Open-cage fullerene derivatives having 11-, 12-, and 13-membered-ring orifices: chemical transformations of the organic addends on the rim of the orifice

A novel open-cage [60]fullerene derivative, having two sulfur atoms on the rim of its 13-membered-ring orifice, has been isolated and characterized. Extensive studies on the N-MEM group reactivity of this as well as other previously reported open-cage [60]fullerene derivatives led to several new open-cage [60]fullerene adducts.     

Hydrolysis of imidazole-2-ylidenes

The direct reaction of an imidazole-2-ylidene in a predominantly aqueous environment [about 0.1 M solution in a H(2)O (>60%)/THF solvent system] was investigated for the first time. The reaction yielded a stable solution of the corresponding imidazolium-hydroxide of pH 13, which is in agreement with results from an ab initio molecular dynamics simulation. In contrast, hydrolysis of the carbene in a mainly aprotic environment (>80% THF) gives a hydrogen-bridged carbene-water complex which could be detected by NMR and IR spectroscopies for the first time. This complex converts slowly to two isomeric ring opened products and is at higher water concentration in dynamic equilibrium with the imidazolium hydroxide. A computational mechanistic study of the carbene hydrolysis with a gradually increasing number of water molecules revealed that the imidazolium-hydroxide structure can only be optimized with three or more water molecules as reactants, and with the increasing number of water molecules its stability is increasing with respect to the carbene-water complex. In agreement with the experimental results, these findings point out that solvent stabilization and basicity of the hydroxide ion plays a crucial role in the reaction. With increasing number of water molecules the barriers connecting the reaction intermediates are getting smaller, and the ring opened hydrolysis products can be derived from imidazolium-hydroxide type intermediates. Computational studies on the hydrolysis of a nonaromatic imidazolidine-2-ylidene analogue clearly indicated the analogous ring-opened product to be by 10-12 kcal/mol more stable than the appropriate ion pair and the carbene-water complex, in agreement with the known aromatic stabilization of imidazol-2-ylidenes. Accordingly, these molecules hydrolyze with exclusive formation of the ring-opened product.     

Multiobjective evolutionary algorithms for complex portfolio optimization problems

This paper investigates the ability of Multiobjective Evolutionary Algorithms (MOEAs), namely the Non-dominated Sorting Genetic Algorithm II (NSGA-II), Pareto Envelope-based Selection Algorithm (PESA) and Strength Pareto Evolutionary Algorithm 2 (SPEA2), for solving complex portfolio optimization problems. The portfolio optimization problem is a typical bi-objective optimization problem with objectives the reward that should be maximized and the risk that should be minimized. While reward is commonly measured by the portfolio’s expected return, various risk measures have been proposed that try to better reflect a portfolio’s riskiness or to simplify the problem to be solved with exact optimization techniques efficiently. However, some risk measures generate additional complexities, since they are non-convex, non-differentiable functions. In addition, constraints imposed by the practitioners introduce further difficulties since they transform the search space into a non-convex region. The results show that MOEAs, in general, are efficient and reliable strategies for this kind of problems, and their performance is independent of the risk function used.     

Realignment strategies for awake-monkey fMRI data

Functional magnetic resonance imaging (fMRI) experiments with awake nonhuman primates (NHPs) have recently seen a surge of applications. However, the standard fMRI analysis tools designed for human experiments are not optimal for NHP data collected at high fields. One major difference is the experimental setup. Although real head movement is impossible for NHPs, MRI image series often contain visible motion artifacts. Animal body movement results in image position changes and geometric distortions. Since conventional realignment methods are not appropriate to address such differences, algorithms tailored specifically for animal scanning become essential. We have implemented a series of high-field NHP specific methods in a software toolbox, fMRI Sandbox (http://kyb.tuebingen.mpg.de/~stoewer/), which allows us to use different realignment strategies. Here we demonstrate the effect of different realignment strategies on the analysis of awake-monkey fMRI data acquired at high field (7 T). We show that the advantage of using a nonstandard realignment algorithm depends on the amount of distortion in the dataset. While the benefits for less distorted datasets are minor, the improvement of statistical maps for heavily distorted datasets is significant.     

Dislocations jam at any density

Crystalline materials deform in an intermittent way via dislocation-slip avalanches. Below a critical stress, the dislocations are jammed within their glide plane due to long-range elastic interactions and the material exhibits plastic response, while above this critical stress the dislocations are mobile (the unjammed phase) and the material flows. We use dislocation dynamics and scaling arguments in two dimensions to show that the critical stress grows with the square root of the dislocation density. Consequently, dislocations jam at any density, in contrast with granular materials, which only jam below a critical density.     

