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排序方式: 共有418条查询结果,搜索用时 15 毫秒
1.
F. S. de Aguiar L. B. Bernardes S. Goulart Rosa Jr. 《Journal of statistical physics》1991,64(3-4):673-682
Metastability in the ferromagneticp-state Potts model defined on the Cayley tree is discussed. It is shown that the sign of the boundary fieldH
s
determines the order of the transition as well as the stability of the low-temperature phase. Lowering the temperature withH
s
>0, a system withp<2 (p>2) will display a second (first)-order transition to a metastable (stable) phase. ForH
s
>0 a second (first)-order transition to a metastable (stable) phase occurs ifp>2 (p<2). In this case the system also has a residual entropy which is negative forp<2. 相似文献
2.
The asymptotic null distribution of the likelihood ratio test for two cases of ordered hypotheses in a particular genetic model is considered. A simple iterative process is proposed in order to get the restricted estimates. It is shown that both tests have asymptotically a chi-bar squared distribution and the same size. A simulation study is also conducted in order to compare the usual unrestricted test with the corresponding one of ordered hypotheses. Finally, the results are extended to some special cases. 相似文献
3.
Gilberto Dini Angela Selvaggi Primicerio 《Rendiconti del Circolo Matematico di Palermo》1989,38(1):60-64
LetR be a Reinhardt domain andD a bounded simply connected strictly pseudoconvex domain withC ∞ boundary. We prove that any proper holomorphic mapF:R →D is, up to biholomorphism ofD, of the form \((z_1^{d_1 } , z_2^{d_2 } , \ldots , z_n^{d_n } )\) withd 1,d 2,…,d n ∈ IN. 相似文献
4.
Cesarino Balsamini Gilberto Spadoni Annalida Bedini Giorgio Tarzia Maurizio Lanfranchi Maria Angela Pellinghelli 《Journal of heterocyclic chemistry》1992,29(6):1593-1598
The alkyl N-(diphenylmethylene)-α,β-dehydroamino acids 1 have been submitted to 1,3-dipolar cycloadditions with nitrile oxides. The reactivity of these compounds depends on the type and on the stereochemistry of the β-substituents. With the unsubstituted terms 1a,b the reaction occurs on the C,C double bond, providing a good method for the synthesis of the 4,5-dihydroisoxazole derivatives 3a,b,c and for the gem-functionalized 4,5-dihydroisoxazoles amino carboxylic ester 5. The β-substituted compounds 1c,d,e , inert to 1,1-dimethylethylnitrile oxide, undergo the reaction to the N,C double bond, thus giving with 2a,b the 4,5-dihydro-1,2,4-oxadiazole derivatives 4. All the reactions occur with high site- and regioselectivity. 相似文献
5.
6.
Gilberto Schiavon Gianni Zotti Gino Bontempelli 《Journal of Electroanalytical Chemistry》1984,161(2):323-335
The electrochemical reduction of [Ni(PPh3)2(p-C6H4Br)Br] in acetonitrile results in a polymeric coating of a nickel-containing poly-p-phenylene, formulated as [-Ni(p-C6H4)n-] (n=6?7) on the basis of elemental analysis, IR, UV, MS and ESCA measurements. This coating is found to undergo a two-electron reversible reduction and a one-electron reversible oxidation with a large potential window (3.6 V), without the polymeric film being destroyed. Moreover, the polymer obtained is shown to be electroactive towards dissolved reactants via permeation or mediated electron transfer, depending on the molecular size of the electroactive species employed. 相似文献
7.
8.
Gino Bontempelli Franco Magno Benedetto Corain Gilberto Schiavon 《Transition Metal Chemistry》1985,10(1):8-11
Summary The reduction of nickel perchlorate in the presence of carbon monoxide and substituted phosphines or diphosphines has been studied in acetonitrile by cyclic voltammetry. The results show that only mono- and bis-carbonylphosphinenickel(O) complexes are formed, while no evidence for the formation of carbonyl-nickel(I) and -nickel(II) species was obtained. Although the oxidation processes are not reversible, a good correlation between the anodic peak potentials relative to nickel(O) complexes and the -donor--acceptor abilities of the phosphines employed was observed. 相似文献
9.
