Elektronenstossinduzierte fragmentierung von polymethylbenzaldehyden—II: Mechanismus der Methyl-Abspaltung aus dem Molekül-Ion von Tri- und Pentamethylbenzaldehyden

The electron-impact-induced elimination of CH₃ from tri-and pentamethylbenzaldehydes can be explained by the mechanism of a vinylogous α-cleavage. Rearrangements can be excluded.     

Thermodynamic suppression of Brownian motion

We have used helium-3 nuclear reaction analysis to measure the Brownian motion (intradiffusion coefficient) of polystyrene in a partially miscible blend with poly(alpha-methylstyrene). In the one-phase region, when the correlation length is close to the polystyrene chain size, the intradiffusion coefficient falls to half of its thermal value. For larger and smaller values of the correlation length, diffusion is normal. These results show that the correlation length of a polymer blend constrains polymer diffusion, as suggested from previous neutron scattering measurements, and mean-field theory.     

Detailed balance and phonon assisted sticking in adsorption and desorption of H2/Si

Recent experimental results on the desorption of D₂ from Si show practically no translational heating indicating a low barrier for adsorption. This seems to be at variance with the extremely low sticking coefficient found in adsorption experiments indicating a very high barrier. In order to understand this apparent discrepancy we consider a simple model of local lattice relaxation allowing for different barriers in adsorption and desorption processes. After taking the dynamics of this relaxation into account it turns out that detailed balance in principle is valid. In practice, however, it can not be applied for very large energy releases from lattice distortions. Our model predicts very strong phonon assisted sticking.     

Luminescence and stability of aqueous thioalkyl acid capped CdSe/ZnS quantum dots correlated to ligand ionization.

The spectroscopic properties of CdSe/ZnS quantum dots (QDs) were observed to change as a function of thioalkyl acid ligand. Experiments were performed using 2, 3, 6, and 11-carbon linear thioalkyl acids, as well as mercaptosuccinic acid (MSA) and dihydrolipoic acid (DHLA). Bathochromic shifts of up to 14 nm in the emission spectra of QDs capped with these ligands were observed. Similarly, hypsochromic or bathochromic shifts up to 7 nm were observed for a specific ligand in acidic or basic solution, respectively. These shifts could be correlated to the number of ionized ligands and the ability of the ligands to act as hole acceptors. It was also found that differences in quantum yield between the ligands were primarily due to variations in radiative decay rate and not nonradiative decay rate. This indicated that different degrees of QD surface passivation were not responsible for the differences, and that the radiative system must be considered as the sum of the ligands and the QD nanocrystal. The stability of QDs capped with mercaptoacetic acid, MSA, and DHLA towards aggregation at low pH was found to correlate with the pK(a) of the ligands. Spectral shifts were also observed during aggregation. Overall, the luminescence of thioalkyl acid capped QDs appears to be a complex function of dielectric constant, electrostatic or hole-acceptor interactions with ionized ligands, and, to a lesser extent, passivation.     

A quinoline based bis-urea receptor for anions: a selective receptor for hydrogen sulfate

A dipodal bis-urea receptor has been synthesized from the reaction of 8-amino quinoline and 1,4-phenylene diisocyanate in dichloromethane, and the anion binding ability of the receptor has been studied using fluoride, chloride, bromide, iodide, perchlorate, nitrate, dihydrogen phosphate and hydrogen sulfate by UV-Vis titrations in DMSO. The results show that the receptor binds each of the anions with a 1:1 stoichiometry, showing high affinity and moderate selectivity for hydrogen sulfate among the anions studied. Ab initio calculations based on density functional theory (DFT) suggest that an anion (X(-)) is bonded within the cleft formed by the two arms of the receptor through two NH...X(-) and two aromatic CH...X(-) interactions. The results from solution and theoretical studies suggest that binding is predominantly influenced by hydrogen bonding interactions and the basicity of anions.     

