Infinitely many reducts of homogeneous structures

It is shown that the countably infinite dimensional pointed vector space (the vector space equipped with a constant) over a finite field has infinitely many first order definable reducts. This implies that the countable homogeneous Boolean-algebra has infinitely many reducts.     

Development of a Neutral Diketopyrrolopyrrole Phosphine Oxide for the Selective Bioimaging of Mitochondria at the Nanomolar Level

Development of novel bioimaging materials that exhibit organelle specific accumulation continues to be at the forefront of research interests and efforts. Among the various subcellular organelles, mitochondria, which are found in the cytoplasm of eukaryotic cells, are of particular interest in relation to their vital function. To date, most molecular probes that target mitochondria utilise delocalised lipophilic cations such as triphenylphosphonium and pyridinium. However, the use of such charged motifs is known to be detrimental to the working function of the mitochondrial transmembrane potential and there remains a strong case for development of neutral mitochondrial fluorescent probes. Herein, we demonstrate for the first time the exploitation of diketopyrrolopyrrole-based chemistries for the realisation of a neutral fluorescent probe that exhibits organelle specific accumulation within the mitochondria at the nanomolar level. The synthesised probe, which bears a neutral triphenylphosphine oxide moiety, exhibits a large Stokes shift and high fluorescence quantum yield in water, both highly sought-after properties in the development of bioimaging agents. In vitro studies reveal no interference with cell metabolism when tested for the human MCF7 breast cancer cell and nanomolar subcellular organelle colocalisation with commercially available mitochondrial staining agent Mitotracker Red. In light of its novelty, neutral structure and the preferential accumulation at nanomolar concentrations we anticipate this work to be of significant interest for the increasingly larger community devoted to the realisation of neutral mitochondrial selective systems and more widely to those engaged in the rational development of superior organic architectures in the biological field.     

Thionylimido Complexes

An improved route to d-block and main group NSO complexes is presented including the synthesis of the first antimony(V) complexes, (Ar₃Sb(NSO)₂), and copper examples [CuBipy(PPh₃)NSO]. The structures of eight complexes are reported. The observed variation in M–N–S bond angles is due to the combination of orbital overlap (ligand-to-metal bonding) and the degree of ionicity of the bonding.     

An effective implementation of a modified Laguerre method for the roots of a polynomial

Numerical Algorithms - Two common strategies for computing all roots of a polynomial with Laguerre’s method are explicit deflation and Maehly’s procedure. The former is only a...     

Extending the Family of V4+ S=${{ 1/2 }}$ Kagome Antiferromagnets

The ionothermal synthesis, structure, and magnetic susceptibility of a novel inorganic–organic hybrid material, imidazolium vanadium(III,IV) oxyfluoride [C₃H₅N₂][V₉O₆F₂₄(H₂O)₂] (ImVOF) are presented. The structure consists of inorganic vanadium oxyfluoride slabs with kagome layers of V⁴⁺ S=${{ 1/2 }}$ ions separated by a mixed valence layer. These inorganic slabs are intercalated with imidazolium cations. Quinuclidinium (Q) and pyrazinium (Pyz) cations can also be incorporated into the hybrid structure type to give QVOF and PyzVOF analogues, respectively. The highly frustrated topology of the inorganic slabs, along with the quantum nature of the magnetism associated with V⁴⁺, means that these materials are excellent candidates to host exotic magnetic ground states, such as the highly sought quantum spin liquid. Magnetic susceptibility measurements of all samples suggest an absence of conventional long‐range magnetic order down to 2 K despite considerable antiferromagnetic exchange.     

