Reversible photochromism of a ferrocenylazobenzene monolayer controllable by a single green light source
Literature Information
Kosuke Namiki, Aiko Sakamoto, Masaki Murata, Shoko Kume, Hiroshi Nishihara
A 3-ferrocenylazobenzene monolayer on an ITO electrode exhibits reversible azobenzene isomerization using a single green light source, assisted by electrochemical control of the ferrocene redox state.
Related Literature
Excited states in large molecular systems through polarizable embedding
Nanna Holmgaard List, Jógvan Magnus Haugaard Olsen, Jacob Kongsted
DOI: 10.1039/C6CP03834D
Facile hydrothermal synthesis of NiMoO4@CoMoO4 hierarchical nanospheres for supercapacitor applications
DOI: 10.1039/C5CP03331D
Formic acid oxidation on platinum: a simple mechanistic study
Kathleen A. Schwarz, Ravishankar Sundararaman, Thomas P. Moffat, Thomas C. Allison
DOI: 10.1039/C5CP03045E
Correction: Kinetics and mechanism of the reaction of perfluoro propyl vinyl ether (PPVE, C3F7OCHCH2) with OH: assessment of its fate in the atmosphere
D. Amedro, L. Vereecken, J. N. Crowley
DOI: 10.1039/C5CP90133B
Light-induced water splitting by titanium-tetrahydroxide: a computational study
Andranik Kazaryan, Rutger van Santen, Evert Jan Baerends
DOI: 10.1039/C5CP01812A
Excited state structural evolution during charge-transfer reactions in betaine-30
W. Ruchira Silva, Renee R. Frontiera
DOI: 10.1039/C5CP06195D
Experimental approach to the fundamental limit of the extinction coefficients of ultra-smooth and highly spherical gold nanoparticles
Dong-Kwan Kim, Yoon Jo Hwang, Cheolho Yoon, Hye-On Yoon, Ki Soo Chang, Gi-Ra Yi
DOI: 10.1039/C5CP02968F
Behaviour of NBD-head group labelled phosphatidylethanolamines in POPC bilayers: a molecular dynamics study
DOI: 10.1039/C5CP01596K
Controlling charge injection properties in polymer field-effect transistors by incorporation of solution processed molybdenum trioxide
Dang Xuan Long, Yong Xu, Huai-xin Wei, Yong-Young Noh
DOI: 10.1039/C5CP03369A
On the lack of evolutionary continuity between prebiotic peptides and extant enzymes
Luciana Raggi, Jeffrey L. Bada, Antonio Lazcano
DOI: 10.1039/C6CP00793G
You might also like
What is 1-(2,4,6-Trifluorophenyl)ethanol (CAS: 1250113-83-7)?
1-(2,4,6-Trifluorophenyl)ethanol is an organic compound with the CAS number 1250...
Is 1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) safe?
1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) is ...
What are the physical and chemical properties of (7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one (CAS: 51419-51-3)?
(7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one is a crystal...
What regulatory guidelines apply to rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3618-04-0)?
The compound rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3...
What is the market or research trend for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3)?
The market for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3) is cur...
What are the main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9)?
The main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9) include research in ...
What precautions should be taken when handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5)?
When handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5), i...
How is 5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) typically synthesized?
5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) can be synthesi...
Are there alternatives to 2,4,6-Trihydroxyisophthalaldehyde (CAS: 4396-13-8) in synthesis?
There are alternative reagents that can be used in the synthesis of 2,4,6-Trihyd...
What is (2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid (CAS: 179461-52-0)?
(2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid is a chemical compound wi...
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














