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排序方式: 共有1466条查询结果,搜索用时 609 毫秒
941.
Kazuki Ogata Daisuke Sasano Tomoya Yokoi Dr. Katsuhiro Isozaki Ryota Yoshida Dr. Toshio Takenaka Dr. Hirofumi Seike Dr. Tetsuya Ogawa Prof. Dr. Hiroki Kurata Dr. Nobuhiro Yasuda Prof. Dr. Hikaru Takaya Prof. Dr. Masaharu Nakamura 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(37):12356-12375
The NCN‐pincer Pd‐complex‐bound norvalines Boc‐D /L ‐[PdCl(dpb)]Nva‐OMe ( 1 ) were synthesized in multigram quantities. The molecular structure and absolute configuration of 1 were unequivocally determined by single‐crystal X‐ray structure analysis. The robustness of 1 under acidic/basic conditions provides a wide range of N‐/C‐terminus convertibility based on the related synthetic transformations. Installation of a variety of functional groups into the N‐/C‐terminus of 1 was readily carried out through N‐Boc‐ or C‐methyl ester deprotection and subsequent condensations with carboxylic acids, R1COOH, or amines, R2NH2, to give the corresponding N‐/C‐functionalized norvalines R1‐D /L ‐[PdCl(dpb)]Nva‐R2 2 – 9 . The dipeptide bearing two Pd units 10 was successfully synthesized through the condensation of C‐free 1 with N‐free 1 . The robustness of these Pd‐bound norvalines was adequately demonstrated by the preservation of the optical purity and Pd unit during the synthetic transformations. The lipophilic Pd‐bound norvalines L ‐ 2 , Boc‐L ‐[PdCl(dpb)]Nva‐NH‐n‐C11H23, and L ‐ 4 , n‐C4H9CO‐L ‐[PdCl(dpb)]Nva‐NH‐n‐C11H23, self‐assembled in aromatic solvents to afford supramolecular gels. The assembled structures in a thermodynamically stable single crystal of L ‐ 2 and kinetically stable supramolecular aggregates of L ‐ 2 were precisely elucidated by cryo‐TEM, WAX, SAXS, UV/Vis, IR analyses, and single‐crystal X‐ray crystallography. An antiparallel β‐sheet‐type aggregate consisting of an infinite one‐dimensional hydrogen‐bonding network of amide groups and π‐stacking of PdCl(dpb) moieties was observed in the supramolecular gel fiber of L ‐ 2 , even though discrete dimers are assembled through hydrogen bonding in the thermodynamically stable single crystal of L ‐ 2 . The disparate DSC profiles of the single crystal and xerogel of L ‐ 2 indicate different thermodynamics of the molecular assembly process. 相似文献
942.
Masataka Nishikawa Tsugio Mizoguchi Yukiko Dokiya Shinichi Bessho Hiroki Haraguchi 《International journal of environmental analytical chemistry》2013,93(4):591-598
Abstract The concentration of mercury in airborne particles was determined in samples collected at heights of 1m and at 175m up the Meteorological Observation Tower (213m) at the Meteorological Research Institute, Tsukuba between August 1985 and April 1986. The concentrations of particulate mercury at the two heights were compared with gaseous mercury levels at a height of 10m and with other chemical components in the particles. The concentrations of particulate mercury at both heights showed no positive correlation with those of gaseous mercury, total suspended particles, sulfate, chloride, sodium or calcium. However, there was some positive correlation between particulate mercury and nitrate concentrations especially at 175m; the concentrations of these components were found to be high when the wind direction was southwesterly. These results suggest that these components were transported from the Tokyo Metropolitan area. 相似文献
943.
Reaction of β-aminothiocarbonyl-α-methylthioenamines (3a-d) derived from ketene-S, N-acetal (1) with benzamidine and guanidine gave 4-arylamino-pyrimidines (4a-d and 5a-d), respectively. 相似文献
944.
9‐Fluorenone (1) smoothly reacts with phenoxyethanol (2) in the presence of Al3+‐montmorillonite catalyst and 3‐mercaptopropionic acid as a cocatalyst under microwave irradiation at 160°C for 10 min to give 9,9‐bis[4‐(2‐hydroxyethoxy)phenyl]fluorene (3) in 81% yield, which was much higher than the yield of 33% obtained by conventional heating using an oil bath. A similar acceleration effect of microwave irradiation was observed in other metal‐cation‐exchanged montmorillonite catalysts as well. 相似文献
945.
Takashi Tomioka Yusuke Takahashi Toshihide Maejima Yuki Yabe Hiroki Iwata Mark T. Hamann 《Tetrahedron letters》2013
Starting from natural d-mannose, a C(42–63) B-ring tetrahydropyran fragment in karlotoxin 2 has been prepared via a common THP intermediate in a concise manner. E-Selective Julia–Kocienski olefination efficiently assembled a C(51–63) chlorodiene subunit and a C(42–50) tetrahydropyran segment. 相似文献
946.
