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Cast aluminum alloys have been successful in a variety of powertrain components in high performance motorcycles (Fig. 1). An example is the water-cooled, 250 cm3 cylinder block (Fig. 2) manufactured [...]

The objective of this symposium at the First International Congress of Respiratory Biology (ICRB) was to enhance communication between comparative biologists and cancer researchers working on [O.sub.2] sensing via the HIF pathway. Representatives from both camps came together on August 13-16, 2006, in Bonn, Germany, to discuss molecular adaptations that occur after cells have been challenged by a reduced (hypoxia) of completely absent (anoxia) supply of oxygen. This brief 'critters-to-cancer' survey discusses current projects and new directions aimed at improving understanding of hypoxic signaling and developing therapeutic interventions.

A new model for analyzing the photophysics of polymer aggregates is introduced taking into account exciton motion along a polymer chain and across polymer chains. Excitonic coupling and vibronic coupling are treated on equal footing using a Holstein-based Hamiltonian represented in a multi-particle basis set. In the HJ-aggregate model the competition between intrachain (through-bond) coupling leading to Wannier-Mott excitons, and interchain (through-space) coupling leading to Frenkel excitons, is studied in detail for two model dimers: one composed of red-phase polydiacetylene (PDA) chains and the other composed of regioregular P3HT chains. The resulting photophysical properties are shown to depend critically on the relative magnitudes of the intrachain and interchain exciton bandwidths. Dominant intraband (interband) coupling favors a photophysical response resembling J-aggregates (H-aggregates). In PDA dimers, where intrachain coupling prevails, the absorption spectrum is dominated by the 0-0 peak, as is characteristic of J-aggregates. The photoluminescence (PL) spectrum displays hybrid character: the ratio of the main (0-0) band to the first vibronic sideband intensities is initially zero at T = 0 K due to the forbidden nature of the 0-0 transition, but then increases with temperature in a manner characteristic of H-aggregates, peaking when kT ≈ ΔE, where ΔE is the interchain splitting. Further increases in temperature result in a decline of the PL ratio, as in a J-aggregate. This remarkable H to J transition is also predicted for the temperature dependence of the radiative decay rate, krad. The maximum (peak) rate scales as, kradmax∼(Wintra/Winter)1/2, where Wintra (Winter) is the intrachain (interchain) exciton bandwidth. Hence, when Wintra is sufficiently larger than Winter the dimer displays thermally activated superradiance. In P3HT the intrachain coupling is far weaker than in PDA making the intrachain and interchain couplings comparable in the crystalline phase. Although the absorption spectral line shape is still well-accounted for by the conventional H-aggregate model, the photoluminescence is more sensitive, with H or J behavior tunable by changes in morphology. Long range intrachain order which coincides with weaker interchain interactions induces J-aggregate behavior, while short range intrachain order and the resulting stronger interchain coupling induces H-aggregate behavior. Our predictions neatly account for the H-like dominance exhibited by the PL from spin-cast films and the J-like dominance exhibited by the PL from highly ordered P3HT nanofibers self-assembled in toluene. [ABSTRACT FROM AUTHOR]

A theory describing vibronic coupling in direct band gap, one-dimensional semiconductors is developed to account for the photophysical properties of isolated, defect-free conjugated polymers. A Holstein-like Hamiltonian represented in a multi-particle basis set is used to evaluate absorption and emission due to Wannier-Mott excitons. The photophysical properties of such quantum wires are shown to strongly resemble those of Frenkel exciton J-aggregates. The 11Bu exciton coherence length and effective mass are readily determined from the ratio of the 0-0 and 0-1 line strengths, I0 - 0/I0 - 1, in the photoluminescence spectrum. I0 - 0/I0 - 1 is shown to follow a T-1/2 dependence, in an excellent agreement with experiments on the red-phase of polydiacteylene. [ABSTRACT FROM AUTHOR]

A theory for polarized absorption in crystalline oligoacenes is presented, which includes Frenkel exciton coupling, the coupling between Frenkel and charge-transfer (CT) excitons, and the coupling of all neutral and ionic excited states to the dominant ring-breathing vibrational mode. For tetracene, spectra calculated using all Frenkel couplings among the five lowest energy molecular singlet states predict a Davydov splitting (DS) of the lowest energy (0-0) vibronic band of only -32 cm-1, far smaller than the measured value of 631 cm-1 and of the wrong sign-a negative sign indicating that the polarizations of the lower and upper Davydov components are reversed from experiment. Inclusion of Frenkel-CT coupling dramatically improves the agreement with experiment, yielding a 0-0 DS of 601 cm-1 and a nearly quantitative reproduction of the relative spectral intensities of the 0-n vibronic components. Our analysis also shows that CT mixing increases with the size of the oligoacenes. We discuss the implications of these results on exciton dissociation and transport. [ABSTRACT FROM AUTHOR]