Upper bound on the decay tau-->microgamma from the Belle detector

We have performed a search for the lepton-flavor-violating decay tau-->microgamma using a data sample of 86.3 fb(-1) accumulated by the Belle detector at KEK. No evidence for a signal is seen, and we set an upper limit for the branching fraction of B(tau-->microgamma)<3.1 x 10(-7) at the 90% confidence level.     

Measurement of the electroweak penguin process B-->X(s)l+l-

We report the first measurement of the branching fraction for the inclusive decay B-->X(s)l(+)l(-), where l is either an electron or a muon, and X(s) is a hadronic recoil system that contains an s quark. We analyzed a data sample of 65.4 x 10(6) B meson pairs collected with the Belle detector at the KEKB e(+)e(-) asymmetric-energy collider. We find B(B-->X(s)l(+)l(-))=[6.1 +/-1.4(stat) +1.4-1.1(syst)] x 10(-6) for dilepton masses greater than 0.2 GeV/c(2).     

Cyclization of α-haloamide with internal double bond by use of the low-valent metal complex

The α-haloamide having internal double bond was allowed to react with a catalytic amount of Pd(PPh₃)₄ in the presence of proton sponge to produce a cyclized product in a fairly good yield possibly through the intermediation of σ-alkylmetal complex although it was not isolated.     

A Residue Calculus for Root Systems

Let V be a finite-dimensional real vector space on which a root system is given. Consider a meromorphic function on V =V+iV, the singular locus of which is a locally finite union of hyperplanes of the form V , = s, , s . Assume is of suitable decay in the imaginary directions, so that integrals of the form _+iV , d make sense for generic V. A residue calculus is developed that allows shifting . This residue calculus can be used to obtain Plancherel and Paley–Wiener theorems on semisimple symmetric spaces.     

Phytophenol Dimerization Reaction: From Basic Rules to Diastereoselectivity and Beyond

Phytophenol dimerization, which is a radical-mediated coupling reaction, plays a critical role in many fields, including lignin biosynthesis. To understand the reaction, 2,2-diphenyl-1-picrylhydrazyl radical was used to initiate a series of phytophenol dimerization reactions in methanol. The products were identified using ultra-performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight tandem mass spectrometry (UHPLC-ESI-Q-TOF-MS/MS) analysis in situ. The identified products mainly included biphenols, magnolol, honokiol, gingerol 6,6′-dimers, 3,6-dimethoxylcatechol β,β′ dimer, euphorbetin, bis-eugenol, dehydrodiisoeugenol, trans-ε-viniferin, (+) pinoresinol, and (−) pinoresinol. Structure–function relationship analysis allowed four basic rules to be defined: meta-excluded, C–C bonding domination, ortho-diOH co-activation, and exocyclic C=C involvement. The exocyclic C=C involvement, however, required conjugation with the phenolic core and the para-site of the -OH group, to yield a furan-fused dimer with two chiral centers. Computational chemistry indicated that the entire process was completed via a radical coupling reaction and an intramolecular conjugate addition reaction. Similar results were also found for the horseradish peroxidase (HRP)-catalyzed coniferyl alcohol dimerization, which produced (+) and (−) pinoresinols (but no (−) epipinoresinol), suggesting that the HRP-catalyzed process was essentially an exocyclic C=C-involved phytophenol dimerization reaction. The reaction was highly diastereoselective. This was attributed to the intramolecular reaction, which prohibited Re-attack. The four basic rules and diastereoselectivity can explain and even predict the main products in various chemical and biological events, especially oxidase-catalyzed lignin cyclization.     

Novel reactor for high volume low-cost silicon epitaxy

The chemical vapor deposition of epitaxial layers of silicon is a widely used process in the electronic industry. It is a batch process and the relatively small capacity (i.e., 20–30 wafers) of epitaxial reactors significantly contributes to the expense of the process. We thus embarked on a research project aimed at a significant expansion of the reactor capacity. The first step was to conduct a complete characterization of the presently used reactors by means of flow visualization, temperature measurements and mass spectrometric studies; results of these studies will be briefly presented and discussed. The main conclusion from these studies was that up-scaling of present reactors is not economical. We thus designed and constructed a novel epitaxial reactor, radically different from current types. In this reactor the susceptor structure consists of parallel graphite discs. Wafers are fastened to one or both sides of these discs. The nutrient gaseous mixture is injected into spaces between discs by a specially designed gas distributor, which delivers the same amount of the mixture to all interdisc spacings, thus insuring the wafer-to-wafer thickness uniformity. A combination of the rotation of the susceptor discs with the gas distributor motion insures the on-the-wafer thickness uniformity. The above described parallel packing allows much higher reactor capacities (e.g., 50–100 wafers). It also results in a more economical reactor in terms of consumption of energy and chemicals. We shall illustrate the application of the novel reactor (known as the “RCA Rotary Disc Reactor”) to epitaxial deposition of silicon from SiCl₂H₂.     

Preparation of a Completely Oriented Molecular Sieve Membrane

Growth of oriented seed crystals on a substrate led to a completely oriented and continuous membrane of LTA-type zeolite. The seed crystals of cubic morphology were dip-coated onto a tilted substrate (see schematic diagram) with the zeolite channels normal to the surface. The substrate was hydrothermally treated in a reaction mixture containing the organic ligand 2,2-bis(hydroxymethyl)-2,2',2"-nitrilotriethanol, which lowers the degree of supersaturation of [Al(OH)(4)](-) ions and preferentially facilitates the intergrowth of the seed crystals.