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101.
102.
103.
Simultaneous Detection of Single Attoliter Droplet Collisions by Electrochemical and Electrogenerated Chemiluminescent Responses 下载免费PDF全文
Jeffrey E. Dick Dr. Christophe Renault Dr. Byung‐Kwon Kim Prof. Dr. Allen J. Bard 《Angewandte Chemie (International ed. in English)》2014,53(44):11859-11862
We provide evidence of single attoliter oil droplet collisions at the surface of an ultra‐microelectrode (UME) by the observation of simultaneous electrochemical current transients (i–t curves) and electrogenerated chemiluminescent (ECL) transients in an oil/water emulsion. An emulsion system based on droplets of toluene and tri‐n‐propylamine (2:1 v/v) emulsified with an ionic liquid and suspended in an aqueous continuous phase was formed by ultrasonification. When an ECL luminophore, such as rubrene, is added to the emulsion droplet, stochastic events can be tracked by observing both the current blips from oxidation at the electrode surface and the ECL blips from the follow‐up ECL reaction, which produces light. This report provides a means of studying fundamental aspects of electrochemistry using the attoliter oil droplet and offers complementary analytical techniques for analyzing discrete collision events, size distribution of emulsion systems, and individual droplet electroactivity. 相似文献
104.
Jihyeon Kim Jongkyoon Park Dr. Seonhwa Park Jeongwook Seo Jeongwook Kwon Hyunsoo Lee Prof. Dr. Seungchul Kim Prof. Dr. Haesik Yang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(43):19364-19370
Distance-dependent electromagnetic radiation and electron transfer have been commonly employed in washing-free fluorescence and electrochemical bioassays, respectively. In this study, we combined the two distance-dependent phenomena for sensitive washing-free DNA detection. A distance-dependent surface plasmonic field induces rapid photoredox catalysis of surface-bound catalytic labels, and distance-dependent mediated electron transfer allows for rapid electron transfer from the surface-bound labels to the electrode. An optimal system consists of a chemically reversible acceptor (Ru(NH3)63+), a chemically reversible photoredox catalyst (eosin Y), and a chemically irreversible donor (triethanolamine). Side reactions with O2 do not significantly decrease the efficiency of photoredox catalysis. Energy transfer quenching between the electrode and the label can be lowered by increasing the distance between them. Washing-free DNA detection had a detection limit of approximately 0.3 nm in buffer and 0.4 nm in serum without a washing step. 相似文献
105.
Hee-Jeong Cha Se-Yeun Hwang Da-Som Lee Dr. Akula Ravi Kumar Prof. Dr. Yong-Uk Kwon Moritz Voß Eva Schuiten Prof. Dr. Uwe T. Bornscheuer Prof. Dr. Frank Hollmann Prof. Dr. Deok-Kun Oh Prof. Dr. Jin-Byung Park 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(18):7090-7094
Long-chain aliphatic amines such as (S,Z)-heptadec-9-en-7-amine and 9-aminoheptadecane were synthesized from ricinoleic acid and oleic acid, respectively, by whole-cell cascade reactions using the combination of an alcohol dehydrogenase (ADH) from Micrococcus luteus, an engineered amine transaminase from Vibrio fluvialis (Vf-ATA), and a photoactivated decarboxylase from Chlorella variabilis NC64A (Cv-FAP) in a one-pot process. In addition, long chain aliphatic esters such as 10-(heptanoyloxy)dec-8-ene and octylnonanoate were prepared from ricinoleic acid and oleic acid, respectively, by using the combination of the ADH, a Baeyer–Villiger monooxygenase variant from Pseudomonas putida KT2440, and the Cv-FAP. The target compounds were produced at rates of up to 37 U g−1 dry cells with conversions up to 90 %. Therefore, this study contributes to the preparation of industrially relevant long-chain aliphatic chiral amines and esters from renewable fatty acid resources. 相似文献
106.
