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11.
Acidolytic cleavage of unsymmetrically substituted dithioacetal monoxides, ArCH(SR)S(O)Me has been used to prepare linear unsymmetrical disulfides RSSMe. Disproportionation was suppressed by the addition of a small amount of benzyl mercaptan. The required starting materials were conveniently obtained from appropriately substituted sulfines ArC(=SO)SR and methyl lithium. The following disulfides were prepared: R =n-C4H9 (73.5%), n-C7H15 (78%), Ph (77.3%), AcO(CH2)10 (81.5%).The unsymmetrical dithioacetal PhCH(SEt)SC7H15-n gave upon oxidation with one equivalent of peracid a mixture of two dithioacetal monoxides which on treatment with HClO4 led to three disulfides. This result is discussed in term of the mechanism of acidolysis. 相似文献
12.
This paper discusses the problem of the thermal properties of flame retarding additives based on phosphazene derivatives and of the commercial agents TomflamB, FlammexT23P and StockhausenW-20949, as well as of flame resistant viscose fibers containing the above agents. Results of this investigation showed the action of FlammexT23P, StockhausenW-20949 and phosphazene derivatives at lower temperature. TomflamB acted within a much wider range of temperatures. The flame retardant additives applied to viscose fibers change the thermal properties of the fiber material. 相似文献
13.
Łada T. Przybylski K. Morawski A. Prażuch J. Brylewski T. 《Journal of Thermal Analysis and Calorimetry》2001,64(2):611-615
The fabrication method of superconducting thin films of compositions HgBa2Ca2Cu3O8+δ (Hg-1223) and Tl2Ba2CuOy (2201) on single-crystalline SrTiO3 and LaAlO3 substrates is reported. The highest obtained T
c was 134 K and J
c over 106 A cm–2 at 77 K. High pressure DTA(HP-DTA) was applied to grow mercury- and thallium-based high-temperature superconducting crystals
and thin films, to identify melting points of particular phases within these oxide systems and determine suitable processing
conditions. The DTA system operates at the: maximum temperature of 1200°C, volume up to 5 cm3, working pressure up to 1.5 GPa and at a working atmosphere — inert gas with up to 25% oxygen.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
14.
Pt(II) and Pd(II) dichloride complexes with 5,7-ditertbutyl-1,2,4-triazolo[1,5-a]pyrimidine (dbtp) have been synthesized and characterized by infrared and 1H, 13C NMR, 13C CPMAS spectroscopy. The structures of the cis-PtCl2(dbtp)2 · EtOH (1) and cis-PdCl2(dbtp)(dmso) (2) has been determined by signal-crystal X-ray diffraction. In both complexes the X-ray crystal structures shows that heterocycle ligand (dbtp) binds the central atom monodentate via nitrogen atom N(3). In addition, compound (2) is interesting for its structural features, because it is the first report of mixed dichloride Pd(II) complexes with N-donor (triazolopyrimidine) and S-donor (dimethylsulfoxide) ligands. In this structure the Pd–Cl distances are: 2.302(1) and 2.281(1) Å, Pd–N 2.041(3) Å and Pd–S 2.245(1) Å. The 1H, 13C NMR studies show clearly that these structures are retained in solution. 相似文献
15.
TERESA HŁADOŃ JAN Pawlaczyk BARBARA Szafran 《Journal of inclusion phenomena and macrocyclic chemistry》2000,36(1):1-8
The ibuprofen--cyclodextrin inclusion complex was prepared by theco-precipitation method. The identity of the obtained product was verified by X-ray and thermogravimetric techniques. The effect of -cyclodextrin on the stability of ibuprofen was analysed. 相似文献
16.
Bicrystals of Fe-6 at.% Si alloy containing <001> 5 tilt grain boundaries with a deposited zinc layer have been annealed at various hydrostatic pressure at four temperatures between 700° and 905°C. After the anneals the dihedral angle of the grain boundary groove formed at the site of the grain boundary intersection with the solid-melt interphase boundary has been measured. The transition from complete to incomplete wetting of the grain boundary by the zinc-rich melt (dewetting phase transition) has been found to occur as the pressure increased at all temperatures studied. The temperature dependence of the dewetting transition pressure p
w
has been determined. That dependence has a minimum at a temperature of 790°C, which is close to the peritectic temperature in the Fe–Zn system (782°C). A thermodynamic analysis of the wetting phenomena in the two-component system, based on Becker's regular solution model for the surface tension of the interphase boundary, explains the minimum in the p
w
(T) dependence. 相似文献
17.
