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References in periodicals archive ?
Application of pesticides and their TPs: Analytical standards of the individual pesticides and the TPs MDIPU and AMPA, dissolved in water: acetonitrile (1:1 v/v), were applied separately to different columns in a single dose at the maximum recommended dose level.
Separation was performed using a gradient elution with mobile phase A consisting of acetonitrile, and mobile phase B consisting of DH2O at a flow-rate of 1.0 ml/min.
Different concentrations of SFV (10 ugmL-1 to 60 ugmL-1) was used to prepare the standard solution as acetonitrile and ammonium acetate buffer (pH 7.6) was used as the mobile phase in a ratio of 50:50.
Grafted copolymers were filtered and thoroughly washed with N,N-dimethylformamide, acetonitrile, ethanol, and diethyl ether to eliminate oligomer and homopolymer that can form in the reaction.
The molar conductance of the nitrate salts of [Ag.sup.+], [Co.sup.2+], [Hg.sup.2+], [Zn.sup.2+], [Ni.sup.2+], [Cu.sup.2+], [Cd.sup.2+], [Mn.sup.2+], [Cr.sup.3+], [Fe.sup.3+] and [Pb.sup.2+] in acetonitrile solvent was monitored as a function of the pyrazoloisoindol derivative ligand to metal ion mole ratio, and the stoichiometry of the complexes in acetonitrile was examined by the mole ratio method at 25[degrees]C temperature.
Figure (5b, 5c) showed heterogeneous, porous surface morphology of Fe-doped TiO2 nanoparticles synthesized in acetonitrile and n-hexane.
The optimum reaction conditions was acetonitrile, temperature reaction 80[degrees]C, [H.sub.2][O.sub.2]/styrene molar ratio equal to 2.5, catalyst loading of 1% mol Ag-1% mol Co, and the catalyst amount of 0.02 g.
Note that the acidity of both analyte and silanol group and thus the dipole-dipole interaction are enhanced in acetonitrile [18].
Figure S2: ECD spectra of VEGF i[M.sub.WT] at pH 5.4 exposed to 0 KCl (mM)/0% acetonitrile, 100 mM KCl by itself, 40% acetonitrile by itself, and both 100 mM KCl/40% acetonitrile present.
Irradiation of azomethine imine 1-4 O solutions in acetonitrile with light of [[lambda].sub.irr] 365 nm results in spectral changes in the characteristic of negative photochromism due to intramolecular photocyclization into diaziridines 1-4 C (Scheme 2), accompanied by a decrease in the intensity of long-wave absorption maxima and the appearance of absorption bands in the short-wave region of the spectrum [10, 30, 31] as shown in Figure 2(a) in the example of compound 1 and in Table 1.
Figure 1(a) displays the absorption spectra of the as-prepared Si-NPs in different coordinating solvents such as ethanol, dimethyl sulfoxide, dimethyl formamide, dioxane, and acetonitrile. In measuring the absorption spectra of NPs in acetonitrile and ethanol, this transition is broadened and splitted into two bands with maxima at 228 nm and 260 nm and 220 nm and 260 nm, respectively.