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81.
Touahir L Galopin E Boukherroub R Gouget-Laemmel AC Chazalviel JN Ozanam F Saison O Akjouj A Pennec Y Djafari-Rouhani B Szunerits S 《The Analyst》2011,136(9):1859-1866
The use of an amorphous silicon-carbon alloy overcoating on silver nanostructures in a localized surface plasmon resonance (LSPR) sensing platform allows for decreasing the detection limit by an order of magnitude as compared to sensors based on gold nanostructures deposited on glass. In addition, silver based multilayer structures show a distinct plasmonic behaviour as compared to gold based nanostructures, which provides the sensor with an increased short-range sensitivity and a decreased long-range sensitivity. 相似文献
82.
Izabela Kaminska Wang Qi Alexandre Barras Janusz Sobczak Joanna Niedziolka‐Jonsson Patrice Woisel Joel Lyskawa William Laure Marcin Opallo Musen Li Rabah Boukherroub Sabine Szunerits 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(26):8673-8678
The large‐scale preparation of graphene is of great importance due to its potential applications in various fields. We report herein a simple method for the simultaneous exfoliation and reduction of graphene oxide (GO) to reduced GO (rGO) by using alkynyl‐terminated dopamine as the reducing agent. The reaction was performed under mild conditions to yield rGO functionalized with the dopamine derivative. The chemical reactivity of the alkynyl function was demonstrated by post‐functionalization with two thiolated precursors, namely 6‐(ferrocenyl)hexanethiol and 1H,1H,2H,2H‐perfluorodecanethiol. X‐ray photoelectron spectroscopy, UV/Vis spectrophotometry, Raman spectroscopy, conductivity measurements, and cyclic voltammetry were used to characterize the resulting surfaces. 相似文献
83.
84.
Abd El-Hamid A. A. Ismail Adel M. E. Attia 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):1231-1240
A series of different acyclo quinazoline nucleosides 6 , 7 , 8 , 10 , 12 , 13 , and 14 have been synthesized. The site of glycosylation was confirmed by 1 H-NMR and 13 C-NMR spectroscopy. 相似文献
85.
86.
The synthesis of two melatonin-derived analogs of the novel 6a,7-dihydro-6H,13H-pyrazino[1,2-a;4,5-a′]diindole ring system is described. The non-methoxy and methoxy analogs, 4a and 4b were prepared in seven steps starting from indoline-2-carboxylic acid 5a and 5-methoxyindoline-2-carboxylic acid 5b, respectively. While 4a exhibited micromolar affinities for both melatonin receptors, the methoxy analog 4b displayed moderate affinity for MT2 receptors (Ki=0.41 μM) being 4.4-fold higher than for the MT1 subtype. 相似文献
87.
Fellah S Boukherroub R Ozanam F Chazalviel JN 《Langmuir : the ACS journal of surfaces and colloids》2004,20(15):6359-6364
Covalent grafting of alkyl chains on silicon can be obtained by thermal treatment in Grignard reagents. Alkyl halide present in the Grignard solution as an impurity appears to play a key role in the grafting process. Grafting efficiency is improved when the alkyl halide concentration is increased. It is also enhanced on n-type substrates as compared to p-type substrates and when alkyl bromides are present in solution rather than alkyl chlorides. The grafting reaction involves a zero-current electrochemical step. A reaction model in which simultaneous Grignard oxidation and alkyl halide reduction take place at the silicon surface accounts for all these observations. Alkyl halide reduction is the rate-determining step. Negative charging of the silicon surface lowers the energetic barrier for this reaction, allowing for efficient grafting on n-Si. 相似文献
88.
The reaction of α-benzoinoxime, H2BNO with FeCl3 in the presence of Et3N as a base gives the mononuclear Fe(III) complex, Fe(HBNO)3 (1). Treatment of 1 with a methanolic solution of KOH at room temperature leads to a dinuclear Fe(III)–Fe(III) complex, [Fe(HBNO)2OH]2 (2). The complexes were initially characterized on the basis of their elemental, mass and thermal analyses. The IR studies were useful in assigning the coordination mode of the benzoinoxime ligand to the iron metal. In addition, the presence of a hydroxo-bridge in the dimeric complex 2 is inferred from the IR spectral studies. Room-temperature Mössbauer studies indicated octahedral, high-spin iron(III). Variable-temperature magnetic susceptibility measurements supported the existence of the μ-dihydroxo-bridging structure core, FeIII(μ-OH)2FeIII in the dinuclear complex 2. Theoretical modelling of the magnetic data indicated a weak antiferromagnetic spin exchange between the iron(III) centers (J = −8.35 cm−1, g = 2.01, ρ = 0.02 and TIP = 1.7 × 10−4 cm3 mol−1 for H = −2JS1 · S2). The electronic spectra of the complexes revealed two bands due to d–d transitions and one band assignable to an oxygen (pπ) → Fe(dπ∗) LMCT transition observed in each complex. An additional charge-transfer transition, assignable to μ-hydroxo(pπ) → Fe(dπ∗), was observed for the dimeric complex 2. The structural and vibrational behaviors of these complexes have been elucidated with quantum mechanical methods. 相似文献
89.
90.
Roya Azad Abolfazl Bezaatpour Mandana Amiri Habibollah Eskandari Sima Nouhi Dereje H. Taffa Michael Wark Rabah Boukherroub Sabine Szunerits 《应用有机金属化学》2019,33(9)
A novel heterogeneous composite material based on reduced graphene oxide (rGO) and bismuth vanadate (BiVO4) was prepared and characterized by various techniques such as powder XRD, HRTEM, EADX, UV–Vis‐DRS, FT‐IR, Raman, BET and XPS analyses. The characterization results reveal that the rGO well decorated by BiVO4. The electrochemical impedance spectroscopy (EIS) shows the increasing of charge transfer of rGO/BiVO4 in presence of light irradiation. In this research, the pure BiVO4 and rGO/BiVO4 composite have been explored for photocatalytic reduction of nitroarenes. Among the prepared nanocomposites, rGO loaded with 10% BiVO4 catalyst (noted as rGO/BiVO4–10%) shows the best performance for the photo‐reduction of various nitroaromatic molecules to their corresponding amine compounds under visible‐light irradiation at room temperature. The catalyst exhibited in particular excellent photocatalytic activity for the conversion of 1,4‐dinitrobenzene to 4‐nitroanilline (100% conversion) in 20 min, 4‐chloronitrobenzene to 4‐chloroaniline and 2‐nitrophenol to 2‐aminophenol (100% conversion) in only 30 min. In addition, the conversion of 4‐bromonitrobenzene, 4‐iodonitrobenzene to their corresponding amine compounds (100% conversion) was achieved in 60 min. The catalyst was recovered for several times and reused without decreasing of its efficiency. 相似文献