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An orthogonal [2 + 2 + <italic>n</italic> ] cycloaddition/alkyne metathesis reaction sequence enables streamlined access to conjugated macrocyclic nanocarbons.
In this paper we present a location service for Beacon Vector Routing (BVR), a point-to-point routing scheme for wireless sensor networks. A location service is necessary for decoupling the static node identifiers and dynamic BVR coordinates. This allows a node to use unique identifiers when communicating with a destination node, instead of using coordinate information directly. Our scheme uses beacons in the network as distributed look-up servers; each containing mappings of identifiers to coordinates. When a node wants to route data to another node, the sending node passes the destination node’s identifier and the payload to the location service. The location service resolves the destination node’s identifier to its associated coordinates and uses BVR to route the payload to that node. We describe our design of the location service and briefly it’s implementation. We evaluate the location service and BVR in simulation and on a sensornet testbed, and compare our results to an existing point-topoint routing scheme for sensornets. In addition, a simplified distributed hash table is implemented on top of the location service and evaluated in simulation. 1
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
The Central Atlantic Magmatic Province (CAMP) is defined by tholeiitic basalts that crop out in once-contiguous parts of North America, Europe, Africa, and South America and is associated with the breakup of Pangea. 40 Ar/ 39 Ar and paleomagnetic data indicate that CAMP magmatism extended over an area of 2.5 million square kilometers in north and central Brazil, and the total aerial extent of the magmatism exceeded 7 million square kilometers in a few million years, with peak activity at 200 million years ago. The magmatism coincided closely in time with a major mass extinction at the Triassic-Jurassic boundary.
We report on the development and exploitation of a new type of chemically amplified resist for 193 nm microlithography. The approach has great versatility as it involves a general structure amenable to radical cyclopolymerization that contains easily interchanged ester functionalities. As the mechanism of polymerization involves free radicals, changes may be made either in the polymerization conditions or in the monomer feed to adjust variables such molecular weight or etch resistance. The latter property is favorably influenced by the formation of new ring structures during polymerization. Variations in the nature of the ester moieties contained in the monomer area easily accomplished to modify the imaging characteristics, surface properties, or etch resistance of the polymers. We report the preparation of a number of novel polymer and copolymer structures and their preliminary testing as resist candidates for 193 nm lithography.
The thinning problem requires that two tasks be implemented: (i) peeling the thick pixels off; (ii) stopping the peeling process when the pixel size reduces to exactly one. The first part can be achieved with relative ease. The main difficulty lies in the second part, because the stopping decision must be done automatically. It is shown that image thinning can be achieved in real-time using a cellular neural network (CNN) with eight planes, each one defined by a set of peeling templates and a set of stopping templates. The thinning processor, which is both analog and parallel, is described and examples are shown.< <ETX xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">></ETX>
Theoretical methods are used to analyze the thermodynamics of ZSM-11 synthesis from amorphous silica and an aqueous solution of tetraalkylammonium hydroxide (TAAOH). The overall process is represented by the reaction 96SiO2(a) + n(TAA+/OH-/200H2O) = (nTAA+/Zn-) + 200nH2O. Both tetrapropylammonium (TPA+) and tetrabutylammonium (TBA+) cations are considered as the structure-directing agents, and calculations are performed for occlusion of either three or four TAA+ cations per unit cell of the zeolite. Both estimates of the change in internal energy and Gibbs free energy reveal that the synthesis of ZSM-11 should be favored by the occlusion of three TBA+ cations per unit cell, consistent with experimental observation. The present analysis also demonstrates the importance of energy and entropy changes associated with the dehydration of TAA+ and OH- ions and with the occlusion of TAA+ cations into the zeolite. The interactions of OH- anions with the zeolite framework to form defects in the form of siloxy (≡SiO-) groups are also considered.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.