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91.
92.
H. R. Acevedo-Parra M. R. Torres-Vitela M. M. Castillo-Ortega F. Bautista J. E. Puig S. M. Nuño-Donlucas 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(10):876-884
The synthesis by emulsion polymerization and the characterization by a battery of techniques of poly(butyl acrylate-co-silver acrylate) [poly(BuAc-co-AgAc)] ionomers are reported here. Reaction rates were fast and conversions around 90% were obtained in less than one hour, regardless of the initial ratio of butyl acrylate and silver acrylate employed (BuAc/AgAc = 90/10, 80/20, 70/30). Particle size was in the range of 176 to 200 nm, depending on the BuAc/AgAc ratio. Ionomers’ formation was corroborated by infrared spectroscopy and inferred by differential scanning calorimetry (DSC). DSC disclosed that the poly(BuAc-co-AgAc) has two glass transition temperatures: one at ca. ?49°C due to relaxation of the ionomer backbone domains rich in BuAc and another ca. 35°C due to the relaxation of the backbone domains where the AgAc-units content was higher. Young moduli increased as the copolymers became richer in AgAc. Antibacterial tests against Escherichia coli with the 90/10 (BuAc/AgAc) ionomer revealed that the bacteria population diminishes from 5 log CFU/mL to less than 0.3 MPN/mL after one hour of contact with the ionomers. Also, we demonstrated that the ionomers are excellent compatibilizers for making semiconductive films of n-dodecylbenzene sulfonic acid-doped polyaniline (PANIDBSA)-poly(BuAc-co-AgAc) and poly(n-butyl methacrylate) (PBMA) blends. The electrical conductivity of the blend films, which were homogeneous, rose as the AgAc content in the films increased. 相似文献
93.
《化学:亚洲杂志》2017,12(6):643-647
A fully conjugated system 4 consisting of two 2‐aza‐21‐carbaporphyrin (NCP) subunits bridged by dipyrrin was synthesized by a highly selective condensation of 3‐pyrrole‐NCP 2 with aryl aldehydes. The free base 4 as well as its silver(III) complex 5 exhibited flexibility of the bridge allowing synergetic binding of AgI, thus leading to a mixed‐valence tetraporphyrinic assembly consisting of eight silver atoms which was characterized both in the solid state and in solution. Binding of chiral acid by 4 and 5 was shown by observation of an induced optical activity of the adducts. 相似文献
94.
Abstract An overview of results on microscopic properties, implantation features and dynamics of Fe ions implanted into Si, Ge and ZnS as investigated with in beam Mößbauer spectroscopy(IBMS) is given. Potential and limitations of the method are discussed. 相似文献
95.
Mieczysław Maciejewski 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(1):77-85
The feasibility of chemical bond formation, especially in the chain-transfer reaction between polymer and β-cyclodextrin (β-CD) molecules in the products of the radiation polymerization of β-CD with vinylidene chloride (VDC) its adducts has been considered. The lack of these bonds in the polymerization products of similar β-CD adducts with methyl methacrylate (MM), styrene (St), a mixture of VDC and allyl chloride (AC) and a mixture of VDC and MM (10:90 molar ratio) has been established. On the basis of the results obtained the lack of chemical bonds in the polymerization product of β-CD· VDC adduct is suggested. 相似文献
96.
97.
98.
Dr. Yong Wu Dr. Shanshan Cao Dr. Iskander Douair Prof. Laurent Maron Prof. Xihe Bi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(19):5999-6006
The [2+1] cycloaddition reaction of a metal carbene with an alkene can produce important cyclopropane products for synthetic intermediates, materials, and pharmaceutical applications. However, this reaction is often accompanied by side reactions, such as coupling and self-coupling, so that the yield of the cyclopropanation product of non-silver transition-metal carbenes and hindered alkenes is generally lower than 50 %. To solve this problem, the addition of a low concentration of diazo compound (decomposition of sulfonyl hydrazones) to alkenes catalyzed by either CuOAc or PdCl2 was studied, but side reactions could still not be avoided. Interestingly, however, the yield of cyclopropanation products for such hindered alkenes were as high as 99 % with AgOTf as a catalyst. To explain this unexpected phenomenon, reaction pathways have been computed for four different catalysts by using DFT. By combining the results of these calculations with those obtained experimentally, it can be concluded that the efficiency of the silver catalyst is due to the barrierless concerted cycloaddition step and the kinetic inhibition of side reactions by a high concentration of alkene. 相似文献
99.
Dayana Borges Bittar Tiago Augusto Catelani Karina Nigoghossian Hernane da Silva Barud Sidney José Lima Ribeiro Leonardo Pezza 《Analytical letters》2017,50(5):829-841
A colorimetric method based on silver nanoparticles was developed for the determination of melamine in milk. Silver nanoparticles were synthesized without any stabilizer, using sodium borohydride as the reducing agent. Optimization of the variables for the formation of the nanoparticles was performed by factorial design, resulting in stable colloidal silver nanoparticles with a mean diameter of 14.0?±?2.7?nm. Spectrophotometric measurements performed at 475?nm showed a linear range from 0.033 to 1.50?mg?L?1 of melamine with limits of detection and quantification of 0.009 and 0.031?mg?L?1, respectively. The method provided highly sensitive determination of melamine in milk. 相似文献
100.
Antibacterial and antibiofilm activity of nanochelating based silver nanoparticles against several nosocomial pathogens 下载免费PDF全文
Seyedeh Mahsan Hoseini‐Alfatemi Abdollah Karimi Shahnaz Armin Saideh Fakharzadeh Fatemeh Fallah Somayeh Kalanaky 《应用有机金属化学》2018,32(5)
The emergence of multi‐drug resistant (MDR) bacteria and dynamic pattern of infectious diseases demand to develop alternative and more effective therapeutic strategies. Silver nanoparticles (AgNPs) are among the most widely commercialized engineered nanomaterials, because of their unique properties and increasing use for various applications in nanomedicine. This study for the first time aimed to evaluate the antibacterial and antibiofilm activities of newly synthesized nanochelating based AgNPs against several Gram‐positive and ‐negative nosocomial pathogens. Nanochelating technology was used to design and synthesize the AgNPs. The cytotoxicity was tested in human cell line using the MTT assay. AgNPs minimal inhibitory concentration (MIC) was determined by standard broth microdilution. Antibiofilm activity was assayed by a microtiter‐plate screening method. The two synthesized AgNPs including AgNPs (A) with the size of about 20‐25 nm, and AgNPs (B) with 30‐35 nm were tested against Staphylococcus aureus, Staphylococcus epidermidis, Acinetobacter baumannii, and Pseudomonas aeruginosa. AgNPs exhibited higher antibacterial activity against Gram‐positive strains. AgNPs were found to significantly inhibit the biofilm formation of tested strains in concentration 0.01 to 10 mg/mL. AgNPs (A) showed significant effective antibiofilm activity compared to AgNPs (B). In summary, our results showed the promising antibacterial and antibiofilm activity of our new nanochelating based synthesized AgNPs against several nosocomial pathogens. 相似文献