Matrix Isolation‐Vibrational Circular Dichroism Spectroscopy of 3‐Butyn‐2‐ol and its Binary Aggregates

Vibrational circular dichroism (VCD) spectroscopy has a unique specificity to chirality and is highly sensitive to the conformational equilibria of chiral molecules. On the other hand, the matrix‐isolation (MI) technique allows substantial control over sample compositions, such as the sample(s)/matrix ratio and the ratio among different samples, and yields spectra with very narrow bandwidths. We combined VCD spectroscopy with the MI technique to record MI‐VCD and MI‐vibrational absorption spectra of 3‐butyn‐2‐ol at different MI temperatures, which allowed us to investigate the conformational distributions of its monomeric and binary species. Good mirror‐imaged MI‐VCD spectra of opposite enantiomers were achieved. The related conformational searches were performed for the monomer and the binary aggregate and their vibrational absorption and VCD spectra were simulated. The well‐resolved experimental MI‐VCD bands provide the essential mean to assign the associated vibrational absorption spectral features correctly to a particular conformation in case of closely spaced bands. By varying the matrix temperature, we show that one can follow the self‐aggregation process of 3‐butyn‐2‐ol and confidently correlate the MI‐VCD spectral features with those obtained for a 0.1 M CCl₄ solution and as a neat liquid at room temperature. Comparison of the aforementioned experimental VCD spectra shows conclusively that there is a substantial contribution from the 3‐butyn‐2‐ol aggregate even at 0.1 M concentration. This spectroscopic combination will be powerful for studying self‐aggregation of chiral molecules, and chirality transfer from a chiral molecule to an interacting achiral molecule and in electron donor–acceptor chiral complexes.     

Desulfurization of sultams with simultaneous methylenation

Alkylation of γ- and δ-sultams with (iodomethyl)trimethylsilane followed by treatment of the resultant silanes with tetrabutylammonium fluoride gave rise to sulfur-free unsaturated amines. In particular, N-THP substituted sultams were found to be useful substrates for the alkylation event. A corresponding one-pot transformation involving sultam α-alkylation with (iodomethyl)magnesium chloride is also reported.     

Modelling the temporal intensity distribution in laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) using scanning and drilling mode

Signal equations basing on dispersion functions describing the measured temporal intensity distribution for laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) used in scanning and drilling mode are developed. Variable ablation rates due to either varying focussing conditions typical for drilling mode and due to the changes of physical and chemical properties in inhomogeneous samples as typically investigated in scanning mode are considered for. The model accounts for intermixing of the sample aerosol within the sampling chamber, the influence of transport in a cylindrical transport channel and the fact that normally not the entire vapour generated and transported to the ICP can be observed. The absolute signal response is influenced by the actually ablated, transported and observed analyte mass. The dispersion functions describing the relative signal response depend on sample chamber volume, the volume of the transport channel, the laser shot frequency, the carrier gas flow rate and the part of observable cross-section at the MS interface compared to the entire cross-section filled by the vapour. All these parameters depend on the experimental set-up and the selected operating conditions only. Using the signal equation the influence of all mentioned parameters on signal course is shown both theoretically and experimentally. The signal equation can be used for calculation of optimal experimental conditions.

On this basis, an algorithm is proposed providing the relative temporal distribution of any analyte with significantly higher temporal resolution than the measured temporal intensity distribution itself. Furthermore, usage of dispersion functions for investigation of a given transport system, for explanation of typical signal deviations, for the proof of homogeneous regions in a heterogeneous sample, for examination of changes in ablation rate and for investigation of fractionation effects is shown.     

