New link between conceptual density functional theory and electron delocalization

In this paper we give a new definition of the softness kernel based on the exchange-correlation density. This new kernel is shown to correspond to the change of electron fluctuation upon external perturbation, thus helping to bridge the gap between conceptual density functional theory and some tools describing electron localization in molecules. With the aid of a few computational calculations on diatomics we illustrate the performance of this new computational tool.     

Selection of a synthetic glycan oligomer from a library of DNA-templated fragments against DC-SIGN and inhibition of HIV gp120 binding to dendritic cells

We report the synthesis of a nucleic acid-encoded carbohydrate library, its combinatorial self-assembly into 37,485 pairs and a screen against DC-SIGN leading to the identification of consensus ligand motifs. A prototypical example from the selected pairs was shown to have enhanced binding. A dendrimer incorporating the selected motifs inhibited gp120's binding to dendritic cells with higher efficiency than mannan.     

A multipurpose gold(I) precatalyst

[Au(tmbn)(2)](SbF(6)) is the first gold(I) complex supported by two nitrile ligands that is indefinitely stable at room temperature. This is a highly versatile precatalyst that can be used for the preparation of active and robust solid-supported gold(I) catalysts.     

Thermal behavior of some vanadyl complexes with flavone derivatives as potential insulin-mimetic agents

Two new complexes having general formula VOL₂·nH₂O [(1) L: 5-hydroxyflavone, n = 1; (2) L: chrysin, n = 4] were synthesized and characterized. Based on IR and electronic data we concluded that studied flavones act as bidentate ligands in complexes with metallic ion coordinated in a square-pyramidal stereochemistry. The thermal analysis (TG, DTA) elucidated the composition and also the number and nature of the water molecules. The thermal behavior also indicated strong interactions between oxovanadium (IV) and these oxygen donor ligands.     

On the reducible character of Haldane-Radić enzyme kinetics to conventional and logistic Michaelis-Menten models

The conceptual and practical issues regarding the reduction of the Haldane-Radi? enzymic mechanism, specific for cholinesterase kinetics, to the consecrated or logistically modified Michaelis-Menten kinetics, specific for some mutant enzymes, are here clarified as due to the limited initial substrate concentration, through detailed initial rate and progress curve analysis, even when other classical conditions for such equivalence are not entirely fulfilled.     

DFT study of structure–properties correlations in [MnTPP][TCNE] quasi-one-dimensional molecular magnets

We report the first band structure calculations of the quasi-one-dimensional [MnTPP][TCNE] compounds (TPP = meso-tetraphenylporphyrinato, TCNE = tetracyanoethylene), based on Density Functional Theory (DFT) methods, in order to interpret the magnetic ordering in these prototypic systems. We compare and contrast the results of broken-symmetry DFT calculations for extended systems, with periodic boundary conditions, and for finite systems, magnetic dimers modeling the actual molecular magnets. By varying systematically the main angles, we are able to determine the geometry dependence of the exchange interaction. Structure–properties correlations in these charge-transfer salts reveal the determinant role of the Mn-(N≡C)_TCNE bond angle on the strength of the ferrimagnetic coupling between the S ₁ = 2 spin located on the Mn^III-porphyrin donor and the S ₂ = 1/2 spin positioned on the cyanocarbon acceptor. When the Mn-(N≡C)_TCNE angle is decreased, the intrachain magnetic coupling strengthens, correlated with the increase in the d_z² - p* d_{{z^{2} }} - \pi * orbital overlap. The exchange coupling constants resulting from DFT calculations of extended systems, with periodic boundary conditions, were found to be consistent with those obtained for the dimers, but systematically smaller. The exchange constants vary strongly with the functional used, hybrid functionals such as B3LYP leading to results that better correlate with the experimental mean-field critical temperatures. The coupling constant varies significantly with the type of broken-symmetry approach, depending on the overlap between magnetic orbitals, but weakly on the basis set once polarization effects are included. The electronic structure calculations for the extended systems provide a density of states consistent with the energy spectrum of the corresponding dimer, allowing for an intuitive explanation of the intrachain ferrimagnetic ordering.     

A material model for cementitious composite materials with an exterior point Eshelby microcrack initiation criterion

A micromechanical model for cementitious composite materials is described in which microcrack initiation, in the interfacial transition zone between aggregate particles and cement matrix, is governed by an exterior-point Eshelby solution. The model assumes a two-phase elastic composite, derived from an Eshelby solution and the Mori–Tanaka homogenization method, to which circular microcracks are added. A multi-component rough crack contact model is employed to simulate normal and shear behaviour of rough microcrack surfaces. The development of the microcrack initiation criterion and the rules adopted for microcrack evolution are a particular focus of the paper. Finally, it is shown, on the basis of several numerical simulations, that the model captures key characteristics of the behaviour of cementitious composites such as concrete.     

A visual proof of a result of Knuth on spanning trees of Aztec diamonds in the case of odd order

The even Aztec diamond AD_n is known to have precisely four times more spanning trees than the odd Aztec diamond OD_n—this was conjectured by Stanley and first proved by Knuth. We present a short combinatorial proof of this fact in the case of odd n. Our proof works also for the more general case of odd-by-odd Aztec rectangles.     

On the classification of complex vector bundles of stable rank

One describes, using a detailed analysis of Atiyah-Hirzebruch spectral sequence, the tuples of cohomology classes on a compact, complex manifold, corresponding to the Chern classes of a complex vector bundle of stable rank. This classification becomes more effective on generalized flag manifolds, where the Lie algebra formalism and concrete integrability conditions describe in constructive terms the Chern classes of a vector bundle. Since deceased.     

The number of spanning trees of plane graphs with reflective symmetry

A plane graph is called symmetric if it is invariant under the reflection across some straight line (called symmetry axis). Let G be a symmetric plane graph. We prove that if there is no edge in G intersected by its symmetry axis then the number of spanning trees of G can be expressed in terms of the product of the number of spanning trees of two smaller graphs, each of which has about half the number of vertices of G.