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41.
42.
Intracavity frequency doubling of a diode-pumped 946-nm Nd:YAG laser with bulk periodically poled MgO LiNbO(3) 总被引:1,自引:0,他引:1
We report what we believe is the first cw quasi-phase-matched intracavity frequency doubling of a diode-pumped 946-nm Nd:YAG laser by use of bulk periodically poled MgO-LiNbO(3). A maximum second-harmonic power of 5.9 mW was obtained at a laser diode power of 500 mW. The blue beam profile showed a TEM(00) single spatial mode of low ellipticity (1:1) because there was no walk-off problem. Bulk periodic domain inversion was accomplished by a corona discharge method with a first-order modulation period of 4.75 microm for a wavelength of 946 nm over a 2-mm interaction length in Z-cut 0.4-mm-thick MgO-LiNbO(3). 相似文献
43.
A new family of pi-conjugated delocalized biradical compound is developed. The solution of 1,4-bis(2,5-diphenylimidazol-4-ylidene)cyclohexa-2,5-diene shows the ESR signal consisting of a moderately broad unresolved line, Delta H(pp) approximately 1 mT, at room temperature. The presence of the thermal equilibrium between a triplet biradical state and a singlet state is confirmed by the ESR measurements, and the spin concentration is determined as 7.90 x 10(21) spin/mol at 300 K. The spin concentration can also be controlled by modifying the molecular planarity. Moreover, the unrestricted DFT/B3LYP calculations suggest the biradical character of the singlet ground state, and the modulation of the energy gap between the singlet state and the triplet state is investigated from the theoretical point of view. Controlling the equilibrium between a diamagnetic state and a paramagnetic state will provide significant progress in the field of biradical chemistry, and the materials with the biradical character in a ground state will lead to a novel development of molecular-based organic magnets. 相似文献
44.
Treatment of nitroarenes having electron-withdrawing groups at the ortho or para position with alkanethiol in the presence of cesium carbonate in dimethyl sulfoxide at 25 °C leads to nucleophilic displacement of the nitro group with the alkylthio group. Cesium carbonate is superior to other bases such as potassium carbonate, sodium carbonate, and triethylamine. The cesium-mediated nucleophilic aromatic substitution reaction provides a mild yet powerful and user-friendly protocol for the synthesis of aryl sulfides. 相似文献
45.
Tomoya Kitazume Kouichi Kawai Takashi Nihei Noriaki Miyake 《Journal of fluorine chemistry》2005,126(1):59-62
Synthetic utility of microreactors and highly stereoselective isomerization (>99:<1) of terminal difluoromethylated alkenes to (E)-difluoromethylated alkenes with TBAF in DMF, are described. 相似文献
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47.
Takuya Takeda Masaki Yanagi Azusa Suzuki Ryuzi Katoh Yoshio Saito 《Tetrahedron letters》2019,60(12):825-830
Novel pyrene-labeled environmentally sensitive fluorescent (ESF) nucleosides [1p3zG (1a) and 2p3zG (1b)] possessing the 3-deazaguanine skeleton were synthesized. Among them, 1p3zG (1a) exhibited longer fluorescence emission wavelengths compared with the previously reported naphthalene-modified ESF nucleoside 3nzG (48–71?nm longer in polar solvents) and showed remarkable solvent-polarity-sensitive fluorescence properties. Oligodeoxynucleotide (ODN) probes containing 1p3zG (1a) clearly discriminated target DNAs by the change in the emission wavelength and intensity through monitoring the microenvironmental change around the DNA minor groove. Thus, these pyrene-labeled ESF nucleosides can be applied in gene detection and molecular diagnostics, as well as in the structural analysis of nucleic acids. 相似文献
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49.
Naokazu Kano Jia-Hua Xing Azusa Kikuchi Seiji Kawa Takayuki Kawashima 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6-7):1685-1687
Reactions of an iminophosphorane bearing the Martin ligand with a ketone, an isothiocyanate, and an alkyne gave the corresponding cycloadducts, 1,3,2 u 5 -oxazaphosphetidine, 1,3,2 u 5 -diazaphosphetidine-4-thione, and 1,2 u 5 -azaphosphetine, respectively, while that with dimethyl acetylenedicarboxylate (DMAD) and successive hydrolysis afforded the 1,2 u 5 -oxaphosphole-(2 H )-one. Thermal reactions of the cycloadducts were also studied. 相似文献
50.