9-BBN: An amino acid protecting group for functionalization of amino acid side chains in organic solvents

9-Borabicyclononane (9-BBN) has been utilized to protect functionalized amino acids for potential chemoselective side chain manipulation. The 9-BBN group imparts organic solubility to otherwise hydrophilic molecules and is tolerant of a wide range of reaction conditions. The high degree of solubility of these molecules in THF is particularly noteworthy. It is cleaved with either aqueous HCl or by exchange with ethylenediamine in methanol. [reaction: see text]     

Time‐Resolved,In Situ DRIFTS/EDE/MS Studies on Alumina‐Supported Rhodium Catalysts: Effects of Ceriation and Zirconiation on Rhodium–CO Interactions

The effects of ceria and zirconia on the structure–function properties of supported rhodium catalysts (1.6 and 4 wt % Rh/γ‐Al₂O₃) during CO exposure are described. Ceria and zirconia are introduced through two preparation methods: 1) ceria is deposited on γ‐Al₂O₃ from [Ce(acac)₃] and rhodium metal is subsequently added, and 2) through the controlled surface modification (CSM) technique, which involves the decomposition of [M(acac)_x] (M=Ce, x=3; M=Zr, x=4) on Rh/γ‐Al₂O₃. The structure–function correlations of ceria and/or zirconia‐doped rhodium catalysts are investigated by diffuse reflectance infrared Fourier‐transform spectroscopy/energy‐dispersive extended X‐ray absorption spectroscopy/mass spectrometry (DRIFTS/EDE/MS) under time‐resolved, in situ conditions. CeO_x and ZrO₂ facilitate the protection of Rh particles against extensive oxidation in air and CO. Larger Rh core particles of ceriated and zirconiated Rh catalysts prepared by CSM are observed and compared with Rh/γ‐Al₂O₃ samples, whereas supported Rh particles are easily disrupted by CO forming mononuclear Rh geminal dicarbonyl species. DRIFTS results indicate that, through the interaction of CO with ceriated Rh particles, a significantly larger amount of linear CO species form; this suggests the predominance of a metallic Rh phase.     

Complex dynamic behavior of fluctuating smectic- A films as studied by scattering with coherent X-rays

Coherent dynamic x-ray scattering has been used to study the thermally excited layer fluctuations in freely suspended smectic films of the compound 4O.8. Using 8-keV x rays and films with a thickness around 0.3 &mgr;m we resolve relaxation times down to a few &mgr;s. A combination of damped and oscillatory behavior is observed for the layer undulations, which can be attributed to inertial effects. These are due to the surface contribution to the free energy which cannot be disregarded for thin films.     

The Franssen effect illusion in budgerigars (Melopsittacus undulatus) and zebra finches (Taeniopygia guttata)

The properties of the Franssen effect (FE) were measured in budgerigars and zebra finches. To elicit the FE, listeners are presented with a signal which has been split into a transient component, carrying an abrupt onset and ramped offset and separated in space from the sustained component which has a slowly rising onset and longer duration. When these two signals are played under certain conditions, the perception is that of a long-duration steady state tone being played at the location of the transient. The birds were trained using operant conditioning methods on a categorization task to peck a left key when presented with a stimulus from a left speaker and to peck a right key when presented with a stimulus from a right speaker. Once training was completed, FE stimuli were presented during a small proportion of trials. The FE was measured at speaker separations of 60 degrees and 180 degrees in both echoic and echoic-reduced conditions. Both species of birds exhibited the FE, although to varying degrees, across conditions. These results show that nonmammals also experience the FE illusion in confusing listening situations in a manner similar to mammals, suggestive of similar auditory processing mechanisms.     

Assignment of the vibrational spectra of lithium hydroxide monohydrate, LiOH·H2O

The assignment of the vibrational spectra of lithium hydroxide monohydrate, LiOH·H(2)O, has been controversial for more than half-a-century. Here we show that only the combination of all three forms of vibrational spectroscopy: infrared, Raman and inelastic neutron scattering spectroscopies coupled with periodic-density functional theory calculations is able to satisfactorily assign the spectra. All previous work based on empirical criteria is, at least partially, incorrect. The librational modes of water do not follow the expected rock > wag > twist order and the calculations indicate that complete or partial deuterium substitution would not be useful in assigning the modes.