Beyond the absorption-limited nonlinear phase shift with microring resonators

We show that the nonlinear phase shift produced by a ring resonator constructed from a given nonlinear optical material can be greater than the phase shift produced by a single pass through an infinite length of the same material when linear and nonlinear absorption are taken into consideration. The figure of merit (defined by the phase shift times the throughput) also improves for the ring resonator over that of the native nonlinear absorbing material. We finally show that these benefits of using the ring resonator as a nonlinear phase-shifting element can enhance the switching characteristics of a Mach-Zehnder interferometer.     

How to Make Drugs Orally Active: A Substrate Template for Peptide Transporter PepT1

By building key structural features into hydrophilic drugs, they can be recognized by the PepT1 transporter system of the small intestine and rendered orally active. The model shown provides, for the first time, a 3D template for all known substrates of PepT1.     

Holomorphic Mappings on C(I), I uncountable

We investigate the relationship between the various topologies that can be defined on spaces of holomorphic functions on C^(I for I uncountable. Our investigation also leads to some interesting results about the space ${\rm C}^{(I)}{{\hat \otimes} \atop \pi}{\rm C}^{(I)}$ .     

Numerical sensitivity of trajectories across conformational energy hypersurfaces from geometry optimized molecular orbital calculations: AM1, MNDO,and MINDO/3

The monocyclic β-lactam [[4(S)-methyl-2-oxo-1-azetidinyl]thia]acetic acid was studied by the semiempirical molecular orbital methods AM1, MNDO, and MINDO/3. Using the reaction coordinate option in the program MOPAC on VAX and Cray X-MP computers, the potential energy curve was calculated for rotation of the C2-N1-S-C torsional angle in the conformationally flexible side chain while optimizing all other geometrical variables in the molecule. The trajectory taken during geometry optimization was found to be sensitive to the computer, the program version, the convergence criteria, and the degree of code optimization used in the calculation. In order to reduce the likelihood of spurious results, conformational or reaction energy hypersurfaces need to be calculated with the more precise SCF convergence and minimization criteria available in programs for MINDO/3, MNDO, and AM1 calculations. The nitrogen in the model β-lactam antibiotic is predicted to invert periodically as the dihedral angle to the exocyclic N-substituent sweeps through 360°.     

Unnatural parity levels populated in the 16O(6Li,d)20Ne reaction

The ¹⁶O(⁶Li, d)²⁰Ne reaction to the 2^?, 4.97 MeV, 3^?, 5.63 MeV, and 4^?, 7.01 MeV members of the K^π = 2^? band has been studied. Angular distributions were measured at 32 MeV from 7.5° to 145° (lab). Excitation functions were measured at 15° (lab) and 145° (lab) from 31 to 33 MeV and 31.75 to 32.5 MeV, respectively. Results of multi-step and compound nuclear calculations are compared to the data. At this incident energy, both mechanisms appear to contribute to the population of the unnatural parity levels.     

The aromaticity of pentalene, heptalene and related bicyclic hydrocarbons

Using an internally consistent LCAO-MO method it is shown that pentalene and heptalene are not electronically stable and will tend to gain or lose two electrons, respectively. The treatment is generalized for bicyclic non-alternant hydrocarbons wih a perimeter of 4n atoms by means of first-order perturbation theory and verified numerically. The energy levels of four selected molecules are presented.     

Searches for B0 decays to combinations of two charmless isoscalar mesons

We search for B meson decays into two-body combinations of eta, eta', omega, and phi mesons from 89 x 10(6) BB pairs collected with the BABAR detector at the PEP-II asymmetric-energy e+e- collider at SLAC. We find the branching fraction B(B0-->etaomega)=(4.0(+1.3)(-1.2)+/-0.4)x10(-6) with a significance of 4.3 sigma. For the other decay modes we set the following 90% confidence level upper limits on the branching fractions, in units of 10(-6): B(B0-->etaeta)<2.8, B(B0-->etaeta')<4.6, B(B0-->eta'eta')<10, B(B0-->eta'omega)<2.8, B(B0-->etaphi)<1.0, B(B0-->eta'phi)<4.5, and B(B0-->phiphi)<1.5.     

Dramatic enhancement of third-harmonic generation in three-dimensional photonic crystals

We have observed a dramatic enhancement of third-harmonic generation in 3D polystyrene-air photonic crystals pumped by a near infrared laser beam. As the pump wavelength is tuned, the peak of the enhancement occurs when the third-harmonic wavelength approaches the short-wavelength edge of the band gap. We show that the origin of the enhancement is phase matching provided by the periodic structure of the photonic crystals.     

Observation of ultraslow light propagation in a ruby crystal at room temperature

We have observed slow light propagation with a group velocity as low as 57.5+/-0.5 m/s at room temperature in a ruby crystal. A quantum coherence effect, coherent population oscillations, produces a very narrow spectral "hole" in the homogeneously broadened absorption profile of ruby. The resulting rapid spectral variation of the refractive index leads to a large value of the group index. We observe slow light propagation both for Gaussian-shaped light pulses and for amplitude modulated optical beams in a system that is much simpler than those previously used for generating slow light.     

Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation

Toluene dioxygenase (TDO)-catalysed sulfoxidation, using Pseudomonas putida UV4, was observed for the thiophene substrates 1A-1N. The unstable thiophene oxide metabolites, 6A-6G, 6K-6N, spontaneously dimerised yielding the corresponding racemic disulfoxide cycloadducts 7A-7G, 7K-7N. Dimeric or crossed [4 + 2] cycloaddition products, derived from the thiophene oxide intermediates 6A and 6D or 6B and 6D, were found when mixtures of thiophene substrates 1A and 1D or 1B and 1D were biotransformed. The thiophene sulfoxide metabolite 6B was also trapped as cycloadducts 17 or 18 using stable dienophiles. Preferential dioxygenase-catalysed oxidation of the substituent on the thiophene ring, including exocyclic sulfoxidation (1H-1J) and cis-dihydroxylation of a phenyl substituent (1G and 1N), was also observed. An enzyme-catalysed deoxygenation of a sulfoxide in P. putida UV4 was noticed when racemic disulfoxide cyclo-adducts 7A, 7B and 7K were converted to the corresponding enantioenriched monosulfoxides 8A, 8B and 8K via a kinetic resolution process. The parent thiophene 1A and the 3-substituted thiophenes 1K-1N were also found to undergo ring dihydroxylation yielding the cis/trans-dihydrodiol metabolites 9A and 9K-9N. Evidence is provided for a dehydrogenase-catalysed desaturation of a heterocyclic dihydrodiol (9Kcis/9Ktrans) to yield the corresponding 2,3-dihydroxythiophene (24) as its preferred thiolactone tautomer (23). A simple model to allow prediction of the structure of metabolites, formed from TDO-catalysed bacterial oxidation of thiophene substrates 1, is presented.