Solar Thermal Energy Storage in a Photochromic Macrocycle

The conversion and efficient storage of solar energy is recognized to hold significant potential with regard to future energy solutions. Molecular solar thermal batteries based on photochromic systems exemplify one possible technology able to harness and apply this potential. Herein is described the synthesis of a macrocycle based on a dimer of the dihydroazulene/vinylheptafulvene (DHA/VHF) photo/thermal couple. By taking advantage of conformational strain, this DHA–DHA macrocycle presents an improved ability to absorb and store incident light energy in chemical bonds (VHF–VHF). A stepwise energy release over two sequential ring‐closing reactions (VHF→DHA) combines the advantages of an initially fast discharge, hypothetically addressing immediate energy consumption needs, followed by a slow process for consistent, long‐term use. This exemplifies another step forward in the molecular engineering and design of functional organic materials towards solar thermal energy storage and release.     

Evaluation of the use of liquid dishwashing compounds to control bacteria in kitchen sponges

A test procedure for evaluating the effect of adding commercial liquid hand dishwashing detergents to kitchen sponges to control microbial growth is described. Claims for this type of application are being made on dishwashing detergents throughout the world. In this evaluation, commercially available kitchen sponges were stripped of antimicrobial compounds. Sponges were then inoculated with a pool of 7 microorganisms which consisted of gram positives, gram negatives, and yeast. Inoculated sponges were treated with the detergent as recommended by the manufacturer and allowed to incubate for 16 h at ambient temperature. Surviving microorganisms were then quantitated using either the spiral or pour plate method. Tests were run using both clean sponges and sponges soiled with 0.5% nonfat dry milk (NFDM). Untreated sponges showed stasis or slightly increased bacterial populations after the incubation period in the absence of NFDM. Significant increases of up to 3 log cfu/mL were observed for untreated sponges when soiled with NFDM. Statistically significant reductions were observed for clean sponges (99.8-99.9998%) and sponges soiled with NFDM (87.6-99.9%) when detergents making "antibacterial sponge" claims were added to the inoculated sponges. Statistically significant differences between detergents making "antibacterial sponge" claims were also observed.     

Spectral properties and absolute rate constants for beta-scission of ring-substituted cumyloxyl radicals. A laser flash photolysis study

A laser flash photolysis study of the spectral properties and beta-scission reactions of a series of ring-substituted cumyloxyl radicals has been carried out. All cumyloxyl radicals display a broad absorption band in the visible region of the spectrum, which decays on the microsecond time scale, leading to a strong increase in absorption in the UV region of the spectrum, which is attributed to the corresponding acetophenone formed after beta-scission of the cumyloxyl radicals. The position of the visible absorption band is red-shifted by the presence of electron-donating ring substituents, while a blue-shift is observed in the presence of electron-withdrawing ring substituents, suggesting that + R ring substituents promote charge separation in the excited cumyloxyl radical through stabilization of the partial positive charge on the aromatic ring of an incipient radical zwitterion. Along this line, an excellent Hammett-type correlation between the experimentally measured energies at the visible absorption maxima of the cumyloxyl radicals and sigma(+) substituent constants is obtained. A red-shift is also observed on going from MeCN to MeCN/H(2)O for all cumyloxyl radicals, pointing toward a specific effect of water. The ring substitution does not influence to a significant extent the rate constants for beta-scission of the cumyloxyl radicals, which varies between 7.1 x 10(5) and 1.1 x 10(6) s(-1), a result that suggests that cumyloxyl radical beta-scission is not governed by the stability of the resulting acetophenone. Finally, k(beta) increases on going from MeCN to the more polar MeCN/H(2)O 1:1 for all cumyloxyl radicals, an observation that reflects the increased stabilization of the transition state for beta-scission through increased solvation of the incipient acetophenone product.     

A pyrrolo-tetrathiafulvalene cage: synthesis and X-ray crystal structure

[reaction: see text] A novel type of tetrathiafulvalene-cage 4 containing three monopyrrolo-tetrathiafulvalene units has been prepared employing a general and efficient synthetic approach. X-ray crystal structure analysis revealed that the cage is able to accommodate solvent molecules within a cavity in the solid state.     

Substituted 1,8-naphthyridin-2(1H)-ones are superior to thymine in the recognition of adenine in duplex as well as triplex structures

The synthesis and evaluation of a series of novel nucleobases based on substituted 1,8-naphthyridin-2(1H)-ones are reported. The nucleobases were designed to meet the requirements for incorporation into peptide nucleic acids (PNAs) and were evaluated as part of PNA duplex and triplex nucleic acid recognition systems. Of the various nucleobases tested, only the 7-chloro-1,8-naphthyridin-2(1H)-one (7-Cl-bT) nucleobase led to consistently increased affinity in all recognition systems, duplex (Watson-Crick) as well as triplex (Hoogsteen). For multiply modified systems, the increase in thermal stability per modification was dependent on the sequence context, ranging from 2.0 degrees C (in separate positions) to 3.5 degrees C (in adjacent positions) in PNA-DNA duplexes and from 1.2 degrees C (in separate positions) to 3.2 degrees C (in adjacent positions) in PNA-RNA duplexes. Singly mismatched oligonucleotide targets were employed to demonstrate uncompromised sequence discrimination. When part of multiply modified triplex (Hoogsteen) recognition systems, the 7-Cl-bT unit gave rise to increases in the thermal stability ranging from 2.7 to 3.5 degrees C when incorporated into separated and adjacent positions, respectively. Our results furthermore indicate that the duplex stabilization is predominantly enthalpic and therefore most likely not a consequence of single-strand preorganization. Finally, and most surprisingly, we find no direct correlation between the end-stacking efficiency of this type of nucleobase and its helix stabilization when involved in Watson-Crick base pairing within a helix.     