Amit Kumar Nitee Kumari Sateesh Dubbu Sumit Kumar Taewan Kwon Jung Hun Koo Jongwon Lim Inki Kim Yoon‐Kyoung Cho Junsuk Rho In Su Lee 《Angewandte Chemie (International ed. in English)》2020,59(24):9460-9469
Interest and challenges remain in designing and synthesizing catalysts with nature‐like complexity at few‐nm scale to harness unprecedented functionalities by using sustainable solar light. We introduce “nanocatalosomes”—a bio‐inspired bilayer‐vesicular design of nanoreactor with metallic bilayer shell‐in‐shell structure, having numerous controllable confined cavities within few‐nm interlayer space, customizable with different noble metals. The intershell‐confined plasmonically coupled hot‐nanospaces within the few‐nm cavities play a pivotal role in harnessing catalytic effects for various organic transformations, as demonstrated by “acceptorless dehydrogenation”, “Suzuki–Miyaura cross‐coupling” and “alkynyl annulation” affording clean conversions and turnover frequencies (TOFs) at least one order of magnitude higher than state‐of‐the‐art Au‐nanorod‐based plasmonic catalysts. This work paves the way towards next‐generation nanoreactors for chemical transformations with solar energy. 相似文献
107.
Taeyeon Kwon Jin Young Koo Hee Cheul Choi 《Angewandte Chemie (International ed. in English)》2020,59(38):16436-16439
Together with high conductivity, high flexibility is an important property required for next generation organic electronic components. Both properties are difficult to achieve together especially when the components are crystalline because of the intrinsic high brittleness of organic molecular crystals. We report an organic radical crystal system that has both high flexibility and high conductivity. The crystal consists of 9,10‐bis(phenylethynyl)anthracene radical cation ( BPEA.+ ) units, and shows flexibility under pressure with high conductivity in ambient condition exhibiting average conductivity of 2.68 S cm?1 when normal linear shape, as well as 2.43 S cm?1 when bent. The structural analysis reveals that both a short π–π distance (3.290 Å) between BPEA.+ units that are aligned along the crystal length direction, and the presence of PF6? counter ions induce flexibility and high electrical conductivity. 相似文献
108.
The effect of a market factor on information flow between stocks using the minimal spanning tree 总被引:1,自引:0,他引:1
We empirically investigated the effects of market factors on the information flow created from N(N−1)/2 linkage relationships among stocks. We also examined the possibility of employing the minimal spanning tree (MST) method, which is capable of reducing the number of links to N−1. We determined that market factors carry important information value regarding information flow among stocks. Moreover, the information flow among stocks showed time-varying properties according to the changes in market status. In particular, we noted that the information flow increased dramatically during periods of market crises. Finally, we confirmed, via the MST method, that the information flow among stocks could be assessed effectively with the reduced linkage relationships among all links among stocks from the perspective of the overall market. 相似文献
109.
Alexander Efremov Youngkeun Kim Hyun-Woo Lee Kwang-Ho Kwon 《Plasma Chemistry and Plasma Processing》2011,31(2):259-271
The effects of HBr/Ar and HBr/Cl2 mixing ratios in the ranges of 0–100% Ar or Cl2 on plasma parameters, densities of active species influencing the dry etch mechanisms were analyzed at fixed total gas flow
rate of 40 sccm, total gas pressure of 6 mTorr, input power of 700 W and bias power of 300 W. The investigation combined plasma
diagnostics by Langmuir probes and the 0-dimensional plasma modeling. It was found that the dilution of HBr by Ar results
in maximum effect on the ion energy flux with expected impact on the etch rate in the ion-flux-limited etch regime, while
the addition of Cl2 influences mainly the relative fluxes of Br and Cl atoms on the etched surface with expected impact on the etch rate in the
reaction-rate-limited etch regime. 相似文献
110.
Min‐kyoung Ham Ji HoYouk Yong‐Ku Kwon Young‐Je Kwark 《Journal of polymer science. Part A, Polymer chemistry》2012,50(12):2389-2397
A photoinitiation process was investigated to develop a rapid and well‐controlled RAFT polymerization method applied to vinyl acetate (VAc) using methyl (ethoxycarbonothioyl)sulfanyl acetate (MESA) and bis(2,4,6‐trimethylbenzoyl)phenylphosphine oxide as the RAFT agent and photoinitiator, respectively. MESA was selected as the photochemically inert RAFT agent to minimize photolysis of the thiocarbonylthio groups during polymerization. Poly(vinyl acetate) with a prespecified well‐controlled molecular weight (MW) and a narrow MW distribution was successfully synthesized. The polymerization reaction proceeded as a living polymerization and was remarkably rapid compared with approaches that use thermally initiated processes with a very short induction period. A detailed kinetic study of the mechanism underlying the polymerization reaction, however, revealed that the chain ends containing xanthate moieties were not perfectly stable upon UV‐irradiation, and they generated radicals via homolytic cleavage. This reaction appeared to proceed by a combination of a degenerative transfer RAFT mechanism and a dissociation‐combination mechanism. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献