Extended X-ray absorption fine structure (EXAFS) characterisation of dilute palladium homogeneous catalysts
Literature Information
John Evans, Mark A. Newton, Thomas Neisius, Robert P. Tooze, Richard Oldman
Highly dilute EXAFS characterisation for the elucidation of species involved in Heck chemistry is demonstrated; the major “monomer” species of Herrmann's acetate-bridged phosphapalladadacycle is characterised and species present during the course of a 50 ppm [Pd] Pd(OAc)2/PBut3 catalysed Heck reaction are presented.
Related Literature
Epitope mapping of imidazolium cations in ionic liquid–protein interactions unveils the balance between hydrophobicity and electrostatics towards protein destabilisation
Micael Silva, Angelo Miguel Figueiredo, Eurico J. Cabrita
DOI: 10.1039/C4CP03534H
Realizing semiconductor–half-metal transition in zigzag graphene nanoribbons supported on hybrid fluorographene–graphane nanoribbons
Shaobin Tang, Xinrui Cao
DOI: 10.1039/C4CP03291H
Femtosecond spectroscopy reveals huge differences in the photoisomerisation dynamics between azobenzenes linked to polymers and azobenzenes in solution
Julia Bahrenburg, Falk Renth, Friedrich Temps, Felix Plamper, Walter Richtering
DOI: 10.1039/C4CP01196A
Probing the dynamics of plasmon-excited hexanethiol-capped gold nanoparticles by picosecond X-ray absorption spectroscopy
Thomas J. Penfold, Maarten Nachtegaal, Chris J. Milne, Majed Chergui
DOI: 10.1039/C4CP03301A
Interband π plasmon of graphene: strong small-size and field-enhancement effects
Jinlian Hu, Haibo Zeng, Cong Wang, Zhigang Li, Caixia Kan, Youwen Liu
DOI: 10.1039/C4CP02299H
Direct measurements of the total rate constant of the reaction NCN + H and implications for the product branching ratio and the enthalpy of formation of NCN
Nancy Faßheber, Johannes Dammeier, Gernot Friedrichs
DOI: 10.1039/C4CP01107D
M(BH3NH2BH2NH2BH3) – the missing link in the mechanism of the thermal decomposition of light alkali metal amidoboranes
K. J. Fijalkowski, T. Jaroń, P. J. Leszczyński, E. Magos-Palasyuk, T. Palasyuk, M. K. Cyrański, W. Grochala
DOI: 10.1039/C4CP03296A
Aggregation-induced chiral symmetry breaking of a naphthalimide–cyanostilbene dyad
Xin Li, Liangliang Zhu, Sai Duan, Yanli Zhao, Hans Ågren
DOI: 10.1039/C4CP04070H
Peculiar surface–interface properties of nanocrystalline ceria–cobalt oxides with enhanced oxygen storage capacity
Nan Qiu, Jing Zhang
DOI: 10.1039/C4CP03390F
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
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










![5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure 5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure](https://static.chemtradehub.com/structs/251/251903-00-1-9cb1.webp)
![1-oxaspiro[4.4]nonan-6-one structure 1-oxaspiro[4.4]nonan-6-one structure](https://static.chemtradehub.com/structs/134/134179-01-4-e051.webp)


