Complete wetting of curved microscopic channels

We have measured the adsorption of argon films on arrays of microscopic nonlinear cusps and of semicircular channels. In the former case, we observe a distinct crossover from a planarlike to a geometry dependent growth behavior near liquid-vapor bulk coexistence, characterized by a growth exponent chi equal to -0.96+/-0.04 in very good agreement with the predictions of a recent scaling theory [C. Rascon and A. O. Parry, J. Chem. Phys. 112, 5175 (2000)]. The crossover location is also consistent with theory. Instead, on the concave channels we find a much steeper growth near saturation that may signal the formation of two menisci at both sides of the channel bottom.     

DNA Binding Studies and Cytotoxicity of a Dinuclear Pt(II) Diazapyrenium-Based Metallo-supramolecular Rectangular Box

The interaction with native DNA of a 2,7-diazapyrenium-based ligand 1 and its Pt(II) rectangular metallacycle 2 is explored through circular and linear dichroism and fluorescence spectroscopies. The metal-free ligand 1 binds through intercalation, with a binding constant of approximately 5×10(5) M(-1) , whereas the metallacycle 2 binds and bends the DNA with a binding constant of 7×10(6) M(-1) . PCR assays show that metallo-supramolecular box 2 interferes with DNA transactions in vitro whereas the intercalator 1 does not. The metallacycle is active against four human cancer cell lines, with IC(50) values ranging between 3.1 and 19.2?μM and shows similar levels of efficacy, but a different spectrum of activity, to cisplatin.     

Preparation of L-Lyxo-Hexos-5-Ulose Through C-3 Epimerization of Bis-Glycopyranosides of L-Arabino-Hexos-5-Ulose1

Abstract

The unreported title compound and its 2,6-di-O-benzyl derivative have been prepared from methyl β-D-galactopyranoside through a sequence involving the bisglycoside methyl 2,6-di-O-benzyl-5-O-methoxv-β-D-galactopyranoside 8, the precursor of L-orabino-hexos-5-ulose, that was converted to the L-lyxo series by inversion at C-3. The inversion was achieved in acceptable yields by selective triflation, followed by displacement with benzoate, and by an oxidation/reduction sequence. Whereas 2,5-di-O-benzyl-L-lyxo-hexos-5-ulose exists entirely as a mixture of the two anomeric 1,4-furanosic forms, the unprotected hexos-5-ulose involves at equilibrium in CD₃CN/D₂O at least eight tautomers, one of which is predominant.     

Simple one-flask method for the preparation of hydroxamic acids

[reaction: see text] A one-step conversion of carboxylic acids to hydroxamic acids under very mild conditions is described. This simple and efficient method has been applied for the synthesis of enantiopure hydroxamate of alpha-amino acids and peptides.     

Synthesis of 1,8-naphthyridine derivatives. Potential antihypertensive agents. 1

Reaction of substituted 7-chloro-1,8-naphthyridines with N-carbethoxypiperazine gave in good yields the corresponding 7-(4-carbethoxypiperazin-1-yl)-1,8-naphthyridines V as potential antihypertensive agents.     

On a generalization of Kantor's likeable planes

Generalizing an idea of Kantor [7], Johnson and Wilke [5] introduced elusive sets of functions over GF(q) to represent translation planes of order q ² that admit a collineation group of order q ² in the linear translation complement and whose kern contains GF(q). In this paper we determine explicitly all elusive sets for q even. We obtain another translation plane of order 8².Deicated to Professors Adriano Barlotti and Luigi Antonio Rosati on the occasion of their 60th birthdayThis research was supported in part by a grant from the M.P.I. (40% funds).     

Mass spectrometric evidence for collisionally induced removal of H2 from monoanions of 10B nido‐carborane derivatives investigated by electrospray ionization quadrupole linear ion trap and Fourier transform ion cyclotron resonance mass spectrometry

Some newly synthesized ¹⁰B nido‐carborane derivatives, i.e., 7,8‐dicarba‐nido‐undecaborane monoanions ([7‐Me‐8‐R‐C₂B₉H₁₀]^‐K⁺, R = H, butyl, hexyl, octyl and decyl), have been fully characterised and examined by electrospray ionization and Fourier transform ion cyclotron resonance mass spectrometry with liquid chromatographic separation (LC/ESI‐FTICR‐MS). These boron‐containing compounds exhibit abundant molecular ions ([M]^?) at m/z 140.22631 [CB₉H₁₄]^?, m/z 196.28883 [CB₉H₂₂]^?, m/z 224.32032 [CB₉H₂₆]^?, m/z 252.35133 [CB₉H₃₀]^? and m/z 280.38354 [CB₉H₃₄]^? at the normal tube lens voltage setting of ?90 V, which was an instrumental parameter value selected in the tuning operation. Additional [M–nH₂]^? (n = 1?4) ions were observed in the mass spectra when higher tube lens voltages were applied, i.e., ?140 V. High‐resolution FTICR‐MS data revealed the accurate masses of fragment ions, bearing either an even or an odd number of electrons. Collision‐induced dissociation of the [M–nH₂]^? ions (n = 0–4) in the quadrupole linear ion trap (LTQ) analyzer confirmed the loss of hydrogen molecules from the molecular ions. It is suggested that the loss of H₂ molecules from the alkyl chain is a consequence of the stabilization effect of the nido‐carborane charged polyhedral skeleton. Copyright © 2009 John Wiley & Sons, Ltd.