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This work demonstrates that optically tunable, SERS-active Ag films can be reproducibly fabricated on glass by the thermal decomposition of layered silver alkanecarboxylates.
The synthesis of silver nanoprisms in aqueous solution using poly(N-vinyl-2-pyrrolidone) (PVP) with different molecular weights (29, 55 and 1300 kg mol(-1)) as a stabilizing agent is described. Low molecular weight PVP (55 kg mol(-1)) is indicated for the preparation of a stable blue solution containing Ag nanoprisms via extended irradiation of a yellow colloidal solution of nanospheres with polychromatic visible light. The fluorescence properties of some cationic dyes (acridine, 9-aminoacridine, Nile Blue and auramine), free and bound to poly(methacrylic acid), have been studied in the presence of different shaped Ag colloidal particles in solution. Only auramine displays an amplification of the fluorescence signal with increasing colloid concentration, while the fluorescence of the other dyes is quenched by interaction with the polymer-stabilized metal nanoparticles.
The synthesis and crystal structure of [tris[2-(benzylamino)ethyl]amine-kappa(4)N]silver(I) perchlorate, [Ag(C(27)H(36)N(4))]ClO(4) or [Ag(bz(3)tren)]ClO(4) [bz(3)tren is tris[2-(benzylamino)ethyl]amine or N,N',N''-tribenzyltris(2-aminoethyl)amine] are reported. The Ag atom is coordinated to four N atoms of the tren unit and is located 0.604 (3) A out of the trigonal plane described by the three secondary amine N atoms, away from the bridgehead N atom. Edge-to-face pi-pi interactions between the aromatic end groups, and weak interactions between Ag and arene, allow the formation of a pseudo-cage complex.
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Large input currents can be generated by an asymmetry in the chloride activity seen by Ag-AgCl electrodes used at the input of intracellular amplifiers because offset compensation no longer takes place at the input of the amplifier but rather later in the circuit in many modern amplifiers. This situation occurs when chloride-free solution, such as potassium acetate, potassium citrate or various intracellular dyes are used as pipette and electrode holder filling solutions. Omitting the agar bridge at the reference electrode, or using a platinum electrode will have similar results. Values of cellular membrane potentials can be significantly contaminated under such conditions, particularly where the amplifier input resistance did not exceed 10(10) omega and where small cells were studied. Unexpected iontophoresis of Cl- can occur when the asymmetry is such as to make the recording pipette negative. These offsets can be avoided in all situations by the use of salt bridges which insure that the two Ag/AgCl junctions are in contact with Cl- of the same activity.
Influence of water Ag(I) speciation on pharmacokinetics of Ag(I) during a post-exposure period was investigated in rainbow trout (Oncorhynchus mykiss) and European eel (Anguilla anguilla). The rainbow trout is sensitive to waterborne ionic Ag(+) whereas the eel is tolerant. The fish were acclimated to either of two chloride concentrations, 10 or 1200 microM, in synthetic soft water and then exposed to a sublethal 24-h pulse of 1.3 microgl(-1) of 110mAg(I) added as 110mAgNO(3) in these waters. The protocol provided exposures to mainly the free ion Ag(+) (low chloride water) or mainly AgCl(aq) (high chloride water). Contents and concentrations of 110mAg(I) in tissues and body fluids were then monitored over a 67-day post-exposure period in Ag(I)-free water of the same chloride levels. Changing the speciation of Ag(I) in the water had no effect on the whole body load of 110mAg(I), but did result in differences in internal distribution. In trout, changing water Ag(I) speciation significantly altered elimination or accumulation of Ag(I) in several body compartments. Notably, trout exposed to AgCl(aq) eliminated 110mAg(I) from the kidney more quickly than trout exposed to Ag(I) primarily as Ag(+). This elimination was matched by higher concentrations of 110mAg in liver of trout exposed to Ag(I) primarily as AgCl(aq). In eel, shifting speciation from Ag(+) to AgCl(aq) hastened elimination of 110mAg(I) from mid and posterior intestine and increased 110mAg(I) retention in kidney. While there was no difference between the two fish species in whole body 110mAg(I) load, most internal body compartments of trout had higher 110mAg(I) concentrations than those in eel early in the experiment. Because tissue-specific elimination times were longer in eel than in trout, these differences were generally cancelled by the end of the 67-day depuration period. The only exception was the liver, which in trout continued to accumulate 110mAg(I) throughout the experiment but in eel remained unchanged. The combined effect of 110mAg(I) movements in the two species was that trout retained all their accumulated 110mAg(I) through the 67-day period, whereas the body burden of 110mAg(I) in eel was reduced to half initial values by day 67.
Nanocomposite crystals, (Ag)(x)(Ag(2)S)(y) with x < y, are synthesized in micellar media. The generation of Ag clusters on Ag(2)S nanocrystals is attributed to the reduction of mobile Ag(+) ions in the Ag(2)S nanocrystals by sulfur derivatives. The proportions in the composite material can be modulated by electron beam irradiation. Using dodecanethiol as surface passivating agent, 2D self-organizations of these nanocomposite crystals are produced.
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