Front cover
Literature Information
A graphical abstract is available for this content
Related Literature
Dynamics of the D+ + H2 and H+ + D2 reactions: a detailed comparison between theory and experiment
J. M. Alvariño, D. Gerlich, M. Hankel, V. J. Herrero, V. Sáez-Rábanos, F. J. Aoiz
DOI: 10.1039/C2CP23479C
Recent developments in the study of ionic liquid interfaces using X-ray photoelectron spectroscopy and potential future directions
Hans-Peter Steinrück
DOI: 10.1039/C2CP24087D
High-pressure spin-crossover in a dinuclear Fe(ii) complex
Patrick Rosa, Laure Vendier, Nicola Casati, Jean-François Létard, Azzedine Bousseksou, Philippe Guionneau, Gábor Molnár
DOI: 10.1039/C2CP23940J
Functionalized corannulene cations: a detailed theoretical survey
Andrey Yu. Rogachev, Alexander S. Filatov, Alexander V. Zabula, Marina A. Petrukhina
DOI: 10.1039/C2CP23442D
On the formation of phenyldiacetylene (C6H5CCCCH) and D5-phenyldiacetylene (C6D5CCCCH) studied under single collision conditions
D. S. N. Parker, F. Zhang, Y. S. Kim, R. I. Kaiser, A. Landera, A. M. Mebel
DOI: 10.1039/C2CP22695B
The importance of the shape of the protein–water interface of a kinesin motor domain for dynamics of the surface atoms of the protein
Anna Kuffel, Jan Zielkiewicz
DOI: 10.1039/C2CP40105C
Switching of fluorescence mediated by a peroxynitrite–glutathione redox reaction in a porous silicon nanoreactor
Beniamino Sciacca, Stephanie Pace, Paola Rivolo, Francesco Geobaldo
DOI: 10.1039/C2CP23996E
Fermi energy level tuning for high performance dye sensitized solar cells using sp2 selective nitrogen-doped carbon nanotube channels
Ga In Lee, Narayan Chandra Deb Nath, Subrata Sarker, Weon Ho Shin, A. J. Saleh Ahammad, Jeung Ku Kang
DOI: 10.1039/C2CP40279C
In situ time-resolved DXAFS study of Rh nanoparticle formation mechanism in ethylene glycol at elevated temperature
Hiroyuki Asakura, Kentaro Teramura, Tetsuya Shishido, Tsunehiro Tanaka, Ning Yan, Chaoxian Xiao, Siyu Yao, Yuan Kou
DOI: 10.1039/C2CP23070D
Multi-structural variational transition state theory: kinetics of the 1,5-hydrogen shift isomerization of the 1-butoxyl radical including all structures and torsional anharmonicity
Xuefei Xu, Ewa Papajak, Jingjing Zheng, Donald G. Truhlar
DOI: 10.1039/C2CP23692C
You might also like
What is 3-Fluoro-2-methylbenzylamine (CAS: 771573-36-5)?
3-Fluoro-2-methylbenzylamine is an organic compound with the CAS number 771573-3...
Is Tert-butyl 2-(oxetan-3-ylidene)acetate (CAS: 1207175-03-8) safe?
Tert-butyl 2-(oxetan-3-ylidene)acetate is considered safe for its intended uses ...
What precautions should be taken when handling 4-Acetyl-2-fluorobenzonitrile (CAS: 214760-18-6)?
Proper personal protective equipment (PPE) such as gloves, goggles, and a lab co...
How is 2-Ethyl-4-methyl-1,3-thiazole (CAS: 15679-12-6) typically synthesized?
2-Ethyl-4-methyl-1,3-thiazole is commonly synthesized via the reaction of thiour...
How should 5',5''-([2,2'-Bithiophene]-5,5'-diyl)bis(([1,1':3',1''-terphenyl]-4,4''-dicarboxylic acid)) (CAS: 1227780-71-3) be stored?
This compound should be stored in a cool, dry place away from direct sunlight an...
What regulatory guidelines apply to L-Lysine Acetate Salt (CAS: 52315-92-1)?
L-Lysine Acetate Salt (CAS: 52315-92-1) is subject to various regulatory guideli...
Is 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) safe?
6-Fluoro-3-hydroxy-2-pyrazinecarboxamide (CAS: 259793-96-9) is generally conside...
What are the physical and chemical properties of 1,1'-Sulfonylbis(1H-imidazole) (CAS: 7189-69-7)?
1,1'-Sulfonylbis(1H-imidazole) is a crystalline solid with a molecular weight of...
What industries use 4-methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5)?
4-Methyl-7-nitro-1H-indole-3-carbonitrile (CAS: 289483-82-5) is primarily used i...
How should waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) be handled?
Waste containing 5-Bromo-3-indolyl-beta-galactoside (CAS: 97753-82-7) should be ...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure 4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure](https://static.chemtradehub.com/structs/362/3627-01-8-79ac.webp)


![(2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure (2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure](https://static.chemtradehub.com/structs/173/173867-04-4-d2d3.webp)
