Abstract: A synthetic method leading to the isolation of ruthenium-based olefin metathesis catalysts relies on the cross metathesis reaction between (L1)Ru(L2)(3-phenylindenylid-1-ene)Cl2 (where L1 and L2 can be two-electron donors) and an olefin. This method leads to the isolation of numerous ruthenium olefin metathesis catalysts.

Abstract: Imidazolium salts are the immediate precursors to N-heterocyclic carbenes (NHC) yet a simple, general synthetic route to a wide variety of imidazolium salts is not yet available. Such a straightforward route is described for two specific members of this family of ligand precursor: 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride (IMes.HCl) and 1,3-Bis(2,6-diispropylphenyl)imidazolium chloride (IPr.HCl). The procedure appears general and similar protocols can be used to isolate various imidazolium salts.

Abstract: A high temperature (on the order of about 90° C. or above) non-aqueous synthetic procedure for the preparation of substantially monodisperse IV-VI semiconductor nanoparticles (quantum dots) is provided. The procedure includes first introducing a first precursor selected from the group consisting of a molecular precursor of a Group IV element and a molecular precursor of a Group VI element into a reaction vessel that comprises at least an organic solvent to form a mixture. Next, the mixture is heated to a temperature of about 90° C. or above and thereafter a second precursor which is different from the first precursor and is selected from the group consisting of a molecular precursor of a Group IV element and a molecular precursor of a Group VI element is added into the heated mixture.

Abstract: A heterogeneous catalytic system for RCM is recyclable, shows reactivity, tolerates functional groups and performs with dienes and highly hindered substrates.

Abstract: A synthetic method leading to the isolation of ruthenium-based olefin metathesis catalysts relies on the cross metathesis reaction between (L1)Ru(L2)(3-phenylindenylid-1-ene)Cl2 (where L1 and L2 can be two-electron donors) and an olefin. This method leads to the isolation of numerous ruthenium olefin metathesis catalysts.

Abstract: By utilizing the sequential synthesis afforded reverse micelles, nanocomposite materials can be synthesized which have a diamagnetic core surrounded by a thin shell of ferromagnetic material passivated with a second shell of a diamagnet. Using gold as the diamagnetic material and iron as the ferromagnetic material, nanocomposites can be synthesized where there is a thin layer of the magnetic material, which is passivated and protected from oxidation. In this case, all of the spins of the magnetic layer lie within the surface of the particle.

Abstract: The cationic iridium carbene complexes [Ir(cod)(N)(L)]X have been synthesized by reaction of [Ir(cod)(py)2]PF6 with L or NL ligands. Complexes of this type are active hydrogenation catalysts capable of hydrogenating simple olefins at room temperature and atmospheric pressure of hydrogen or by transfer hydrogenation.

Abstract: An attachable vertical bow plate set a distance ahead of the existing bow, preferably extending above and below the water surface, helps to reduce drag associated with a vessel. The plate's lower edge is preferably set at a depth corresponding to the depth where the existing bow begins to have its cut away.

Abstract: The magnetic and magnetotransport properties of field-aligned single domain half-metallic CrO2 powders have been studied. Needle-shaped nanoparticles of CrO2 have been aligned in a strong magnetic field. The aligned powder sample shows a strong anisotropy along the alignment direction. The conduction mechanism of the aligned CrO2 powder sample has been examined and is consistent with the intergranular spin dependent tunneling. Negative tunneling magnetoresistance (TMR) of about 41% is achieved in a small field in the vicinity of the coercive field at 5 K. The magnetoresistance (MR) versus field curve shows two well-separated narrow peaks at the coercive fields and resembles that of a magnetic tunnel junction. This junction-like MR results from the narrow switching field distribution of the aligned powders. The results suggest that the aligned magnetic CrO2 particles may find novel applications in spin transport structures and devices.

Abstract: Uniaxial magnetic anisotropy was found in the Fe/Co/Cu/Co magnetoresistive structures deposited on Si (100) substrates. Samples magnetized along an easy anisotropy axis showed extremely sharp magnetization and magnetoresistance switching at low fields and maximum giant magnetoresistance of 9.5% at 5K (5.5% at room temperature) for the samples with 5 nm of Fe,5 nm of Co, 2.5 nm of Cu and 2 nm of Co. These results were advantageous compared to Co/Cu/Co trilayers grown on Cr/Cu buffer which did not exhibit uniaxial anisotropy. Deposition on spinning wafers allowed excluding substrate related anisotropy. An existing magnetic field in the magnetron sputtering system with the strength of 32 Oe at the sample location was found the most probable source of the induced uniaxial anisotropy.

Abstract: A process for conducting coupling reactions of aryl halides with unsaturated silanes is described. The processes use N-heterocyclic carbenes as ancillary ligands in these coupling reactions. A coupling of an aryl halide with an unsaturated silane can be carried out by mixing, in a liquid medium, at least one strong base; at least one aryl halide or aryl pseudohalide in which all substituents are other than silyl groups, wherein the aryl halide has, directly bonded to the aromatic ring(s), at least one chlorine atom, bromine atom, or iodine atom; at least one silane wherein the silicon atom is quaternary, wherein one group bound to the silicon atom is unsaturated at the alpha or beta position, and wherein each of the remaining groups bound to the silicon atom is a saturated hydrocarbyl or a saturated hydrocarbyloxy group; at least one nickel, palladium, or platinum compound, wherein the formal oxidation state of the metal is zero or two; and at least one N-heterocyclic carbene.

