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31.
32.
Shigekazu Ito Hideaki Miyake Hiroki Sugiyama Masaaki Yoshifuji 《Heteroatom Chemistry》2005,16(5):357-360
Kinetically stabilized 2‐lithio‐1‐(2,4,6‐tri‐t‐butylphenyl)‐1‐phosphapropene was allowed to react with a bulky phosphaalkyne Mes*CP (Mes* = 2,4,6‐t‐Bu3C6H2) followed by quenching with iodomethane or benzyl bromide to give the corresponding 1,3‐diphosphabuta‐1,3‐dienes. The presence of the bulky Mes* group on the 1‐phosphorus atom prevents intramolecular [2+2] cyclization and gave the PC PC skeleton, whereas Mes*CP reacted with half an equivalent of nucleophile to afford the PCPC four‐membered ring compounds. X‐ray crystallography of 4‐benzyl‐1,3‐diphosphabuta‐1,3‐diene confirmed the molecular structure showing conjugation on the 1,3‐diphosphabuta‐1,3‐diene moiety. © 2005 Wiley Periodicals, Inc. Heteroatom Chem 16:357–360, 2005; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20104 相似文献
33.
Hisami Yumoto Shigekazu Onozumi Yoshinori Kato Masatou Ishihara Kiyoshi Kishi 《Crystal Research and Technology》1996,31(2):159-164
Indium tin oxide (ITO) whiskers were grown by VLS (vapour-liquid-solid) mechanism, using the electron shower method. The whiskers were grown above 200 °C, and the deposition rate was above 0.6 nm/s. The electron shower controlled the size of the whiskers, and the size was 30 nm in diameter and 600 nm in length. The whiskers grew along the substrate at t < 300 s, but grew in a direction perpendicular to the substrate at t > 300 s. When the ITO whiskers grown along the substrate were used as NO2 gas sensor, the sensitivity was 340, and about 300 times higher than those of the whiskers grown in a direction perpendicular to the substrate and plate-like ITO crystallites. 相似文献
34.
Shigekazu Ito 《Tetrahedron letters》2018,59(1):1-13
This minireview summarizes recent findings on isolable congeners of cyclobutane-1,3-diyl from the views of structural characters, usefulness for organo electronics, and activation of small molecules. Recent findings on isolable cyclopentane-1,3-diyl, 2,4-dimethylene-1,3-cyclobutanediyl, and cyclobutadiene are also overviewed. This article focuses on the reports on the isolable biradicals that have been published since 2013. 相似文献
35.
Ken-ichi Okamoto Norikazu Oda Akira Itaya Shigekazu Kusabayashi 《Chemical physics letters》1975,35(4):483-486
Magnetic fields were found to increase the photocurrent in poly-N-vinylcarbazole (PVCz) films by up to 5–6% at 1 kG. This positive magnetic field effect was sensitive to both applied voltage and temperature, and was enhanced with dimethyl-terephthalate (DMTP) doping by a factor of two. Magnetic fields were also found to increase the prompt exciplex fluorescence of PVCz films doped with DMTP by up to 2% at 500 G. The observations made clear that a carrier generation process via an exciplex state has an important role in photo-carrier generation even in undoped PVCz films. 相似文献
36.
Sato M Nagata T Tanemura A Fujihara T Kumakura S Unoura K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(9):2166-2178
Ruthenocene-terminated butadienes and hexatrienes were prepared by the Wittig reaction of 3-ruthenocenyl-2-propenals with ruthenocenylmethylphosphonium salts and the Mukaiyama coupling of the propenals, respectively. Cyclic voltammetry of these complexes indicated that they were involved in a stable two-electron redox process. The oxidation potentials for ruthenocene-terminated oligoenes shifted progressively to lower potential with the increasing CH==CH units as follows: Rc--Rc (0.32 V)>RcCH==CHRc (+0.09 V)>Rc(CH==CH)(2)Rc (-0.06 V)>Rc(CH==CH)(3)Rc (-0.07 V), (Rc=ruthenocene). The tendency is in remarkable contrast to that in the successive one-electron redox process. These complexes were chemically oxidized to give stable crystalline solids, whose structures were confirmed by NMR spectroscopy and X-ray analysis to be oligoene analogues of a bis(fulvene) complex, for example, [(eta(5)-C(5)Me(5))Ru[mu(2)-eta(6):eta(6)-C(5)H(4)CH(CH==CH)(n)CHC(5)H(4)]Ru(eta(5)-C(5)Me(5))](2+) (n=1 or 2). The DFT calculation of the two-electron-oxidized species reproduced well the fulvene-complex structure for the ruthenocene moieties. Since both the neutral and oxidized species are stable and chemically reversible, this redox system may be serviceable as a two-electron version of the ferrocene one-electron redox system. 相似文献
37.
Shigekazu Kumakura Satoshi Shiraishi Masaru Izawa Mitsuyasu Hanamura 《International journal of quantum chemistry》1992,41(6):785-792
Second-order multiconfigurational self-consistent field (MCSCF ) calculation has been programmed on the basis of CNDO /INDO molecular orbital bases, in which the configuration space employed is restricted within pair-excitations. Test calculations have been carried out for 17 small molecules. All the MCSCF ground states of these molecules have been successfully converged to their respective optimal states by employing a simple weighting scheme. This procedure provides a great savings in computer time. The MCSCF calculation on azetidine required only 27 min on a HITAC M-680H. The MCSCF energies of HF, F2, and BH show improved behaviors up to large atomic distances (~7au). 相似文献
38.
Hiroshi Masuhara Satoshi Ohwada Noboru Mataga Akira Itaya Ken-ichi Okamoto Shigekazu Kusabayashi 《Chemical physics letters》1978,59(2):188-192
Ionic photodissociation processes of vinyl polymers with pendant carbazolyl groups in solution have been studied by nonsecond laser photolysis. The ionic dissociation yield decreases in the order of monomer, oligomers, and polymers. 相似文献
39.
40.
Keisuke Sekine Dai Akaishi Kakeru Konagaya Prof. Dr. Shigekazu Ito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(32):e202200657
Optically active cyclopropanes have been widely investigated especially from the views of pharmaceutical and agrochemical industries, and substituting one of the methylenes with the difluoromethylene unit should be promising for developing novel biologically relevant compounds and functional materials. In this paper, the copper-catalyzed enantioselective hydrosilylation of gem-difluorocyclopropenes to provide the corresponding chiral gem-difluorocyclopropanes is presented. The use of copper(I) chloride, chiral ligands including bidentate BINAPs and monodentate phosphoramidites, and silylborane Me2PhSi-Bpin accompanying sodium tert-butoxide in methanol was appropriate for the enantioselective hydrosilylation of the strained C=C double bond, and the resultant chiral difluorinated three-membered ring was unambiguously characterized. Subsequent activation of the silyl groups in enantio-enriched gem-difluorocyclopropanes showed substantial reduction of the enantiopurity, indicating cleavage of the distal C−C bond leading to the transient acyclic intermediates. 相似文献