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11.
12.
Summary Mercuric ions may be determined by titration with ethylenedithiodiacetic acid at a wavelength of 260 nm at any pH less than 1. The method is simple, rapid, and selective, and is applicable in solutions of high electrolyte concentration. Mercury(II) can be determined down to 1.5×10–5
M with a relative standard deviation less than 2%.
Zusammenfassung Quecksilber (II) läßt sich mit Äthylendithiodiessigsäure bei 260 nm und pH1 titrieren. Das Verfahren ist einfach, rasch und selektiv. Es läßt sich auch für Lösungen mit hoher Elektrolytkonzentration anwenden. Hg(II)-Konzentrationen über 1,5×10–5 M sind mit einer relativen Standardabweichung unter 2% bestimmbar.相似文献
13.
Let X be a nonsingular complex projective surface and let D be an ample divisor on X such that the associated invertible sheaf is spanned by its global sections. We prove that D is 2-connected apart from a few cases we explicitly describe. We also provide a corresponding result for the 3-connectedness when D210 and for the 4-connectedness when D217 and D is very ample. 相似文献
14.
Mauro Beltrametti 《Annali di Matematica Pura ed Applicata》1987,147(1):151-172
Sunto In questo lavoro si studiano le varietà non singolari di dimensione d il cui divisore canonico non è numericamente effettivo e si estendono alcuni dei risultati ottenuti da Mori nel caso d=3. CiÒ viene ottenuto mediante un uso sistematico della teoria di Mori dei raggi estremali e di un forte teorema di Kawamata-Shokurov. Quest'ultimo risultato fornisce una varietà normale Y e un morfismo : X Y che contrae un raggio estremale R e che dá la struttura di X. Se R è numericamente effettivo, dimY 相似文献
15.
Maurizio Lanfranchi Antonio Tiripicchio Giuliano Giuliano Mauro Ghedini 《Transition Metal Chemistry》1980,5(1):21-25
Summary The structure of [Ir(NCMe)3(NO)(PPh3)2][PF6]2 has been ] determined by x-ray methods. Crystals are orthorhombic, space groupPca 21 , witha = 21.753(14),b = 11.678(10),c = 18.474(12) Å and Z = 4. The structure has been solved from diffractometer data and refined by full-matrix leastsquares to R = 0.076 for 2776 observed reflections. The cation is a hexacoordinate and not a pentacoordinate species as expected. The extra acetonitrile molecule,trans to the nitrosyl ligand, is much more weakly bound to the metal atom [Ir-N 2.360(26) against 1.965(20) and 1.912(14) Å for the other two acetonitriles]. The nitrosyl is bent [Ir-N-O 111(1)° Å] and acts as the formally one-electron donor NO–. 相似文献
16.
Rudovsky J Hermann P Botta M Aime S Lukes I 《Chemical communications (Cambridge, England)》2005,(18):2390-2392
A marked increase of relaxivity has been observed upon rigidifying the internal frame of Gd-containing PAMAM dendrimers: the effect has been attained by either protonation of the dendrimer or by forming supramolecular adducts with cationic polyaminoacids. 相似文献
17.
Luis C. Mendes Andrea D. Tedesco Mauro S. Miranda Marcia R. Benzi Beatriz S. Chagas 《Polymer Testing》2005,24(8):963-968
In this third work, we evaluated the degree of conversion (DC) versus depth of dental filling composite named Prodigy Condensable™ using infrared spectroscopy. Confirming previous results, there was a gradual reduction of DC with increasing depth but the composite exhibited extreme values of DC, an upper value (45.9%) on the surface and a lower one (6.1%) at a depth of 5 mm. The composite presented the worst performance among materials studied. The composite formulation was 80% of inorganic fillers and BisfenolA/dimethacrylate (BisGMA) (18%)/triethyleneglycoldimethacrylate (TEGDMA) (2.0%) as monomers. As stated before, type/ratio/viscosity of monomers and type, amount, size and size distribution of fillers all together had an important role in the cure reaction contributing to the final performance of the composite. 相似文献
18.
