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11.
Hereditarily finite sets and hypersets are characterized both as algorithmic data structures and by means of a first-order axiomatization which, despite being rather weak, suffices to make the following two problems decidable:
- (1) Establishing whether a conjunction r of formulae of the form: ? y1 ?? ym((y1?W1& ?&ym ?Wm) ←q), with q quantifier-free and involving only the relators =, ? and propositional connectives, and each yi distinct from all wj's, is satisfiable.
- (2) Establishing whether a formula of the form ? y q, q quantifier-free, is satisfiable.
12.
Paolesse R Monti D La Monica L Venanzi M Froiio A Nardis S Di Natale C Martinelli E D'Amico A 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(11):2476-2483
Porphyrin diad 1 was synthesized by reaction of the acyl chloride of porphyrin 2 and trans-1,2-dithiane-4,5-diol. The Co complex of this diad was studied as a potential enantioselective receptor for chiral recognition in solution and in the solid state. In solution both enantiomers of limonene induce significant changes in the visible and circular dichroism (CD) spectra of [Co2(1)], while a different behavior is observed in the case of the enantiomeric pair of trans-1,2-diaminocyclohexane. A different efficiency of [Co2(1)] chiral recognition is obtained for these compounds, with a remarkable degree of enantiodiscrimination observed in the case of limonene. Self-assembled monolayers of [Co2(1)] were deposited onto the gold electrodes of quartz crystal microbalances to be used as sensing materials of nanogravimetric sensors operating in the gas phase. The enantiodiscrimination properties of these sensors towards the enantiomeric pairs of chiral analytes have been studied. While in the case of analytes bearing donor ligand atoms we did not observe a remarkable enantioselectivity, a significant degree of chiral discrimination was observed in the case of limonene; this result is particularly encouraging for the potential development of enantioselective chemical sensors for use in an array configuration. 相似文献
13.
David D. Díaz Henk J. Bolink Luca Cappelli Eugenio Coronado 《Tetrahedron letters》2007,48(27):4657-4660
A series of new light emitting subphthalocyanines, lower homologues of phthalocyanines, were synthesized having color points covering the red-orange region of the visible spectrum. Additionally, they were found to be of potential use as narrow band emitters for red-light emitting diodes. 相似文献
14.
Guido Barone Giuseppina Castronuovo Vittorio Crescenzi Vittorio Elia Eugenio Rizzo 《Journal of solution chemistry》1978,7(3):179-192
In order to clarify some aspects of the hydrophobic interactions, the enthalpies of dilution of monoethylurea, 1,3-dimethylurea,
and 1,3-diethylurea have been determined calorimetrically at 25°C. The calorimetric data, expressed in terms of excess enthalpy,
permit the evaluation of the pair and triplet interaction coefficients. The analyses of these and of the analogous coefficientsg
xx andg
xxx, derived from osmotic data, indicate a driving force favorable to the interactions among the hydrated solute molecules. Nevertheless,
the positive values of theh
xx andh
xxx coefficients seem to suggest that the source of the effect is a rearrangement of the water molecules rather than a direct
association of the solute molecules. There are evidences of a strict correlation between the enthalpic and the entropic effects.
Preliminary data were presented at the International Conferences on Chemical Thermodynamics at Baden (1973) and Montpellier
(1975). The experimental part was carried out at the Istituto Chimico of the University of Trieste.
To whom correspondence should be addressed. 相似文献
15.
Zamudio-Rivera LS George-Tellez R López-Mendoza G Morales-Pacheco A Flores E Höpfl H Barba V Fernández FJ Cabirol N Beltrán HI 《Inorganic chemistry》2005,44(15):5370-5378
The one pot reaction of salicylaldehyde 1, beta-amino alcohols 2a-2c, and di-n-butyltin(IV) oxide 3a or diphenyltin(IV) oxide 3b produced five diorganotin(IV) compounds, 4a-4c, 5a, and 5c, in good yields. All compounds were characterized by IR, (1)H, (13)C, and (119)Sn NMR spectroscopy, and elemental analysis; furthermore, compounds 4b, 4c, 5a, and 5c were characterized by X-ray diffraction analysis. After the structural characterization, all of the compounds were tested in vitro against Bacillus subtilis (Gram-positive, strain ATCC 6633), Escherichia coli (Gram-negative, strain DH5alpha), Pseudomonas aeruginosa (Gram-negative, strain BH3), Desulfovibrio longus (strain DSM 6739), and Desulfomicrobium aspheronum (strain DSM 5918) to assess their antimicrobial activity. Compounds 4 and 5 demonstrated a wide range of bactericidal activities against the tested aerobic (one Gram-positive and two Gram-negative subtypes) and anaerobic bacteria (two sulfate-reducing bacteria, SRB). Compound 5 had better bactericidal performances than compound 4. For all of the compounds, the acute toxicity was measured using luminescent bacteria toxicity (LBT-Microtox) tests to track their further environmental impact. According to these results and in order to fulfill environmental regulations, the toxicity of the compounds studied herein can be modulated through the proper selection of the disubstituted tin(IV) moiety. 相似文献
16.
