Contrasting dynamic responses of supported Rh nanoparticles to H2S and SO2 and subsequent poisoning of NO reduction by H2
Literature Information
Mark A. Newton, Andrew J. Dent, Sofia Diaz-Moreno, Steven G. Fiddy, Bhrat Jyoti
H2S induces rapid sulfidation of the Rh nanoparticles at room temperature and completely poisons NO reduction by H2; SO2 elicits an equally rapid but subtle modification of nanoparticle structure but has little effect upon NO reduction at 523 K.
Related Literature
A physical picture for mechanical dissociation of biological complexes: from forces to free energies
Rafael Tapia-Rojo, Juan J. Mazo, Fernando Falo
DOI: 10.1039/C6CP07508H
Controlling the kinetic and thermodynamic stability of cationic clusters by the addition of molecules or counterions
Anne Strate, Thomas Niemann
DOI: 10.1039/C7CP02227A
Characterising molecules for fundamental physics: an accurate spectroscopic model of methyltrioxorhenium derived from new infrared and millimetre-wave measurements
Thérèse R. Huet, Laurent Margulès, Roman Motiyenko, Richard J. Hendricks, Michael R. Tarbutt
DOI: 10.1039/C6CP08724H
Photocleavage of coumarin dimers studied by femtosecond UV transient absorption spectroscopy
Man Jiang, Nicholas Paul, Nikolai Bieniek, Tiago Buckup, Norbert Hampp, Marcus Motzkus
DOI: 10.1039/C6CP08076F
Silver–gold alloy nanoparticles as tunable substrates for systematic control of ion-desorption efficiency and heat transfer in surface-assisted laser desorption/ionization
Samuel Kin-Man Lai, Yu-Hong Cheng, Ho-Wai Tang, Kwan-Ming Ng
DOI: 10.1039/C7CP04033D
Growth and structure of ultrathin praseodymium oxide layers on ruthenium(0001)
Jan Höcker, Julian Cambeis, Alexei Zakharov, Yuran Niu, Gang Wei, Andreas Schaefer
DOI: 10.1039/C6CP06853G
Remarkable influence of ‘phane effect’ on the excited-state properties of cofacially oriented coumarins
Arindam Mukhopadhyay, Vijay Kumar Maka, Jarugu Narasimha Moorthy
DOI: 10.1039/C6CP07720J
The influence of heteroatoms on the aromatic character and the current pathways of B2N2-dibenzo[a,e]pentalenes
Maria Dimitrova, Heike Fliegl, Dage Sundholm
DOI: 10.1039/C7CP02964K
You might also like
How should waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3) be handled?
Waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3...
How should N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine (CAS: 1318338-47-4) be stored?
N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine should be stored in a tightly sealed c...
What is the market or research trend for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1)?
The market for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1) is...
How should Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) be stored?
Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) ...
What regulatory guidelines apply to 2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3)?
2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3) is regulated under the Glob...
What regulatory guidelines apply to 1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 119462-56-5)?
1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 11946...
Are there alternatives to 5-Fluoro-2-(1-pyrrolidinyl)pyridine (CAS: 1287217-79-1) in synthesis?
Several alternatives can be used in the synthesis of 5-Fluoro-2-(1-pyrrolidinyl)...
What precautions should be taken when handling 1-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione (CAS: 153631-19-7)?
Proper personal protective equipment (PPE) must be worn when handling this compo...
What precautions should be taken when handling 6-Bromoimidazo[1,2-a]pyridin-8-amine (CAS: 676371-00-9)?
When handling 6-Bromoimidazo[1,2-a]pyridin-8-amine, it is important to wear appr...
Are there alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride (CAS: 1049740-22-8) in synthesis?
Alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochlo...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry












![2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure 2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure](https://static.chemtradehub.com/structs/127/1279090-25-3-1b84.webp)

