Studies of silicon nanocluster ligand coating by solid-state NMR

Silicon nanoclusters were studied by ²⁹Si and ¹³C MAS NMR (magic angle spinning) spectroscopy. We for the first time confirmed the cleavage of ordinary ether C—O bonds of the solvent in the process of the synthesis of nanoclusters and the “binding” of the decomposition products to the surface of silicon nanoparticles as ligands. The applicability of MAS NMR spectroscopy in the studies of silicon nanocluster ligand coating and in the determination of the processes leading to the formation of the nanoparticle ligand shell was demonstrated.     

ToF‐SIMS characterization of glyoxal surface oxidation products by hydrogen peroxide: A comparison between dry and liquid samples

As one of the simplest volatile organic compounds, glyoxal and its oxidation products were considered to be important precursors to aqueous secondary organic aerosol formation. Herein, we analyzed products from glyoxal oxidation by hydrogen peroxide in dry and liquid samples using time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS). ToF‐SIMS spectra and spectral principal component analysis (PCA) were used to investigate surface oxidation products. Dry samples were prepared on clean silicon wafers. Liquid samples consisting of glyoxal and hydrogen peroxide (H₂O₂) were introduced to a vacuum compatible microfluidic reactor prior to UV illumination or dark aging followed by in situ liquid SIMS analysis. A number of reaction products were observed in both dry and liquid samples; different oligomers and carboxylic acids could be formed depending on reaction conditions. In addition, hydrolyzed products were observed in the liquid samples, but not in the dry samples. Although dry samples reveal some products of the aqueous process, they are not fully representative as results from those of the aqueous samples. Our findings suggest that the ability to characterize the liquid surface reaction products provides more realistic information of the reaction products associated with aqueous secondary organic aerosol formation in the atmosphere. Meanwhile, the high mass resolution spectra from the dry sample SIMS measurement are helpful to identify oxidation products in the liquid samples.     

Photochlorination of tetramethylsilane and hexamethyldisilane in the gas phase

Preliminary studies of the reaction of chlorine with tetramethylsilane and hexamethyldisilane in the gas phase show that the photochlorination of tetramethylsilane is complex, giving different products from the corresponding reaction in solution and having an explosion boundary. At pressures below the explosion boundary the main products are ethylene, hydrogen chloride, dimethylchlorosilane, and more highly chlorinated methylsilanes. Above the explosion boundary main products after explosion are methane, acetylene, ethylene, hydrogen chloride, and silicon tetrachloride. Hexamethyldisilane reacts rapidly with chlorine in the dark, as it does in solution, forming mainly trimethylchlorosilane along with similar products to those found with tetramethylsilane. Subsequent photochlorination of trimethylchlorosilane follows a similar course to that of tetramethylsilane in the gas phase. Tentative mechanisms involving “hot” molecules are suggested.     

Transfer of functionalized carbon fragments via substituted 5, 10-methylentetetrahydrofolate models. : Approach to dihydroindole and indole alkaloids.

4-(2-N(1)-tosyl-N(3)-methyl-4-,4-dimethylimidazolidyl)-3-ketobutanoate reacts with tryptamine, in the presence of acetic acid, to give primary “carbon transfer” products, which can be conveniently converted to synthetically useful indole and dihydroindole derivatives.     

Surface phases and nanostructures on silicon surface

The paper gives definitions of conventional terms related to silicon surface science, such as surface, surfaced phase, adatoms, “in phase” and “on phase” atoms. The formation methods of surface phases are illustrated as well as their role in physical processes on the surface. The influence of surface phases on diffusion, desorption, adsorption, and phase interface formation at the silicon surface is described.     

