Synthesis of 1-(4-substituted)benzyl-6-hydroxyisoquinolines with potential activity on NA+,K+-atpase

The synthesis of 1-(4-substituted)benzyl-6-hydroxyisoquinolines, to be evaluated in the displacement of the specific ³H-ouabain binding to Na⁺,K⁺-ATPase, is described. The key step involved a cyclization to the isoquinoline ring under Pictet-Gams conditions which was best performed with the 6-hydroxy group protected as the benzyl ether. When an unsaturated ester group was present in position 4 of the 1-benzyl group, this was best introduced before the cyclization step, since the IIeck reaction on 1-(4-bromobenzyl)-6-hydroxyisoquinoline ( 8 ) with acrylic acid derivatives was not successful in all cases.     

On the instability of the equilibrium for a Lagrangian system with gyroscopic forces

We consider a Lagrangian Differential System (L.D.S.) with Lagrangian function L(q, )=T(q, )+U(q), sufficiently smooth in a neighbourhood of the critical pointq=0 of the potential functionU(q). The kinetic function T(q, ) is a non homogeneous quadratic function of the 's, i.e. the L.D.S. contains the so-called gyroscopic forces. The potential functionU(q) starts with a degenerate (but non zero), semidefinite-negative, quadratic form. Moreover,q=0 is not a proper maximum ofU, and this property has to be recognized in a suitable way. By analizing the problem of the existence of solutions of the L.D.S., which asymptotically tend to the equilibrium solution, (q, )=(0,0), we provide a sufficient criterium for its instability.Work performed under the auspices of M.U.R.S.T. (Ministero dell'Universitá e della Ricerca Scientifica e Tecnologica) and G.N.F.M. (Gruppo Nazionale di Fisica Matematica of the National Research Council (C.N.R.)).     

Unbiased Bayes estimates and improper priors

Given two random variables (X, Y) the condition of unbiasedness states that:E(X |Y=y)=y andE(Y |X=x)=x both almost surely (a.s.). If the prior onY is proper and has finite expectation or non-negative support, unbiasedness impliesX=Y a.s. This paper examines the implications of unbiasedness when the prior onY is improper. Since the improper case can be meaningfully analysed in a finitely additive framework, we revisit the whole issue of unbiasedness from this perspective. First we argue that a notion weaker than equality a.s., named coincidence, is more appropriate in a finitely additive setting. Next we discuss the meaning of unbiasedness from a Bayesian and fiducial perspective. We then show that unbiasedness and finite expectation ofY imply coincidence betweenX andY, while a weaker conclusion follows if the improper prior onY is only assumed to have positive support. We illustrate our approach throughout the paper by revisiting some examples discussed in the recent literature.This work was partially supported by C.N.R. grant N.80.02970.10 (G.C.) and by C.N.R. grant altri interventi (P.V.). A preliminary draft was written while the Authors were visiting the Department of Statistics at Carnegie Mellon University.The paper is the result of close cooperation between the two authors. However subsections 3.1 and 3.3 are mainly due to G.C. while subsection 3.2 and section 4 are mainly due to P.V.     

Synthesis of new tren-based tris-macrocycles. Anion cluster assembling inside the cavity generated by a bowl-shaped receptor

The synthesis of three new tris-macrocycles, containing three [12]aneN(4) (L1), [12]aneN(3)O (L2), or [14]aneN(4) (L3) moieties appended to a tren unit, is reported. The crystal structure of the [(Na(ClO(4))(6)) subset L1(2)H(13)]Na(6)Cl(2)(ClO(4))(12) compound shows the anionic cluster [Na(ClO(4))(6)](5)(-) assembled inside the cavity defined by two bowl-shaped polyammonium receptors, held by multiple charge-charge and hydrogen bond interactions.     

Catalysis in aprotic solvents. Effect of the polarity of the catalyst.

The catalytic constants for the $\text{n}$-butylaminolysis of sultones in aprotic-apolar solvents are linearly correlated with a combination of the hydrogen-bonding parameter and the polarity parameter of the catalyst.     

