A highly porous interpenetrated metal-organic framework from the use of a novel nanosized organic linker

The initial use of a novel elongated tricarboxylic acid H(3)hmpib in metal-organic framework (MOF) chemistry resulted in a [Zn(4)O(hmpib)(2)] MOF (UCY-1) with pyrite topology. The compound displays a remarkably high internal surface area despite its double-interpenetrated structure as well as high CO(2) uptake and selective adsorption for it over CH(4).     

Are hydrotropes distinct from surfactants?

The physicochemical properties of a homologous series of sodium p-n-alkylbenzoates have been investigated. The objective was to determine whether there is a clear transition point from hydrotropic to surfactant-like behavior with increasing alkyl chain length n, so as to shed clear light on the aggregation mechanism of so-called "hydrotropes". Electrical conductivity measurements were used for a first estimation of the critical aggregation concentrations (cac). As for classical surfactants, log(cac) depends on alkyl chain length n, but two branches of behavior were observed: one having a gradient typical of long chain fatty acid salts and the other with a more shallow dependence. Surface tension (γ) measurements of high purity aqueous solutions were used to generate limiting headgroup areas A(cac), which were in the range (40-50 ?(2)) being consistent with monolayer formation. Small-angle neutron scattering conclusively shows that the lower chain length homologues (classed as hydrotropes) exhibit sharp transitions in aggregation as a function of bulk concentration, typical of regular surfactants. As such, there is little to suggest from this study that hydrotropes differ in association behavior from regular surfactants.     

Micro-immunohistochemistry using a microfluidic probe

A flexible method to extract more high-quality information from tissue sections is critically needed for both drug discovery and clinical pathology. Here, we present micro-immunohistochemistry (μIHC), a method for staining tissue sections at the micrometre scale. Nanolitres of antibody solutions are confined over micrometre-sized areas of tissue sections using a vertical microfluidic probe (vMFP) for their incubation with primary antibodies, the key step in conventional IHC. The vMFP operates several micrometres above the tissue section, can be interactively positioned on it, and even enables the staining of individual cores of tissue microarrays with multiple antigens. μIHC using such a microfluidic probe is preservative of tissue samples and reagents, alleviates antibody cross-reactivity issues, and allows a wide range of staining conditions to be applied on a single tissue section. This method may therefore find broad use in tissue-based diagnostics and in research.     

Critical scaling properties at the superfluid transition of 4He in aerogel

We study the superfluid transition of 4He in aerogel by Monte Carlo simulations and finite size scaling analysis. Aerogel is a highly porous silica glass, which we model by a diffusion limited cluster aggregation model. The superfluid is modeled by a three dimensional XY model, with excluded bonds to sites on the aerogel cluster. We obtain the correlation length exponent nu=0.73+/-0.02, in reasonable agreement with experiments and with previous simulations. For the heat capacity exponent alpha, both experiments and previous simulations suggest deviations from the Josephson hyperscaling relation alpha=2-dnu. In contrast, our Monte Carlo results support hyperscaling with alpha=-0.2+/-0.05. We suggest a reinterpretation of the experiments, which avoids scaling violations and is consistent with our simulation results.     

Anti-Cancer Activity and Phenolic Content of Extracts Derived from Cypriot Carob (Ceratonia siliqua L.) Pods Using Different Solvents

Extracts derived from the Ceratonia siliqua L. (carob) tree have been widely studied for their ability to prevent many diseases mainly due to the presence of polyphenolic compounds. In this study, we explored, for the first time, the anti-cancer properties of Cypriot carobs. We produced extracts from ripe and unripe whole carobs, pulp and seeds using solvents with different polarities. We measured the ability of the extracts to inhibit proliferation and induce apoptosis in cancer and normal immortalized breast cells, using the MTT assay, cell cycle analysis and Western Blotting. The extracts’ total polyphenol content and anti-oxidant action was evaluated using the Folin–Ciocalteu method and the DPPH assay. Finally, we used LC-MS analysis to identify and quantify polyphenols in the most effective extracts. Our results demonstrate that the anti-proliferative capacity of carob extracts varied with the stage of carob maturity and the extraction solvent. The Diethyl-ether and Ethyl acetate extracts derived from the ripe whole fruit had high Myricetin content and also displayed specific activity against cancer cells. Their mechanism of action involved caspase-dependent and independent apoptosis. Our results indicate that extracts from Cypriot carobs may have potential uses in the development of nutritional supplements and pharmaceuticals.     

