Highlights
Literature Information
The first page of this article is displayed as the abstract.
Related Literature
Phase diagrams of diblock copolymers in electric fields: a self-consistent field theory study
Ji Wu, Xianghong Wang, Yongyun Ji, Linli He, Shiben Li
DOI: 10.1039/C5CP08030D
Electrochemical oxidation of 2-propanol over platinum and palladium electrodes in alkaline media studied by in situ attenuated total reflection infrared spectroscopy
Takeou Okanishi, Yu Katayama, Ryota Ito, Hiroki Muroyama, Toshiaki Matsui, Koichi Eguchi
DOI: 10.1039/C5CP07518A
Sulfur antisite-induced intrinsic high-temperature ferromagnetism in Ag2S:Y nanocrystals
Pan Wang, Tianye Yang, Rui Zhao, Mingzhe Zhang
DOI: 10.1039/C5CP07690K
Thermal optical non-linearity of nematic mesophase enhanced by gold nanoparticles – an experimental and numerical investigation
O. Kurochkin, Y. K. Murugesan, T. P. Bennett, G. D'Alessandro, Y. Reznikov, B. J. Tang, G. H. Mehl, M. Kaczmarek
DOI: 10.1039/C6CP00116E
Nonlinear optical chromophores based on Dewar's rules: enhancement of electro-optic activity by introducing heteroatoms into the donor or bridge
Shuhui Bo, Xinhou Liu
DOI: 10.1039/C5CP04959H
On the structure and bonding in the B4O4+ cluster: a boron oxide analogue of the 3,5-dehydrophenyl cation with π and σ double aromaticity
Ting Ou, Wen-Juan Tian, Xue-Rui You, Kang Wang
DOI: 10.1039/C5CP04519C
Density functional investigation and some optical experiments on dye-sensitized quantum dots
Kalpna Jain, Sreejith Kaniyankandy, Shyam Kishor, Ida Josefsson, Hirendra N. Ghosh, Khundrakpam S. Singh, Sumit Mookerjee, Michael Odelius, Lavanya M. Ramaniah
DOI: 10.1039/C5CP03816B
Charge transport in a liquid crystalline triphenylene polymer monolayer at air–solid interface
H. N. Gayathri, Bharat Kumar, K. A. Suresh, H. K. Bisoyi, Sandeep Kumar
DOI: 10.1039/C5CP07531A
Reproducible, stable and fast electrochemical activity from easy to make graphene on copper electrodes
Zachary P. L. Laker, Jonathan P. Rourke, Neil R. Wilson
DOI: 10.1039/C5CP04070A
Theoretical evidence of charge transfer interaction between SO2 and deep eutectic solvents formed by choline chloride and glycerol
Hongping Li, Yonghui Chang, Wenshuai Zhu, Changwei Wang, Chao Wang, Sheng Yin, Ming Zhang
DOI: 10.1039/C5CP04172D
You might also like
What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?
(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...
What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?
5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...
What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?
Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...
Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?
1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...
What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?
[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...
What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?
6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...
What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?
This compound is primarily used in the pharmaceutical industry for the developme...
What are the main uses of 1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (CAS: 1228013-15-7)?
1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2...
Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?
Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...
What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?
3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...
Source Journal
Green Chemistry

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.














