[2,6‐(Trip)2H3C6 ](Cp*)Si: A Stable Monomeric Arylsilicon(II) Compound

Si takes a rest : A bulky σ‐bound terphenyl substituent and a π‐bound Cp* ligand enable the isolation and full characterization of the first aryl‐substituted, monomeric silicon(II) compound 1 , which can be regarded as the “resting state” of a true silylene containing a σ‐bound Cp* group. The conformation of the aryl group prevents aryl–Si π back‐bonding.

     

Regular patterns stabilize auditory streams

The auditory system continuously parses the acoustic environment into auditory objects, usually representing separate sound sources. Sound sources typically show characteristic emission patterns. These regular temporal sound patterns are possible cues for distinguishing sound sources. The present study was designed to test whether regular patterns are used as cues for source distinction and to specify the role that detecting these regularities may play in the process of auditory stream segregation. Participants were presented with tone sequences, and they were asked to continuously indicate whether they perceived the tones in terms of a single coherent sequence of sounds (integrated) or as two concurrent sound streams (segregated). Unknown to the participant, in some stimulus conditions, regular patterns were present in one or both putative streams. In all stimulus conditions, participants' perception switched back and forth between the two sound organizations. Importantly, regular patterns occurring in either one or both streams prolonged the mean duration of two-stream percepts, whereas the duration of one-stream percepts was unaffected. These results suggest that temporal regularities are utilized in auditory scene analysis. It appears that the role of this cue lies in stabilizing streams once they have been formed on the basis of simpler acoustic cues.     

Modification of acrylic bone cements by poly(ethylene glycol) with different molecular weight

The high polymerization temperature of acrylic bone cements can cause arthroplasty failure because of the thermal necrosis of surrounding bone tissue. To reduce this undesired effect we have developed novel acrylic bone cement composites containing a phase change material (PCM). As PCM poly(ethylene glycol) (PEG) of different molecular weight was applied and the effect of its incorporation on curing parameters, mechanical and morphological properties of acrylic bone cement was investigated. A significant decrease in maximum temperature from 65.8°C to 47.4°C and slight increase of setting time were observed. PEG introduction also contributed to the thermal stability of acrylic bone cement increase. SEM investigation of modified bone cement confirmed that the microstructure does not alter considerably because of PEG content. It was found that both PEG addition and incubation test contribute to an inconsiderable decrease in mechanical strength of bone cement. However, the mechanical strength increase can be caused by the fresh bone tissue incorporation into the pores appearing in bone cement. Copyright © 2016 John Wiley & Sons, Ltd.     

Monolayers of an amphiphilic para-carboxy-calix[4]arene act as templates for the crystallization of acetaminophen

The title compound, 5,11,17,23-tetra-carboxy-25,26,27,28-tetradodecyloxy-calix[4]arene, 1, has been studied at the air–water interface, self-assembled as Langmuir monolayers, for its ability to interact with an active pharmaceutical ingredient (API), acetaminophen (APAP), and to initiate its crystallization. The Π/A isotherm study shows that there is a clear interaction between 1 and APAP causing an expansion of the monolayer. In addition to the known phase transition occurring at a surface tension of 38 mN m^?1, an additional kink is observed in the compression isotherm for concentrations of APAP above 40 mM suggesting that this API is causing an additional phase transition of the monolayer. Interface-initiated crystallization studies show that the presence of a monolayer spread on a supersaturated solution of APAP (26 g L^?1) triggers this API crystal growth from the interface. The transfer of 1-based monolayers on glass surfaces has been carried out using the Langmuir–Blodgett technique. The so-produced monolayers have been shown to template the crystallization of APAP. LB films of 1 have characterized using imaging and spectroscopic ellipsometry. The results suggest that each monolayer has an average thickness of 18 Å, which is consistent with the molecular structure of 1 self-organized parallel to the interface with the alkyl chains pointing out parallel to the axis of the macrocycle and without interdigitation of the alkyl chains. The presence of APAP in the subphase during the LB transfer causes a limited but relevant increase in the layer thickness. The study of the capabilities of the LB films to initiate crystallization of APAP is also demonstrated showing the influence of the monolayer packing on the quantity of formed crystals.     

Azinyl sulfides. L.

The title compound, C₁₉H₁₃N₃S, is folded, with the central ring in a boat conformation. The folding angle between the two quinoline rings is 150.2 (1)°. The 14‐methyl substituent is in a quasi‐axial orientation with respect to the thia­zine ring. The S?N—C_methyl angle is 120.1 (1)°.     

Water molecules in the crystal structure of tricyclic acyclovir

The biologically important mol­ecule tricyclic acyclo­vir, presented here as 3‐[(2‐hydroxy­ethoxy)­methyl]‐6‐methyl‐3H‐imidazolo­[1,2‐a]­purin‐9(5H)‐one dihydrate, C₁₁H₁₃N₅O₃·2H₂O, shows conformational flexibility, which is observed in the solid state as two symmetrically independent mol­ecules with different side‐chain conformations. Additionally, one of these mol­ecules exhibits side‐chain disorder, such that there are three different conformations in the crystal. Water mol­ecules found in the crystal form (H₂O)₈ clusters which are located between mol­ecules of tricyclic acyclovir. The complex hydrogen‐bond network formed between water and tricyclic acyclovir in the solid state may be related to the solvation of the mol­ecules in solution.     

Lipophilicity study of eight cephalosporins by reversed‐phase thin‐layer chromatographic method

The lipophilicity (R_M0) and specific hydrophobic surface area for the representatives of four generation cephalosporins have been determined by reversed‐phase thin‐layer chromatography, and the effect of different mobile‐phase modifiers (such as methanol, acetonitrile, acetone, 1,4‐dioxane and 2‐propanol) on the retention has been studied. The compounds studied showed typical retention behavior; their R_M values decreased linearly with increasing concentration of the organic modifier in the eluent. The linear correlations between the volume fraction of the organic solvent and the R_M values over a limited range were established for each solute, resulting in high values of correlation coefficients (>0.95 in most cases). R_M values were determined by various concentrations of organic modifier, and the correlation obtained was extrapolated to 0% of organic modifier. Chromatographically established logP (R_M0) parameters were compared with computationally calculated partition coefficients values (AClogP, ALOGP, KOWWIN, ALOGPs, XLOGP2, MLOGP and XLOGP3) and experimental octanol–water logP values (measured by the shake flask method). The received results demonstrate that RP‐TLC may be a good alternative technique for analytics in describing the lipophilic nature of investigated cephalosporins as well as the activity. Copyright © 2015 John Wiley & Sons, Ltd.     

Electron — Phonon interaction in thin films

The electron-phonon interaction decoupling scheme in thin films is considered. The decoupled Green functions satisfy the equations containing the additional interaction terms calculated in a self-consistent way for the local quantities such as the mean square displacements of atoms and the occupation numbers of electrons. In particular, the appearance of these additional terms of the mass operator character allows us to expect that the electron phonon interaction is responsible for the stable structure of films.