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81.
Single crystals of CeAgAs2 have been obtained by chemical transport reactions starting from a pre‐reacted powder sample. The crystal structure was solved using X‐ray diffraction (space group Pmca, No. 57, a = 5.7586(4) Å, b = 5.7852(4) Å, c = 21.066(3) Å, Z = 8) and refined to a residual of R(F) = 0.029 for 46 refined parameters and 1020 reflections. The structure of CeAgAs2 represents a new distorted and ordered variant of the HfCuSi2 type. The characteristic feature of this structure are infinite cis‐trans chains of As atoms with As—As distances of 2.563(1) Å and 2.601(1) Å. CeAgAs2 is paramagnetic (μeff = 2.37 μB, θ = —10.5(2) K), with antiferromagnetic ordering at 5.5(2) K and exhibits a metamagnetic transition starting at 4.6 kOe and T = 1.8 K.  相似文献   
82.
When crystallized from appropriate solvents, the complex aqua-bis(dimethylglyoximato)nitrocobalt (III) may incorporate solvent molecules, thus forming a variety of mixed crystals. In the resulting host-guest crystals, the space groupP2l/m and the packing motif of the pure host compound are retained. Lattice constantsa andb remain essentially unaltered upon intercalation, whereasc and the monoclinic angle depend largely on the clathrated guest. Space filling and intermolecular contacts are discussed.Dedicated to Professor Peter Paetzold at the occasion of his 60th birthday. A preliminary account of this work has been given at the Spring Meeting of the British Crystallographic Association, Newcastle upon Tyne, 1994.  相似文献   
83.
Picó  Y.  Vreuls  J. J.  Ghijsen  R. T.  Brinkman  U. A. Th. 《Chromatographia》1994,38(7-8):461-469
Summary A small cartridge containing a drying agent is inserted between a solid phase extraction (SPE) column and a gas chromatograph (GC) to enable the introduction of water-free desorption solvent into the GC in on-line liquid chromatography (LC)-type enrichment of trace-level analytes from water samples. Some characteristics of the drying agents, such as their capacity to retain water and their re-usability after heating, have been tested. Possible interactions of the drying agent with the analytes, e.g., irreversible adsorption or catalyzed degradation, have been checked for a wide range of alkanes, alkylbenzenes chlorobenzenes, chlorophenols and phthalate esters. Using the on-line SPE-GC system with flame ionization detection (FID) and spiked samples containing different levels of the test compounds, the repeatability was shown to be satisfactory (6–17%). For 10 mL samples, the detection limits were lower than 0.1 g/L. The on-line SPE-GC-FID system here presented can be used for the repeated analysis of water samples without exchange of the dyring cartridge. The technique is applied to the analysis of tap water.  相似文献   
84.
Sub-Doppler electronic spectra with hundreds of resolved rotational lines are now available for benzene-Ar dimers and trimers. From their analysis the structure of these clusters is precisely determined. The analysis of two bands, 6 0 1 and 16 0 2 , of C6H6 · Ar is presented in detail. It leads to accurate values of the van der Waals bond length in the electronic ground and excited state. The change in frequency upon clustering is found to be a factor of 17 larger for the overtone of the out-of-plane modev 16 than for the in-plane vibrationv 1. This can be tentatively explained by an interaction of the low frequency out-of-plane motion of the ring with the van-der-Waals motion of the Ar atom.  相似文献   
85.
Starting from the para‐phenylenediamine derivative HN(SiMe3)‐C6H4‐NH(SiMe3), a lithiation and subsequent borylation give [(MeO)2B]N(SiMe3)‐C6H4‐N(SiMe3)[B(OMe)2] ( 1 ), the hydridation of which yields Li2[(H3B)N(SiMe3)‐C6H4‐N(SiMe3)(BH3)] ( 2 ). Applying ZrCl4 upon 2 initiates a condensation to give the title compound [‐N(SiMe3)‐p‐C6H4‐N(SiMe3)‐BH‐]2, a hetero[3, 3]paracyclophane with two N‐B‐N chains that connect the para‐phenylene units. The product 3 crystallizes in the orthorhombic space group P212121.  相似文献   
86.
Summary Comprehensive gas chromatography is an excellent technique for separating complex mixtures. If, however high-boiling compounds such as polychlorinated biphenyls have to be analysed, proper adjustiment of the temperature of the modulator turns out to be very important in maintaining the performance of the system. It is shown that miniaturisation of the column-to-modulator coupling, adequate selection of the modulating conditions and, for halogenated compound mixtures, the use of a micro electron-capture detector, can solve experimental problems previously encountered with high boilers.  相似文献   
87.
Summary Micellar phase-transfer catalysis (MPTC) offers the opportunity to derivatize carboxylic acids directly in an aqueous matrix without prior extraction of the acids into a suitable aprotic solvent. The currently developed MPTC system consists of a non-ionic surfactant, Arkopal N-130, an ion-pair agent, tetrakis-(decyl)-ammonium bromide, and a novel fluorescence reagent, 9-bromomethylacridine. The MPTC system can be applied to the derivatization of many types of carboxylic acids. The reaction rate is affected by the lipophilicity of the acid and by the presence of other functional groups. For lipophilic carboxylic acids the reaction is complete within 5 min at 60°C and pH 7.0.  相似文献   
88.
The vibrational spectra of compounds Ln2WO6 and Ln2MoO6 (Ln = lanthanide, including Y and Bi) are reported. Neglecting details it is possible to assign the internal vibrations of the molybdate and tungstate group. The results are in agreement with the structural data known up till now and suggest further that tungsten in the unknown Y2WO6 structure is in six-coordination, that Bi2MoO6 shows still another modification than koechlinite and that vibrational spectroscopy may yield additional structural information for compounds like those under consideration.  相似文献   
89.
A new oxidimetric titrant, bis(trifluoroacetoxy)iodobenzene is proposed for potentiometric titrations in acetonitrile and water-acetonitrile media. The general analytical conditions for using this titrant and the results for the potentiometric titrations of various inorganic and organic reductants are described.  相似文献   
90.
We describe the synthesis of two cyclobutadiene(cyclopentadienyl)cobalt-containing poly(p-phenylene ethynylene)s (PPEs) and their use as precursors for stable ceramic surface coatings. Organometallic PPEs were shaped into hexagonally ordered assemblies by using the breath-figure method. Such breath figures can be washed away with an appropriate solvent. Upon pyrolysis at 500 degrees C under either nitrogen or air, the bubble arrays persist as ceramics and are insoluble in organic solvents or water. The formed pyrolyzed bubble arrays were analyzed by optical and scanning electron microscopy, as well as energy dispersive X-ray microanalysis (EDX). The composition of the ceramic materials is discussed based on EDX and IR data.  相似文献   
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