我们利用具有不同对称性的同分异构体,通过改变分子间氢键网络,操控单链磁体行为,成功合成了2 例化合物:[NiⅡ(L1)][FeⅢ(Tp)(CN)3]2·3.5H2O (1)和[NiⅡ(L2)][FeⅢ(Tp)(CN)3]2·3H2O (2),其中Tp=hydrotris(pyrazolyl)borate,L1=3,4-bis(1H-imid-azol-1-yl)thiophen,L2=1,2-bis(1H-imidazol-1-yl)thiophen)。磁性研究表明,1和2表现为具有不同矫顽场的单链磁体行为。1的矫顽场为8.41 kOe,而2的矫顽场为3.84 kOe。 相似文献
947.
Hiroki IwasakiNozomi Tsutsui Toru EguchiHiroaki Ohno Masayuki Yamashita Tetsuaki Tanaka 《Tetrahedron letters》2011,52(15):1770-1772
We report a samarium(II)-mediated tandem spirocyclization reaction to provide dispiro[4.2.4.2]tetradecadiene and dispiro[4.2.5.2]pentadecadiene skeletons. The reaction was achieved by intramolecular addition of a ketyl radical onto an aromatic ring bearing an electrophilic moiety followed by reductive capture of the spirohexadienyl radical intermediate with SmI2 in the presence of HMPA. 相似文献
948.
We developed an atomistic model of octamethylcyclotetrasiloxane (OMCTS) liquid confined within the nanospace between two flat mica surfaces. Molecular dynamics simulation was carried out for the liquidlike state where OMCTS liquid is not frozen, while forming molecular layers parallel to the surface. With the aid of a layer by layer analysis of the intra- and interlayer microscopic structures and the dynamics, it is found that the difference in the properties of the inner layers and the bulk liquid are relatively small in spite of the clear differences in the structure. This leads to the conclusion that the layered structure itself is an appearance of the microscopic structure that already exists in the bulk liquid. The most striking difference from the bulk liquid is mainly seen in the contact layer, where characteristic molecular orientations that are not seen in the crystalline phase appeared, and the dynamics of the liquid becomes 2-3 orders of magnitude slower than that of the bulk. 相似文献
949.
Fujii T Aoki Y Habazaki H 《Langmuir : the ACS journal of surfaces and colloids》2011,27(19):11752-11756
Hierarchical dual pillar surfaces with optimized pillar intervals are fabricated by a novel combined process of the oblique angle magnetron sputtering deposition of Al-Nb alloys and their anodizing. The pillar intervals are controlled by the deposition angle and cell size of a scalloped substrate for oblique angle deposition. Anodizing of the deposited pillar surfaces develops a nanopillar oxide layer, producing the hierarchical dual pillar surfaces. After being coated with a fluoroalkyl phosphate layer to reduce the surface free energy, hierarchical surfaces with submicrometer pillar intervals greater than 400 nm show super liquid repellency even for hexadecane with a low surface tension of 27.5 mN m(-1), although the submicrometer pillar surfaces with smaller submicrometer pillar intervals and without nanopillars were not super-oil-repellent. In contrast, the dual pillar surfaces show superhydrophobicity regardless of the submicrometer pillar intervals. Thus, the present study demonstrates the importance of the pillar intervals (gap size between pillars) to realize the superoleophobicity. 相似文献
950.
Rao KP Kondo M Sakamoto R Kusamoto T Nishikawa M Kume S Nihei M Oshio H Nishihara H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(50):14010-14019
The donor-acceptor-donor (D-A-D) conjugated molecules 1,4-bis(diarylaminophenylethynyl)anthraquinone (1,4-Am(2)Aq) and 1,4-bis(ferrocenylethynyl)anthraquinone (1,4-Fc(2)Aq), undergo a double proton cyclization reaction with bis(trifluoromethanesulfone)imide acid (TFSIH) to yield 1,4-bis(diarylaminophenyl or ferrocenyl) dipyrylium salts [1,4-R(2)Pyl(2)](TFSI)(2) (R=Am or Fc) with novel planar pentacyclic structures similar to the aromatic benzo[e]pyrene-type skeleton. [1,4-Am(2)Pyl(2)](TFSI)(2) could be reduced to give the neutral molecule [1,4-Am(2)Pyl(2)](0), which is stable and maintains the benzo[e]pyrene-type skeleton. To the best of our knowledge, this is the first oxygen-atom-containing polycyclic aromatic hydrocarbon with 22 (4n+2) π-electrons. The obtained condensed-ring benzo[e]pyrene-type skeleton compounds show physical and chemical properties that are significantly different from those of [1,5-Am(2)Pyl(2)](TFSI)(2), which has a perylene-type skeleton. 相似文献