Controlling the self-assembly of a deoxiguaninosine on mica

We report a tapping mode scanning force microscopy investigation on the growth from solutions of a lipophilic deoxiguanosine derivative on the basal plane of a muscovite mica surface. By varying the chemical composition of the substrate surface it is possible to drive the self-assembly towards either layered thin films, which are very likely to consist of guanosine quartets, or nanoribbons, comprising hydrogen bonded networks. Both these two architectures, which are peculiar to the guanine base itself, are of notable importance for the fabrication of molecular nanowires. Moreover, the first arrangement provides evidence that the guanosine is able to behave as ionophore, thus, suggesting its utilization in the development of solid-state ion selective sensors.     

Investigation of anthropic effects connected with metal ions concentration, organic matter and grain size in Bormida river sediments

An investigation on the sediment composition and grain size was carried out along the Bormida river (Piedmont, Northern Italy). The samples were taken both in the riverbed and on its banks. Multivariate statistical exploratory methods permitted to identify possible sources of primary pollution. In particular, principal component analysis (PCA) showed that there are probably at least three anthropogenic main causes of pollution, one connected with Cr, Ni and Sn, the second with cadmium and the last one with mercury. Some correlations were found between heavy metal ion concentrations and organic matter and/or the sediment grain size. Differences between the samples collected in the riverbed and on the banks were identified and the relationships between the principal components and the distance of the samples from the riverbed and from the hot spot represented by the ACNA industrial site were also analyzed.     

Dielectric Shielding of Ionic Charges in Aqueous Solutions of Different Ionic Strength

The thermodynamic functions of the proton transfer H₂tn²⁺+tn → 2 Htn⁺ (tn = 1,3-diaminopropane) have been determined in aqueous solutions containing different amounts of KCl (0.05 ? μ ? 3.01). The free energy (?ΔG) of the process decreases, whereas the enthalpy (-ΔH) increases with μ. There is reason to believe that the reaction is entirely controlled by the Coulomb forces between the two protonic charges. The electrostatic energy involved can be described in terms of a model incorporating an effective dielectric constant εe, such that δε_e/δμ and δ²ε_e/δμδT are both positive. The polarisation of pure water is produced by orientation of hydrogen-bonded dipole molecules H₂O, whereas the electrolyte solution is polarised in addition by dislocation of the ions K⁺ and Cl^?. Our results demonstrate that the former type of polarisation is much more temperature dependent than the latter.     

Reactivity of 2-methyl-4-(1-pyrrolidinyl)-2H-1,2-benzothiazine 1,1-dioxide towards p-toluenesulphonyl azide

The 2-methyl-2H-1,2-benzothiazin-4-(3H)-one 1,1 dioxide ( 2 ), obtained according to a new, one-pot method, is transformed into the pyrrolidino enamine 3 . Reaction of p-toluenesulphonyl azide with 3 gives, via an unstable triazoline adduct which loses nitrogen, the two isomeric tosylamino derivatives 4 and 5 . The structures have been assigned by exhaustive nmr analysis and some aspects on their formation and chemical behaviour are discussed.     

Inorganic coordination polymers. XIV. Chromium(III) phosphinate perfluorocarboxylate polymers

A series of polymers, {Cr(OH)(OPRR′O)[OOC(CF₂)_nCF(CF₃)₂]}_x has been prepared and studied. The polymers with R = R′ = C₆H₅ are soluble in CCl₂FCClF₂, whereas those with R = CH₃ and R′ = C₆H₅ and with R = R′ = C₈H₁₇ are insoluble in all solvents. Attempts to prepare similar materials without hydroxyl groups gave the polymers {Cr(OH)_r(OPRR′O)_p[OOC(CF₂)_nCF(CF₃)₂]_q}_x with 0 < r < 1. The latter polymers are much more tractable than the former; however they are also less thermally stable. The perfluoro-carboxylate groups in these materials can either be chelating or bridging, depending on the other ligands present.