A review of the Aharonov-Carmi thought experiment concerning the inertial and electromagnetic vector potentials

We review and elaborate upon a thought experiment of Aharonov and Carmi concerning the inertial and electromagnetic vector potentials. We discuss several conclusions suggested by this experiment which involve extensions of the equivalence principle, and then emphasize the use of the experiment as a predictive tool.     

Molybdenum blue: binding to collagen fibres and microcrystal formation

Collagen fibres have been shown by transmission electron microscopy to progressively bind the polyoxomolybdate ring-complex, termed molybdenum blue. Nucleation of cuboidal molybdenum blue microcrystals occurs on the surface of the collagen fibres, leading eventually to extensive coating of the fibres with microcrystals.     

Surface products and coverage dependence of dissociative ethane adsorption on Pt{110}-(1 x 2)

The dissociation of ethane on Pt{110}-(1 x 2) has been studied using supersonic molecular beam and temperature-programmed reaction techniques. The study unequivocally shows that the stable dissociation product of ethane on Pt{110}-(1 x 2) at all coverages is CCH2 at 350-400 K and CCH at 440 K. Temperature-programmed-reaction (TPR) experiments indicate that the CCH2 species decomposes to CCH with a reaction-limited peak temperature of 430 K. Above 450 K, the CCH species becomes unstable and decomposes with a peak temperature of 540 K. By 600 K, ethane dehydrogenates completely to form a surface carbon layer. The sticking probability is initially 0.02 at 370 K and 0.03 at 600 K and follows a linear (1-2theta) dependence for coverages of up to theta = 0.4 ML, where theta is defined as the number of C2Hx units per (1 x 2) unit cell. However, a much weaker coverage dependence at 800 K suggests that the carbon agglomerates into high-density islands.     

Factors affecting d-block metal-ligand bond lengths: toward an automated library of molecular geometry for metal complexes

Metal-ligand (M-L) bond lengths for a range of ligands (carboxylates, chlorides, pyridines, water, tertiary phosphines, and alkenes) and a variety of metals have been retrieved from the Cambridge Structural Database, CSD. Analysis of the factors which affect M-L bond lengths (for example, ligand coordination mode, oxidation state, metal coordination number and geometry, spin and Jahn-Teller effects, and ligand trans to M-L bond) shows that it is generally possible to subdivide the M-L data sets systematically to obtain better defined, unimodal, bond length distributions with means and sample standard deviations (SSDs) which reflect the nature of the bond in question. Typically, the SSDs for the M-L data sets can be reduced to 0.04-0.05 A by these methods. This work is an extension to tables of bond lengths in organometallic compounds and coordination complexes published in 1989. The importance of the factors which affect M-L bond lengths for particular metal-ligand groups are discussed. From the case studies reported, an algorithm is proposed by which compilation of a library of molecular geometry for metal complexes may be automated. The points that need to be considered to produce such a molecular library from the data stored in the CSD are discussed. The development of such a library would allow users to retrieve chemically well-defined geometric data rapidly and accurately. This should be of use, for example, to crystallographers and molecular modelers.     

Magnetically driven ferroelectric order in Ni3V2O8

We show that long-range ferroelectric and incommensurate magnetic order appear simultaneously in a single phase transition in Ni3V2O8. The temperature and magnetic-field dependence of the spontaneous polarization show a strong coupling between magnetic and ferroelectric orders. We determine the magnetic symmetry using Landau theory for continuous phase transitions, which shows that the spin structure alone can break spatial inversion symmetry leading to ferroelectric order. This phenomenological theory explains our experimental observation that the spontaneous polarization is restricted to lie along the crystal b axis and predicts that the magnitude should be proportional to a magnetic order parameter.     

Electronic control of chiral quaternary center creation in the intramolecular asymmetric heck reaction

The Boehringer-Ingelheim phosphinoimidazoline (BIPI) ligands were applied to the formation of chiral quaternary centers in the asymmetric Heck reaction. Several different substrates were examined in detail, using more than 70 members of this new ligand class. Hammett relationships were determined through systematic variation of the ligand electronics. All substrates showed essentially the same Hammett behavior, where enantioselectivity increased as the ligands were made more electron-deficient. Ligand optimization has led to catalysts which give the highest enantioselectivities reported to date for these difficult systems.     

Nuclear magnetic shielding and chirality IV. The odd and even character of the shielding response to a chiral potential

We investigate the odd and even character of the shielding response in a chiral molecule (modeled by a Ne8 helix) when subjected to a chiral potential. We establish that the diastereomeric splittings are a measure of odd powers of Vodd. Implications for diastereomeric, splittings of Xe in handed cages with handed tethers are discussed.     

Exploiting independent filter bandwidth of human factor cepstral coefficients in automatic speech recognition

Mel frequency cepstral coefficients (MFCC) are the most widely used speech features in automatic speech recognition systems, primarily because the coefficients fit well with the assumptions used in hidden Markov models and because of the superior noise robustness of MFCC over alternative feature sets such as linear prediction-based coefficients. The authors have recently introduced human factor cepstral coefficients (HFCC), a modification of MFCC that uses the known relationship between center frequency and critical bandwidth from human psychoacoustics to decouple filter bandwidth from filter spacing. In this work, the authors introduce a variation of HFCC called HFCC-E in which filter bandwidth is linearly scaled in order to investigate the effects of wider filter bandwidth on noise robustness. Experimental results show an increase in signal-to-noise ratio of 7 dB over traditional MFCC algorithms when filter bandwidth increases in HFCC-E. An important attribute of both HFCC and HFCC-E is that the algorithms only differ from MFCC in the filter bank coefficients: increased noise robustness using wider filters is achieved with no additional computational cost.     

Interlaboratory evaluation of hydrophone sensitivity calibration from 0.1 to 2 MHz via time delay spectrometry

Knowing the low-frequency response of hydrophones, down to 100 kHz at least, is important for accurate biomedical ultrasound measurements. However, current international standards do not extend below 500 kHz. Furthermore, commercial hydrophone sources typically do not supply sensitivity data below 1-2 MHz. Therefore, to help identify and validate practical calibration methods below 2 MHz, the authors have extended their previous individual efforts in an interlaboratory evaluation of sensitivity calibration using the swept-frequency technique, time delay spectrometry (TDS). Calibrations were performed for needle and membrane PVDF hydrophones using each laboratory's TDS system. Each site employed the same purpose-built broadband source transducers, comprising both plano-concave and biconcave 1-3 piezocomposite elements 4 cm in diameter, with maximum and minimum thicknesses of approximately 1.5 and 0.1 cm. Agreement between laboratories was within the estimated measurement precision of +/-0.6 dB. The results demonstrated that a TDS system employing such transducers constitutes a viable method for hydrophone calibrations in this frequency range.