Stability and disturbance of coating films

In the studies of two-roll metering and application systems, two types of disturbances were observed. These were termed “ring type” and “irregular” disturbances. This research established that the physical reason for the appearance of the ring type instability is the competition between surface tension and centrifugal forces at the liquid-air interface. The rings are generated at the surface of the dynamic liquid meniscus, in the gap between the rolls, because of the very large centrifugal forces there. Considering conditions of a constant interfacial pressure difference (pressure jump), one can reduce the problem to one with only one free parameter, viz., the radius of the meniscus, and calculate the wavelength of the disturbances. There is no single formula which will adequately describe the dynamic meniscus. Its curvature depends on the rheological properties of the fluid and on the kinematic conditions in the process. Dimensional analysis is combined with experimental findings to yield a formula for the radius of the meniscus for fluids having a high yield stress for the case of two counter-rotating rolls.The rheological behavior of a flowing starch adhesive in the dynamical meniscus is analyzed. The theoretical and experimental studies show that systems using two counter-rotating rolls practically always produced ring-type instabilities with all types of fluids.The picture is more complex for co-rotating roll systems. When non-Newtonian adhesives are used, ring type disturbances are observed in one zone of roll speed ratios, and irregular disturbances are observed in another zone. The two zones are separated by a speed ratio zone (a “speed window”) where a more or less perfectly stable fluid layer is observed. When Newtonian oils are used, there are two such speed windows. The first one corresponds to very low metering roll speeds and a minimum of liquid transfer to the applicator roll. The second stable zone occurs at high metering roll speeds and yields a maximum of liquid transfer. The physical reason for the high transfer rate in the high speed “window” is considered and shown to be the thin air layer following the surface of the metering roll. The air pumped into the metering gap returns along the applicator roll and accelerates the film on the applicator roll in the process. Under these conditions the fluid-air interface may become unstable, leading to the “irregular” type of disturbance.     

Effect of Atomic Oxygen on the Surface Morphology of Polyethylene

The chemical species created in a low-pressure electrical discharge in oxygen attack the polymer at the surface, converting it to gaseous products. This process is interesting because: 1) the chemical changes on the resulting surface facilitate the formation of strong adhesive bonds and provide sites for the chemical attachment of other molecules, 2) significant morphological features lying below the surface may be revealed, 3) polymer can be cleanly removed from surfaces which are resistant to oxidation, and 4) dielectric breakdown frequently is preceded by the attack on the polymer of chemical species created in a corona discharge. Atomic oxygen is an important chemical species created in such a discharge. It reacts with organic substances rapidly at room temperature, but lives long enough in the low-pressure gas that it can be separated from many other reactive species created in the discharge. “Titration” with NO₂ provides a straightforward chemiluminescent means for determining the concentration of atomic oxygen to which the sample is exposed. This paper characterizes the attack of atomic oxygen, perhaps in the presence of long lived but less reactive species such as excited O₂molecules, on polymer surfaces, using electron microscopic observations of known morphological features of polyethylene to observe the changes produced by atomic oxygen. Lamellar polyethylene crystals were attacked both at the edges and the fold surfaces. Layers many microns thick were removed from spherulitic samples and replicas obtained from the surfaces thus exposed. Thick samples were thinned to the point at which they were transparent to an electron beam and interior morphological features were directly observed.     

Adsorption of trimethoxysilane and of 3-mercaptopropyltrimethoxysilane on silica and on silicon wafers from vapor phase: an IR study

The interaction of trimethoxysilane (TMS) and of 3-mercaptopropyltrimethoxysilane (MPTMS) with silica and silicon wafers has been studied by the mean of transmission FTIR spectroscopy. TMS vapor adsorption on silica's silanols results in the formation of Si-O-Si bonds at room temperature, mainly through the elimination of one methanol molecule per TMS molecule. Similarly, MPTMS vapor reacts with the surface through "hydroxolysis" of one of Si-O-CH3 bonds, and most of the molecules have their SH group free. The same species is formed over the silicon wafer surface. On the other side, deposition of liquid MPTMS over silicon surface leads to the detection of spectral features characterizing a condensed layer.     

Geochemical Continuity and Catalyst/Cofactor Replacement in the Emergence and Evolution of Life

The origin of life is mostly divided into “genetics first” and “metabolism first” hypotheses. The former is based on spark‐tube tests and organic species from meteorites and comets, and proposes a heterotrophic origin of life also consistent with the “RNA World” concept. The “metabolism first” hypothesis posits that life began autotrophically on minerals and/or hydrothermal vents. The lack of direct evidence means it is not possible to lend solid support to either hypothesis but the “metabolism first” option can be explored if a continuous geochemical, catalytically dynamic process is assumed. Using this approach, it is speculated that purine and pyrimidine synthesis originated on a mineral surface, which was later replaced by ATP. The same applies to redox processes where metal‐bound hydrides could have been replaced by NAD.     