Stefano Vecchio Alessia Catalani Vanessa Rossi Mauro Tomassetti 《Thermochimica Acta》2004,420(1-2):99-104
The thermal behaviour of acetanilide (Ac) and two of its analogues, namely the para-ethoxyacetanilide (p-Eto Ac) and the para-bromoacetanilide (p-Br Ac), which are used as analgesics in the pharmaceutical industry was studied with a simultaneous TG/DSC unit. The examined analgesics showed two endothermic DSC peaks due to melting and vaporization. By combining the experimental TG data with the corresponding reference vapour pressure data obtained with the Antoine equation the plot of P versus v was derived. From the slope of this equation the constant k-value was determined for Ac. Then, using the same k-value the vapour pressures of p-Eto Ac and p-Br Ac were determined in the same temperature range. The vaporization enthalpies for all the studied compounds were obtained from different methods and a very good agreement was found. Vaporization follows a zero-order kinetics. The activation energy of vaporization (Evap) was calculated from the dynamic TG experiments, using the Arrhenius equation. 相似文献
19.
Maurizio Lenarda Renzo Ganzerla Adriana Lisini Mauro Graziani Tristano Boschi 《Transition Metal Chemistry》1981,6(4):199-203
Summary Platinum(0) and palladium(0) complexes of the type: P2M(R1R2C=CR3R4) (P=trisubstituted phosphine; R1, R2, R3 and R4 are different groups having electron acceptor or electron donor properties; M=Pt or Pd) with so called pushpull olefins, have been prepared and characterized. In some cases unusual patterns in the n.m.r. spectra of olefinic protons were observed. The spectra were analyzed by computer simulation and general rules for ABMX patterns for this type of complexes are given. 相似文献
20.
Bottamauro M Casellato U Scalco C Tamburini S Tomasin P Vigato PA Aime S Barge A 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(17):3917-3926
Heterodinuclear lanthanide(III)-sodium(I) complexes [LnNa(L)(Cl)(2)(CH(3)OH)] (Ln=La[bond]Nd, Sm[bond]Lu), where H(2)L is a [1+1] asymmetric compartmental macrocyclic ligand containing a N(3)O(2) Schiff base and a O(3)O(2) crown-ether-like coordination site, have been prepared and characterized by IR, (1)H, (13)C, and (23)Na NMR spectroscopy, mass spectrometry, and electron microscopy. In the solid state, the lanthanide(III) ions coordinate the Schiff-base N(3)O(2) site, and the sodium ion occupies the O(3)O(2) crownlike cavity, as shown by the X-ray crystal structures of the Nd, Eu, Gd, and Yb derivatives. In these complexes, the lanthanide(III) ion is coordinated by two chlorine atoms in the trans position and by three nitrogen and two negatively charged phenol oxygen atoms of the Schiff base, and the ion is heptacoordinated with a pentagonal bipyramidal geometry. The sodium ion is coordinated by three etheric oxygen atoms and the two phenolic oxygens that act as a bridge. A methanol molecule is also coordinated in the apical position of the resulting pentagonal pyramidal polyhedron. A detailed (1)H and (13)C NMR study was carried out in CD(3)OD for both diamagnetic and paramagnetic heterodinuclear complexes [LnNa(L)(Cl)(2)(CH(3)OH)]. The complexes are also isostructural in solution, and their structures parallel those found in the solid state. Moreover, some significative distances determined in the solid state and in solution are comparable. Finally, the potential use of these complexes as molecular probes for the selective recognition of specific metal ions has been tested. In particular, their ability to act as shift reagents and the selectivity of the O(3)O(2) site towards Li(+), Ca(2+), and K(+) were investigated by (23)Na NMR spectroscopy. 相似文献