Single domain antibody–quantum dot conjugates for ricin detection by both fluoroimmunoassay and surface plasmon resonance

The combination of stable biorecognition elements and robust quantum dots (QDs) has the potential to yield highly effective reporters for bioanalyses. Llama-derived single domain antibodies (sdAb) provide small thermostable recognition elements that can be easily manipulated using standard DNA methods. The sdAb was self-assembled on dihydrolipoic acid (DHLA) ligand-capped CdSe–ZnS core–shell QDs made in our laboratory through the polyhistidine tail of the protein, which coordinated to zinc ions on the QD surface. The sdAb–QD bioconjugates were then applied in both fluorometric and surface plasmon resonance (SPR) immunoassays for the detection of ricin, a potential biothreat agent. The sdAb–QD conjugates functioned in fluoroimmunoassays for the detection of ricin, providing equivalent limits of detection when compared to the same anti-ricin sdAb labeled with a conventional fluorophore. In addition, the DHLA-QD–sdAb conjugates were very effective reporter elements in SPR sandwich assays, providing more sensitive detection with a signal enhancement of ∼10-fold over sdAb reporters and 2–4 fold over full sized antibody reporters. Commercially prepared streptavidin-modified polymer-coated QDs also amplified the SPR signal for the detection of ricin when applied to locations where biotinylated anti-ricin sdAb was bound to target; however, we observed a 4-fold greater amplification when using the DHLA-QD–sdAb conjugates in this format.     

Calculation of peak-to-total ratios for high purity germanium detectors using Monte-Carlo modeling

Summary In order to estimate by calculation the magnitude of the true coincidence summing losses that may be affecting the observed gamma-ray spectrum of a given nuclide, measured using a spectrometer, knowledge of the total detection efficiencies at the gamma-ray energies within the cascades is essential. The total efficiency can be determined from the full energy peak efficiency, provided the peak-to-total ratio is known. For a given high purity germanium (HPGe) detector, one can establish an intrinsic peak-to-total (P/T) efficiency curve using a set of measurements performed with “single” (ideally monoenergetic) gamma-emitting nuclides (e.g., ²⁴¹Am, ¹⁰⁹Cd, ⁵⁷Co, ¹¹³Sn, ¹³⁷Cs, ⁶⁵Zn). Some of these nuclides are short lived and so have to be replaced periodically. Moreover, the presence of low energy gamma-rays and X-rays in most of the decay schemes complicate the empirical determination of the P/T ratios. This problem is especially severe if measurements are made using HPGe detectors that have a very thin dead layer. The problems posed by low energy gamma-rays and X-rays can be avoided by using absorbers, but then one has to be careful not to perturb the intrinsic value of the P/T ratio being sought. This paper addresses these problems. Measurement related limitations are avoided if one can use a computational technique instead. In the work presented here, the feasibility of using a Monte-Carlo based technique to determine the P/T ratios at a wide range of energies (60 keV to 2000 keV) is explored. The Monte-Carlo code MCNP (version 4B) is used to simulate gamma-ray spectra from various nuclides. Measured P/T ratios are compared to calculated ratios for several HPGe detectors to demonstrate the generality of the approach. Reasons for observed disagreement between the two are discussed.     

Nitroxide/substrate weak hydrogen bonding: attitude and dynamics of collisions in solution

The study of intermolecular collisions and bonding interactions in solutions is of critical importance in understanding and predicting solute/solvent properties. Previous work has established that stable paramagnetic nitroxide molecules are excellent probes of intermolecular interactions for hydrogen bonding in polar solvents. In this study, 1H, 2H, 13C, 15N NMR and liquid/liquid intermolecular transfer dynamic nuclear polarization (L2IT DNP) results are obtained for the paramagnetic probe molecule, TEMPO, interacting with the common aprotic and protic polar solvents, CH3CN and CH3CONH2, yielding a profile of both dipolar and scalar interactions. A significant scalar contact hyperfine is observed for the N-O...H-C interaction (13CH3 hyperfine, a/h=0.66 MHz) in the CH3CN/TEMPO system, whereas the N-O...H-C and N-O...H-N interactions for the TEMPO/CH3CONH2 system yield 13CH3 and 15N hyperfine couplings of a/h=0.16 and -0.50 MHz, respectively. The distance and attitude of the scalar interaction for the nitroxide hydrogen bonding at the methyl group in CH3CN and the amino group in CH3CONH2 are computed using density functional theory (DFT), yielding good agreement with the experimental results. These results show that the hyperfine coupling provides a sensitive probe of weak hydrogen-bonding interactions in solution.