Synthesis and characterization of quasi-two-coordinate transition metal dithiolates M(SAr*)2 (M = Cr, Mn, Fe, Co, Ni, Zn; Ar* = C6H3-2,6(C6H2-2,4,6-Pri3)2

A sequence of first row transition metal(II) dithiolates M(SAr)(2) (M = Cr(1), Mn(2), Fe(3), Co(4), Ni(5) and Zn(6); Ar = C(6)H(3)-2,6-(C(6)H(2)-2,4,6-Pr(i)(3))(2)) has been synthesized and characterized. Compounds 1-5 were obtained by the reaction of two equiv of LiSAr with a metal dihalide, whereas 6 was obtained by treatment of ZnMe(2) with 2 equiv of HSAr. They were characterized by spectroscopy, magnetic measurements, and X-ray crystallography. The dithiolates 1, 2, and 4-6 possess linear or nearly linear SMS units with further interactions between M and two ipso carbons from C(6)H(2)-2,4,6-Pr(i)(3) rings. The iron species 3, however, has a bent geometry, two different Fe-S distances, and an interaction between iron and one ipso carbon of a flanking ring. The secondary M-C interactions vary in strength in the sequence Cr(2+) approximately Fe(2+) > Co(2+) approximately Ni(2+) > Mn(2+) approximately Zn(2+) such that the manganese and zinc compounds have essentially two coordination but the chromium and iron complexes are quasi four and three coordinate, respectively. The geometric distortions in the iron species 3 suggested that the structure represents the initial stage of a rearrangement into a sandwich structure involving metal-aryl ring coordination. The bent structure of 3 probably also precludes the observation of free ion magnetism of Fe(2+) recently reported for Fe{C(SiMe(3))(3)}(2). DFT calculations on the model compounds M(SPh)(2) (M = Cr-Ni) support the higher tendency of the iron species to distort its geometry.     

Anomalous structure-luminescence relationship in phosphorescent gold(I) isonitrile neutral complexes

A new compound that exhibits the shortest intermolecular Au...Au distance ever reported for neutral RNCAuX complexes is found to exhibit a counterintuitive higher-energy Au-centered phosphorescence than that in an analogous compound with a much longer Au...Au distance, presumably due to a different extent of excited-state distortion in dimers vs. extended chains.     

Dynamic Stereochemistry of a Biphenyl-Bisprolineamide Model Catalyst and its Imidazolidinone Intermediates

In this study, we characterize the dynamic stereochemistry of a biphenyl-2,2’-bis(proline amide) catalyst in chloroform and DMSO as representative weakly and strongly hydrogen bonding solvents. Using vibrational circular dichroism (VCD) spectroscopy and density functional theory (DFT) based spectra calculations, we show that the preferred axial stereochemistry of the catalyst is determined by solute-solvent interactions. Explicitly considering solvation with DMSO molecules is found to be essential to correctly predict the conformational preferences of the catalyst. Furthermore, we investigate the stereochemistry of the corresponding enamines and imidazolidinones that are formed upon reaction with isovaleraldehyde. The enamines are found to rapidly convert to endo-imidazolidinones and the thermodynamically favored exo-imidazolidinones are formed only slowly. The present study demonstrates that the stereochemistry of these imidazolidinones can be deduced directly from the VCD spectra analysis without any further detailed analysis of NMR spectra. Hence, we herein exemplify the use of VCD spectroscopy for an in situ characterization of intermediates relevant in asymmetric catalysts.     

Fast functionalization of multi-walled carbon nanotubes by an atmospheric pressure plasma jet

The afterglow of an atmospheric pressure plasma has been used for the fast oxidative functionalization of multi-walled carbon nanotubes (MWCNTs). Scanning electron microscopy and Raman spectroscopy demonstrate that the MWCNT morphology is mostly preserved when the MWCNTs are dispersed in a solvent and injected as a spray into the plasma. Contact angle measurements show that this approach enhances the wettability of MWCNTs and reduces their sedimentation in an aqueous dispersion. X-ray photoelectron spectroscopy, IR spectroscopy, and electrokinetic measurements show that oxygen plasma incorporates about 6.6 at.% of oxygen and creates mainly hydroxyl and carboxyl functional groups on the MWCNT surface. The typical effective treatment time is estimated to be in the range of milliseconds. The approach is ideally suited for combination with the industrial gas phase CVD synthesis of MWCNTs.