5-dimensional braneworld with gravitating Nambu–Goto matching conditions

We continue the investigation of a recent proposal on alternative matching conditions for self-gravitating defects which generalize the standard matching conditions. The reasoning for this study is the need for consistency of the various codimension defects and the existence of a meaningful equation of motion at the probe limit, things that seem to lack from the standard approach. These matching conditions arise by varying the brane–bulk action with respect to the brane embedding fields (and not with respect to the bulk metric at the brane position) in a way that takes into account the gravitational back-reaction of the brane to the bulk. They always possess a Nambu–Goto probe limit and any codimension defect is seemingly consistent for any second order bulk gravity theory. Here, we consider in detail the case of a codimension-1 brane in five-dimensional Einstein gravity, derive the generic alternative junction conditions and find the Z₂$Z_2$-symmetric braneworld cosmology, as well as its bulk extension. Compared to the standard braneworld cosmology, the new one has an extra integration constant which accounts for the today matter and dark energy contents, therefore, there is more freedom for accommodating the observed cosmic features. One branch of the solution possesses the asymptotic linearized LFRW regime. We have constrained the parameters so that to have a recent passage from a long deceleration era to a small today acceleration epoch and we have computed the age of the universe, consistent with current data, and the time-varying dark energy equation of state. For a range of the parameters it is possible for the presented cosmology to provide a large acceleration in the high energy regime.     

Azafullerenes encapsulated within single-walled carbon nanotubes

Methods of insertion of azafullerenes in single-walled carbon nanotubes (SWNTs) at different temperatures were investigated, while the effects of the conditions applied on the structure of azafullerene-based peapods, namely, C59N@SWNTs, were explored. Morphological characteristics of C59N@SWNTs were assessed and evaluated by means of high-resolution transmission electron microscopy (HR-TEM). Pathways and chemical reactions that occur upon encapsulation of C59N within SWNTs were evaluated. Monomeric azafullerenyl radical C59N. as inserted into SWNTs at high temperature, from purified (C59N)2 in the gas phase, can undergo a variety of different transformations forming dimers, oligomers or existing in its monomeric form inside SWNTs due to the stabilization effect by nanotube side walls. However, under milder conditions, that is, at lower temperature, bisazafullerene (C59N)2 can be inserted into SWNTs in its pristine dimeric form.     

(Terpyridine)copper(II)-carbon nanohorns: metallo-nanocomplexes for photoinduced charge separation

New metallo-nanostructured materials of carbon nanohorns (CNHs), within the family of elongated carbon nanotubes, have been prepared by the coordination of copper(II)-2,2':6',2' '-terpyridine (Cu(II)tpy) with oxidized carbon nanohorns (CNHs-COOH). The resulted CNHs-COO-Cu(II)tpy metallo-nanocomplexes have been characterized by diverse analytical spectroscopic tools and cyclic and differential pulse voltammetry. Scanning transmission electron microscopy (STEM), dynamic light scattering (DLS), and energy dispersive X-ray spectroscopy (EDX) measurements have been employed to probe the morphological characteristics and particle-size distribution of CNHs-COO-Cu(II)tpy as well as to investigate the elemental composition of the metallo-nanocomplex. Steady-state and time-resolved fluorescence emission studies have shown efficient fluorescence quenching, suggesting that electron transfer occurs from the singlet excited state of Cu(II)tpy to CNHs. Photoexcitation of Cu(II)tpy resulted in the one-electron reduction of nanohorns with a simultaneous one-electron oxidation of the Cu(II)tpy unit (CNHs(*-)-COO-(Cu(II)tpy)*+) as revealed by transient absorption measurements. The charge-separated state of CNHs(*-)-COO-(Cu(II)tpy)*+ has been confirmed with the aid of an electron mediator, such as hexyl-viologen dication (HV2+) and an electron-hole shifter in polar solvents.     

Liquid chromatography and ultra-performance liquid chromatography-mass spectrometry fingerprinting of human urine: sample stability under different handling and storage conditions for metabonomics studies

Typically following collection biological samples are kept in a freezer for periods ranging from a few days to several months before analysis. Experience has shown that in LC-MS-based metabonomics research the best analytical practice is to store samples as these are collected, complete the sample set and analyse it in a single run. However, this approach is prudent only if the samples stored in the refrigerator or in the freezer are stable. Another important issue is the stability of the samples following the freeze-thaw process. To investigate these matters urine samples were collected from 6 male volunteers and analysed by LC-MS and ultra-performance liquid chromatography (UPLC)-MS [in both positive and negative electrospray ionization (ESI)] on the day of collection or at intervals of up to 6 months storage at -20 degrees C and -80 degrees C. Other sets of these samples underwent a series of up to nine freeze-thaw cycles. The stability of samples kept at 4 degrees C in an autosampler for up to 6 days was also assessed, with clear differences appearing after 48h. Data was analysed using multivariate statistical analysis (principal component analysis). The results show that sample storage at both -20 and -80 degrees C appeared to ensure sample stability. Similarly up to nine freeze thaw cycles were without any apparent effect on the profile.     

Hydrogen on hybrid MoS2/graphene nanostructures

Transition metal dichalcogenides are rising candidates for the replacement of Pt catalysts in water splitting. In this theoretical study we focus on the hydrogen evolution reaction part of this process and on how hydrogen (H) interacts with MoS₂ nanostructures, free‐standing or positioned on a graphene substrate. Density functional theory calculations confirm the stability of such nanostructures and our results for H on several configurations, from 2D infinite monolayers to quasi‐1D MoS₂ ribbons and quasi‐0D MoS₂ flakes, are presented. We calculate the adsorption energy of H atoms on various sites of the MoS₂ nanostructures, notably at Mo and S active edges. Comparing free‐standing and MoS₂/graphene hybrid systems we find that the effect of the support on the adsorption of H on MoS₂ nanostructures is quite significant when the substrate induces strain. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)