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101.
Corrigendum: An NMR‐Driven Crystallography Strategy to Overcome the Computability Limit of Powder Structure Determination: A Layered Aluminophosphate Case 下载免费PDF全文
102.
Alkoxyallene‐ynes: Selective Preparation of Bicyclo[5.3.0] Ring Systems Including a δ‐Alkoxy Cyclopentadienone 下载免费PDF全文
Dr. Aurélien Tap Camille Lecourt Sabrina Dhambri Mathieu Arnould Dr. Gilles Galvani Dr. Olivier Nguyen Van Buu Dr. Morgan Jouanneau Dr. Jean‐Pierre Férézou Prof. Janick Ardisson Dr. Marie‐Isabelle Lannou Dr. Geoffroy Sorin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(14):4938-4944
The development of an intramolecular rhodium(I)‐catalyzed Pauson–Khand reaction of alkoxyallene‐ynes with a proximal alkoxy group is reported. This reaction, in the presence of a [Rh(cycloocta‐1,5‐diene)Cl]2/propane‐1,3‐diylbis(diphenylphosphane) system under a CO atmosphere, constitutes a powerful tool for selectively accessing carbo‐ and heterobicyclo[5.3.0] frameworks featuring an enol ether moiety. Through this procedure, a straightforward access to guaiane skeletons with a tertiary hydroxy group at the C10 position was achieved. 相似文献
103.
104.
We obtain the convergence in law of a sequence of excited (also called cookies) random walks toward an excited Brownian motion. This last process is a continuous semi-martingale whose drift is a function, say ??, of its local time. It was introduced by Norris, Rogers and Williams as a simplified version of Brownian polymers, and then recently further studied by the authors. To get our results we need to renormalize together the sequence of cookies, the time and the space in a convenient way. The proof follows a general approach already taken by Tóth and his coauthors in multiple occasions, which goes through Ray-Knight type results. Namely we first prove, when ?? is bounded and Lipschitz, that the convergence holds at the level of the local time processes. This is done via a careful study of the transition kernel of an auxiliary Markov chain which describes the local time at a given level. Then we prove a tightness result and deduce the convergence at the level of the full processes. 相似文献
105.
106.
Guillem Aromí Leoní A. Barrios Olivier Roubeau Patrick Gamez 《Coordination chemistry reviews》2011,255(5-6):485-546
The current great interest in preparing functional metal-organic materials is inevitably associated with tremendous research efforts dedicated to the design and synthesis of new families of sophisticated multi-nucleating ligands. In this context, the N-donor triazole and tetrazole rings represent two categories of ligands that are increasingly used, most likely as the result of the recent dramatic development of “click chemistry” and Zeolitic Imidazolate Frameworks (ZIFs). Thus, azole-based complexes have found numerous applications in coordination chemistry.In the present review, we focus on the utilization of 1,2,3-triazole, 1,2,4-triazole and tetrazole ligands to create coordination polymers, metal complexes and spin-crossover compounds, reported to the end of 2009. In the first instance, we present a compendium of all the relevant ligands that have been employed to generate coordination polymers and Metal-Organic Frameworks (MOFs). Due to the huge amount of reported MOFs and coordination polymers bearing these azole rings, three representative examples for each category (therefore nine in total) are described in detail. The second section is devoted to the use of the bridging abilities of these azole ligands to prepare metal complexes (containing at least two metal centers). Given the large number and the great structural diversity of the polynuclear compounds found in the literature, these have been grouped according to their nuclearity. Finally, in the last section, the triazole- and tetrazole-containing coordination compounds exhibiting spin-crossover properties are presented. 相似文献
107.
Eugene Olivier Trevor M. Letcher Paramespri Naidoo Deresh Ramjugernath 《The Journal of chemical thermodynamics》2011,43(6):829-833
Activity coefficients at infinite dilution were determined for 27 solutes: n-alkanes, alk-1-enes, alk-1-ynes, cycloalkanes, alkylbenzenes, alcohols, and ketones in the ionic liquid 1-butyl-3-methylimidazolium hexafluoroantimonate, [BMIM][SbF6], by gas–liquid chromatography at three different temperatures, T = (313.15, 323.15, and 333.15) K. The results are compared to published data on related compounds. The partial molar excess enthalpy values at infinite dilution were calculated from the experimental data over the same temperature range. Selectivities and capacities at infinite dilution were calculated for the hexane/benzene and methanol/benzene systems from experimental infinite dilution activity coefficients and compared to the literature values for related ionic liquids, as well as to data on industrial molecular solvents. 相似文献
108.
Dr. Iwona Olejniczak Dr. Andrzej Łapiński Prof. Roman Świetlik Dr. Jean Olivier Dr. Stéphane Golhen Dr. Lahcène Ouahab 《Chemphyschem》2011,12(11):2124-2130
The room‐temperature infrared and Raman spectra of a series of four isostructural polymeric salts of 2,3,6,7‐tetrakis(2‐cyanoethylthio)‐tetrathiafulvalene (TCE‐TTF) with paramagnetic (CoII, MnII) and diamagnetic (ZnII, CdII) ions, together with BF4? or ClO4? anions are reported. Infrared and Raman‐active modes are identified and assigned based on theoretical calculations for neutral and ionized TCE‐TTF using density functional theory (DFT) methods. It is confirmed that the TCE‐TTF molecules in all the materials investigated are fully ionized and interact in the crystal structure through cyanoethylthio groups. The vibrational modes related to the C?C stretching vibrations of TCE‐TTF are analyzed assuming the occurrence of electron–molecular vibration coupling (EMV). The presence of the antisymmetric C?C dimeric mode provides evidence that charge transfer takes place between TCE‐TTF molecules belonging to neighboring polymeric networks. 相似文献
109.
Abdelmounaim Safer Mustapha Rahmouni François Carreaux Ludovic Paquin Olivier Lozach Laurent Meijer Jean Pierre Bazureau 《Chemical Papers》2011,65(3):332-337
A series of nine 5-arylidenerhodanine derivatives was prepared in good yields and purity without the use of a solvent or catalyst
under microwave-assisted condensation with some substituted isatins. All 5-arylidenerhodanines were evaluated as possible
inhibitors of the CK1α/β, CDK5/p25, and GSK-3α/β kinases. None of them showed substantive inhibitory activity against these kinases when evaluated at the concentration of
10 μM. 相似文献
110.
Charif Tamin Denis Chaumont Olivier Heintz Mohamed Adnane 《Surface and interface analysis : SIA》2020,52(12):985-990
This paper aims to estimate the band alignment to CdS/CZTS hetero-interface by direct X-ray photoelectron spectroscopy (XPS) measurements. XPS was used to determinate the valence-band offset (VBO) directly by determining the valence band positions at the hetero-interface. The conduction band offset (CBO) value was estimated based on the band gap measurements by UV/Visible spectroscopy and VBO measurements. The position of valence band (VB) changes close to the CdS-CZTS interface and the CBO is cliff-like. The band alignment diagram indicates that the CdS-CZTS interface heterojunction is type II. 相似文献