Alessandro D'Aprano Dorina I. Donato Eugenio Caponetti 《Journal of solution chemistry》1979,8(2):135-146
Dielectric constants (measured at 1 MHz) are reported for solutions of water (concentration range 0 to 0.2 mole fraction)
in 1-propanol at 25°C, and in 1-butanol, 1-pentanol, and 1-hexanol at 15, 25, 35, and 45°C. These results, together with literature
values for solutions of water in methanol, ethanol, 1-heptanol, and 1-octanol, show that water interacts with alcohols in
at least two ways: (1) it can participate in the formation of dynamic hydrogen-bonded chains, thereby raising the polarizability;
(2) it can form relatively stable structures such as H2O(ROH)4 which have zero net dipole moment and consequently diminish volume polarizability. For C
n
H
2n+1
OH alcohols,n≥4, most of the initially added water forms complexes: consequently, addition of water to these alcohols lowers the dielectric
constant. 相似文献
17.
Guillermo Restrepo Eugenio J. Llanos Héber Mesa 《Journal of mathematical chemistry》2006,39(2):401-416
We carried out a mathematical study of 72 chemical elements taking advantage of the chemotopological method. We selected 128
properties to define the elements (physico-chemical, geochemical and chemical properties). Then, we looked for correlated
properties and we reduced the number of them to 90. In this way we defined each element as a 90-tuple. Afterwards, we applied
principal component analysis and cluster analysis (4 similarity functions and 5 grouping methodologies). Then, we calculated
a consensus tree for the 20 dendrograms generated by the CA. Afterwards, we extracted the similarity relationships from the
consensus tree and built up a basis for a topology on the set of chemical elements. Finally, we calculated some topological
properties (closures, derived sets, boundaries, interiors and exteriors) of several subsets of chemical elements. We found
that alkali metals, alkaline earth metals and noble gases appear not related to the rest of the elements. Also, we found that
the boundary of non-metals are the semimetals with a stair-shape on the periodic table 相似文献
18.
Miguel Clemente-León Eugenio Coronado Carlos J. Gómez-García Eugenia Martínez-Ferrero 《Journal of Cluster Science》2002,13(3):381-407
The use of polyoxometalates (pOM's) as inorganic component in the synthesis of new molecular hybrid materials is presented. Here we show that the combination of organic molecules of the tetrathiafulvalene (TTF) type or perylene (per) with POM's yields new radical salts with unprecedented structures that present interesting magnetic and/or electrical properties or coexistence of both. The first true metallic radical salt containing a POM has been prepared and characterized. We also describe the recent results obtained by combining magnetic POM's with the organometallic cation decamethylferrocene. 相似文献
19.
Coronado E Gómez-García CJ Nuez A Romero FM Rusanov E Stoeckli-Evans H 《Inorganic chemistry》2002,41(18):4615-4617
The combination of hexacyanoferrate(III) anions, [Fe(CN)(6)](3)(-), with nickel(II) complexes derived from the chiral ligand trans-cyclohexane-1,2-diamine (trans-chxn) affords the enantiopure layered compounds [Ni(trans-(1S,2S)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (1) and [Ni(trans-(1R,2R)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (2). These chiral systems behave as ferromagnets (T(c) = 13.8 K) with a relatively high coercive field (H(c) = 0.17 T) at 2 K. They also exhibit an unusual magnetic behavior at low temperatures that has been attributed to the dynamics of the magnetic domains in the ordered phase. 相似文献
20.
Aresta M Tommasi I Quaranta E Fragale C Mascetti J Tranquille M Galan F Fouassier M 《Inorganic chemistry》1996,35(14):4254-4260
Extended labeling experiments have shown that formation of rhodium peroxocarbonate from CO(2) and [RhCl(eta(2)-O(2))(P)(3)] (P is PEt(2)Ph or PEtPh(2)) proceeds through O-O bond cleavage and CO(2) insertion. O-transfer to ancillary phosphine ligand to give R(3)P=O selectively (>85%) involves the Rh-linked O atom of the peroxo group of RhCl(CO(4))(P)(3). 相似文献