Pseudorapidity distributions of charged particles from Au + Au collisions at the maximum RHIC energy,square root[s(NN)] = 200 GeV

We present charged-particle multiplicities as a function of pseudorapidity and collision centrality for the 197Au+197Au reaction at square root[s(NN)] = 200 GeV. For the 5% most central events we obtain dN(ch)/deta/(eta = 0) = 625+/-55 and N(ch)/(-4.7< or =eta < or =4.7) = 4630 +/- 370, i.e., 14% and 21% increases, respectively, relative to square root[s(NN)] = 130 GeV collisions. Charged-particle production per pair of participant nucleons is found to increase from peripheral to central collisions around midrapidity. These results constrain current models of particle production at the highest RHIC energy.     

Stringent neutron-star limits on large extra dimensions

Supernovae (SNe) are copious sources for Kaluza-Klein (KK) gravitons which are generic for theories with large extra dimensions. These massive particles are produced with average velocities approximately 0.5c so that many of them are gravitationally retained by the SN core. Every neutron star thus has a halo of KK gravitons which decay into nu(nu), e(+)e(-), and gammagamma on time scales approximately 10(9) years. The EGRET gamma-flux limits (E(gamma) approximately 100 MeV) for nearby neutron stars constrain the compactification scale for n = 2 extra dimensions to M > or = 500 TeV, and M > or = 30 TeV for n = 3. The requirement that neutron stars are not excessively heated by KK decays implies M > or = 1700 TeV for n = 2, and M > or = 60 TeV for n = 3.     

A multi-domain Chebyshev collocation method for predicting ultrasonic field parameters in complex material geometries

The use of ultrasound to measure elastic field parameters as well as to detect cracks in solid materials has received much attention, and new important applications have been developed recently, e.g., the use of laser generated ultrasound in non-destructive evaluation (NDE). To model such applications requires a realistic calculation of field parameters in complex geometries with discontinuous, layered materials. In this paper we present an approach for solving the elastic wave equation in complex geometries with discontinuous layered materials. The approach is based on a pseudospectral elastodynamic formulation, giving a direct solution of the time-domain elastodynamic equations. A typical calculation is performed by decomposing the global computational domain into a number of subdomains. Every subdomain is then mapped on a unit square using transfinite blending functions and spatial derivatives are calculated efficiently by a Chebyshev collocation scheme. This enables that the elastodynamic equations can be solved within spectral accuracy, and furthermore, complex interfaces can be approximated smoothly, hence avoiding staircasing. A global solution is constructed from the local solutions by means of characteristic variables. Finally, the global solution is advanced in time using a fourth order Runge-Kutta scheme. Examples of field prediction in discontinuous solids with complex geometries are given and related to ultrasonic NDE.     

Phase transition in gauge theories and multiple-point model

The phase transition in the regularized U(1) gauge theory is investigated by using the dual Abelian Higgs model of scalar monopoles. The corresponding-renormalization-group-improved effective potential, analogous to the Coleman-Weinberg one, is considered in the two-loop approximation for β functions, and the phase-transition (critical) dual and nondual couplings are calculated in the U(1) gauge theory. It is shown that the critical value of the renormalized electric fine-structure constant,α _crit≈0.208, obtained in this study agrees with the lattice result for compact QED: α _crit ^lat ≈0.20±0.015. This result and the behavior of α in the vicinity of the phase-transition point are compared with the multiple-point-model prediction for the values of α near the Planck scale. Such a comparison is very encouraging for the multiple point model assuming the existence of the multiple critical point at the Planck scale.     

Contacting and forming singularities: Distinguishing examples

A thin film bridge breaks in a way that starts at one equilibrium state and ends at another equilibrium state. The dynamical trajectory that carries it from connected to disconnected provides rare evidence regarding the singularity of passage through topological change. This nonequilibrium trajectory, called a "forming" flow, is discussed in an attempt to frame it within the larger class of singularities for which bounding surfaces do not remain material surfaces. As a contrast, the weaker "contacting" singularity is illustrated by a stagnation flow where material points reach the stagnation point in finite time. A classification scheme based on pathology of the nonunique Lagrangian motions is suggested. New results for the disconnection example include healing of surgery in post-disconnection simulations, different dynamical scalings of the just-disconnected components and a comparison of post-disconnection simulation to experiment. (c) 1999 American Institute of Physics.