Studies in the cycloproparene series: cycloaddition reactions of diarylmethylidenecycloproparenes

Journal ArticleDiarylmethylidenecyclopropanaphthalenes 4b-d add diphenylisobenzofuran (DPIBF) and α-pyrone across the exocyclic double bond to give ring expanded products 11b-d and 13b-d that result from subsequent relief of ring strain in the non-isolable spirocyclic intermediates 10 and 12, respectively. The benzene homologues 3b and 3c add DPIBF across the bridge bond to give the norcaradiene adducts 19b and 19c

Review and statistical analysis of the ultrasonic velocity method for estimating the porosity fraction in polycrystalline materials

A review and statistical analysis of the ultrasonic velocity method for estimating the porosity fraction in polycrystalline materials is presented. Initially, a semi-empirical model is developed showing the origin of the linear relationship between ultrasonic velocity and porosity fraction. Then, from a compilation of data produced by many researchers, scatter plots of velocity versus percent porosity data are shown for Al2O3, MgO, porcelain-based ceramics, PZT, SiC, Si3N4, steel, tungsten, UO2,(U0.30Pu0.70)C, and YBa2Cu3O(7-x). Linear regression analysis produced predicted slope, intercept, correlation coefficient, level of significance, and confidence interval statistics for the data. Velocity values predicted from regression analysis for fully-dense materials are in good agreement with those calculated from elastic properties

One-dimensional coordination polymers based on first-row transition metals: a solid-state study of weak backbone interactions

Journal ArticleWe present further data on the solid-state structures of one-dimensional coordination polymers based upon dipositive transition metal hexafluoroacetylacetonate (hfacac) complexes. A variety of linking subunits are employed in order to investigate and probe the relatively weak interactions that make up the backbones of these polymers. Reported in this study are metal complexes containing manganese, zinc, copper, and cobalt and a range of donor building blocks encompassing an array of bonding motifs, including pyridyl-metal, pyridyl(N-oxide)-metal, and hydrogen bonding. The specific linkers utilized are 4,4′-dipyridyl N,N′- dioxide hydrate, 2,5-bis(4-ethynylpyridyl)furan, 4,4′-trimethylenedipyridine, and trans-1-(2-pyridyl)-2-(4-pyridyl)-ethylene. A detailed discussion of the products is presented, as is a comparison to known compounds of a similar nature. All compounds are characterized via single-crystal X-ray diffraction and elemental analysis for the bulk of the sample

Self-selected formation of single discrete supramolecules with flexible, bidentate ligands in the coordination-driven self-assembly

Journal ArticleFlexible donor ligands like 1,2-bis(3-pyridyl)ethyne or 1,4-bis(3-pyridyl)-1,3-butadiyne selfassemble into discrete 2-D supramolecules instead of infinite networks upon combination with organoplatinum 90, 120, and 180 degree acceptor units. These systems are unique examples of versatile pyridine donors adjusting their bonding directionality to accommodate rigid platinum acceptors in the formation of closed macrocycles. Discrete, nanoscopic 3-D cages are also prepared in high yield via coordination-driven self-assembly from bidentate 3-substituted pyridines and tripod organoplatinum acceptors. Flexible, bidentate 3-substituted pyridine donors and a rigid organopalladium acceptor are also exclusively selfassembled into discrete 2-D macrocycles. Moreover, discrete supramolecules are successfully prepared from ambidentate donor ligands and platinum containing acceptors. Despite the possibility of forming more than one product, ambidentate ligands prefer to self-assemble predominantly into one species. Flexible, ambidentate pyridyl-carboxylate based donor ligands like sodium 3-(3-pyridyl)benzoate, sodium 4-(3-pyridyl)benzoate and potassium 4-(3-pyridyl)ethynylbenzoate self-assemble into discrete [2+2] macrocyclic species instead of infinite networks when combined with a 90 degree organoplatinum acceptor. In each case only one isomeric ensemble is selectively formed in high yield. All products are characterized by electrospray ionization mass spectrometry (ESI-MS), 31P{1H} and 1H NMR spectroscopy. They are the first examples of discrete supramolecules incorporating flexible, bidentate donor ligands. Despite their potential versatility, these flexible donors adjust their bonding directionality to accommodate a rigid acceptor in the formation of one discrete ensemble

Self-assembly of coordinative supramolecular polygons with open binding sites

ManuscriptThe design and synthesis of coordinative supramolecular polygons with open binding sites is described. Coordination-driven self-assembly of 2,6-bis(pyridin-4-ylethynyl)pyridine with 60? and 120? organoplatinum acceptors results in quantitative formation of a supramolecular rhomboid and hexagon, respectively, both bearing open pyridyl binding sites. The structures were determined by multinuclear (31P and 1H) NMR spectroscopy and electrospray ionization (ESI) mass spectrometry, along with a computational study

Supramolecular chemistry and molecular design: self-assembly of molecular squares

Journal ArticleModem supramolecular chemistry has been described as organized polymolecular systems held together by noncovalent interactions and represents one of the major frontiers in the chemical sciences.'-' At present the field is dominated by the hydrogen bonding motif that mimics biological systems and the classical covalent macrocyclics such as crown ethers, cyclophanes, cyclodextrins, calixarenes, etc., that represent the roots of the field!?' Much less is known about the use of coordination and transition metals as a motif for the assembly of supramolecular species

Incorporation of flexible pyridine-functionalized ligands into discrete supramolecules via coordination-driven self-assembly

Journal ArticleFlexible, pyridine-functionalized ligands were self-assembled into discrete supramolecules of differing stoichiometries upon combination with various organoplatinum molecules. They are characterized by electrospray ionization mass spectrometry, 31P(iHI and 'H NMR. Despite its inherent flexibility, 3-substituted pyridines 1 and di-pynrdyl substituted 18-membered diaza-crown ligand 8 prefer to self-assemble into closed systems when reacted with platinum-containing acceptors

A coded aperture imaging system optimized for hard X-ray and gamma ray astronomy

A coded aperture imaging system was designed for the Gamma-Ray imaging spectrometer (GRIS). The system is optimized for imaging 511 keV positron-annihilation photons. For a galactic center 511-keV source strength of 0.001 sq/s, the source location accuracy is expected to be + or - 0.2 deg

The Gamma-Ray Imaging Spectrometer (GRIS): A new balloon-borne experiment for gamma-ray line astronomy

High resolution gamma-ray spectroscopy is a relatively new field that holds great promise for further understanding of high energy astrophysical processes. When the high resolution gamma-ray spectrometer (GRSE) was removed from the GRO payload, a balloon program was initiated to permit continued development and improvement of instrumentation in this field, as well as continued scientific observations. The Gamma-Ray Imaging Spectrometer (GRIS) is one of the experiments selected as part of this program. The instrument contains a number of new and innovative features that are expected to produce a significant improvement in source location accuracy and sensitivity over previous balloon and satellite experiments