Effects of base pairing on the one-electron reduction rate of cytosine
Literature Information
Kiyohiko Kawai, Aya Yokoohji, Sachiko Tojo, Tetsuro Majima
Using nucleoside derivatives, which are soluble in dichloromethane, we have experimentally demonstrated that the reduction potential of cytosine is lowered by base pairing with guanine.
Related Literature
The electronic structure of perfluorodecalin studied by soft X-ray spectroscopy and electronic structure calculations
M. Agåker, C. Schwanke, T. Petit, K. M. Lange, J.-E. Rubensson
DOI: 10.1039/C4CP03153A
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
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
Effects of kinetic and transport phenomena on thermal explosion and oscillatory behaviour in a spherical reactor with mixed convection
Filipa Gonçalves de Azevedo, John F. Griffiths, Silvana S. S. Cardoso
DOI: 10.1039/C4CP02990A
Understanding the adsorption mechanism of noble gases Kr and Xe in CPO-27-Ni, CPO-27-Mg, and ZIF-8
O. V. Magdysyuk, F. Adams, H.-P. Liermann, I. Spanopoulos, P. N. Trikalitis, M. Hirscher, R. E. Morris, M. J. Duncan, L. J. McCormick, R. E. Dinnebier
DOI: 10.1039/C4CP03298E
Noble-metal-free BODIPY–cobaloxime photocatalysts for visible-light-driven hydrogen production
Geng-Geng Luo, Kai Fang, Ji-Huai Wu, Jing-Cao Dai, Qing-Hua Zhao
DOI: 10.1039/C4CP03343D
Electron spin-polarization and spin lattices in the boron- and nitrogen-doped organic framework COF-5
Xiaobiao Liu, Jie Tan, Aizhu Wang, Xiaoming Zhang, Mingwen Zhao
DOI: 10.1039/C4CP03478C
Photoelectrochemical reduction of aqueous protons with a CuO|CuBi2O4 heterojunction under visible light irradiation
Hyun S. Park, Chong-Yong Lee, Erwin Reisner
DOI: 10.1039/C4CP03883E
Probing molecular interaction in ionic liquids by low frequency spectroscopy: Coulomb energy, hydrogen bonding and dispersion forces
Koichi Fumino, Sebastian Reimann
DOI: 10.1039/C4CP01476F
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