Reactions of elemental phosphorus and phosphine with electrophiles in superbasic systems: XX. Phosphorylation of 4-vinylbenzyl chloride with elemental phosphorus

4-Vinylbenzyl chloride reacts with white and red phosphorus, as well as with nanostructured “activated” red phosphorus (complex organophosphorus polymer prepared from white phosphorus under ionizing radiation) in the system concentrated aqueous KOH-dioxane-phase-transfer catalyst (20–50°C, argon) to form tris(4-vinylbenzyl)phosphine oxide, along with (4-vinylbenzyl)- and bis(4-vinylbenzyl)phosphinic acids, the yield and product ratio being dependent on both the reaction conditions and the nature of the phosphorylating agent. The nanostructured “activated” red phosphorus is more reactive than ordinary commercial red phosphorus.     

Surface Molding of Microscale Hydrogels with Microactuation Functionality

This work describes the fabrication of numerous hydrogel microstructures (μ‐gels) via a process called “surface molding.” Chemically patterned elastomeric‐assembly substrates were used to organize and manipulate the geometry of liquid prepolymer microdroplets, which, following photo‐initiated crosslinking, maintained the desired morphology. By adjusting the state of strain during the crosslinking process, a continua of structures could be created using one pattern. These arrays of μ‐gels have stimuli‐responsive properties that are directly applicable to actuation where the basis shape and array geometry of the μ‐gels can be used to rationally generate microactuators with programmed motions. As a method, “surface molding,” represents a powerful addition to the soft‐lithographic toolset that can be readily applied to the simultaneous synthesis of large numbers of geometrically and functionally distinct polymeric microstructures.     

“Grafting through” polymerization involving surface-bound monomers

“Grafting through” polymerization represents copolymerization of free monomers in solution and polymerizable units bound to a substrate. Free polymer chains are formed initially in solution and can incorporate the surface-bound monomers, and thereby, get covalently bonded to the surface during the polymerization process. As more growing chains attach to the surface-bound monomers, an immobilized polymer layer is formed on the surface. We use a combination of computer simulation and experiments to comprehend this process for monomers bound to a flat impenetrable substrate. We concentrate specifically on addressing the effect of spatial density of the surface-bound monomers on the formation of the surface-attached polymers. We employ a lattice-based Monte Carlo model utilizing the bond fluctuation model scheme to provide molecular-level insight into the grafting process. For experimental validation, we create gradients of density of bound methacrylate units on flat silicon wafers using organosilane chemistry and carry out “grafting through” free radical polymerization initiated in bulk. We report that the proximity of the surface-bound polymerizable units promotes the “grafting through” process but prevents more free growing chains to “graft through'' the polymerizable units. The “grafting through” process is self-limiting in nature and does not affect the overall density of the surface-bound polymer layer, except in case of the highest theoretical packing density of surface-bound monomers. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 263–274     

Are There Carbenes in N‐Heterocyclic Carbene Organocatalysis?

Azolium cations are widely employed in organocatalysis to catalyse highly valuable synthetic processes in the presence of a base. These reactions are called “N‐heterocyclic carbene catalysis”, based on the assumption that they are initiated by the formation of a free carbene through deprotonation, which can then react with the substrates and thereby affect their reactivity to obtain the desired products. However, we herein provide evidence that an electrophilic aromatic substitution mechanism is energetically more favourable, in which the azolium cation reacts directly with the substrate, avoiding the formation of the free carbene in solution.     

