The reaction of 5-arylidene-4-arylimino-2-thiazolidinones 4 with GRIGNARD reagents effected 1,4-addition to the exocyclic CC bond with the formation of 5 . Alkylation of the arylidene derivatives 4 with diazomethane or methyl iodide results in the formation of the N-methyl derivatives 6 . Treatment of 6 with phenylmagnesium bromide effects addition of the reagent to the double bond of the lateral chain to yield products, proved to have structure 8 . The 5-arylazo derivatives 9 of 4-arylimino-2-thiazolidinones were obtained by coupling 4 with aromatic diazonium chlorides. Compounds 9 were N-methylated with diazomethane to yield 10 . 相似文献
4-Arylidene-2-phenyl-1-substituted-2-imidazolin-5-ones 1a – d react with organomagnesium compounds, in ether at room temperature, to yield, as the main isolable products, the 4-disubstituted-methyl derivatives 2a – h . On the other hand, 1a – d react with phenylmagnesium bromide in a boiling ether-benzene mixture to give, among the reaction products, 2a – d and the 4-diarylmethylene derivatives 3a – d . Spectral data of 2 and 3 are discussed. Treatment of the GRIGNARD products 2a – c with formaldehyde and piperidine or morpholine effects aminomethylation at C-4 with the formation of the MANNICH bases 6a – f . 相似文献
We present a novel Partial Virtual channel Sharing (PVS) NoC architecture which reduces the impact of faults on performance and also tolerates faults within the routing logic. Without PVS, failure of a component impairs the fault-free connected components, which leads to considerable performance degradation. Improving resource utilization is key in enhancing or sustaining performance with minimal overhead when faults or overload occurs. In the proposed architecture, autonomic virtual-channel buffer sharing is implemented with a novel algorithm that determines the sharing of buffers among a set of ports. The runtime allocation of the buffers depends on incoming load and fault occurrence. In addition, we propose an efficient technique for maintaining the accessibility of a processing element (PE) to the network even if its router is faulty. Our techniques can be used in any NoC topology and for both, 2D and 3D NoCs. The synthesis results for an integrated video conference application demonstrate 22 % reduction in average packet latency compared to state-of-the-art virtual channel (VC) based NoC architecture. Extensive quantitative simulation has been carried out with synthetic benchmarks. Simulation results reveal that the PVS architecture improves the performance significantly in presence of faults, compared to other VC-based NoC architectures. 相似文献
Abstract Production of fish fingers was achieved by using fish species such as sardine (Sardina pilchardus, Walbaum, 1792), whiting (Merlangius merlangus, Linnaeus, 1758) and pike perch (Sander lucioperca, Linnaeus, 1758). Quality changes of battered fish patties during a period of 8 months at –18 °C were investigated. According to the results of microbiological and chemical analysis, fish fingers were found to be within acceptable limits during frozen storage for 8 months. However, sensory analysis showed that, at the end of the frozen storage, fish fingers made from sardine could not be consumed because of rancidity. 相似文献
The structure and surface morphology of Ni-incorporated diamond like carbon (Ni:DLC) films have been investigated. These films were deposited on Si substrates using pulsed laser deposition (PLD) technique. A KrF Excimer laser (λ = 248 nm) was used for co-ablation from multi component Ni–graphite target. The concentration of Ni was varied by ablating the Ni part of the target with various numbers of laser pulses. The SEM and AFM analysis reveals that the surface is composed of segregates of Ni which increases with the increase in Ni content during the growth process. The structural investigations by XRD and Raman spectroscopy provided information about the orientation of the incorporated constituent and the ordering of the carbon species. Maximum height of the nano structures which were observed on the surface was ∼50 nm. The G-peak of the graphite was shifted towards higher wave number due to enhancement in SP2 sites which have been increased due to the increase in the Ni concentration. A small change in the surface roughness ranging from 7.78 nm to 13.1 nm due to increased Ni concentration was also observed. 相似文献
Internet of Things (IoT) is changing the way many sectors operate and special attention is paid to promoting healthy living by employing IoT based technologies. In this paper, a novel approach is developed with IoT prototype of Wireless Sensor Network and Cloud based system to provide continuous monitoring of a patient’s health status, ensuring timely scheduled and unscheduled medicinal dosage based on real-time patient vitals measurement, life-saving emergency prediction and communication. The designed integrated prototype consists of a wearable expandable health monitoring system, Smart Medicine Dispensing System, Cloud-based Big Data analytical diagnostic and Artificial Intelligence (AI) based reporting tool. A working prototype was developed and tested on few persons to ensure that it is working according to expected standards. Based on the initial experiments, the system fulfilled intended objectives including continuous health monitoring, scheduled timely medication, unscheduled emergency medication, life-saving emergency reporting, life-saving emergency prediction and early stage diagnosis. In addition, based on the analysis reports, physicians can diagnose/decide, view medication side effects, medication errors and prescribe medication accordingly. The proposed system exhibited the ability to achieve objectives it was designed using IoT to alleviate the pressure on hospitals due to crowdedness in hospital care and to reduce the healthcare service delays.
Propylsulfonic acid-functionalized partially crystalline silicalite-1 materials were synthesized via one step co-condensation technique by varying the molar ratio of organosilane source, 3-mercaptopropyltrimethoxysilane (3MP) to tetraethylorthosilicate (TEOS) in the range of 0.05–0.30, and subsequent oxidation of thiol group to propylsulfonic acid using hydrogen peroxide (H2O2). These materials were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM) and nitrogen adsorption–desorption method. The structure of these materials was determined by Fourier transform infrared spectroscopy (FT-IR) and 29Si and 13C solid state NMR. XRD results show that % crystallinity of the materials decreased with the increase in 3MP concentration in the synthesis mixture. Selected area electron diffraction (SAED) showed the presence of crystalline and amorphous phases in the samples. An amorphous phase was formed when 3MP concentration was 30 mol% of the total silica source. After elimination of the structure directing agent (SDA) by calcination at 420 °C, thermogravimetric analysis (TGA) shows that the structure was thermally stable up to 550 °C. Ammonia temperature-programmed desorption (NH3-TPD) shows that the acid capacity of these materials was in the range of 1.19–1.83 mmol H+/g, which shows that these materials could be used as potential heterogeneous acid catalyst. 相似文献
In this article, time–frequency representation of Wigner–Ville is used to analyse the acoustic signal backscattered by a thin elastic tube of radii ratio b/a. This analysis allows to determine the reduced cutoff frequency of the circumferential antisymmetric wave A1 propagating around the tube. The evolution of this reduced cutoff frequency in function of b/a is reported. The values obtained of reduced cutoff frequency are compared to the values computed from the proper modes method. 相似文献
ABSTRACT A model study on the hydrodesulphurization of dimethyl sulphide, di n-prophyl sulphide, di n-butyl sulphide and dimethyl disulphide on Co-Mo-A12O3 surface was conducted using stopped-flow chromatographic technique. The plots for the rates of hydrocarbon formation agreed well with the first order reaction at the surface of the catalyst. Activation energies for the hydrodesulphurization of (C2H5)2S, (C3H7)2S, n-(C4H9)2S and (CH3)2S2 are 57.55, 70.67, 72.74 and 37.80 Kj mole?1 respectively. 相似文献