Live cell refractometry using microfluidic devices

Using Hilbert phase microscopy for extracting quantitative phase images, we measured the average refractive index associated with live cells in culture. To decouple the contributions to the phase signal from the cell refractive index and thickness, we confined the cells in microchannels. The results are confirmed by comparison with measurements of spherical cells in suspension.     

The mechanisms of the homogeneous,unimolecular, elimination kinetics of several β‐substituted diethyl acetals in the gas‐phase

The rates of gas‐phase elimination of several β‐substituted diethyl acetals have been determined in a static system and seasoned with allyl bromide. The reactions, inhibited with toluene, are homogeneous, unimolecular, and follow first‐order law kinetics. These elimination processes involve two parallel reactions. The first parallel reaction yields ethanol and the corresponding ethyl vinyl ether. The latter product is an unstable intermediate and further decomposes to ethylene and the corresponding substituted aldehyde. The second parallel reaction gives ethane and the corresponding ethyl ester. The kinetics has been measured over the temperature range of 370–441 °C and pressure range of 23–160 torr. The rate coefficients are given by the following Arrhenius equations: The differences in the rates of ethanol formation may be attributed to electronic transmission of the β‐substituent. The comparative kinetic and thermodynamic parameters of the parallel reactions suggest two different concerted polar four‐membered cyclic transition state types of mechanisms. Copyright © 2010 John Wiley & Sons, Ltd.     

Transfer of naturally occurring radionuclides to wheat under laboratory controlled conditions

Knowledge of soil–plant transfer of naturally occurring radionuclides can be essential to assure an adequate radiological protection. Available data are mainly for anthropogenic radionuclides and biased for temperate climates. Wheat plantlets were grown using soil collected in Mediterranean regions and transfer factors, TF, for ^234,238U, ²²⁶Ra, ²¹⁰Po and stable elements (K, Na, Ca and Mg) were determined. U, Ra and Po were mainly located in roots. Calcium presented the highest TF values, whereas for radionuclides were much lower. Uranium TFs were correlated with total and exchangeable potassium concentration in soil. Calcium and radium TFs were correlated with total calcium concentration in soil.

     

Nature's Combinatorial Biosynthesis Produces Vatiamides A–F

Hybrid type I PKS/NRPS biosynthetic pathways typically proceed in a collinear manner wherein one molecular building block is enzymatically incorporated in a sequence that corresponds to gene arrangement. In this work, genome mining combined with the use of a fluorogenic azide‐based click probe led to the discovery and characterization of vatiamides A–F, three structurally diverse alkynylated lipopeptides, and their brominated analogues, from the cyanobacterium Moorea producens ASI16Jul14‐2. These derive from a unique combinatorial non‐collinear PKS/NRPS system encoded by a 90 kb gene cluster in which an upstream PKS cassette interacts with three separate cognate NRPS partners. This is facilitated by a series of promiscuous intermodule PKS‐NRPS docking motifs possessing identical amino acid sequences. This interaction confers a new type of combinatorial capacity for creating molecular diversity in microbial systems.     

High Molecular Weight Polystyrene Obtained by Cationic Emulsion Polymerization Catalyzed by Imidazolium‐Based Ionic Liquid

The ionic liquid 1‐n‐butyl‐3‐methylimidazolium heptachlorodiferrate (BMI.Fe₂Cl₇) is efficiently used as catalyst in the cationic emulsion polymerization of styrene. The effect of different reaction temperatures, surfactant, and ionic liquid concentrations on polymer properties as molecular weight distribution and particle size is evaluated. High weight average molecular weights, above 1000 kDa, are achieved at 70% of conversion in 100 nm polystyrene particles formed mainly by micellar nucleation. Particle sizes and molecular weights increase with the decrease of the amount of surfactant. Even at low concentrations, BMI.Fe₂Cl₇/styrene molar ratio equal to 1/1000, the ionic liquid proves to be efficient for the emulsion polymerization of styrene, and lower ionic liquid concentrations lead to the formation of longer polymer chains.     

Gravity,antimatter and the Dirac-Milne universe

We review the main arguments against antigravity, a different acceleration of antimatter relative to matter in a gravitational field, discussing and challenging Morrison’s, Good’s and Schiff’s arguments. Following Price, we show that, very surprisingly, the usual expression of the Equivalence Principle is violated by General Relativity when particles of negative mass are supposed to exist, which may provide a fundamental explanation of MOND phenomenology, obviating the need for Dark Matter. Motivated by the observation of repulsive gravity under the form of Dark Energy, and by the fact that our universe looks very similar to a coasting (neither decelerating nor accelerating) universe, we study the Dirac-Milne cosmology, a symmetric matter-antimatter cosmology where antiparticles have the same gravitational properties as holes in a semiconductor. Noting the similarities with our universe (age, SN1a luminosity distance, nucleosynthesis, CMB angular scale), we focus our attention on structure formation mechanisms, finding strong similarities with our universe. Additional tests of the Dirac-Milne cosmology are briefly reviewed, and we finally note that a crucial test of the Dirac-Milne cosmology will be soon realized at CERN next to the ELENA antiproton decelerator, possibly as early as fall 2018, with the AEgIS, ALPHA-g and Gbar antihydrogen gravity experiments.     