Structural Insights into the Role of β3 nAChR Subunit in the Activation of Nicotinic Receptors

The β3 subunit of nicotinic acetylcholine receptors (nAChRs) participates in heteropentameric assemblies with some α and other β neuronal subunits forming a plethora of various subtypes, differing in their electrophysiological and pharmacological properties. While β3 has for several years been considered an accessory subunit without direct participation in the formation of functional binding sites, recent electrophysiology data have disputed this notion and indicated the presence of a functional (+) side on the extracellular domain (ECD) of β3. In this study, we present the 2.4 Å resolution crystal structure of the monomeric β3 ECD, which revealed rather distinctive loop C features as compared to those of α nAChR subunits, leading to intramolecular stereochemical hindrance of the binding site cavity. Vigorous molecular dynamics simulations in the context of full length pentameric β3-containing nAChRs, while not excluding the possibility of a β3 (+) binding site, demonstrate that this site cannot efficiently accommodate the agonist nicotine. From the structural perspective, our results endorse the accessory rather than functional role of the β3 nAChR subunit, in accordance with earlier functional studies on β3-containing nAChRs.     

Linear stability diagrams for the shear flow of an Oldroyd-B fluid with slip along the fixed wall

We consider the time-dependent shear flow of an Oldroyd-B fluid with slip along the fixed wall. Slip is allowed by means of a generic slip equation predicting that the shear stress is a non-monotonic function of the velocity at the wall. The complete one-dimensional stability analysis to one-dimensional disturbances is carried out and the corresponding neutral stability diagrams are constructed. Asymptotic results for large values of the elasticity number and finite element calculations are also presented. The instability regimes are within or coincide with the negative-slope regime of the slip equation. The numerical calculations agree with the linear stability results when the size of the initial perturbation is small. Large perturbations may destabilize a linearly stable steady state, leading to a periodic solution. The period and the amplitude of the periodic solutions increase with elasticity. Received: 19 June 1997 Accepted: 22 September 1997     

Rigid sphere molecular model enables an assessment of the pore curvature effect upon realistic evaluations of surface areas of mesoporous and microporous materials

A gas adsorption rigid spheres model (RSM) was incorporated into the CPSM model (corrugated pore structure model) to correlate the pore surface areas obtained from the BET and CPSM methods. The latter is a method simulating the gas sorption hysteresis loop and enables the evaluation of surface areas S(CPSM) through the integration of the pertinent pore size distributions. Thus, S(CPSM) values are inherently influenced by pore curvature. The new CPSM-RSM version estimates surface areas S(CPSMfs) that are independent of pore curvature and can be compared with the pertinent S(BET) values. The RSM exploits the fact that a curved pore surface accommodates fewer molecules, assumed to behave as rigid spheres, than an equal flat one. Thus, the RSM accounts for a higher molecular surface coverage Ac (nm2/molec.) in pores with marked curvature than that (i.e., Af) on a flat surface. The ratio Ac/Af for nitrogen adsorbed on single pore sizes varies in the range Ac/Af = 1.44-1.03 for pore sizes D = 1.5-15 nm, respectively. Also for D = 1.5-5.0 nm the S(CPSMfs) and S(BET) values are lower by approximately 10-45% than the S(CPSM) estimates. From the application of the CPSM-RSM model on several porous materials exhibiting all known types of sorption hysteresis loops, it was confirmed that S(BET) approximately S(CPSMfs) (+/-5%) and (S(CPSM) - S(BET))/S(BET) = 3-68% for the materials examined. In conclusion, the BET method may produce quite conservative surface area estimates for materials exhibiting pore structures with appreciable pore curvature, whereas the CPSM-RSM model can reliably predict both S(CPSM) and S(CPSMfs) = S(BET) values.     

