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Thais R. Cruz Eliada A. Silva Douglas P. Oliveira Daniele M. Martins Patrik D.S. Gois Antonio E.H. Machado Pedro Ivo S. Maia Beatriz E. Goi Benedito S. Lima-Neto Valdemiro P. Carvalho-Jr 《应用有机金属化学》2020,34(5):e5602
Arene ruthenium(II) complexes bearing the cyclic amines RuCl2(η6-p-cymene)(pyrrolidine)] ( 1 ), [RuCl2(η6-p-cymene)(piperidine)] ( 2 ), and [RuCl2(η6-p-cymene)(peridroazepine)] ( 3 ) were successfully synthesized. Complexes 1 – 3 were fully characterized by means of Fourier transform infrared, UV–visible, and NMR spectroscopy, elemental analysis, cyclic voltammetry, computational methods, and one of the complexes was further studied by single crystal X-ray crystallography. These compounds were evaluated as catalytic precursors for ring-opening metathesis polymerization (ROMP) of norbornene (NBE) and atom-transfer radical polymerization (ATRP) of methyl methacrylate (MMA). NBE polymerization via ROMP was evaluated using complexes 1 – 3 as precatalysts in the presence of ethyl diazoacetate (EDA) under different [NBE]/[EDA]/[Ru] ratios, temperatures (25 and 50°C), and reaction times (5–60 min). The highest yields of polyNBE were obtained with [NBE]/[EDA]/[Ru] = 5000/28/1 for 60 min at 50°C. MMA polymerization via ATRP was conducted using 1 – 3 as catalysts in the presence of ethyl-α-bromoisobutyrate (EBiB) as initiator. The catalytic tests were evaluated as a function of the reaction time using the initial molar ratio of [MMA]/[EBiB]/[Ru] = 1000/2/1 at 95°C. The increase in molecular weight as function of time indicates that complexes 1–3 were able to mediate the MMA polymerization with an acceptable rate and some level of control. Differences in the rate of polymerization were observed in the order 3 > 2 > 1 for the ROMP and ATRP. 相似文献
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Luisa C. Melo Murilo S. S. Julião Maria A. L. Milhome Ronaldo F. do Nascimento Djenaine De Souza Pedro de Lima-Neto Adriana N. Correia 《Journal of Analytical Chemistry》2018,73(7):695-704
This work describes the electroanalytical determination of Chlorpyriphos pesticide in natural waters using hanging mercury drop electrode allied to square wave adsorptive cathodic stripping voltammetry. The best responses were obtained in Britton?Robinson buffer solutions at pH 2.0, using a frequency of 100 s–1, a scan increment of 5 mV, a square wave amplitude of 25 mV and an accumulation potential of–0.4 V during 60 s. Therefore, voltammetric responses showed the presence of one well-defined and irreversible reduction peak, at–1.08 V vs. Ag/AgCl/KCl 1.0 M, which involves two electrons in the reduction of carbon?nitrogen bond in the N-heterocyclic system with the participation of protonation equilibrium preceding the electron transfer reaction. Analytical curves were constructed and compared to similar curves performed by gas chromatograph coupled to a selective nitrogen?phosphorus detector, which demonstrates that the proposed methodology is suitable for determining contamination by Chlorpyriphos in complex samples. 相似文献
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J?RG?FELDVOSSEmail author SALVATORE?SICILIANO THOMAS?WEIGEL 《Transformation Groups》2016,21(2):377-398
In this paper it is shown that the projective cover of the trivial irreducible module of a finite-dimensional solvable restricted Lie algebra is induced from the one dimensional trivial module of a maximal torus. As a consequence, the number of the isomorphism classes of irreducible modules with a fixed p-character for a finite-dimensional solvable restricted Lie algebra L is bounded above by p MT(L), where MT(L) denotes the maximal dimension of a torus in L. Finally, it is proved that in characteristic p > 3 the projective cover of the trivial irreducible L-module is induced from the one-dimensional trivial module of a torus of maximal dimension, only if L is solvable. 相似文献
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CO activation in the [Ru(NH3)5CO]2+ ion has been demonstrated under nucleophilic conditions in pyridine or 2-ethoxyethanol solution at 100 °C. In the presence
of Me3NO the observed pseudo-first order rate constants were found to be sensitive only to auxiliary ligand concentration (pyridine
or methyl pyridines), but with a tendency towards rate saturation and the same limiting rate at large excess of each entering
ligand. A mechanism is proposed in which the rate-limiting step is viewed as an auxiliary ligand-assisted CO2 elimination, preceded by a fast reversible addition of Me3NO. This reaction pathway is also supported by the values determined for ΔH
‡ (81 ± 13 kJ mol−1) and ΔS
‡ (−114 ± 36 J mol−1 K−1).
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
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ER Badman GE Patterson JM Wells RE Santini RG Cooks 《Journal of mass spectrometry : JMS》1999,34(8):889-894
Dual-detector differential non-destructive Fourier transform detection in a quadrupole ion trap is shown to improve signal intensity and reduce noise compared with spectra recorded using a single detector. A larger area detector in each end-cap electrode is machined to fit its hyperbolic shape and so minimize field imperfections on the z-axis. Argon, acetophenone and bromobenzene spectra were recorded to allow a comparison between single- and dual-detector (differential) modes of detection and to demonstrate the improvement achieved with differential detection. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
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Darshan C Kundaliya Reeta Vij AA Tulapurkar U Vaidya R Pinto RG Kulkarni 《Pramana》2002,58(5-6):1041-1044
Electrical resistance (R) measurements of a bulk La0.33Nd0.33Ca0.33MnO3 perovskite in magnetic fields up to 40 kOe have revealed anomalous temperature hysteretic effects both in 0 Oe and 20 kOe
magnetic fields. The sharp peak observed in the R vs. T plot indicates the occurrence of metal-to-insulator (M-I) transition at a temperature of T
MI=110 K and 140 K, for cooling and warming paths, respectively. An applied magnetic field of 20 kOe reduces the resistance
and shifts T
MI to 160 K and 185 K for cooling and warming, respectively. We have observed a much higher resistance in the cooling path than
in the warming path leading to the hysteretic resistance ratio (R
cool/R
warm) of 200 at 110 K and 1.8 at 160 K for 0 Oe and 20 kOe, respectively. Record values of colossal magnetoresistance (CMR) have
been achieved. The CMR value reaches nearly 99% in the temperature ranges of 90 K to 140 K and 90 K to 170 K for 20 kOe and
40 kOe magnetic fields in the cooling mode, respectively. The observed unusual behavior is attributed to the co-existence
of La-rich and Nd-rich domains assumed to be distributed randomly in the compound. 相似文献