A three-dimensional simulation of wind flow around buildings

The steady Navier–Stokes equation is solved to simulate the wind-flow environment of three-dimensional configurations of buildings. The method assumes an incident wind described by a power-law velocity profile. A new method for controlling the two-part nested solution iteration is introduced. The simulation is compared to some published wind-tunnel measurements.     

Diode-laser absorption measurements of CO2, H2O, N2O, and NH3 near 2.0 μm

2 , H₂O, N₂O, and NH₃ concentrations in various flowfields using absorption spectroscopy and extractive sampling techniques. An external-cavity diode laser with a tuning range of 1.953–2.057 μm was used to record absorption lineshapes from measured transitions in the CO₂ 4ν₂ ⁰+ν₃, ν₁+2ν₂ ⁰+ν₃, and 2ν₁+ν₃ bands, H₂O ν₂+ν₃and ν₁+ν₂ bands, N₂O 2ν₁+4ν₂ ⁰, ν₂ ¹+2ν₃, 3ν₁+2ν₂ ⁰, and 4ν₁ bands, and NH₃ν₁+ν₄ and ν₃+ν₄ bands. Measured CO₂, H₂O, and N₂O survey spectra were compared to calculations to verify the HITRAN96 database and used to determine optimum transitions for species detection. Individual lineshape measurements were used to determine fundamental spectroscopic parameters including the line strength, line-center frequency, and self-broadening coefficient of the probed transition. The results represent the first measurements of CO₂, H₂O, N₂O, and NH₃ absorption near 2.0 μm using room-temperature near-IR diode lasers. Received: 12 March 1998/Revised version: 7 May 1998     

Absorption of CO laser radiation by NO

Absorption of CO i.r. laser radiation by NO has been studied over the temperature range 300°–4000°K using a grating-tunable CO laser in conjunction with a room-temperature absorption cell and a shock tube. The CO laser line with strongest absorption at elevated temperatures was determined to be the V = 7 → 6, J = 12 → 13 line at 1935.4817 cm^-1, which is nearly coincident with the ²Π_{$\text{3}\text{2}$}V = 0 → 1, J = 37/2 → 39/2 transition in NO. The absorption cell measurements (300°K) were used to infer the position of the NO absorption line (a Λ-doublet at 1935.492 and 1935.497 cm^-1) as well as collision-broadening parameters in pure NO and NO dilute in foreign gases: 2γ° (collision-broadened full width at half maximum in cm^-1 atm^-1 at 300°K) = 0.110, NO-NO; 0.072, NO in Ar; 0.069, NO in Kr; 0.109, NO in N₂. Calculations of the NO absorption coefficient at 1935.4817 cm^-1 are presented for a range of conditions applicable to current studies in combustion and NO_x kinetics. Shock tube measurements (630°–4000°K) supporting these calculations are also reported.     

Sulfotransferases: structure, mechanism, biological activity, inhibition, and synthetic utility

The sulfonation (also known as sulfurylation) of biomolecules has long been known to take place in a variety of organisms, from prokaryotes to multicellular species, and new biological functions continue to be uncovered in connection with this important transformation. Early studies of sulfotransferases (STs), the enzymes that catalyze sulfonation, focused primarily on the cytosolic STs, which are involved in detoxification, hormone regulation, and drug metabolism. Although known to exist, the membrane-associated STs were not studied as extensively until more recently. Involved in the sulfonation of complex carbohydrates and proteins, they have emerged as central players in a number of molecular-recognition events and biochemical signaling pathways. STs have also been implicated in many pathophysiological processes. As a result, much interest in the complex roles of STs and in their targeting for therapeutic intervention has been generated. Progress in the elucidation of the structures and mechanisms of sulfotransferases, as well as their biological activity, inhibition, and synthetic utility, are discussed in this Review.     

Stark effects on the phosphorescent states of l-indanone,l-tetralone,and 2,4,5-Trimethylbenzaldehyde

The differences in dipole moments between the ground and the phosphorescent states of l-indanone, l-tetralone, and 2,4,5-trimethylbenzaldehyde using durene and hexamethylbenzene host crystals are determined from spectral line splittings in a static electric field and from intensity modulation in an alternating field. It is concluded that the magnitude of the vector difference in dipole moments characteristic of a ³nπ^* excited state for l-indanone is ?2.2 ± 0.1 D and for l-tetralone is ?1.8 ± 0.1 D while the difference characteristic of a ³ππ^* excited state for trimethylbenzaldehyde is ± 1.1 ±0.1 D.     

Advanced surface modification of indium tin oxide for improved charge injection in organic devices

A new method is described for surface modification of ITO with an electroactive organic monolayer. This procedure was done to enhance hole injection in an electronic device and involves sequential formation of a monolayer of a pi-conjugated organic semiconductor on the indium tin oxide (ITO) surface followed by doping with a strong electron acceptor. The semiconductor monolayer is covalently bound to the ITO, which ensures strong adhesion and interface stability; reduction of the hole injection barrier in these devices is accomplished by formation of a charge-transfer complex by doping within the monolayer. This gives rise to very high current densities in simple single layer devices and double layer light emitting devices compared to those with untreated ITO anodes.