Rosanna Toniolo Alan Valentino G. Bontempelli Gilberto Schiavon 《Fresenius' Journal of Analytical Chemistry》1998,360(2):260-262
A simple method for the analysis of nanoliter droplets is proposed, which is profitable when larger samples cannot be collected
as, for instance, in the case of several biological fluids and particularly in clinical chemistry. A glass capillary associated
to a micromanipulator is used to collect submicroliter volumes which are partially transferred into transparent polymeric
tubings with known internal diameters (120–178 μm), where the volumes sampled are measured by meniscus collimations with a
collimator microscope at suitable magnification. Both ends of these tubings are preliminarily equipped with ferrules and fittings,
so as to make them suitable for connection as the loop to a conventional high-pressure injection valve. The reliability of
this procedure has been tested for the analysis of Na+, K+ and Ca2+ present in minute synthetic standard samples (10–200 nL) by a conventional ion-chromatographic instrumentation. Relative
standard deviations in peak area measurements (5–6%) are discussed in terms of the whole approximation affecting volume measurements,
which depends on both the inconstancy of the inner diameter of the polymeric tubings employed and the uncertainty characterizing
meniscus collimations. The proposed procedure can be easily extended to the determination of any organic or inorganic species
present in very small samples, provided that their detection can be achieved by any chromatographic approach or, more generally,
by flow injection analysis.
Received: 16 June 1997 / Revised: 12 August 1997 / Accepted: 14 August 1997 相似文献
10.
Iris A. Bermejo Claudio D. Navo Jorge Castro-Lpez Ana Guerreiro Ester Jimnez-Moreno Elena M. Snchez Fernndez Fayna García-Martín Hiroshi Hinou Shin-Ichiro Nishimura Jos M. García Fernndez Carmen Ortiz Mellet Alberto Avenoza Jesús H. Busto Gonalo J. L. Bernardes Ramn Hurtado-Guerrero Jesús M. Peregrina Francisco Corzana 《Chemical science》2020,11(15):3996
The Tn antigen (GalNAc-α-1-O-Thr/Ser) is a well-known tumor-associated carbohydrate determinant. The use of glycopeptides that incorporate this structure has become a significant and promising niche of research owing to their potential use as anticancer vaccines. Herein, the conformational preferences of a glycopeptide with an unnatural Tn antigen, characterized by a threonine decorated with an sp2-iminosugar-type α-GalNAc mimic, have been studied both in solution, by combining NMR spectroscopy and molecular dynamics simulations, and in the solid state bound to an anti-mucin-1 (MUC1) antibody, by X-ray crystallography. The Tn surrogate can mimic the main conformer sampled by the natural antigen in solution and exhibits high affinity towards anti-MUC1 antibodies. Encouraged by these data, a cancer vaccine candidate based on this unnatural glycopeptide and conjugated to the carrier protein Keyhole Limpet Hemocyanin (KLH) has been prepared and tested in mice. Significantly, the experiments in vivo have proved that this vaccine elicits higher levels of specific anti-MUC1 IgG antibodies than the analog that bears the natural Tn antigen and that the elicited antibodies recognize human breast cancer cells with high selectivity. Altogether, we compile evidence to confirm that the presentation of the antigen, both in solution and in the bound state, plays a critical role in the efficacy of the designed cancer vaccines. Moreover, the outcomes derived from this vaccine prove that there is room for exploring further adjustments at the carbohydrate level that could contribute to designing more efficient cancer vaccines.An anti-cancer vaccine based on an unnatural antigen with an sp2-iminosugar fragment. 相似文献