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91.
Red–Green–Blue Trichromophoric Nanoparticles with Dual Fluorescence Resonance Energy Transfer: Highly Sensitive Fluorogenic Response Toward Polyanions 下载免费PDF全文
Jinjia Xu Dr. Atsuro Takai Prof. Dr. Masayuki Takeuchi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(37):13014-13018
A red–green–blue (RGB) trichromophoric fluorescent organic nanoparticle exhibiting multi‐colour emission was constructed; the blue‐emitting cationic oligofluorene nanoparticle acted as an energy‐donor scaffold to undergo fluorescence resonance energy transfer (FRET) to a red‐emitting dye embedded in the nanoparticle (interior FRET) and to a green‐emitting dye adsorbed on the surface through electrostatic interactions (exterior FRET). Each FRET event occurs independently and is free from sequential FRET, thus the resultant dual‐FRET system exhibits multi‐colour emission, including white, in aqueous solution and film state. A characteristic white‐emissive nanoparticle showed visible responses upon perturbation of the exterior FRET efficiency by acceptor displacement, leading to highly sensitive responses toward polyanions in a ratiometric manner. Specifically, our system exhibits high sensitivity toward heparin with an extremely low detection limit. 相似文献
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Zhengxiao Zhang Prof. Eiji Nakata Dr. Huyen Dinh Dr. Masayuki Saimura Prof. Arivazhagan Rajendran Prof. Kazunari Matsuda Prof. Takashi Morii 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(72):18118-18128
Recognition-driven modification has been emerging as a novel approach to modifying biomolecular targets of interest site-specifically and efficiently. To this end, protein modular adaptors (MAs) are the ideal reaction model for recognition-driven modification of DNA as they consist of both a sequence-specific DNA-binding domain (DBD) and a self-ligating protein-tag. Coupling DNA recognition by DBD and the chemoselective reaction of the protein tag could provide a highly efficient sequence-specific reaction. However, combining an MA consisting of a reactive protein-tag and its substrate, for example, SNAP-tag and benzyl guanine (BG), revealed rather nonselective reaction with DNA. Therefore new substrates of SNAP-tag have been designed to realize sequence-selective rapid crosslinking reactions of MAs with SNAP-tag. The reactions of substrates with SNAP-tag were verified by kinetic analyses to enable the sequence-selective crosslinking reaction of MA. The new substrate enables the distinctive orthogonality of SNAP-tag against CLIP-tag to achieve orthogonal DNA-protein crosslinking by six unique MAs. 相似文献
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Kumagai Yuta Kimura Atsushi Taguchi Mitsumasa Watanabe Masayuki 《Journal of Radioanalytical and Nuclear Chemistry》2018,316(1):341-348
Journal of Radioanalytical and Nuclear Chemistry - This study aims to demonstrate that zeolite has the potential to increase the efficiency of radiolysis treatment of aqueous organic pollutants by... 相似文献
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Masayuki Kirihara Takuya Noguchi Nobuhiro Okajima Sayuri Naito Yuki Ishizuka Aiko Harano Hiroyuki Tsukiji Ryu Takizawa 《Tetrahedron》2012,68(5):1515-1520
The reaction of dithioacetals with 30% hydrogen peroxide in the presence of catalytic amounts of tantalum(V) and iodide ion effectively produced carbonyl compounds in high yields. Dithioacetals also can be deprotected using the niobium(V) catalyzed oxidation of iodide ion by hydrogen peroxide under mild conditions. 相似文献
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Inside Back Cover: Carbon Dioxide to Methanol: The Aqueous Catalytic Way at Room Temperature (Chem. Eur. J. 44/2016) 下载免费PDF全文