated triphenylphosphine (RhCl(TPPMS)3, 0.52 mmol L-1) catalysed the hydrogenation of NBR (50 g L-1) with a 95% conversion to HNBR in 9 hours at 1000 psi and 100 °C. The solubility of the Rhodium catalyst was critical to the success of the reaction, creating an effective relative partition between the water and polymer phases.  The authors also found that NBR starting materials containing gel resulted in lower conversions because this structure limits contact between the active catalyst and substrate.

To read more, follow the link below:

Hydrogenation of acrylonitrile-butadiene copolymer latex using water-soluble rhodium catalysts

Yin Liu, Hanmiroo Kim, Qinmin Pan, and Garry L. Rempel

Catal. Sci. Technol., 2013, Advance Article, DOI: 10.1039/c3cy00257h

Tien Nguyen is a web contributor working towards her PhD in David Nicewicz’s research  group at the University of North Carolina at Chapel Hill, USA. Her current area of research  focuses on anti-Markovnikov hydroamination of alkenes using photoredox catalysis.

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Homogeneous catalyst made to act more like an enzyme

Homogeneous catalytic systems which display selectivity in a mixture of similar substrates are rare. Now scientists in Italy and the Netherlands have shown that encapsulating a homogeneous catalyst in a supramolecular host can give it a more discerning nature.

 Alessandro Scarso at the University of Venice and colleagues found that putting a catalyst within a supramolecular host makes it act more like an enzyme – only specific substrates can fit into the cavity and reach the catalyst. Supramolecular interactions between the substrate, host and catalyst provide additional levels of electronic restriction.

Read the full story at Chemistry World

Substrate Selectivity in the Alkyne Hydration Mediated by NHC-Au(I) controlled by Encapsulation of the Catalyst within a Hydrogen Bonded Hexameric Host

Substrate Selectivity in the Alkyne Hydration Mediated by NHC-Au(I) controlled by Encapsulation of the Catalyst within a Hydrogen Bonded Hexameric Host
Alessandro Scarso, Alessandra Cavarzan, Francesco Trentin, Joost Reek and Giorgio Strukul
Catal. Sci. Technol., 2013, DOI: 10.1039/C3CY00300K, Communication

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HOT articles for August

Comparison of methane activation and catalytic ethylene formation on free gold and palladium dimer cations: product binding determines the catalytic turnover
Sandra M. Lang, Anja Frank and Thorsten M. Bernhardt

Catal. Sci. Technol., 2013, Advance Article
DOI: 10.1039/C3CY00286A, Paper

Comparison of methane activation and catalytic ethylene formation on free gold and palladium dimer cations: product binding determines the catalytic turnover


Total oxidation of naphthalene at low temperatures using palladium nanoparticles supported on inorganic oxide-coated cordierite honeycomb monoliths
Francisco J. Varela-Gandía, Ángel Berenguer-Murcia, Dolores Lozano-Castelló, Diego Cazorla-Amorós, David R. Sellick and Stuart H. Taylor

Catal. Sci. Technol., 2013, Advance Article
DOI: 10.1039/C3CY00323J, Paper

Total oxidation of naphthalene at low temperatures using palladium nanoparticles supported on inorganic oxide-coated cordierite honeycomb monoliths


Development of a 4,4′-biphenyl/phosphine-based COF for the heterogeneous Pd-catalysed telomerisation of 1,3-butadiene
Peter J. C. Hausoul, Tamara M. Eggenhuisen, Deepak Nand, Marc Baldus, Bert M. Weckhuysen, Robertus J. M. Klein Gebbink and Pieter C. A. Bruijnincx

Catal. Sci. Technol., 2013, Advance Article
DOI: 10.1039/C3CY00188A, Paper

Development of a 4,4’-biphenyl/phosphine-based COF for the heterogeneous Pd-catalysed telomerisation of 1,3-butadiene


Superior activity of rutile-supported ruthenium nanoparticles for HCl oxidation
Evgenii V. Kondratenko, Amol P. Amrute, Marga-Martina Pohl, Norbert Steinfeldt, Cecilia Mondelli and Javier Pérez-Ramírez

Catal. Sci. Technol., 2013, Advance Article
DOI: 10.1039/C3CY00372H, Communication

Superior activity of rutile-supported ruthenium nanoparticles for HCl oxidation


Recent advances in the photocatalytic CO2 reduction over semiconductors
Jin Mao, Kan Li and Tianyou Peng

Catal. Sci. Technol., 2013, Advance Article
DOI: 10.1039/C3CY00345K, Perspective

Recent advances in the photocatalytic CO2 reduction over semiconductors

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Pd Nanocubes: A new customizable weapon for enantioselective hydrogenation

Ever heard of a customizable catalyst? A catalyst with a unique shape? A catalyst which with a change in size can provide different activity? If not, then here is a catalyst- an easy to prepare Pd nanocube which you can customize as per the activity desired: racemic or enantioselective hydrogenation of α,β-unsaturated carboxylic acids.

The enantioselective hydrogenation of aliphatic α,β-unsaturated carboxylic acids faces the obstacle of lower enantioselectivities as the aliphatic substituent is not armed to curb the inevitable isomerization of the double bonds in the structure. High enantioselectivities have been observed in cases of aryl substituted α,β-unsaturated carboxylic acids owing to the stabilizing effect of the aryl substituent at the β-position. With no effective solutions up-to-date, the researchers at Chinese Academy of Sciences tried to find the answer to this problem in the world of micromeretics and morphology.

Considering the previous instances where the sizes and shape of the catalysts did play a role in the enantioselectivity, the researchers tried to capitalize on this and were indeed rewarded with fruitful results. They decided to study the effects of shape and size, by preparing both cubic and spherical Pd nanoparticles as catalysts for the enantioselective hydrogenation of unsaturated carboxylic acids. The studies conducted by the Shen group clearly indicate that the Pd nanocubes have a upperhand, as they provide good enantioselectivities as compared to the spherical nanoparticles. They also found that the Pd nanocubes of larger size provided with excellent enantioselecctivities as compared to the smaller nanocubes. The dynamics of this can be explained by the fact that larger nanocubes, which have more flat sites, can easily accommodate the chiral modifier (like cinchonidine) on its surface along with the substrate, thus resulting in higher enantioselectivities. Meanwhile, the smaller nanocubes provided higher yields, as they are equipped with more edge sites, which accelerates the process of hydrogenation. The present study provides with a customizable formula with both small and large nanocubes put to different use.

Activity desired Pd Nanocubes customized to
Racemic Hydrogenation at High yields Small  size
Enantioselective Hydrogenation at Lower yields Large size

Thus, the present paper brings forward the fresh concept of customized Pd nanocubes, which can be an effective weapon in the armory of catalysts for enantioselective hydrogenation of α,β-unsaturated carboxylic acids.

Palladium nanocubes as customizable weapons for enantioselective hydrogenation

Customizable Palladium Nanocubes for Racemic/Enantioselective hydrogenation

To read more, follow the link below:

Enantioselective hydrogenation of α,β-unsaturated carboxylic acids on Pd nanocubes
Chunhui Chen, Ensheng Zhan, Na Ta, Yong Li and  Wenjie Shen

Catal. Sci. Technol., 2013, Advance Article
DOI:
10.1039/C3CY00314K

Shreesha Bhat, Web Writer Shreesha Bhat is a M.S.(Pharm.) in Medicinal Chemistry from National Institute of Pharmaceutical        Education and Research, India. His area of interests include chemical synthesis of biologically important  molecules and developing newer methods for organic synthesis using novel catalysts.

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