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991.
Summary A direct titrimetric method for the estimation of iron(III) has been developed, which involves the adjustment of concentration of iron(III) andPh, dilution, addition of 1 ml of 2% indicator solution and titration with EDTA (30° to 35° C). It is based on the fact that the iron(III) forms a blue coloured complex which is destroyed at the 11 molar ratio making the end-point of the titration. Quantity of iron(III) as small as 23.2 mg can be titrated accurately when present in a volume of 100 ml. Study of interferences revealed that quite a number of elements like Be2+, Mg2+, Ca2+, Sr2+, Ba2+, UO2
2+ and Mn2+ does not interfere, whereas much interference is caused by Cu2+, Zn2+, Pb2+, Fe2+, Co2+, Ni2+, ZrO2+, V02+, Al3+, Cr3+, Ti4+, Ce4+ and Th4+. The method proposed for iron(III) is selective and should be of considerable use in many cases.Part III: See Z. analyt. Chem. 167, 332 (1959). 相似文献
992.
R. A. English S. G. Davidson Z. L. Miskovic F. O. Goodman A. T. Amos B. L. Burrows 《Progress in Surface Science》1996,53(2-4):323-330
A recursive Green-function (RGF) technique is used to study the surface states of an electrified solid. The concatenating nature of the method leads to a continued-fraction form of the RGF, which can be expressed as a ratio of Bessel functions. The surface density of states (SDOS), derived from the RGF, reveals a quasi-Stark-ladder distribution of the energy levels at the surface atom. The dependence of the SDOS on the applied field and surface perturbation parameters is discussed. 相似文献
993.
Goldfuss B Löschmann T Rominger F 《Chemistry (Weinheim an der Bergstrasse, Germany)》2001,7(9):2028-2033
Not the expected phosphinofenchol 1 but phosphorane 2 is obtained after reaction of 2-lithio(diphenylphosphino)benzene with (-)-fenchone. Surprisingly, ONIOM(B3LYP/6-31G*:UFF) computations of 1 and 2 as well as B3LYP analyses of smaller model systems point to a lower thermodynamic stability of phosphoranes relative to their isomeric alkoxyphosphines. An analogue inherent instability is computed for the methylphosphorane 10, which is also synthesized and characterized by X-ray analysis. Decreasing ring size in cyclic phosphoranes, that is, from five- to four-membered ring systems, destabilizes cyclic phosphoranes even more. This computational prediction is verified experimentally by reaction of lithiomethyl(diphenylphosphine) with (-)-fenchone and subsequent isolation of the corresponding phosphinofenchol. Protonation or alkylation of phosphoranide intermediates can account for the formation of metastable phosphoranes. 相似文献
994.
Kozikowski AP Tückmantel W Böttcher G Romanczyk LJ 《The Journal of organic chemistry》2003,68(5):1641-1658
We report an improved synthesis of bis(5,7,3',4'-tetra-O-benzyl)epicatechin 4beta,8-dimer (3) from 5,7,3',4'-tetra-O-benzylepicatechin (1) and 5,7,3',4'-tetra-O-benzyl-4-(2-hydroxyethoxy)epicatechin (2) by replacing the previously employed Lewis acid, titanium tetrachloride, with the clay mineral Bentonite K-10. Under the same conditions, the benzyl-protected all-4beta,8-trimer, -tetramer, and -pentamer were obtained regioselectively from their lower homologues, albeit in rapidly decreasing yields. Reaction of 2 with an organoaluminum thiolate generated from 2-mercaptobenzothiazole and trimethylaluminum followed by acetylation produced 3-O-acetyl-4-[(2-benzothiazolyl)thio]-5,7,3',4'-tetra-O-benzylepicatechin (12). Medium-sized protected oligomers with 4beta,8-interflavan linkages are obtained in improved yields by using this compound as the electrophile and silver tetrafluoroborate as activator and are isolated by reversed-phase HPLC. Their deprotection by ester saponification followed by hydrogenolysis yielded the free procyanidins, which were characterized as their peracetates. The synthetic procyanidins are identical by normal-phase HPLC with fractions isolated from cocoa. The principle of chain extension by two members was demonstrated using a dimeric electrophile obtained by self-condensation of compound 12. Both the synthetic and natural pentamer 32 inhibit the growth of several breast cancer cell lines. Using the MDA MB 231 line, it was established that this outcome is based on the induction of cell cycle arrest in the G0/G1 phase. Subsequent cell death is more likely necrotic rather than apoptotic. Control experiments demonstrate that the polyphenol itself, rather than hydrogen peroxide potentially formed by its autoxidation, is the causative agent. 相似文献
995.
Optical electron transfer in the mixed-valence cation of biferrocenylacetylene (BF+) has been examined in CD2Cl2 solvent. The intervalence absorption line shape is relatively narrow at both low and high chromophore concentrations, but broader at intermediate concentrations. The transition energy for metal-to-metal charge transfer increases from ≈4440 cm−1 at infinite dilution to 5995 cm−1 for 3.8 mM BF+. Related effects exist due to added electrolyte. Neither the electrolyte nor chromophore concentration effects are expected from a simple reading of electron transfer theories. Nevertheless, both phenomena can be understood and within the context of theory upon careful consideration of the effects of ion-pairing (and tripling) equilibria upon electron-transfer energetics. 相似文献
996.
997.
A method is presented for the determination of 2-10M nitric acid based on the fact that the presence of high nitric acid concentration causes an enhancement of the intensity of some bands in the fluorescence spectra of rare earth ions in solution. The 616-nm band of Eu(3+) shows the most dramatic intensity enhancement with increasing nitric acid concentration. The present method, based on the measurement of the ratio of Eu(3+) fluorescent band intensities is shown to be independent of Eu(3+) concentration and relatively free of interference. This robust method allows the presence of an interferent to be determined from the experimental data. 相似文献
998.
Based on the method of SAMSAHL a programmed, semi-automated processing system has been developed and tested for the neutron
activation analysis of the following elements: As, Se, Sb, Br, Sn and Te. The main characteristics of the procedure are the
following: wet ashing of the sample (by means of digestion in a mixture of concentrated sulphuric acid and hydrogen peroxide),
bromination, and chlorination. The procedure is controlled via the appropriate dosage of the reagents and a carefully managed
thermal balance. The chemical yield and its reproducibility were determined by tracer techniques using exactly the same parameters
as for the active runs. According to the results the method can be used for the routine determination of the given elements
except antimony.
Presented at the 4th Symposium on the Recent Developments in Neutron Activation Analysis, 1975, Cambridge. 相似文献
999.
It has been shown by a series of experiments on 5-alkyl, 5-halo-, and other 5-substituted 1-naphthol derivatives that the product ratio of the ortho- and para-naphthoquinones formed on oxidation with Fremy's salt is controlled by the bulkiness of the C5-substituent. 相似文献
1000.
The vapor-phase Raman spectrum of cyclopentene has been recorded and eleven lines corresponding to the Δν=2 transitions of the ring-puckering have been observed. A difference band sequence with 3070.4cm−1 as the reference band has also been observed. 相似文献