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911.
The111Cd quadrupole coupling in the spinel CdCr2Se4 is investigated by TDPAC after different sample treatments. The experiments are consistent with Se vacancies causing the non-cubic probe environments and with the assumption that the majority of the111In atoms are positioned at A-sites. 相似文献
912.
V. Balek L. A. Pérez-Maqueda J. Poyato Z. Černý V. Ramírez-Valle I. M. Buntseva J. L. Pérez-Rodríguez 《Journal of Thermal Analysis and Calorimetry》2007,88(1):87-91
The effect of grinding
on thermal behavior of pyrophyllite and talc as commonly used ceramic clay
minerals was investigated by DTA, TG, emanation thermal analysis (ETA), B.E.T.
surface area (s.a.) measurements, X-ray diffraction (XRD) and scanning electron
microscopy (SEM).
A vibratory mill was used in this study, grinding
time was 5 min. It was found that the grinding caused an increase in surface
area and a grain size reduction of the samples. From TG and DTA results it
followed that grinding caused a decrease of the temperature at which the structure
bound OH groups released. The formation of high temperature phases was enhanced
with the ground samples. For the ground talc sample the crystallization of
non-crystalline phase into orthorhombic enstatite was observed in the range
of 800°C. For ground pyrophyllite a certain agglomeration of grains was
observed in the range above 950°C. Moreover, for both clays the ETA characterized
a closing up of subsurface irregularities caused by grinding as a decrease
of the emanation rate in the range 250–400°C. The comparison of
thermal analysis results with the results of other methods made it possible
to better understand the effect of grinding on the ceramic clays. 相似文献
913.
Milan Melník Peter Mikuš 《Phosphorus, sulfur, and silicon and the related elements》2020,195(5):367-370
AbstractIn this review, the structural data of monomeric platinum(II) complexes with inner coordination spheres of Pt(η2-P2L)(SiL)2, Pt(η2-P2L)(η2-Si2L) and Pt(η2-P,SiL)2 are classified and analyzed. These complexes crystallize in three crystal systems: monoclinic (8 examples), triclinic (4 examples) and orthorhombic (4 examples). Distorted square-planar environments about the Pt(II) atoms are built up by combination of homobi-P,P with two monodentate Si donor ligands; homobi-PP with homo-Si,Si donor ligands, or heterobi-P,Si donor ligands. The chelating ligands create metallacycles with the following angles: 65.0° (SiOSi) < 83.1° (SiC2Si) < 85.2° (PC2P) < 88.8° (SiSi2Si)). The mean Pt-P and Pt-Si bond distances in Pt(η2-P2L)·(SiL)2 complexes are 2.319 and 2.365?Å; in Pt(η2-P2L)(η2-Si2L) the values are 2.316 and 2.360?Å. The complex [Pt{η2-Me2P(C2B10H10)SiMe2}2] exists in two isomeric forms, a monoclinic cis- and a triclinic trans-isomer. The structural data are compared and discussed with the complexes of inner coordination spheres: Pt(η2-P2L)(XL)2 (X?=?O, N, CN, BL, Cl, SL, SeL, Br, or I) and Pt(η2-P2L)(η2-X2L) (X?=?OL, NL, SL or SeL). 相似文献
914.
C. Díaz M. L. Valenzuela E. Spodine Y. Moreno O. Peña 《Journal of Cluster Science》2007,18(4):831-844
Pyrolysis of the organometallic polymer: {{[N=P(R1)]0.8[N=P(OC6H4CH2CN[Ru])2]0.15[N=P((OC6H5)(OC6H4CH2CN[Ru]]0.05}{Cl}0.31}
n
, [Ru]=CpRu(PPh3)2, R1 = O2C12H8 (1) as well of the cyclic specie {N3P3 (OC6H5)5(OC6H4CH2CN[Ru])}{PF6} (2) under a flow of air at 800°C affords nanostructured RuO2. Nanoparticles near to 10 nm were observed. The differences in the use of cyclic or polymeric phosphazenes, as solid state
template, influence strongly the morphology and slightly the composition of the pyrolytic product. Temperature variable (SQUID)
measurements in the range of 5–300 K of the material obtained from the polymer, indicate an antiferromagnetic interaction
between the Ru atoms, although lower than that found for the crystalline ruthenium oxide, probably due to some amorphous product
present in the pyrolytic material. The possible formation mechanism is discussed and the differences in using the cyclic or
the polymeric compound as precursor is analyzed in terms of the relative content of Ru to P, N. A general formation method
of nanostructured metal oxides is proposed. 相似文献
915.
