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231.
Jean Escudie Claude Couret Henri Ranaivonjatovo Mohamed Lazraq Jacques Satge 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2):27-31
Abstract Two new diphosphenes 7 and 10 have been synthesized by action of DBU on trichlorogermylphosphines 4 and 8; this route involves the intermediate formation of chlorophosphines 5 and 9. Diphosphenes 7 and 10 are stabilized by the 2,6-bis(trifuoromethyl)phenyl group which presents both steric and electronic effects and is used for the first time in phosphorus chemistry. 相似文献
232.
Antonin Desmecht Dr. Debobrata Sheet Claude Poleunis Prof. Sophie Hermans Prof. Olivier Riant 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(6):1436-1440
The chemical functionalization of carbon nanotubes is often a prerequisite prior to their use in various applications. The covalent grafting of 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (BPin) functional groups directly on the surface of multi- and single-walled carbon nanotubes, activated by nucleophilic addition of nBuLi, was carried out. Thermogravimetric analysis (TGA) coupled with mass spectrometry, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ions mass spectrometry (ToF-SIMS) confirmed the efficiency of this methodology and proved the integrity and covalent grafting of the BPin functional groups. These groups were further reacted with various nucleophiles in the presence of a copper(II) source in the conditions of the aerobic Chan–Lam–Evans coupling. The resulting materials were characterized by TGA, XPS and ToF-SIMS. This route is efficient, reliable and among the scarce reactions that enable the direct grafting of heteroatoms at carbonaceous material surfaces. 相似文献
233.
Maxwell D. Cummings Tse‐I Lin Lili Hu Abdellah Tahri David McGowan Katie Amssoms Stefaan Last Benoit Devogelaere Marie‐Claude Rouan Leen Vijgen Jan Martin Berke Pascale Dehertogh Els Fransen Erna Cleiren Liesbet vanderHelm Gregory Fanning Kristof VanEmelen Origne Nyanguile Kenny Simmen Pierre Raboisson Sandrine Vendeville 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2012,124(19):4715-4718
234.
235.
Maud Jenart Claude Niebel Jean-Yves Balandier Julie Leroy Alix Mignolet Sara Stas Antoine Van Vooren Jérôme Cornil Yves Henri Geerts 《Tetrahedron》2012,68(1):349-355
Two quaterthiophene-based dimers including an ethylene bridge have been designed and efficiently prepared; experimental and computational studies show a promising potential as semiconducting material with a charge transport of higher dimensionality compared to quaterthiophene. 相似文献
236.
James Courmarcel Gildas Le Gland Loic Toupet Fr d ric Paul Claude Lapinte 《Journal of organometallic chemistry》2003,670(1-2):108-122
The synthesis of the new (η2-dppe)(η5-C5Me5)Fe---CC---1,3-(C6H4X) (m-2a/2b; X=F/Br) and (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4I) (2c) complexes, as well as the solid-state structure of the known (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4F) (2a) complex are described. The catalytic coupling reactions of the bromo complexes with various alkynes were next investigated. Starting from the known (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4Br) complex (2b), the synthesis of the (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)---CC---H complex (6d) and of the corresponding silyl-protected precursors (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)CC---SiR3 (6b/6c; R=iPr/Me) are reported. By use of lithium---bromine exchange reactions on 2b, the silyl- (7a; E=Si; R=Me) and tin- (7b–7d; E=Sn; R=Me, Bu, Ph) substituted analogues (η2-dppe)(η5-C5Me5)Fe---CC---1,4-(C6H4)ER3 are also isolated. The spectroscopic and electrochemical characterisations of all these new Fe(II)/Fe(III) redox-active building blocks are presented and the electronic substituent parameters for the “(η2-dppe)(η5-C5Me5)Fe---CC” group are determined by means of 19F-NMR. 相似文献
237.
