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101.
102.
Under the Pummerer reaction conditions, N-(1-cyclohexenyl)-N-methyl-α-(methylsulfinyl)acetamide () cyclized in a 5-endo trigonal fashion through the intermediary cation () to give the tetrahydro-4H-oxindole (). The reaction was successively applied to a novel synthesis of erythrinane skeleton. 相似文献
103.
104.
The growth, movement and nature of outside dislocation, which propagate from heavily phosphorus (>1015 ions/cm2) implanted (111), (100), and (110) silicon layers into unimplanted outside regions by a compressive strain induced during
1100° C wet O2 annealing, are investigated using transmission electron microscopy and x-ray diffraction topography. Outside dislocations
are formed, mainly on (111) planes., by the glide motion of dislocation networks formed in implanted layers during early annealing.
This results in dislocations extending into the unimplanted areas to different degrees, in the order of, from the largest
to smallest, (111), (110), and (100) wafers. In (110) wafers, the [001] oriented dislocations in the implanted regions rise
to the surface at the implant and unimplant boundary. On the other hand, the [110] dislocations penetrate into the unimplanted
region. Two sets of orthogonal 〈110〉 oriented dislocations generated in (100) implanted wafers behave in the same manner as
the [001] dislocations in (110) wafers. Some sources of the compressive strain related to the generation of these dislocations
are discussed. 相似文献
105.
Ikuma N Tsue H Tsue N Shimono S Uchida Y Masaki K Matsuoka N Tamura R 《Organic letters》2005,7(9):1797-1800
[reaction: see text] Enantiomerically enriched samples of chiral cyclic nitroxides with a 4-hydroxyphenyl group on the stereogenic center bearing the NO radical group undergo unprecedented spontaneous racemization and/or epimerization in aprotic solvents, which can be well accounted for by the multistep equilibrations involving planar quinoid intermediates. 相似文献
106.
Tamura R Takeuchi T Aoki C Takeuchi S Kiss T Yokoya T Shin S 《Physical review letters》2004,92(14):146402
Ca 2p-3d resonant photoemission spectroscopy of a Cd6Ca crystalline approximant unambiguously demonstrates that the low-lying unoccupied 3d levels of calcium are lowered below the Fermi energy by the formation of the approximant, as suggested from electronic structure calculations [Phys. Rev. Lett. 87, 206408 (2001)]]. Moreover, the Ca 3d partial density of states (DOS) obtained near the Fermi energy is in reasonable agreement with theoretical Ca 3d DOS. These results verify the unconventional picture that the origin of the pseudogap in the Cd-based quasicrystals is due to hybridization of the Ca 3d band with the Cd 5p band. 相似文献
107.
A new class of molecular beacons were developed in which pyrene fluorophores were connected both at 3' and 5' ends of a single-stranded oligonucleotide. The two pyrene-based fluorophores were synthesized from the same starting material, so that the preparation of the beacons was simplified. The detection strategy of the beacons for target DNAs is based on "excimer-monomer emission switching" of the pyrene fluorophores: excimer emission of the pyrene moieties changed to monomer one when the beacons hybridized with the targets. This type of two-state mode of fluorescence allows unambiguous detection of the target DNAs because strict 1:1 correlation between the nonhybridized and the hybridized beacons can be monitored by the presence of isoemissive points of the fluorescence changes. The beacons can detect target 19-mer DNAs and can discriminate the targets from their single-nucleotide mismatches at 1 nM concentration. Advantages of the excimer-monomer switching molecular beacons were discussed in comparison with conventional ones. 相似文献
108.
Shibata T Fujimoto T Yokota K Takagi K 《Journal of the American Chemical Society》2004,126(27):8382-8383
An asymmetric [2+2+2] cycloaddition of an alpha,omega-diyne, possessing ortho-substituted aryl groups on its terminus, and a monoalkyne with oxygen functionalities gave various axially chiral teraryl compounds. The coupling proceeded with extremely high enantio- (>99.5% ee) and diastereoselectivities (dl/meso = >95/5) when catalyzed by an iridium-chiral phosphine complex. As the products were readily transformed into diol compounds by deprotection without racemization, the present procedure provides access to a new chiral pool of diol compounds with C2 symmetry. 相似文献
109.
cis-Decalin (2) and perylene (3) are co-enclathrated by a self-assembled M6L4-coordination cage (1) to give 1 superset(2.3) although each of them is not enclathrated. This phenomenon is termed as AND bimolecular recognition because enclathration occurs only if 2 and 3 coexist. Cage 1 also coenclathrates azulene (8) and 1,4-naphthoquinone (9) to give 1 superset(8.9). In this case, 1 superset(8)2 and 1 superset(9)2 are formed by treating 1 with 8 and 9 individually. This case is termed as OR bimolecular recognition because enclathration occurs if 8 or 9 exists. Accordingly, we have shown that the self-assembled cage 1 experiences both AND and OR bimolecular recognition. 相似文献
110.
Shigendo Enomoto Ken-ichi Kumagai Taro Tamura Miki Hasegawa Kyoko Nakada Toshihiko Hoshi Michio Kobayashi 《Monatshefte für Chemie / Chemical Monthly》2004,29(1):471-481
Fluoranthene (FA) forms a 1:1 van der Waals complex with benzene in cyclohexane. The 1H NMR spectrum of this complex shows that the FA moiety in the complex state has five kinds of hydrogen atoms and that the 1H NMR peaks assigned to the protons attached to the naphthalene skeleton are largely shifted to higher magnetic field on complex formation with benzene. These observations indicate that the complex takes the structure of CS symmetry, in which the benzene molecule mainly interacts with the electronic system localized on the naphthalene moiety of FA. The present ab initio calculations reproduce well the 1H NMR spectral shifts mentioned above and the experimentally predicted CS structure of the complex. According to the PPP calculations for the electronic absorption spectral changes on the complex formation, the FA-benzene complex is considered to take a sandwich type structure. 相似文献