Influence of ligand shape and steric hindrance on the composition of the nanocrystal ligand shell

Organic ligands play a key role in the synthesis of colloidal semiconductor nanocrystals or quantum dots. Generally they consist of a functional group and an aliphatic chain, with carboxylic acids, thiols and phosphonic acids as typical examples. The functional group ensures the binding to the nanocrystal surface, while the stability of the dispersion strongly depends on the interactions between the organic chains of the adjacent ligands. A number of studies already addressed the binding strength and the type of binding between the nanocrystal surface and the ligand yet none discuss the effect of the organic chain on the ligand exchange. By means of NMR spectroscopy, we examine the ligand shell composition of CdSe nanocrystals originally capped with oleic acid (OA), when exposed to a linear carboxylic acid. Regardless of chain length, we see a one-to-one exchange between the carboxylic acids. The composition of the ligand shell closely matches that of the ligand mixture in solution, indicating that the ligand shell can be seen as an ideal mixture of both ligands. As a consequence, a mixed ligand shell can easily be prepared by adding a ligand mixture with desired composition to the nanocrystal dispersion. On the other hand, when the CdSe nanocrystals are exposed to a branched carboxylic acid with two long aliphatic chains, like 2-hexyldecanoic acid, the ligand shell mainly consists of OA moieties. We interpret these results using an exchange process where the incoming ligand not only displaces oleic acid but also occupies additional space in the ligand shell to accommodate both aliphatic chains. Hence, given a one-for-one exchange reaction, steric hindrance in a fully packed ligand shell will prevent complete ligand exchange. These results can be very useful in view of producing nanocrystals with lower ligand densities by means of synthesis with these branched carboxylic acids

Atomically Precise Nanocrystals

Nanocrystals are a state-of-matter in the border area between molecules and bulk materials. Unlike bulk materials, nanocrystals have size-dependent properties, yet the question remains whether nanocrystal properties can be analyzed, understood, and controlled with atomic precision, a key characteristic of molecules. Acknowledging the inclination of nanocrystals to form defect structures, we first outline the prospects of atomically precise analysis. A broad spectrum of analytical methods has become available over the last five years, such that for heterogeneous nanocrystal ensembles, a single, atomically precise representative structure can be determined to explore structure-property relations. Atomically precise synthesis, on the other hand, remains an outstanding challenge that may well face fundamental limitations. However, to amplify properties and prepare nanocrystals for specific applications, full atomic precision may not be needed. Examples of an atomic precision light approach, focusing on exact thickness or facet control, exist and can inspire scientists to explore atomic precision in nanocrystal research further

Use of nile blue-doped silica nanoparticles as labels in heterogeneous immunoassays for antibiotic determination

III Encuentro sobre Nanociencia y Nanotecnología de Investigadores y Tecnólogos Andaluce

Long-wavelength homogeneous fluoroimmunoassay for the veterinary antibiotic monensin using nile-blue doped silica nanoparticles

II Encuentro sobre nanociencia y nanotecnología de investigadores y tecnólogos de la Universidad de Córdoba. NANOUC

iSLIM: a comprehensive approach to mapping and characterizing gene regulatory networks

Mapping gene regulatory networks is a significant challenge in systems biology, yet only a few methods are currently capable of systems-level identification of transcription factors (TFs) that bind a specific regulatory element. We developed a microfluidic method for integrated systems-level interaction mapping of TF-DNA interactions, generating and interrogating an array of 423 full-length Drosophila TFs. With integrated systems-level interaction mapping, it is now possible to rapidly and quantitatively map gene regulatory networks of higher eukaryote

Quantum Rod Emission Coupled to Plasmonic Lattice Resonances: A Collective Directional Source of Polarized Light

We demonstrate that an array of optical antennas may render a thin layer of randomly oriented semiconductor nanocrystals into an enhanced and highly directional source of polarized light. The array sustains collective plasmonic lattice resonances which are in spectral overlap with the emission of the nanocrystals over narrow angular regions. Consequently, different photon energies of visible light are enhanced and beamed into definite directions.Comment: 4 pages, 3 figure

Health-related costs in a sample of premenopausal non-diabetic overweight or obese females in Antwerp region : a cost-of-illness analysis

Background: People with overweight or obesity are at increased risk for disease later in life which cause important health costs. The aim of this study was to estimate the health status and the corresponding costs in a sample of females with overweight or obesity which were participating in a Randomized Controlled Trial (RCT) exploring the effect of lifestyle habits changes on ectopic adipose tissue. Methods: Sixty-two non-diabetic premenopausal females without major comorbidities of overweight and obesity were recruited among patients visiting endocrinologists at the obesity clinic of the University Hospital of Antwerp and the University of Antwerp. A RCT-embedded cost-of-illness approach with societal perspective, based on self-reported questionnaires and cost diaries (3 months recall) was applied to estimate the prevalence of different comorbidities and the related direct and indirect costs in this sample of overweight or obese females. The European Quality-of-Life-5D questionnaire was used to define the health state and the corresponding utility index of the participants. Results: The average direct health costs and health utilities observed in this sample were comparable with the general Flemish female population. This may partially be explained by the strict inclusion criteria of the RCT (i.e. overweight or obesity without diabetes type 2 or cardiovascular diseases). However, 15% of the participants had five or more comorbidities resulting in higher average costs and lower average health utility as compared to the general population, only 3 participants were diagnozed with the metabolic syndrome. In this subsample productivity was low due to high average absenteeism, yielding important total costs for the society. Conclusion: Secondary prevention to avoid health deterioration in overweight or obese females without major comorbidies is needed to contain health care costs. Trial registration: ClinicalTrials.gov: NCT02831621, approval of the ethics committee of the University Hospital of Antwerp (number: 14/17/205 -ref: 7543075363)

Casein genetic variants in ovine Merino breed

The genetic polymorphism on Merina ewe milk was investigated, using polyacrylamide gel electrophoresis at pH 8.6 and ultra thin-layer isoelectric focusing techniques, according to Krause et al. (1988), and Chianese et al. (1992). The casein fractions identified were: - Seven as1-casein phenotypes: CC, BB, BC, AB, AC, BD and CD (Chianese et al.,1996). - Three as2-casein phenotypes, provisionally nominated F, S, and I. - Three b-casein phenotypes, also provisionally nominated K, L and M, because their genetic segregation is not well known yet. The phenotypical distribution of the observed casein fractions and their adjustment to a normal distribution is presented.El polimorfismo genético de la leche de oveja Merina fue investigado mediante electroforesis en gel de poliacrilamida a pH 8,6 (PAGE) e isoelectroenfoque en gel ultrafino (UTLIEF), siguiendo las técnicas descritas por Krause et al. (1988) y Chianese et al. (1992). Dentro de las fracciones caseínicas se identificaron siete fenotipos de as1-caseína (CC, BB, BC, AB, AC, BD y CD), según la nomenclatura establecida por Chianese et al. (1996). Mientras que, a nivel de as2- y b-caseína se han observado tres perfiles electroforéticos, denominados provisionalmente F, S e I; K, L y M respectivamente, ya que no se conoce su segregación genética. Se presenta la distribución fenotípica de las fracciones caseínicas estudiadas, así como su ajuste a la distribución normal