Effects of modification of molecular structure on Raman spectral depolarization ratios: aqueous betaine (CH3)3NCH2CO2*29D2O versus (CH3)4NBr*29D2O

Replacement of a CH in (CH3)4N+ by a CO2- group raises rho from 0.012 to 0.034 for symmetric N-C stretching and from ca. 0.026 to 0.031 for all-in-phase methyl C-H stretching. rho for antisymmetric C-H stretching and CH3 bending remains in the 0.73-0.75 range. No significant effect on rho attributable to the failure of solvation sheath symmetry to match the symmetry of the solute molecule is seen either near rho=0 or near p=3/4. The drastic change in charge distribution on going from cation to zwitterion, too, does not cause a major change near rho=0. Corroborative evidence of weakness of interaction between most surrounding D2O molecules and the Me3N+ portion of the zwitterion, derived from the O-D stretching region of the Raman spectrum, and implying the absence of symmetry in the solvation sheath, is discussed in Appendix A.     

In Process Citation

The authors attribute to the existence of high polymers the decrease in reactivity and the appearance of cloudiness in aged alkaline niobate solutions. Gel permeation and ultracentrifugation can be used to determine the order of magnitude (10(4) and 6 x 10(4)) of the molecular weight of these particles and their proportion (5%). The structure of these ions is used to explain this exceptional behaviour of the solutions.     

Coenzyme F430 from Methanogenic Bacteria: Complete Assignment of Configuration Based on an X-Ray Analysis of 12,13-Diepi-F430 Pentamethyl Ester and on NMR Spectroscopy

The structure of a derivative of coenzyme F430 from methanogenic bacteria, the bromide salt of 12,13-diepi-F430 pentamethyl ester ( 5 , X = Br), was determined by X-ray structure analysis. It reveals a more pronounced saddle-shaped out-of-plane deformation of the macrocycle than any hydroporphinoid Ni complex investigated so far. The crystal structure confirms the constitution proposed for coenzyme F430 ( 2 ) and shows that in the epimer 5 , the three stereogenic centers in ring D, C(17), C(18), and C(19), have the (17S)-, (18S)-, and (19R)-configuration, respectively. Deuteration and 2D-NMR studies independently demonstrate that native coenzyme F430 (2) has the same configuration in ring D as the epimer 5 . Therefore, our original tentative assignment of configuration at C(19) and C(18) [1] has to be reversed. This completes the assignment of configuration for all stereogenic centers in coenzyme F430, which has the structure shown in Formula 2 .     

Comment on 'new infrared spectra and tautomeric studies of purine and alpha L-alanine with an innovative sampling technique.'.

IR spectra claimed [Spectrochim. Acta A 55 (1999) 2329] to be those of NH2CHMeCO2H and N(7)H purine, as isolated molecules in KBr. are those of cationic species formed in the acid media used.     

Three layers of neutrinos

In this Letter we point out that in a class of models for spontaneous R-parity breaking based on gauged B−L$B-L$, the spectrum for neutrinos is quite peculiar. We find that those models generally predict three layers of neutrinos: one heavy sterile neutrino, two massive active neutrinos, and three nearly massless (one active and two sterile) neutrinos.     

Raman-spectral depolarisation ratios of ions in concentrated aqueous solution. The next-to-negligible effect of highly asymmetric ion surroundings on the symmetry properties of polarisability changes during vibrations of symmetric ions. Ammonium sulphate and tetramethylammonium bromide

Depolarisation ratios rho have been measured for the Raman spectra of solutions of composition (NH4)2 SO4*11H2O and (CH3)4NBr*29D2O. Even though the former's vibration spectrum shows clear evidence of lowered ion symmetries (presence of nu1 of SO4(2-) in the IR spectrum, IR versus R nu(max) shifts for nu3 and nu4 of SO4(2-) and nu4 of NH4+) nu1 of SO4(2-) has (apparent) rho of only 0.014, while nu2, nu3 and nu4 of SO4(2-) and nu4 (probably also nu2) of NH4+ have rho in the range 0.73-0.77; within the experimental error and base line uncertainty the latter are equal to 0.75, i.e. to rho(max) with the geometry of the optics used. For (CH3)4NBr symmetric N+-C stretching has rho 0.012; all-in-phase C-H stretching and four overtones in Fermi resonance with it have rho in the range 0.02-0.035, but the deviation from zero here is in part due to underlying or overlapping depolarised bands. The sufficiently well isolated antisymmetric CH stretching and degenerate CH bending bands again have rho in the range 0.74-0.76. These results show that the selection rules in respect of rho, which apply strictly only to isolated molecules, are for practical purposes still valid for molecules in strongly symmetry-distorting external environments in the liquid phase. More specifically: (A) During vibrations in which quasi-spherical intramolecular symmetry is retained, the externally caused aspherical component of the polarizability ellipsoid does not change aspherically to a sufficient extent for an appreciably intense anisotropic Raman band to appear. (B) During intramolecularly anti-symmetric vibrations of symmetric molecules, the portion of the externally caused distortion of the polarizability ellipsoid that fails to cancel over a whole vibration period is not large enough to give rise to an appreciably intense isotropic component of the Raman band. This means in practice rho for these Raman bands is still rho(max), even for concentrated aqueous solutions.     

Determination of drugs of abuse in bovine dentin using liquid chromatography–electrospray ionization tandem mass spectrometry

Drugs deposited in human teeth are well preserved; the spectrum of toxicological investigations may therefore be supplemented by an analysis method for drugs in teeth. A liquid chromatography–electrospray ionization tandem mass spectrometry assay for the detection and quantification of basic drugs of abuse in bovine dentin samples was developed and validated. The drugs and metabolites amphetamine, methamphetamine, methylenedioxymethylamphetamine, methylenedioxyethylamphetamine, codeine, morphine, cocaine and benzoylecgonine were extracted from 50 mg ground dentin powder by ultrasonication for 60 min in methanol 3 times. The extracts were analyzed on a triple‐quadrupole mass‐spectrometer in multiple reaction monitoring mode. The method was validated and proved to be accurate, precise, selective, specific and stable with good linearity within the calibration range and a lower limit of quantification of 10 to 20 pg/mg. To artificially load bovine dentin samples with drugs, the natural process of de‐ and remineralization in the oral cavity was mimicked by a pH‐cycling experiment. The artificially drug‐loaded dentin samples showed drug concentrations of 20 to 80 pg/mg. The method can be applied in further in vitro experiments as well as in post‐mortem cases, especially where limited sample tissue is available. Copyright © 2014 John Wiley & Sons, Ltd.     

Testing the mechanism for the LSP stability at the LHC

The lightest supersymmetric particle (LSP) is a natural candidate for the cold dark matter of the universe. In this Letter we discuss how to test the mechanism responsible for the LSP stability at the LHC. We note that if R-parity is conserved dynamically one should expect a Higgs boson which decays mainly into two right-handed neutrinos (a “leptonic” Higgs) or into two sfermions. The first case could exhibit spectacular lepton number violating signals with four secondary vertices due to the long-lived nature of right-handed neutrinos. These signals, together with the standard channels for the discovery of SUSY, could help to establish the underlying theory at the TeV scale.