Inversion twinning in a second polymorph of the hydrochloride salt of the recreational drug ethylone

A second polymorph of the hydrochloride salt of the recreational drug ethylone, C₁₂H₁₆NO₃⁺·Cl⁻, is reported [systematic name: (±)‐2‐ethylammonio‐1‐(3,4‐methylenedioxyphenyl)propane‐1‐one chloride]. This polymorph, denoted form (A), appears in crystallizations performed above 308 K. The originally reported form (B) [Wood et al. (2015). Acta Cryst. C 71 , 32–38] crystallizes preferentially at room temperature. The conformations of the cations in the two forms differ by a 180° rotation about the C—C bond linking the side chain to the aromatic ring. Hydrogen bonding links the cations and anions in both forms into similar extended chains in which any one chain contains only a single enantiomer of the chiral cation, but the packing of the ions is different. In form (A), the aromatic rings of adjacent chains interleave, but pack equally well if neighbouring chains contain the same or opposite enantiomorph of the cation. The consequence of this is then near perfect inversion twinning in the structure. In form (B), neighbouring chains are always inverted, leading to a centrosymmetric space group. The question as to why the polymorphs crystallize at slightly different temperatures has been examined by density functional theory (DFT) and lattice energy calculations and a consideration of packing compactness. The free energy (ΔG) of the crystal lattice for polymorph (A) lies some 52 kJ mol⁻¹ above that of polymorph (B).     

A classification of orbits admitting a unique invariant measure

We consider the space of countable structures with fixed underlying set in a given countable language. We show that the number of ergodic probability measures on this space that are $S_{\infty }$-invariant and concentrated on a single isomorphism class must be zero, or one, or continuum. Further, such an isomorphism class admits a unique $S_{\infty }$-invariant probability measure precisely when the structure is highly homogeneous; by a result of Peter J. Cameron, these are the structures that are interdefinable with one of the five reducts of the rational linear order $(\mathbb{Q},<)$.     

Synthesis and Single Crystal Structures of N-Substituted Benzamides and Their Chemoselective Selenation/Reduction Derivatives

A series of N-aryl-N-(2-oxo-2-arylethyl) benzamides and cinnamides has been prepared. The reaction of the benzamides with Woollins’ reagent, a highly efficient chemoselective selenation/reduction reagent, gave the corresponding N-aryl-N-(arylenethyl) benzoselenoamides in good yields. Five representative single crystal X-ray structures are discussed.     

Bimodules in crossed products of von Neumann algebras

In this paper, we study bimodules over a von Neumann algebra M   in the context of an inclusion M⊆M_?αG$M\subseteq M{?}_{\alpha }G$, where G is a discrete group acting on a factor M by outer ?-automorphisms. We characterize the M  -bimodules X⊆M_?αG$X\subseteq M{?}_{\alpha }G$ that are closed in the Bures topology in terms of the subsets of G  . We show that this characterization also holds for w^?$w^{?}$-closed bimodules when G has the approximation property (AP  ), a class of groups that includes all amenable and weakly amenable ones. As an application, we prove a version of Mercer's extension theorem for certain w^?$w^{?}$-continuous surjective isometric maps on X.     

Comparative study of Euler/Euler and Euler/Lagrange approaches simulating evaporation in a turbulent gas–liquid flow

This study deals with the Reynolds‐averaged Navier–Stokes simulation of evaporation in a turbulent gas–liquid flow in a three‐dimensional duct, focussing on the results obtained by a four‐equation turbulence model within the framework of the Euler/Euler approach for multiphase flow calculations: in addition to the two‐equation k?ε model describing the turbulence of the continuous (C) phase, the computational model employs transport equations for the turbulence kinetic energy of the disperse (D) phase and for the velocity covariance q=〈{u}^D{u}^C〉^D. In the present study, the evaporation model according to Abramzon and Sirignano (Int. J. Heat Mass Transfer 1989; 32 :1605–1618) has been extended by introducing an additional transport equation for a newly defined quantity ā, defined as the phase‐interface surface fraction. This allows the change in the drop diameter to be quantified in terms of a probability density function. The source term in the equation describing the dynamics of the volumetric fraction of the dispersed phase α^D is related to the evaporation time scale τ_Γ. The performance of the new model is evaluated by performing a comparative analysis of the results obtained by simulating a polydispersed spray in a three‐dimensional duct configuration with the results of the Euler/Lagrange calculations performed in parallel. Prior to these calculations, some selected (solid) particle‐laden flow configurations were computationally examined with respect to the validation of the background, four‐equation, eddy‐viscosity‐based turbulence model. Copyright © 2008 John Wiley & Sons, Ltd.