The Elastic Continuum Limit of the Tight Binding Model

The authors consider the simplest quantum mechanics model of solids, the tight binding model, and prove that in the continuum limit, the energy of tight binding model converges to that of the continuum elasticity model obtained using Cauchy-Born rule. The technique in this paper is based mainly on spectral perturbation theory for large matrices.

Binding Model and 3D-QSAR of 3-（2-Chloropyrid-5- ylmethylamino）-2-cyanoacrylates as PSⅡ Electron Transport Inhibitor

The binding model of 3-（2-chloropyrid-5-ylmethylamino）-2-cyanoacrylate photosystem Ⅱ （PSⅡ） electron transport inhibitors with the D 1 protein of PSII was built. The high herbicidal activity of this kind of inhibitors was explained by docking studies： in addition to usual factors, the N atom on the pyridine ring could form an H-bond with the backbone amide of Phe265 on the D1 protein. 3D-QSAR analysis on sixteen 3-（2-chloropyrid-5-yl- methylamino）-2-cyanoacrylate compounds was performed using CoMFA method to explain the nature of interactions between the compounds and D1 protein. These studies may provide useful insights for designing new PSII electron transport inhibitors.

Surface brightens up Si quantum dots: direct bandgap-like size-tunable emission

Colloidal semiconductor quantum dots(QDs)constitute a perfect material for ink-jet printable large area displays,photovoltaics,light-emitting diode,bio-imaging luminescent markers and many other applications.For this purpose,efficient light emission/absorption and spectral tunability are necessary conditions.These are currently fulfilled by the direct bandgap materials.Si-QDs could offer the solution to major hurdles posed by these materials,namely,toxicity(e.g.,Cd-,Pb-or As-based QDs),scarcity(e.g.,QD with In,Se,Te)and/or instability.Here we show that by combining quantum confinement with dedicated surface engineering,the biggest drawback of Si—the indirect bandgap nature—can be overcome,and a‘direct bandgap’variety of Si-QDs is created.We demonstrate this transformation on chemically synthesized Si-QDs using state-of-the-art optical spectroscopy and theoretical modelling.The carbon surface termination gives rise to drastic modification in electron and hole wavefunctions and radiative transitions between the lowest excited states of electron and hole attain‘direct bandgap-like’(phonon-less)character.This results in efficient fast emission,tunable within the visible spectral range by QD size.These findings are fully justified within a tight-binding theoretical model.When the C surface termination is replaced by oxygen,the emission is converted into the well-known red luminescence,with microsecond decay and limited spectral tunability.In that way,the‘direct bandgap’Si-QDs convert into the‘traditional’indirect bandgap form,thoroughly investigated in the past.

A molecularly imprinted polymer receptor for the enantiomeric recognition of amino acid hydantoins mimicking cooperative hydrogen bonds between nucleotide bases

Using acrylamide as hydrogen bonding functional monomer and (5R)-5-benzylhydantoin as template, a molecularly imprinted polymer was prepared in a polar solvent, which exhibited good enantiomeric recognition properties. The binding characteristics and selectivity of the polymer were evaluated by batch methods. Scatchard analysis showed that two classes of binding sites were produced in the polymer matrix and their dissociation constants were calculated to be 3.5 × 10?5mol/L and 4.3 × 10?4 mol/L, respectively, by utilizing the model of multiple independent classes of binding sites. These results were more reasonable than those obtained by Scatchard analysis, which was in agreement with the prediction of the binding characteristics of the polymer by exploring the effect of acrylamide on UV spectra of (5R)-5-benzylhydantoin. The substrate and enantio-selectivity of the polymer was investigated. Finally, the study of effect of water on the chiral separation factor of the polymer further proved that the hydrogen bonding interactions played an important role in the recognition of the acrylamide-based molecularly imprinted polymers.