Energy Minimization for Real-Time Data Gathering in Wireless Sensor Networks

This paper studies the challenging problem of energy minimization for data gathering over a multiple-sources single-sink communication substrate in wireless sensor networks by exploring the energy-latency tradeoffs using rate adaptation techniques. We consider a real-time scenario for mission-critical applications, where the data gathering must be performed within a specified latency constraint. We first propose an offline numerical optimization algorithm with performance analysis for a special case with a complete binary data gathering tree. Then, by discretizing the transmission time, we present a simple, distributed on-line protocol that relies only on the local information available at each sensor node. Extensive simulations were conducted for both long and short-range communication scenarios using two different source placement models. We used the baseline of transmitting all packets at the highest speed and shutting down the radios afterwards. Our simulation results show that compared with this baseline, up to 90% energy savings can be achieved by our techniques (both off-line and on-line), under different settings of several key system parameters     

AN INEXPENSIVE STIRRING DEVICE FOR THE 'MERRY-GO-ROUND' PHOTOREACTOR FOR THE DETERMINATION OF REACTION QUANTUM YIELDS

A simple bar magnet is employed to effect stirring of the contents of reaction cells in a'merry-go-round'photoreactor.     

Microwave-assisted solid-phase synthesis of peptoids

Microwave irradiation reduces the reaction time for the solid-phase synthesis of peptoids. Under these conditions, coupling of each residue requires only 1 min. The purity and yields of peptoids synthesized in this way are as good as or better than those achieved using standard methods. [reaction: see text]     

Simultaneously multiply-configurable or superposed molecular logic systems composed of ICT (internal charge transfer) chromophores and fluorophores integrated with one- or two-ion receptors

Integrated "ICT chromophore-receptor" systems show ion-induced shifts in their electronic absorption spectra. The wavelength of observation can be used to reversibly configure the system to any of the four logic operations permissible with a single input (YES, NOT, PASS 1, PASS 0), under conditions of ion input and transmittance output. We demonstrate these with dyes integrated into Tsien's calcium receptor, 1-2. Applying multiple ion inputs to 1-2 also allows us to perform two- or three-input OR or NOR operations. The weak fluorescence output of 1 also shows YES or NOT logic depending on how it is configured by excitation and emission wavelengths. Integrated "receptor(1)-ICT chromophore-receptor(2)" systems 3-5 selectively target two ions into the receptor terminals. The ion-induced transmittance output of 3-5 can also be configured via wavelength to illustrate several logic types including, most importantly, XOR. The opposite effects of the two ions on the energy of the chromophore excited state is responsible for this behaviour. INHIBIT and REVERSE IMPLICATION are two of the other logic types seen here. Integration of XOR logic with a preceding OR operation can be arranged by using three ion inputs. The fluorescence output of these systems can be configured via wavelength to display INHIBIT or NOR logic under two-input conditions. The superposition or multiplicity of logic gate configurations is an unusual consequence of the ability to simultaneously observe multiple wavelengths.     

Stereocontrolled formation of beta-glucosides and related linkages in the absence of neighboring group participation: influence of a trans-fused 2,3-O-carbonate group

[reaction: see text] Phenyl 4,6-di-O-benzyl-2,3-O-carbonyl-beta-D-glucothiopyranoside and the regiosiomeric phenyl 2,6-di-O-benzyl-3,4-O-carbonyl-beta-D-glucothiopyranoside were prepared and studied as glucosyl donors at -60 degrees C in dichloromethane with preactivation by 1-benzenesulfinyl piperidine before addition of the acceptor alcohol. The 2,3-O-carbonate protected donor showed moderate to excellent beta-selectivity under these conditions depending on the acceptor employed, thereby providing a means for 1,2-trans-equatorial glycosidic bonds without recourse to neighboring group participation and its associated problem of ortho ester formation. In contrast, the 3,4-O-carbonate protected donor showed moderate to no beta-selectivity under the conditions employed. The results obtained in this study with carbonate protected glucopyranosyl donors are contrasted with those obtained previously in the manno- and rhamnopyranosyl series when the 2,3-O-carbonate protected is alpha-selective and the 3,4-O-carbonate is beta-selective.     

Report on the Einstein Centenary Symposium at Ahmedabad

We consider the question of whether the correct theory of gravity is a metric theory. The metric hypothesis is shown to place severe restrictions on the form of the equation of motion for the one-body problem. By relaxing these restrictions we include nonmetric contributions to the equation of motion, and the solution in the post-Newtonian approximation is given. The solution given here contains five arbitrary parameters in place of the usual two (, ) of metric theories. One of them produces a secular change in the eccentricity; the others contribute to the perihelion advance and to periodic terms. Only certain combinations of these parameters can be determined even from orbits with different eccentricities.