A Gauge Invariant Description for the General Conic Constrained Particle from the FJBW Iteration Algorithm

We consider a second-degree algebraic curve describing a general conic constraint imposed on the motion of a massive spinless particle. The problem is trivial at classical level but becomes involved and interesting concerning its quantum counterpart with subtleties in its symplectic structure and symmetries. We start with a second-class version of the general conic constrained particle, which encompasses previous versions of circular and elliptical paths discussed in the literature. By applying the symplectic FJBW iteration program, we proceed on to show how a gauge invariant version for the model can be achieved from the originally second-class system. We pursue the complete constraint analysis in phase space and perform the Faddeev-Jackiw symplectic quantization following the Barcelos-Wotzasek iteration program to unravel the essential aspects of the constraint structure. While in the standard Dirac-Bergmann approach there are four second-class constraints, in the FJBW they reduce to two. By using the symplectic potential obtained in the last step of the FJBW iteration process, we construct a gauge invariant model exhibiting explicitly its BRST symmetry. We obtain the quantum BRST charge and write the Green functions generator for the gauge invariant version. Our results reproduce and neatly generalize the known BRST symmetry of the rigid rotor, clearly showing that this last one constitutes a particular case of a broader class of theories.     

The kinetics and mechanism of the homogeneous,unimolecular gas‐phase elimination of 2‐(4‐substituted‐phenoxy)tetrahydro‐2H‐pyranes

The gas‐phase elimination kinetics of tetrahydropyranyl phenoxy ethers: 2‐phenoxytetrahydro‐2H‐pyran, 2‐(4‐methoxyphenoxy)tetrahydro‐2H‐pyran, and 2‐(4‐tert‐butylphenoxy)tetrahydro‐2H‐pyran were determined in a static system, with the vessels deactivated with allyl bromide, and in the presence of the free radical inhibitor toluene. The working temperature and pressure were 330 to 390°C and 25 to 89 Torr, respectively. The reactions yielded DHP and the corresponding 4‐substituted phenol. The eliminations are homogeneous, unimolecular, and satisfy a first‐order rate law. The Arrhenius equations for decompositions were found as follows:

• 2‐phenoxytetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.18 ± 0.21) ? (211.6 ± 0.4) kJ mol^?1 (2.303 RT)^?1
• 2‐(4‐methoxyphenoxy)tetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.11 ± 0.18) ? (203.6 ± 0.3) kJ mol^?1 (2.303 RT)^?1
• 2‐(4‐tert‐butylphenoxy)tetrahydro‐2H‐pyran
• log k₁ (s^?1) = (14.08 ± 0.08) ? (205.9 ± 1.0) kJ mol^?1 (2.303 RT)^?1

The analysis of kinetic and thermodynamic parameters for thermal elimination of 2‐(4‐substituted‐phenoxy)tetrahydro‐2H‐pyranes suggests that the reaction proceeds via 4‐member cyclic transition state. The results obtained confirm a slight increase of rate constant with increasing electron donating ability groups in the phenoxy ring. The pyran hydrogen abstraction by the oxygen of the phenoxy group appears to be the determinant factor in the reaction rate.     

Theoretical calculations for neighboring group participation in gas‐phase elimination kinetics of 2‐hydroxyphenethyl chloride and 2‐methoxyphenethyl chloride

Theoretical calculation of the kinetics and mechanisms of gas‐phase elimination of 2‐hydroxyphenethyl chloride and 2‐methoxyphenethyl chloride has been carried out at the MP2/6‐31G(d,p), B3LYP/6‐31G(d,p), B3LYP/6‐31 + G(d,p), B3PW91/6‐31G(d,p) and CCSD(T) levels of the theory. The two substrates undergo parallel elimination reactions. The first process of elimination appears to proceed through a three‐membered cyclic transition state by the anchimeric assistance of the aromatic ring to produce the corresponding styrene product and HCl. The second process of elimination occurs through a five‐membered cyclic transition state by participation of the oxygen of o‐OH or the o‐OCH₃ to yield in both cases benzohydrofuran. The B3PW91/6‐31G(d,p) method was found to be in good agreement with the experimental kinetic and thermodynamic parameters for both substrates in the two reaction channels. However, some differences in the performance of the different methods are observed. NBO analysis of the pyrolysis of both phenethyl chlorides implies a C? Cl bond polarization, in the sense of C^δ+…Cl^δ?, which is a rate‐determining step for both parallel reactions. Synchronicity parameters imply polar transition states of these elimination reactions. Copyright © 2009 John Wiley & Sons, Ltd.