Efficient kinetic experiments in continuous flow microreactors
文献情報
Kosi C. Aroh, Klavs F. Jensen
Flow chemistry is an enabling technology that can offer an automated and robust approach for the generation of reaction kinetics data. Recent studies have taken advantage of transient flows to quickly generate concentration profiles with various online analytical tools. In this work, we demonstrate an improved method where temperature and flow are transient throughout the reaction. It was observed that only two orthogonal temperature ramp experiments under the same transient flow condition were sufficient to characterize a Paal–Knorr (one step bimolecular) reaction within our chosen reaction space. This method further shortens the time and decreases the materials needed to collect sufficient kinetic data and provides a framework with which more complex kinetic studies could be performed.
関連文献
A photoinduced charge transfer composite of graphene oxide and ferrocene
Subash Sharma, Koichi Wakita, Masayoshi Umeno, Yasuhiko Hayashi, Masaki Tanemura
DOI: 10.1039/C2CP43427J
Organic ultra-thin film transistors with a liquid gate for extracellular stimulation and recording of electric activity of stem cell-derived neuronal networks
Tobias Cramer, Beatrice Chelli, Mauro Murgia, Marianna Barbalinardo, Eva Bystrenova, Dago M. de Leeuw, Fabio Biscarini
DOI: 10.1039/C3CP44251A
A new hematite photoanode doping strategy for solar water splitting: oxygen vacancy generation
Tae-Youl Yang, Ho-Young Kang, Uk Sim, Young-Joo Lee, Ji-Hoon Lee, Byungjin Koo, Ki Tae Nam, Young-Chang Joo
DOI: 10.1039/C2CP44352J
Metal centered oxidation or ligand centered oxidation of metal dithiolene? Spectral, electrochemical and structural studies on a nickel-4-pyridine-1,2-dithiolate system
Xin-Yu Li, Yong-Gang Sun, Peng Huo, Ming-Yan Shao, Shu-Fang Ji
DOI: 10.1039/C3CP44054K
Polyallylamine-directed green synthesis of platinum nanocubes. Shape and electronic effect codependent enhanced electrocatalytic activity
Gengtao Fu, Ke Wu, Xian Jiang, Lin Tao, Yu Chen, Jun Lin, Yiming Zhou, Shaohua Wei, Yawen Tang, Tianhong Lu, Xinghua Xia
DOI: 10.1039/C3CP44191A
Visualization of clusters in polymer electrolyte membranes by electron microscopy
Sergey Yakovlev, Kenneth H. Downing
DOI: 10.1039/C2CP42969A
Hydrogen oxidation at the Pt–BaZr0.1Ce0.7Y0.1Yb0.1O3−δ (BZCYYb) interface
Mingfei Liu, Shi Feng, Wei Liu, Hyeon Cheol Park, Meilin Liu
DOI: 10.1039/C3CP44225J
The catalytic mechanism of glyceraldehyde 3-phosphate dehydrogenase from Trypanosoma cruzi elucidated via the QM/MM approach
Cláudio Nahum Alves, Jerônimo Lameira, Iñaki Tuñón, Sergio Martí, Vicent Moliner
DOI: 10.1039/C3CP43968B
Method/basis set dependence of NICS values among metallic nano-clusters and hydrocarbons
Zahra Badri, Cina Foroutan-Nejad, Parviz Rashidi-Ranjbar
DOI: 10.1039/C2CP23205G
こちらもおすすめ
間溴苯甲酰腈の市場動向や研究トレンドはどうですか?
間 brom 苯甲酰腈は、合成化学や薬物化学において重要な Intermediate として使用されています。市場動向としては、その合成性と機能性により、研究開...
Methyl 2-amino-5-(trifluoromethyl)benzoateに適用される法規ガイドラインは何ですか?
CAS番号117324-58-0の塩酸メチル2アミノ-5-トリフルオロメチルベンゼートは、GHS分類により腐食性物質と判定されます。REACH規則では、製造、販...
3-ブロモ-1,3,4,5-四水化-2H-1-ベンザアゼピン-2-オンは安全ですか?
毒性があるため、適切な安全対策が必須です。皮膚や粘膜への刺激性が強く、吸入や誤飲により健康被害を引き起こす可能性があります。取扱時にはガスマスクや手袋、眼鏡を使...
三氟甲基ピリジン-2-甲アミン塩酸塩は安全ですか?
三氟甲基ピリジン-2-甲アミン塩酸塩は安全性に注意が必要です。毒性は低レベルですが、直接的接触や吸入は避けるべきです。適切な手袋や防塵マスクを着用し、密閉された...
1-エチル-4-(4-硝基フェニル)ピペリジンは安全ですか?
1-エチル-4-(4-硝基フェニル)ピペリジンは有毒であり、取扱には注意が必要です。保管や作業中に手袋を着用し、目や皮膚に接触しないように注意する必要があります...
1,1-ジメトキシプロパン-2-オンは安全ですか?
1,1-ジメトキシプロパン-2-オンは一般的に低毒性ですが、皮膚や目への刺激性があるため、取扱いには注意が必要です。蒸気や液体の吸入には有害な可能性があり、適切...
コバルト(II) 3,3'-{[(1S,2S)-1,2-ジメチルフENCYCLICALE-1,2-エチエンジイル]ビス[ニトロリルメチルイリデン]}ビス[4-オキソ-2-ペンテン-2-olate]について「に適用される法規ガイドラインは何ですか?
この化合物はCAS番号259259-80-8に対応しています。GHS分類では、毒性、燃焼性、反応性、炎症性を考慮に入れ、適切な危険性分類が行われます。REACH...
「カーバミル酸, N-[8-[[2-[[2-(2,6-ジオキソ-3-ピペリジニル)-2,3-ジオキソ-1,3-ジヒドロ-1H-イソイソインドール-4-イルオキシ]アセチル]アミノ]オクチル]-1,1-ジメチレチルエステル」はどのように保存すればよいですか?
この化合物は、冷却庫で-20℃の温度、乾燥した容器に保管し、直日光から保護する必要があります。湿度の高い環境や高温は避けてください。
掲載誌
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.














![(1S,4aR,5R,7S,7aS)-1-(beta-D-Glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl alpha-D-galactopyranoside structure (1S,4aR,5R,7S,7aS)-1-(beta-D-Glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl alpha-D-galactopyranoside structure](https://static.chemtradehub.com/structs/817/81720-07-2-4ffd.webp)