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1.
Jnos Szanyi Ja Hun Kwak Sarah Burton Jose A. Rodriguez Charles H.F. Peden 《Journal of Electron Spectroscopy and Related Phenomena》2006,150(2-3):164-170
Adsorbed ionic NOx species formed upon the interaction of NO2 with dehydrated or hydrated Na- and Ba-Y, FAU zeolites were characterized using FT-IR/TPD, solid state NMR, and XANES techniques. NO2 disproportionates on both dehydrated catalyst materials forming NO+ and NO3− species. These ionic species are stabilized by their interactions with the negatively charged zeolite framework and the charge compensating cations (Na+ and Ba2+), respectively. Although the nature of the adsorbed NOx species formed on the two catalysts is similar, their thermal stabilities are strongly dependent on the charge compensating cations. In the presence of water in the channels of these zeolite materials new paths open for reactions between NO+ and H2O, and NO2 and H2O, resulting in significant changes in the adsorbed ionic species observed. These combined spectroscopic investigations afforded the understanding of the interactions between water and NO2 on these zeolite catalysts. 相似文献
2.
It was studied the tin phase composition of the electrodeposited alloys produced at different temperatures and current densities from an acid chloride/fluoride electrolyte and an acid chloride bath. Mössbauer spectra were consistent with a Ni3Sn4 intermetallic compound, dissolved tin, and a Cu?Sn intermetallic compound formed at the interface of the copper substrate. 相似文献
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5.
Wojciech Bocian Jarosław Jaźwínski Lech Stefaniak Graham A. Webb 《Chemistry of Heterocyclic Compounds》1995,31(9):1103-1107
1H,13C,14N and15N NMR measurements are reported for four mesoionic 1-oxa-2, 3, 4-triazoles containing exocyclic nitrogenous groups. The NMR signal assignments are discussed and compared with those previously published for some corresponding oxatriazoles. The results obtained support the proposed cyclic mesoionic structures for the compounds studied. The questions of possible charge delocalization and valence tautomerism are addressed. Compound with N– H as a exocyclic group (Fig. 1) is found to be relatively unstable, this is attributed to proton migration in the corresponding non-cyclic form of this molecule.Published in Khimiya Geterotsikiicheskikh Soedinenii, No. 9, pp. 1260–1263, September, 1995. 相似文献
6.
Zusammenfassung Die komplexe Koazervation im SystemG-A-H2O kann als zweistufiger Prozeß aufgefaßt werden. Das erste Stadium ist die Bildung des elektrisch neutralen Komplexes zwischen G und A unter Einfluß der elektrostatischen Anziehungskräfte. Die Stöchiometrie der gewonnenen Verbindung wird durch die Äquivalenz der Makroionen bestimmt.Nur elektrisch neutrale Komplexe können die neue Phase, d. h. das komplexe Koazervat bilden. Deshalb muß die Zusammensetzung der koazervaten Phase von pH abhängen und bei Veränderung des Verhältnisses der Polymere im Gemisch unveränderlich bleiben.Bei einem Verhältnis der Polymere, kleiner als das stöchiometrische, ist die Bildung geladener Komplexe möglich.Den Prozeß der komplexen Koazervation kann man mittels der Methode der Trübungsmessung bei Cs<6·10–3 g/100 g untersuchen. Hierbei ist die optische Dichte proportional der Menge des komplexen Koazervats oder des elektrisch neutralen Komplexes im System. 相似文献
7.
Chester M. Mikulski Scott Grossman Chung Ja Lee Nicholas M. Karayannis 《Transition Metal Chemistry》1987,12(1):21-25
Summary Complexes of the general types Pd(L)(LH)Cl (LH=hxH, xnH, or tbH) and Pt(L)(LH)Cl3 (LH=hxH, or xnH) are formed by boiling under reflux 21 molar mixtures of hypoxanthine (hxH), xanthine (xnH) or theobromine (tbH) and PdCl2 or PtCl4 in ethanol-triethyl orthoformate. These complexes appear to be linear chain polymeric species, characterized by single monoanionic L– ligands bridging between adjacent Pd2+ or Pt4+ ions. Inclusion of one terminal neutral LH and one terminal chloro-ligand completes the coordination sphere in the square-planar Pd2+ complexes, while the Pt4+ complexes aretrans-octahedral, involving three terminal chloro and one terminal LH ligand per platinum. The possible binding sites of the bidentate bridging L– and the unidentate terminal LH are discussed. 相似文献
8.
W. Bocian J. Jaźwiński O. Staszewska J. W. Wiench L. Stefaniak G. A. Webb 《Chemistry of Heterocyclic Compounds》1996,32(11-12):1358-1366
Multinuclear1H,13C,14N,15N, and17O NMR data are presented for some sydnones, isosydnones and isothiosydnones. The type of valence tautomerism shown in (Fig. 1) is not observed for the compounds studied. At high pH compounds2 and12 are found to undergo transformations. The more suitable NMR parameters are reported for establishing the structures of mesoionic compounds containing three heteroatoms in the five-membered conjugated ring. Someab initio GIAO calculations on a model structure of sydnones and related compounds have been performed. 相似文献
9.
F. Pérez-Giménez G. M. Antón-Fos F. J. García-March M. T. Salabert-Salvador R. A. Cercós-del-Pozo J. Jaén-Oltra 《Chromatographia》1995,41(3-4):167-174
Summary The possible relation existing between RF values obtained by thin-layer chromatography for a group of anilines with connectivity indices proposed by Kier and Hall has been studied. Using multivariable regression the corresponding connectivity functions, selected for their respective correlation coefficients, standard deviations, Snedecor's F and Student's t were obtained. Regression analysis of the connectivity functions gives a correct prediction of the experimental elution sequence for this group of substances on silica gel stationary phases and various mobile phases of different polarity. The corresponding random and stability studies of the different prediction models selected were carried out, showing good stability and null randomness in all cases. 相似文献
10.
Hong SB Lee SH Shin CH Woo AJ Alvarez LJ Zicovich-Wilson CM Camblor MA 《Journal of the American Chemical Society》2004,126(42):13742-13751
Here, we report that synthetic gallosilicate molecular sieves with the NAT topology and Si/Ga ratios close to but slightly higher than 1.50 undergo an in situ transformation under their crystallization conditions. The materials have been studied ex situ by using powder X-ray diffraction, elemental and thermal analyses, and multinuclear MAS NMR. The transformation is characterized by a change in the distribution of Si and Ga of the NAT framework, from a quite (but not completely) disordered phase to a very highly (but not completely) ordered one, accompanied by a change from tetragonal to orthorhombic symmetry. During most of the solution-mediated transformation, no noticeable signs of fresh precipitation, phase segregation, or changes in the chemical composition are detected. Intermediate materials show variations in the degree of Si-Ga ordering and orthorhombic distortion and are not physical mixtures of the disordered and ordered phases. Ab initio calculations strongly suggest a preferential siting of Si in the tetrahedral sites involved in a smaller number of 4-rings in the NAT topology (i.e., the low multiplicity site). The cost of violations of Loewenstein's rule has also been calculated. For this topology and chemical composition the preferential siting and Loewenstein's rule drive together the system to the ordered configuration. A Monte Carlo sampling procedure affords a reasonable model for the initial, mainly disordered state, which fits well within the experimental disorder-order series. 相似文献