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101.
Enzo Benedetti Francesco Posar Aldo D'Alessio Piergiorgio Vergamini Giovanni Pezzin Maria Pizzoli 《Journal of Polymer Science.Polymer Physics》1985,23(6):1187-1192
Infrared studies of the poly(vinyl chloride) (PVC)/di-n-butylphthalate (DBP) system are reported. Spectra of DBP in different solvents seem to be indicative of the ability of DBP to interact with PVC chains in the same way as with polyesters and of competitive interactions between DBP molecules and DBP with PVC. Plots of the width at half-height of the carbonyl stretching vibration, measured at 25 and at ?180°C, as a function of composition, show a sudden change of slope at about 60% PVC concentration by weight, indicating that above this polymer composition interaction between DBP and PVC dominates that between DBP molecules. This change corresponds to a “singularity” observed in the dependence of the glass transition temperature on composition. 相似文献
102.
E. Milaré F. L. Fertonani A. V. Benedetti M. Ionashiro 《Journal of Thermal Analysis and Calorimetry》2000,59(3):617-624
Thermogravimetry (TG) and other analysis techniques (EDX, SEM, Mapping surface, X-ray diffraction, inductively coupled argon
plasma emission spectroscopy and atomic spectrometry with cold vapor generation) were used to study the reaction of Hg with
Rh. The results permitted the suggestion that, when subjected to heat, an electrodeposited Hg film reacts with Rh to form
intermetallic products with different stabilities, as indicated by at least three mass loss steps. In the first step, between
room temperature and 160°C, only the bulk Hg is removed. From this temperature up to about 175°C, the mass loss can be attributed
to the desorption of a film of metallic Hg. The last step, from 175 to 240°C, can be ascribed to the removal of Hg from a
thin dark film of RhHg2 .
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
103.
Adriano Benedetti Pier G. De Benedetti Antonio C. Fabretti Giancarlo Franchini Corrado Gatti 《Transition Metal Chemistry》1984,9(12):457-460
Summary A series of cobalt(II) and nickel(II) 2-X-1,3,4-thiadiazole complexes (X=Cl or Br) were investigated by electronic, n.m.r., Raman and i.r. spectroscopy, and by thermogravimetric analyses, magnetic moments and conductivity measurements.The complexes havepseudo-tetrahedral or pseudo-octa-hedral stereochemistries with MN2X2 (X=Cl or Br), MN4X2 (X=Cl, Br or O) or MN3O3 chromophores.The ligands are mono- or bi-dentate without involving the sulphur atom. Surprisingly, the chloro-derivative ligand seems to be more nucleophilic than the bromo-analogue.The computed (CNDO/2) molecular orbital indices for the uncomplexed ligands indicate that the coordination sites are the nitrogen atoms.In connection with our previous work(1) on the coordination ability of heterocyclic ligands with interesting biological(2,3) and pharmaceutical(4) properties and containing endocyclic nitrogen and sulphur donor atoms, we have considered the 1,3,4-thiadiazole ring, which is the main framework of a very important class of diuretic drugs, the sulphonamide inhibitors(5) of the zinc m tallo-enzyme carbonic anhydrase.In this study we have investigated the coordination behaviour of the 2-chloro-1,3,4-thiadiazole(ctz) and the 2-bromo-1,3,4-thiadiazole (btz). 相似文献
104.
Semisynthesis of dimeric proteins by expressed protein ligation 总被引:1,自引:0,他引:1
A one-pot synthesis of homodimeric proteins is described. The synthetic strategy is based on a double expressed protein ligation reaction between thioester peptides and a new bis-cysteinyl linker. The protocol was also applied to the synthesis of heterodimers. 相似文献
105.
This paper defines the pressure metric on the Moduli space of Margulis spacetimes without cusps and shows that it is positive definite on the constant entropy sections. It also demonstrates an identity regarding the variation of the cross-ratios. 相似文献
106.
