VUV Fourier-transform absorption study of the Lyman and Werner bands in D2

An extensive survey of the D(2) absorption spectrum has been performed with the high-resolution VUV Fourier-transform spectrometer employing synchrotron radiation. The frequency range of 90,000-119,000 cm(-1) covers the full depth of the potential wells of the B (1)Σ(u)(+), B' (1)Σ(u)(+), and C (1)Π(u) electronic states up to the D(1s) + D(2l) dissociation limit. Improved level energies of rovibrational levels have been determined up to respectively v = 51, v = 13, and v = 20. Highest resolution is achieved by probing absorption in a molecular gas jet with slit geometry, as well as in a liquid helium cooled static gas cell, resulting in line widths of ≈0.35 cm(-1). Extended calibration methods are employed to extract line positions of D(2) lines at absolute accuracies of 0.03 cm(-1). The D (1)Π(u) and B' (1)Σ(u)(+) electronic states correlate with the D(1s) + D(3l]) dissociation limit, but support a few vibrational levels below the second dissociation limit, respectively, v = 0-3 and v = 0-1, and are also included in the presented study. The complete set of resulting level energies is the most comprehensive and accurate data set for D(2). The observations are compared with previous studies, both experimental and theoretical.     

Supramolecular binding of protonated amines to a receptor microgel in aqueous medium

Polyanionic microgels containing negatively charged tetrazole binding sites show supramolecular binding of various protonated amines (e.g. dibucaine and spermine) in a competitive aqueous medium at millimolar concentration.     

Towards standardization of external quality assessment schemes by using bias values based on biological variation

The precision and trueness of current instruments and methods in clinical laboratories is much better than in the past. However, the z-score and other comparison variables that are currently used in external quality assessment programs are based on relative data. Thus, they may change from program to program and also change over time within the same program and consequently may not be useful or cost-effective. We therefore devised a test-specific decision limit for accepting or rejecting test results based on a combination of the data of within- and between-subject biological variations. We then applied these limits to a group of tests performed in our laboratory and compared our results with those of external quality assessment programs. In addition, we combined external and internal quality control data on the same graph and prepared a two-dimensional graph for different levels of control sera. Inspection of all results of control sera on this new graph was more useful for decision making. We concluded that the z-score is not reliable for comparisons of test results in external quality assessment. As a substitute for this currently accepted practice, we assert that control limits based on biological variation are more reliable, and can be useful in the evaluation of both external and internal quality assessments and their combination on this new graph.     

Block copolymers and telechelic oligomers by end group reaction of polymethacrylates

Block copolymers and telechelic oligomers bearing methacrylate moities were obtained by means of a new highly selective end group reaction. Starting from polymethacrylates that were prepared by radical polymerization in the presence of mercaptanes as chain transfer agents, the resulting ester end group linked to the terminal tertiary carbon atom of the polymer backbone can be either transesterified or saponified selectively. The selectivity of the end group reactions was determined by MALDI-TOF-mass spectrometry. Polymethacrylate-b-poly(ethylene oxide)-, polymethacrylate-b-poly(methacrylic acid)- and polymethacrylate-b-polysiloxane-b-polymethacrylate-copolymers as well as α,ω-dihydroxy- and α,ω-dicarboxy-telechelic polymethacrylates were prepared by applying end group transesterification or end group saponification.     

Telechelic Polyisobutenes with Asymmetrical Reactivity

3-Chlorocyclopentene-(1) has been used as initiator in the quasiliving cationic polymerization of isobutene. Polyisobutenes in the molecular weight range Mw = 300 - 60000 Dalton with a molecular weight distribution MWD between 1.17 and 1.34 have been synthesized. The linear polymer was selectively hydrosilated on one or both ends. With a furan coupling agent, the PIB (polyisobutene) was dimerized, yielding polymers with a cyclopentene head- and tail group.     

ChemInform Abstract: The Extended Stability Range of Phosphorus Allotropes.

A complete stability range of known and new crystalline allotropes of phosphorus including recently discovered tubular modifications and not‐yet‐known crystal structures of [P₁₂] nanorods, and not‐yet‐isolated [P₁₄] nanorods is given using quantum chemical DFT calculations.