Marek Trojanowicz Joanna Szpunar-Łobińska Zdzislaw Michalski 《Mikrochimica acta》1991,103(3-4):159-169
An original computer-controlled solid-state photometer has been developed and its potential for simultaneous multicomponent flow-injection analysis of binary and ternary mixtures is demonstrated. The device is simple in construction. Its principle of operation is based on rapid sequential measurements of the absorbance of the complexes formed by the analytes with chromogenic reagents at the wavelengths corresponding to the emission maxima of three light emitting diodes (563, 580 and 638 nm). 相似文献
18.
S. I. Kozlov G. Łapienis G. V. Rakova K. S. Kazanskii 《Polymer Science Series A》2006,48(10):1022-1034
Soluble comb-shaped and swelling network polymers based on monomethacrylate (M = 2080) and bismethacrylate (M = 4000) poly(ethylene oxide) macromonomers, have been synthesized by the controlled atom-transfer radical polymerization in aqueous media. PEG 2000 methyl ether ethyl-2-bromoisobutyrate and 2-bromoisobutyrate, in combination with CuBr, CuBr2, and 2,2′-bipyridyl, have been used as initiators. The length of the main chain of comb-shaped polymers, as estimated with multidetector chromatography, is in good agreement with the calculated values in the 15–20 range at M w /M n = 1.42–1.89. The polymerization of the methacrylate macromonomer proceeds at a high rate and with a nearly quantitative conversion. The replacement of 10–80 mol % CuBr with CuBr2 appreciably decelerates polymerization and decreases polydispersity to 1.14–1.21, while the experimental and calculated values of chain lengths remain equal. This finding indicates a higher level of process control. The polymer networks thus prepared manifest Gaussian elastic behavior, as is evident from the relationship between the elastic modulus G and the swelling degree Q that is consistent with the classical prediction G ~ Q m , where m = ?1/3. Within the framework of the accepted model of networks of this type, this fact suggests the short length of polymethacrylate chains. In addition, the relationship between the time of attainment of the gelation point and the composition of the initiation system agrees with the atomtransfer controlled polymerization mechanism. The efficiencies of various radical polymerization methods for controlling the network structure are compared. 相似文献
19.
Dagmara Jacewicz Agnieszka Łapińska Aleksandra Dąbrowska Lech Chmurzyński 《Transition Metal Chemistry》2006,31(1):111-117
The kinetics of the reaction between gaseous CO2 and the cis-[Cr(phen)2(OH2)2]3+ ion leading to the formation of the carbonato complex ion, have been studied over the pH and temperature ranges: 3 < pH <
6 and 5 < T < 25 °C, respectively, at a constant ionic strength of 1 m (NaClO4). Investigations were carried out using the stopped-flow spectrophotometry technique in the UV–Vis range: 340–700 nm. The
major reactant species in the pH range studied was cis-[Cr(phen)2(OH)(OH2)]2+ ion, which underwent reaction with CO2 to form cis-[Cr(phen)2(OH2)(HCO3)]2+ ion. Subsequently, slower ring closure of the latter species to form the bidentate carbonato chelate was observed. The possible
mechanism has been discussed and the activation parameters ΔH† and ΔS† were also determined for the reaction studied. 相似文献
20.
Joanna Szpunar-Łobińska Michiel Ceulemans Wilfried Dirkx Claudia Witte Ryszard Łobiński Freddy C. Adams 《Mikrochimica acta》1994,113(3-6):287-298
Interferences in trace and ultratrace speciation analysis of organotin and organolead compounds in various samples by gas chromatography coupled with atomic absorption spectrometry (AAS) and/or microwave induced plasma atomic emission spectrometry (MIP AES) are investigated. Particular attention is given to the effects of matrix co-extractives and reagents impurities introduced during sample preparation. Their influence on the detection limits is discussed in terms of baseline noise level, blank value, formation of artefacts and signal suppression. Loss of column resolution during the analysis of some matrices is observed. 相似文献