I. Benedetti M.H. Aliabadi G. Davì 《International Journal of Solids and Structures》2008,45(7-8):2355-2376
In this paper a fast solver for three-dimensional BEM and DBEM is developed. The technique is based on the use of hierarchical matrices for the representation of the collocation matrix and uses a preconditioned GMRES for the solution of the algebraic system of equations. The preconditioner is built exploiting the hierarchical arithmetic and taking full advantage of the hierarchical format. Special algorithms are developed to deal with crack problems within the context of DBEM. The structure of DBEM matrices has been efficiently exploited and it has been demonstrated that, since the cracks form only small parts of the whole structure, the use of hierarchical matrices can be particularly advantageous. Test examples presented show that, with the proposed technique, substantial increase in number of elements over the crack surfaces leads only to moderate increases in memory storage and solution time. 相似文献
107.
We give a new definition of the relative topological degree for multimaps compositions of approximable multimaps and continuous map. We apply this notion to prove an existence result for variational inequalities of Stampacchia’s type in finite dimensional vector spaces. Finally we obtain the same results also for multimaps compositions of selectionable multimaps and continuous map. 相似文献
108.
Riassunto Viene presentato un algoritmo atto a verificare se un grafo è domistabile, tale essendo ogni grafo in cui qualsiasi insieme
dominante minimale di nodi è indipendente. L’algoritmo, che implica un numero di confronti polinomiale, rispetto al numero
dei nodi, si basa sulla ricerca di insiemi di nodi dotati di particolari proprietà.
Summary In the present paper an algorithm is proposed which verifies ?domistability? in graphs. A graph is called domistable when each minimal dominating set of nodes is also an independent one. The algorithm, polynomial in the number of nodes, is based on the systematic search for node subsets with particular properties.相似文献
109.
Marcelo Aguiar Carlos André Carolina Benedetti Nantel Bergeron Zhi Chen Persi Diaconis Anders Hendrickson Samuel Hsiao I. Martin Isaacs Andrea Jedwab Kenneth Johnson Gizem Karaali Aaron Lauve Tung Le Stephen Lewis Huilan Li Kay Magaard Eric Marberg Mike Zabrocki 《Advances in Mathematics》2012,229(4):2310-2337
We identify two seemingly disparate structures: supercharacters, a useful way of doing Fourier analysis on the group of unipotent uppertriangular matrices with coefficients in a finite field, and the ring of symmetric functions in noncommuting variables. Each is a Hopf algebra and the two are isomorphic as such. This allows developments in each to be transferred. The identification suggests a rich class of examples for the emerging field of combinatorial Hopf algebras. 相似文献
110.
Johanna Wordsworth Tania M. Benedetti Ali Alinezhad Richard D. Tilley Martin A. Edwards Wolfgang Schuhmann J. Justin Gooding 《Chemical science》2020,11(5):1233
Electrocatalytic nanoparticles that mimic the three-dimensional geometric architecture of enzymes where the reaction occurs down a substrate channel isolated from bulk solution, referred to herein as nanozymes, were used to explore the impact of nano-confinement on electrocatalytic reactions. Surfactant covered Pt–Ni nanozyme nanoparticles, with Ni etched from the nanoparticles, possess a nanoscale channel in which the active sites for electrocatalysis of oxygen reduction are located. Different particle compositions and etching parameters allowed synthesis of nanoparticles with different average substrate channel diameters that have varying amounts of nano-confinement. The results showed that in the kinetically limited regime at low overpotentials, the smaller the substrate channels the higher the specific activity of the electrocatalyst. This is attributed to higher concentrations of protons, relative to bulk solution, required to balance the potential inside the nano-confined channel. However, at higher overpotentials where limitation by mass transport of oxygen becomes important, the nanozymes with larger substrate channels showed higher electrocatalytic activity. A reaction-diffusion model revealed that the higher electrocatalytic activity at low overpotentials with smaller substrate channels can be explained by the higher concentration of protons. The model suggests that the dominant mode of mass transport to achieve these high concentrations is by migration, exemplifying how nano-confinement can be used to enhance reaction rates. Experimental and theoretical data show that under mass transport limiting potentials, the nano-confinement has no effect and the reaction only occurs at the entrance of the substrate channel at the nanoparticle surface.Nanoparticles mimicking the three-dimensional architecture of enzymes where the reaction occurs down a channel isolated from bulk solution, referred here as nanozymes, were used to explore the impact of nano-confinement on electrocatalytic reactions. 相似文献