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131.
Photokilling Squamous Carcinoma Cells SCCVII with Ultrafine Particles of Selected Metal Oxides 总被引:1,自引:0,他引:1
Ivanković Siniša Gotić Marijan Jurin Mislav Musić Svetozar 《Journal of Sol-Gel Science and Technology》2003,27(2):225-233
The ability of ultrafine particles of TiO2, WO3 and iron-doped TiO2 to kill cancer cells in the presence of UV irradiation was investigated. The best photokilling effect on carcinoma cells SCVII cultured in vitro showed iron-doped TiO2 ultrafine particles synthesized by the sol-gel procedure with starting chemicals Ti(IV)-isopropoxide and anhydrous Fe(II)-acetate. It was found that a small particle size and high dispersity influenced citotoxicity and photocatalytic efficiency. The remarkable photokiling effect of highly iron-doped TiO2 ultrafine particles (the molar ratio Fe/Ti = 0.136) in the presence of UV irradiation was observed. The influence of ultrafine metal oxide particles on the inhibition of cancer cell proliferation was measured using a 3H-thymidine incorporation test. The possible mechanism involved in the photokilling of carcinoma cells with ultrafine particles of selected metal oxides was discussed. 相似文献
132.
Lichens are bioaccumulators of divalent metal ions and the interaction between the lichens and five heavy metals was studied. In order to have a better understanding of the metal-uptake process by the lichens, data from atomic absorption spectroscopy were used to calculate the apparent coordination constants of the lichen–metal ion interactions by means of the Langmuir elaboration and microcalorimetric measurements to obtain enthalpimetric information. The results showed a correlation between the Langmuir constants and enthalpimetric measurements. 相似文献
133.
Catherine J. Murphy 《Journal of Cluster Science》1996,7(3):341-350
One of the most exciting frontiers in materials chemistry in recent years is the optoelectronics of quantum-confined semiconductor nanoclusters. These nanoclusters are 10–200 A in diameter, and in this size regime exhibit extra-ordinarily interesting quantum mechanical effects. Cadmium sulfide is a popular semiconductor for these studies, and reviewed here is the synthesis and charac-terization of such CdS nanoclusters, with emphasis on how chemical control of the surface by thiolates influences product formation and properties. Also described are the syntheses and structures of true molecular clusters of CdS capped with thiolate ligands. 相似文献
134.
Summary Polyethylene oxide (PEO)-based polymers with hydroxy, methoxy, and aminopropoxy terminal groups were coated on diol functionalized and hexamethyldisilazane end-capped silica particles. Proton-donor and proton-acceptor test solutes, including carboxylic acids, hydroxy-containing compounds, arylamines, and alkylamines were used to evaluate the chromatographic performances of these polymer coated particles under SFC conditions with neat CO2 as mobile phase. It was found that the particles coated with hydroxy-terminated PEO were suitable for the separation of proton-donor compounds such as hydroxy-containing compounds and carboxylic acids, and the particles coated with aminopropoxy-terminated PEO could be used for the separation of amines. That is, the proton-accepting stationary phase is suitable for the separation of proton accepting solutes, including strong basic alkylamines (pKb4), using neat CO2 as mobile phase, while the protondonating stationary phase is suitable for the separation of proton-donating compounds such as carboxylic acids (pKa4). Hydrogen bond basicity was found to be a critical factor for the chromatography of basic amines. Low volatility acidic and basic drugs were chromatographed using the new stationary phases. The stability of the PEO coated particles was determined by measuring the loss of organic carbon under SFC conditions. It was found that approximately 18 % of the coating (average molecular weight of 15,000) was washed out of the particles by supercritical CO2 after 7 h at 350 atm and 50°C 相似文献
135.
The essential features (geometries of the minima and of the saddle points, energy barriers) of the potential energy surface of the four hydrides YXH4 mentioned in the title have been determined with two basis sets, of minimal and DZ quality respectively. The importance of the different extent of the deformation of the XH4 group in the different structures of the four hydrides is brought out and discussed. The aspects of charge distribution and bonding are examined drawing on population analysis, comparison of the electrostatic molecular potentials and decomposition of the interaction energy (this last referred to the Y+ + XH
4
–
YXH4 process). The capability of XH3 in effecting the etherolytic disruption of the Y-H bond is finally brought out. 相似文献
136.
Rolf Niedermayer 《Angewandte Chemie (International ed. in English)》1975,14(4):212-218
Synthesis of organometallic materials can be accomplished in many cases by cocondensation of metal atoms and organic molecules at low temperatures. The reaction kinetics is determined by the competition between metal cluster growth and formation of the organometallic compound. Interesting compounds may contain one or more metal atoms; the latter type could be obtained by reaction between a cluster containing the desired number of metal atoms and an organic molecule. A precise knowledge of the events occurring on condensation of metal atoms and cluster formation can therefore be of value in the control of chemical synthesis. These phenomena have been investigated in connection with the study of the growth of thin metallic films, both experimentally and theoretically. Direct observation of the formation of very small clusters is difficult. The good agreement between experimental results and recent calculations for the development of large clusters, however, allows reliable theoretical conclusions for the first stages of adsorption and cluster formation. The present contribution describes experimental work on film growth and relevant theoretical concepts, and an attempt is made to develop applications to organometallic synthesis. 相似文献
137.
Paola Ceroni Mauro Maestri Sang-kyu Lee Marius Gorka 《Journal of organometallic chemistry》2004,689(24):4375-4383
Suitably designed luminescent dendrimers can play a role of ligands for luminescent and non-luminescent metal ions. This combination leads to species capable of exhibiting interesting and unusual properties, including (i) shielding excited states from quenching processes, (ii) light harvesting, (iii) conversion of incident UV light into visible or infrared emission, and (iv) metal ions sensing with signal amplification. 相似文献
138.
139.
Zauresh S. Nurkeeva Al-Sayed Abdel Aal Vitaliy V. Khutoryanskiy Grigoriy A. Mun Aida G. Beksyrgaeva 《Radiation Physics and Chemistry》2003,67(6):717-722
Gamma-radiation grafting of vinyl ether of monoethanolamine and vinyl ether of ethyleneglycol (VEEG) on polyethylene films has been studied from binary monomer mixtures. The effect of co-monomer composition and total exposure radiation dose on the grafting process is investigated. A combination of potentiometric and gravimetric techniques is applied to determine the grafting degree of each monomer in the final graft copolymer. The presence of more active monomer VEEG in the mixture was found to enhance the grafting of both monomers because the increasing of copolymerization rate which in turn increases the total grafting degree. The modification of the hydrophilic properties of the graft copolymer is studied by examining the grafted films for water- and copper (II) ions uptake. 相似文献
140.
Recently, we reported that multi-hollow polymer particles can be prepared from carboxylated polymer particles by the stepwise
alkali/acid method. In this article, an attempt was made to prepare similar particles from acid-swellable polymer particles
by the stepwise treatment with acid and alkali, which was named the stepwise acid/alkali method. The acid-swellable particles
were produced by emulsion terpolymerization of styrene, butyl acrylate, and dimethyl 2-amino ethyl methacrylate. The effects
of initial pH value, temperature, and time in the acid and alkali treatment processes on the multi-hollow structure were examined.
Received: 18 December 1996 Accepted: 11 March 1997 相似文献