Massenspektrometrische untersuchungen zur elementaranalyse organischer verbindungen—III: Verbrennungsvorgänge im leeren rohr

A measuring system is described which permits study of all stages of combustion processes as functions of carrier gas, temperature, residence time and tube filling. The organic sample is fed at constant speed into a stream of carrier gas. The mixture reaches the combustion chamber within a few milliseconds via a transfer capillary. With the help of a viscous inlet system, a sample of the resulting reaction products is taken and fed into a mass spectrometer. Reaction time and temperature can be adjusted within wide ranges or varied continuously. A plot of the extent of reaction of the various combustion products against temperature at a chosen reaction time yields an oxidation-thermogram which gives a clear picture of the combustion process. It is evident from thermograms of selected compounds that the samples decompose in the presence of oxygen at appreciably lower temperatures than in inert gas. The primary step of the decomposition is “oxidative pyrolysis” which often leads to other products than “inert pyrolysis”. The intermediate products found are partly structurally specific and, especially with nitrogen-containing samples, are numerous and long-lived (for example, carbon monoxide, nitric oxide, cyanogen, hydrocyanic acid, cyanic acid and methyl cyanate). The notorious “difficult combustibility” is largely due to the fact that carbon monoxide, cyanic and hydrocyanic acids undergo complete combustion only at very high temperature. The combustion properties of the “empty tube” can be improved noticeably by a filling of quartz wool and markedly by partly filling with platinum wool.     

Preparation of tris(trimethylsilyl)methyl (“trisyl”) derivatives of silicon

Treatment of (Me₃Si)₃CLi (“trisyl”lithium, TsiLi) with appropriate silicon halides has given a range of compounds of the type (Me₃Si)₃CSiRR′X; e.g., TsiSiCl₃, TsiSiMeCl₂, TsiSiMe₂X (X = Cl, OMe), TsiSiPh₂X (X = F, Cl, OMe), and TsiSiPhMeH. The trisyl group causes very large steric hindrance to nucleophilic displacements at the silicon to which it is attached, so that (unless one or more hydride ligands are present) most of the common displacements at silicon do not occur. However, halides can be reduced to hydrides by LiAlH₄, and the hydrides can be converted into halides in electrophilic displacements by hallogens. The presence of even one hydride ligand markedly reduces the hindrance, so that, for example, TsiSiPhHI reacts with refluxing methanol to give TsiSiPhH(OMe).     

Linear calibrations in chromatography: The incorrect use of ordinary least squares for determinations at low levels,and the need to redefine the limit of quantification with this regression model

Ordinary least squares is widely applied as the standard regression method for analytical calibrations, and it is usually accepted that this regression method can be used for quantification starting at the limit of quantification. However, it requires calibration being homoscedastic and this is not common. Different calibrations have been evaluated to assess whether ordinary least squares is adequate to quantify estimates at low levels. All calibrations evaluated were linear and heteroscedastic. Despite acceptable values for precision at limit of quantification levels were obtained, ordinary least squares fitting resulted in significant and unacceptable bias at low levels. When weighted least squares regression was applied, bias at low levels was solved and accurate estimates were obtained. With heteroscedastic calibrations, limit values determined by conventional methods are only appropriate if weighted least squares are used. A “practical limit of quantification” can be determined with ordinary least squares in heteroscedastic calibrations, which should be fixed at a minimum of 20 times the value calculated with conventional methods. Biases obtained above this “practical limit” were acceptable applying ordinary least squares and no significant differences were obtained between the estimates measured using weighted and ordinary least squares when analyzing real‐world samples.     

Mechanical properties of high‐density polyethylene and crosslinked high‐density polyethylene in crude oil and its components

The tensile and stress‐relaxation properties of an uncrosslinked and a loosely silane‐crosslinked high‐density polyethylene exposed to organic “crude‐oil” penetrants were assessed. The measurements were performed on penetrant‐saturated samples, surrounded by the organic liquid throughout the experiment. The penetrant solubilities in the two polymers were similar and in accordance with predicted values based on the solubility parameter method. The stiffness and strength of the swollen samples were significantly less than those of the dry samples, indicating a plasticization of the amorphous component. Raman spectroscopy on polyethylene exposed to deuterated n‐hexane revealed a penetrant‐induced partial melting/dissolution of the crystal surface and an intact crystal core component. The stress‐relaxation rates, within the time frame of the experiment (～1 s to 18 h), were approximately the same, independent of silane‐crosslinks and the presence of penetrants. This indicated that the mechanical α‐relaxation, which is the main relaxation process occurring in the measured time interval, was not affected by the penetrants. Consequently, its rate seemed to be independent of the crystal surface dissolution (decrease in the content of crystal‐core interface). The shape of the “log stress–log time” curves of the swollen samples was, however, different from that of the dry samples. This was most likely attributed to a time‐dependent saturation of penetrant to a higher level associated with the stretched state of the polymer sample. The silane crosslinks affected only the elongation at break, which was less than that of the uncrosslinked material. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 641–648, 2006     