Asthma is a heterogeneous disorder and one of the most common chronic childhood diseases. An improved characterization of asthma phenotypes would be invaluable for the understanding of the pathogenic mechanisms and the correct treatment of this disease. The aim of this pilot study was to explore the potential of metabolomics applied to urine samples in characterizing asthma, and to identify the most representative metabolites. Urine samples of 41 atopic asthmatic children (further subdivided in sub-groups according to the symptoms) and 12 age-matched controls were analyzed. Untargeted metabolic profiles were collected by LC-MS, and studied by multivariate analysis. The group of the asthmatics was differentiated by a model that proved to be uncorrelated with the chronic assumption of controller drugs on the part of the patients. The distinct sub-groups were also appropriately modeled. Further investigations revealed a reduced excretion of urocanic acid, methyl-imidazoleacetic acid and a metabolite resembling the structure of an Ile-Pro fragment in the asthmatics. The meaning of these findings was discussed and mainly correlated with the modulation of immunity in asthma. Metabolic profiles from urines have revealed the potential to characterize asthma and enabled the identification of metabolites that may have a role in the underlying inflammation. 相似文献
238.
Dr. Delphine Crozet Dr. Aitor Gual Dr. David McKay Dr. Chiara Dinoi Dr. Cyril Godard Prof. Martine Urrutigoïty Dr. Jean‐Claude Daran Prof. Laurent Maron Prof. Carmen Claver Prof. Philippe Kalck 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(23):7128-7140
The reactivity of [Rh(CO)2{(R,R)‐Ph? BPE}]BF4 ( 2 ) toward amine, CO and/or H2 was examined by high‐pressure NMR and IR spectroscopy. The two cationic pentacoordinated species [Rh(CO)3{(R,R)‐Ph? BPE}]BF4 ( 4 ) and [Rh(CO)2(NHC5H10){(R,R)‐Ph‐BPE}]BF4 ( 8 ) were identified. The transformation of 2 into the neutral complex [RhH(CO)2{(R,R)‐Ph? BPE}] ( 3 ) under hydroaminomethylation conditions (CO/H2, amine) was investigated. The full mechanisms related to the formation of 3 , 4 and 8 starting from 2 are supported by DFT calculations. In particular, the pathway from 2 to 3 revealed the deprotonation by the amine of the dihydride species [Rh(H)2(CO)2{(R,R)‐Ph? BPE}]BF4 ( 6 ), resulting from the oxidative addition of H2 on 2 . 相似文献
239.
Claude St. Thomas Hortensia Maldonado‐Textle Antal Rockenbauer Laszlo Korecz Nora Nagy Ramiro Guerrero‐Santos 《Journal of polymer science. Part A, Polymer chemistry》2012,50(14):2944-2956
Two different initiator/transfer agents (inifers) containing an alkoxyamine and a dithiobenzoate were synthetized and used to trigger out either reversible addition‐fragmentation chain transfer (RAFT) polymerization or nitroxide‐mediated polymerization (NMP). α‐Dithiobenzoate‐ω‐alkoxyamine‐difunctional polymers were produced in both cases which were subsequently used as precursors in the formation of block copolymers. This synthetic approach was applied to N‐isopropylacrylamide (NIPAM) or polyethylene oxide methacrylate (EOMA) to form α,ω‐heterodifunctional homopolymers via RAFT at 60°C which were chain extended with styrene by activating the alkoxyamine moiety at 120°C. Under such temperature conditions, it is proposed that a tandem NMP/RAFT polymerization is initiated producing a simultaneous growth of polystyrene blocks at both chain‐ends. Self‐assembled nanostructures of these amphiphilic block copolymers were evidenced by scanning electron microscopy. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
240.
The voltammogram of aryldiazonium tetrafluoroborates in acetonitrile (ACN), at low concentration, shows a first one-electron wave followed at a more negative potential by a small second wave; this last one corresponds to the reduction of the radical formed at the level of the first wave. Simulation of the voltammogram permits one to determine the standard redox potential of the radical/anion couple Eo(Ph./Ph-) = 0.05 V/SCE and the reduction mechanism of the diazonium cation. An electron transfer concerted with the cleavage of the C-N bond furnishes the aryl radical; this radical undergoes two competitive reactions: reduction at the electrode and H-atom transfer. 相似文献