Analysis of endosulfan and its metabolites in human serum using gas chromatography-tandem mass spectrometry 总被引:5,自引:0,他引:5
Arrebola FJ Martínez Vidal JL Fernández-Gutiérrez A 《Journal of chromatographic science》2001,39(5):177-182
A new analytical method combining solid-phase extraction and gas chromatography-tandem mass spectrometry (GC-MS-MS) is proposed to determine the insecticide endosulfan as well as its metabolites endosulfan-ether, -lactone, and -sulfate in human serum. Most matrix interferences are avoided using a cleanup step included in the sample treatment and an instrumental technique such as GC-MS-MS, which presents a high sensitivity and selectivity. Recoveries of spiked compounds range between 94.8 and 100.4% and 93.4 and 99.7% at fortification levels of 10 and 30 ng/mL, respectively. The relative standard deviation is lower than 17.6% in all cases, and the limits of detection calculated range from 6 to 19 pg/mL. Serum samples of nine agricultural workers that spray endosulfan into greenhouses in Almería (Spain) and two nonoccupationally exposed people are analyzed, and endosulfan is found in all the samples studied. 相似文献
916.
Román-Bravo P López-Cardoso M y García PG Höpfl H Cea-Olivares R 《Chemical communications (Cambridge, England)》2004,(17):1940-1941
The molecular structures of two lipophilic polyion aggregates derived from tetraphenyl imidodiphosphinate are described: [Na(crown ether)][MNa(2)[Ph(2)P(O)NP(O)Ph(2)](4)] with crown ether = 15-crown-5 for 1and benzo-15-crown-5 for (M = Na(+) for 1 and Na(H(2)O)(+) for 2). 相似文献
917.
Imre T Schlosser G Pocsfalvi G Siciliano R Molnár-Szöllosi E Kremmer T Malorni A Vékey K 《Journal of mass spectrometry : JMS》2005,40(11):1472-1483
A new anionic surfactant (RapiGest SF) was successfully used for site-specific analysis of glycosylation in human alpha-1-acid glycoprotein (AGP). By means of this analytical approach combined with capillary HPLC-mass spectrometry (and tandem mass spectrometry), the N-linked glycosylation pattern of AGP was explored. On the basis of mass matching and MS/MS experiments ca 80 different AGP-derived glycopeptides were identified. Glycosylation shows a markedly different pattern for the various glycosylation sites. At sites I and II, triantennary complex-type oligosaccharides predominate and at sites III, IV and V, tetra-antennary complex-type oligosaccharides predominate. Sites IV and V show the presence of additional N-acetyl lactosamine (Gal-GlcNAc) units (even higher degree of branching and/or longer antennae are also present). 相似文献
918.
Gregorio López María D. Santana Gabriel García Gregorio Sánchez Joaquín García 《Transition Metal Chemistry》1987,12(2):130-133
Summary The organopalladium(II) complexes: Pd(2,4,6-C6F3H2)2L2 [L=triphenylphosphine(PPh3), methyldiphenylphosphine(PPh2Me), dimethylphenylphosphine-(PPhMe2) or pyridine(py); L2=1,2-bis(diphenylphosphino)ethane(dpe), 2,2-bipyridine(bipy), 1, 10-phenanthroline(phen) or ethylenediamine(en)] have been prepared by addition of the appropriate compound to the THF-dioxane solution resulting from the arylation of potassium tetrachloropalladate(II) with (2,4,6-C6F3H2)MgBr. The i.r. data suggest that the py and PPhMe2 compounds are thecis-isomers, whereas the PPh3 and PPh2Me compounds have thetrans configuration.1H- and19F-n.m.r. data for the compounds are reported. 相似文献
919.
920.
Brown SP Pérez-Torralba M Sanz D Claramunt RM Emsley L 《Journal of the American Chemical Society》2002,124(7):1152-1153
A new method for detecting hydrogen bonds in the solid state is presented. Using two-dimensional NMR correlation experiments, it is shown that a hydrogen-bond mediated J coupling can be observed in a powder under magic-angle spinning conditions, even though the J coupling is 2 orders of magnitude smaller than the dominant anisotropic interactions encountered in solid-state NMR. Specifically, the observation of a pair of peaks in a two-dimensional 15N-15N solid-state INADEQUATE experiment due to two nitrogens that have no covalent connectivity is attributed to the presence of a J coupling across a linking hydrogen bond. 相似文献