On the streaming potential arising from flows having axial symmetry and the determination of zeta potential therefrom

Determining the zeta potential of macroscopic surfaces helps predict the surfaces' attractiveness to charged particles or cells, or tells whether the surface is clean or contaminated, among other applications. Typically, one pumps the test solution through a narrow channel formed by the test surface and measures the streaming current or streaming potential engendered thereby. It is worth considering alternative geometries: 1. The “spincoat” design, in which the test liquid is directed as a narrow jet to the axis of a disk-shaped sample rotating on its axis, offers a large signal with a small liquid flow rate, e.g. 1 mL/min. The validity of assumptions underlying the simplest analysis of this design improves as the flow rate decreases at constant rotation rate. 2. The “rotating disk”, in which the sample is spun on its axis while immersed in solution, offers much reduced surface conductance and uniform accessibility to charged entities in solution. This design also provides a means for determining the zeta potential of open porous structures without requiring compression of the sample into a plug. 3. The “impinging jet,” in which a jet of liquid is directed to a nonrotating sample, allows an arbitrary sample shape and detection of spatial variations of zeta potential. Deceleration of the radially expanding film causes a “hydraulic jump instability” some distance from the axis; the radius of the jump defines the probed area.     

Problems on the Evaluation of the Critical Wavelength of Sunscreens for “Broad Spectrum” Approval Brought on by Viscous Fingering During Sunscreen Application

When a viscous liquid is applied to a solid substrate, a patterned liquid layer is usually formed by the phenomenon called viscous fingering, since the moving liquid surface is in far‐from‐equilibrium conditions to let the morphological fluctuation to grow. Pseudosunscreen solutions were prepared and applied on a flat quartz plate. A spatially periodic stripe pattern was formed on the pseudosunscreen layer when a block applicator was used, whereas a flat surface layer was formed when a four‐sided applicator was used. UV absorbance of the patterned layer was lower than that of the flat layer having the same average thickness. In addition, a larger decrease in the UV absorbance by the pattern formation was observed at wavelengths at which the UV absorbance of the flat layer was large, which was consistent with theoretical simulations. In 2011, US FDA introduced a new rule using the term “Broad Spectrum” for labeling the sunscreens. The different decrease in the UV absorbance at each wavelength was found to change the critical wavelength, which is a criterion for sunscreens to be labeled as “Broad Spectrum” protection. The result of this study makes the problem on the evaluation of the critical wavelength come to the surface.     

The characteristics of component transfer through barrier membrane layers

A uniform matrix with randomly distributed impurity centers, which create an effective field repulsing particles that diffuse in the membrane and prevent the formation of “percolation” paths in “thick” membranes, is considered as a barrier layer model. Two repulsive potential types were analyzed, one decreasing according to a power law depending on the distance between the localization center of an impurity and the diffusing particle and the other decreasing exponentially as a function of this distance. An exponential dependence of the permeability constants of the desired components on the membrane layer thickness was predicted. According to this dependence, the components to be separated effectively pass through membrane layers only in local regions, where the force field that retards particles is weakened because of a fluctuation decrease in the concentration of centers repulsing the diffusing particles. The process is then characterized by nonequilibrium transmembrane transfer conditions, under which particles have time to be effectively “sorbed” only in regions of increased membrane permeability. Under these conditions, the selectivity of membrane separation can be influenced by the state of the surface of membranes. For this reason, the modification of the surface of barrier structures can be used to control their selective permeability to the desired products. Equations for the rate of component transfer through barrier membrane layers under the most general boundary conditions were obtained. These equations can be used to analyze separation on membranes with barrier structures subjected to surface modification.