Mercury Porosimetry: Contact Angle Hysteresis of Materials with Controlled Pore Structure

Mercury Porosimetry (MP) hysteresis is a commonly observed phenomenon in which mercury retention disguises further the overall hysteresis picture. This article introduces a new interpretation of the MP hysteresis based on the combined effect of pore structure networking and mercury contact angle variation occurring between the mercury penetration and retraction operations. To distinguish the contribution of each factor the following investigations were carried out. Nitrogen sorption (NP) and MP experiments were performed on samples of an anodic aluminum membrane and the results were interpreted in terms of the Corrugated Pore Structure Model (CPSM), i.e., CPSM-Nitrogen and CPSM-Mercury models, respectively. The simulation of the observed hysteresis data using the CPSM model enabled the evaluation of an identical for the two methods intrinsic pore size distribution (PSD) and cumulative surface area in perfect agreement with the respective BET value. Additionally, the CPSM analysis of data resulted in the evaluation of mercury contact angles, i.e., θ(p)=143 degrees and θ(r)=101.7 degrees for the MP penetration and retraction branches of the hysteresis loop, respectively. Moreover, CPSM-Mercury simulations of literature MP hysteresis data, valid for controlled-pore glasses and nuclepore membranes, led to the evaluation of contact angles, i.e., glasses: θ(p)=143 degrees, θ(r)=100.5-107.5 degrees and nuclepore: θ(p)=143 degrees, θ(r)=118- 121 degrees. The latter values are comparable with relevant literature data and approximate those determined for the anodic aluminum membrane. The CPSM model employed herein proved to be a flexible and reliable model for simulating the pertinent hysteresis loops by combining pore networking and contact angle hysteresis phenomena. Copyright 2001 Academic Press.     

Synthesis, structure, magnetic properties and aqueous solution characterization of p-hydroquinone and phenol iminodiacetate copper(II) complexes

The reaction of Cu2+ acetate monohydrate with 2-[N,N'-bis(carboxymethyl)aminomethyl]-4-carboxyphenol (H4cacp), 2-[N,N-bis(carboxymethyl)aminomethyl]hydroquinone (H4cah) and the dinucleating 2,5-bis[N,N-bis(carboxymethyl)aminomethyl]hydroquinone (H6bicah) in water results in the formation of several Cu2+ species, which are in dynamic equilibrium in aqueous solution and their stability is pH dependent. A systematic crystallographic study of these species was pursued, resulting in the characterization of most of the species. Additional techniques were employed to characterize the molecules in the solid state (infrared spectroscopy) and in solution (UV-vis spectroscopy and electrochemistry). These measurements show that the Cu2+ ions are ligated mainly to the iminodiacetate at pH < 6, exhibiting only weak interactions with the phenol oxygen. At pH > 6, the phenol oxygen was deprotonated and dinuclear-bridged species, from the phenolate oxygen complexes exhibiting a Cu2+ 2O2 core, were isolated. The coordination environment around the copper ions varies between trigonal bipyramidal, tetragonal pyramidal and distorted octahedral geometries. The two unpaired electrons of the Cu2+ ions are found to be antiferromagnetically coupled. A survey of the magnetic and structural properties of the dinuclear phenoxide bridged Cu2+ complexes shows that the strength of the antiferromagnetic coupling is linearly dependent on the Cu-Ophenolate bond lengths, at bond distances below 1.98 angstroms. The effect of the Cu-O-Cu angles on the magnetic properties of the complexes is also discussed.