Abstract: A Pd(OAc)2/diazabutadiene system has been developed for the catalytic cross-coupling of aryl halides with arylboronic acids. A combination of the diazabutadiene DAB-Cy (1, N,N′-Dicyclohexyl-1,4-dizabutadiene) and Pd(OAc)2 was found to form an excellent catalyst for the Suzuki-Miyaura cross-coupling of various aryl bromides and activated aryl chlorides with arylboronic acids.

Abstract: A metal stearate denitrification system utilizes insoluble and hydrophobic metal stearates as a carbon source for the bacterial substrate. The system in a long-term, low-maintenance denitrification cell is a flow-through plastic container having a replaceable porous liner filled with a porous and permeable mixture of metal stearate and volcanic scoria and a small amount of soil as a bacteria source. Oxidized effluent from an aerated home septic tank enters the container near its base and exits near its top. The insoluble and hydrophobic metal stearate remains in place as the fluid flows through the container. Over a time span of years, the metal stearate is gradually destroyed by bacteria using stearate as a metabolic food source. The aerobic bacteria first remove the dissolved oxygen in the entering fluid and then the anaerobic bacteria denitrify the nitrate.

Abstract: A method of oxidizing organic pollutants in a solution comprises chelating a catalytic metal with cyclodextrins (CD) and/or derivatized cyclodextrins (dCD), and simultaneously complexing an organic pollutant with cyclodextrins (CD) and/or derivatized cyclodextrins (dCD). The CD or dCD is capable of removing the pollutant from sorption sites (either in solution, in soil/sediment, or on surfaces). Furthermore, the CD/dCD is also capable of competing with other metal chelators that may be present in the system. The ability of the CD/dCD to bind both the pollutant and the metal in the presence of competing binding sites is essential for the success of the technique.

Abstract: A corrosion-resistant coating for aluminum alloys preferably includes lithium molybdate and cerium. A conversion coating has been developed for aluminum surfaces that can substitute for the conventional chromate containing conversion coating. This new coating contains compounds such as lithium molybdate and cerium. The initial process consisted of two steps. Coated surface was tested to ASTM B117 requirement for 168 hours, showing little corrosion. Paint adhesion tests were also conducted with good results. Subsequent tests indicated that one step is adequate, but additional tests are needed.

Abstract: A method for making a patterned magnetic recording disk uses patterned ion implantation of the disk substrate. Energetic ions, such as He, N or Ar ions, are directed to the disk substrate through a mask, preferably a non-contact mask. They are implanted into the substrate, and the process causes localized topographic distortions in the substrate surface. A magnetic layer is then deposited over the substrate in the conventional manner, such as by sputtering. The result is a disk with patterned magnetic regions that are raised above the substrate surface. Because these regions are elevated, they are closer to the recording head in the disk drive and can thus be individually recorded to form discrete magnetic bits. Depending on the type of substrate used, the ion implantation can cause either localized swelling to form pillars or localized compaction to form pits. The patches of magnetic material on the tops of the pillars, or on the substrate surface between the pits, form the discrete magnetic bits.

Abstract: This invention provides a process for conducting amination reactions. The processes of the present invention make use of N-heterocyclic carbenes as ancillary ligands in aminations of aryl halides and aryl pseudohalides. An amination can be carried out by mixing, in a liquid medium, at least one strong base; at least one aryl halide or aryl pseudohalide in which all substituents are other than amino groups, wherein the aryl halide has, directly bonded to the aromatic ring(s), at least one halogen atom selected from the group consisting of a chlorine atom, a bromine atom, and an iodine atom; at least one primary amine and/or at least one secondary amine; at least one metal compound comprising at least one metal atom selected from nickel, palladium, and platinum, wherein the formal oxidation state of the metal is zero or two; and at least one N-heterocyclic carbene.

Abstract: This invention provides a process for conducting Suzuki coupling reactions. The processes of the present invention make use of N-heterocyclic carbenes as ancillary ligands in Suzuki couplings of aryl halides and aryl pseudohalides. A Suzuki coupling can be carried out by mixing, in a liquid medium, at least one strong base; at least one aryl halide or aryl pseudohalide in which all substituents are other than boronic acid groups, wherein the aryl halide has, directly bonded to the aromatic ring(s), at least one halogen atom selected from the group consisting of a chlorine atom, a bromine atom, and an iodine atom; at least one arylboronic acid in which all substituents are other than chlorine atoms, bromine atoms, iodine atoms, or pseudohalide groups; at least one metal compound comprising at least one metal atom selected from nickel, palladium, and platinum, wherein the formal oxidation state of the metal is zero or two; and at least one N-heterocyclic carbene.

Abstract: This invention provides a process for conducting Kumada coupling reactions. The processes of the present invention make use of N-heterocyclic carbenes as ancillary ligands in Kumada couplings of aryl halides. A Kumada coupling can be carried out by mixing, in a liquid medium, at least one aryl halide, wherein the aryl halide has, directly bonded to the aromatic ring(s), at least one halogen atom selected from the group consisting of a chlorine atom, a bromine atom, and an iodine atom; at least one Grignard reagent; at least one metal compound comprising at least one metal atom selected from nickel, palladium, and platinum, wherein the formal oxidation state of the metal is zero or two; and at least one N-heterocyclic carbene.

Abstract: This invention provides a process for conducting Stille coupling reactions. The processes of the present invention make use of N-heterocyclic carbenes as ancillary ligands in Stille couplings of aryl halides.