Evidence for C–C bond cleavage by H2O2 in a mesoporous CMK-5 type carbon at room temperature
Literature Information
An-Hui Lu, Wen-Cui Li, Nelli Muratova, Bernd Spliethoff, Ferdi Schüth
We reported an evidence for C–C bond cleavage by milder oxidizing agent H2O2 in a mesoporous CMK-5 type carbon at room temperature.
Related Literature
Metathesis polymerization of monomers containing two diphenylacetylene units: synthesis and properties of poly(diphenylacetylene)s bearing diphenylacetylene units on the side chain
Toshikazu Sakaguchi, Hikaru Shimada, Tamotsu Hashimoto
DOI: 10.1039/D0PY01182G
Forced gradient copolymerisation: a simplified approach for polymerisation-induced self-assembly
Sihao Xu, Nathaniel Corrigan, Cyrille Boyer
DOI: 10.1039/D0PY00889C
An in-depth analysis approach enabling precision single chain nanoparticle design
Ralf Schweins, Hartmut Komber
DOI: 10.1039/D0PY01045F
Amphiphobic polyHIPEs with pH-triggered transition to hydrophilicity–oleophobicity for the controlled removal of water from oil–water mixtures
Xiaomin Li, Zhiguang Xu, Huanjie Chi, Zhu Wu, Yan Zhao
DOI: 10.1039/D0PY01144D
Semifluorinated, kinked polyarylenes via direct arylation polycondensation
Fabian Kempe, Felix Riehle, Hartmut Komber, Rukiya Matsidik, Michael Walter, Michael Sommer
DOI: 10.1039/D0PY00973C
One-step synthesis of well-dispersed polypyrrole copolymers under gamma-ray irradiation
Yuqing Qiao, Yusen Meng, Ming Yu, Bowu Zhang
DOI: 10.1039/D0PY01566K
Retracted Article: Non-thermal microwave effects in radical polymerization of bio-based terpenoid (meth)acrylates
Amaia Agirre, José M. Asua
DOI: 10.1039/D0PY01192D
Facile topological transformation of ABA triblock copolymers into multisite, single-chain-folding and branched multiblock copolymers via sequential click coupling and anthracene chemistry
Yanzhe He, Zhigang Wang, Peng Liu, Xiangdong Zhou, Youliang Zhao
DOI: 10.1039/D0PY01649G
One-component rapid Norrish Type II photoinitiation of bulk photo-CuAAC polymer networks
Abhishek U. Shete, Bryan P. Sutherland
DOI: 10.1039/D0PY01310B
You might also like
What are the main uses of 1H-Indazole-6-carbonitrile (CAS: 141290-59-7)?
1H-Indazole-6-carbonitrile finds applications in pharmaceuticals, where it serve...
How should waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) be handled?
Waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) should be collecte...
What industries use Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide (CAS: 68291-98-5)?
Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide is primarily used in pharmac...
Are there alternatives to Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxylate (CAS: 741709-66-0) in synthesis?
Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxyla...
How should waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) be handled?
Waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) should be manage...
What is 6-Formyl-2-pyridinecarboxylic acid (CAS: 499214-11-8)?
6-Formyl-2-pyridinecarboxylic acid is an organic compound with the molecular for...
What is the market or research trend for 3-(3,4-dimethoxyphenyl)-2,5-dimethyl-N-(2-morpholin-4-ylethyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS: 900874-91-1)?
Research trends for this compound indicate a focus on its potential applications...
How is 9H-Tribenzo[b,d,f]azepine (CAS: 29875-73-8) typically synthesized?
9H-Tribenzo[b,d,f]azepine is typically synthesized via a multi-step process invo...
How is 1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (CAS: 1797982-51-4) typically synthesized?
1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxyli...
How should waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: 671820-52-3) be handled?
Waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: ...
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














