Redox cycling of iron by carbon dot enhanced chemiluminescence: mechanism of electron–hole induction in carbon dot
文献情報
Syed Niaz Ali Shah, Ling Lin, Yongzan Zheng, Dingkun Zhang, Jin-Ming Lin
The chemiluminescence (CL) of the Fenton system with nitrogen doped carbon dots (N-CDs) was significantly enhanced. The introduction of N-CDs improved the utilization of H2O2 and drastically enhanced the generation of ˙OH, which resulted in enhanced CL emission of the Fenton system through energy and electron transfer processes. The oxidation of N-CDs by ˙OH led to rapid incorporation of oxygen into N-CDs. The mechanism relied on the production of •OH radicals through the Fenton reaction and clearly indicated the important role of peroxide-induced redox cycling of Fe2+ ⇔ Fe3+ in the presence of N-CDs. The CL intensity of the system containing Fe2+ was higher than that containing Fe3+ because the rate of the Fe3+ reaction was much slower than that of the Fe2+ reaction. The CL signal remained constant after some time due to redox cycling, which established equilibrium, irrespective of the form of iron. This study provides a feasible approach to greatly enhance the weak CL of the Fenton system with the introduction of environmentally friendly N-CDs, and initiates an inspiring research in the domain of catalysis, CL and the mechanism of the Fenton system, which will be helpful in various applied research areas.
関連文献
Thiophene-benzothiadiazole based D–A1–D–A2 type alternating copolymers for polymer solar cells
Quoc Viet Hoang, Mohammad Afsar Uddin, Han Young Woo
DOI: 10.1039/C7PY00696A
A facile strategy for manipulating micellar size and morphology through intramolecular cross-linking of amphiphilic block copolymers
Ryoto Tanaka, Kodai Watanabe, Takuya Yamamoto, Kenji Tajima, Takuya Isono, Toshifumi Satoh
DOI: 10.1039/C7PY00646B
Green chain-shattering polymers based on a self-immolative azobenzene motif
DOI: 10.1039/C5PY01937K
Multifunctional porous Tröger's base polymers with tetraphenylethene units: CO2 adsorption, luminescence and sensing properties
Yuanzheng Cui, Yuchuan Liu, Jiancong Liu, Jianfeng Du, Yue Yu, Shun Wang, Zhiqiang Liang, Jihong Yu
DOI: 10.1039/C7PY00856B
Enhanced stability of conductive polyacetylene in ladder-like surface-grafted brushes
Michał Szuwarzyński, Karol Wolski, Szczepan Zapotoczny
DOI: 10.1039/C6PY00977H
Development of a polymer theranostic for prostate cancer
Barbara E. Rolfe, Pamela J. Russell, Brian W.-C. Tse
DOI: 10.1039/C4PY00999A
Self-assembled micelles prepared from amphiphilic copolymers bearing cell outer membrane phosphorylcholine zwitterions for a potential anti-phagocytic clearance carrier
Yuping Zhao, Guiqiang He, Weihong Guo, Lili Bao, Meijun Yi, Yongkuan Gong, Shiping Zhang
DOI: 10.1039/C6PY00845C
Correction: Transition from smectic nanofibers to smectic vesicles in the self-assemblies of PEG-b-liquid crystal polycarbonates
Lu Zhou, Dapeng Zhang, Sabrina Hocine, Alessia Pilone, Sylvain Trépout, Sergio Marco, Christophe M. Thomas, Jia Guo
DOI: 10.1039/C7PY90126G
Long-subchain Janus-dendritic copolymers from locally confined click reaction and generation-dependent micro-phase separation
Peng-Yun Li, Jia-Min Li, Lian-Wei Li, Xiao-Dong Ye, Wei-Dong He
DOI: 10.1039/C7PY00551B
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.










![(2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure (2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure](https://static.chemtradehub.com/structs/250/2505001-54-5-c1e9.webp)



