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81.
Murashima K Watanabe T Kanegawa S Yoshihara D Inagaki Y Karasawa S Koga N 《Inorganic chemistry》2012,51(9):4982-4993
N,N-Dipyridilaminoxyl, NOpy(2), having a stable aminoxyl, was prepared as a new magnetic coupler for heterospin systems. Solutions of NOpy(2) were mixed with those of bis{1,1,1,5,5,5, hexafluoro-4-(phenylimino)-2-pentanonate}cobalt derivatives, Co(hfpip-X)(2), at a 1:1 ratio to afford the polymeric cobalt(II) complexes, [Co(hfpip-X)(2)(NOpy(2))](n); X = H (1), F (2), F(3) (3), F(5) (4), Cl (5), Cl(3) (6), Br (7), and I (8) as single crystals. In all complexes, the local structures of the cobalt-complex units were compressed octahedra and the pyridine ligands in NOpy(2) units coordinated to the cobalt ions in trans configuration to form linear chains for 1-4 and in cis configuration to form helical chains for 5-8. In the chains, the aminoxyl in NOpy(2) ferromagnetically interacted with the cobalt ions to produce the ferromagnetic chains with J(intra)/k(B) = 9-14 K. In the magnetic susceptibility experiments of aligned sample of 6, the magnetic easy axis was determined to be the a* axis, which was the direction perpendicular to the b axis of the chain axis. The resulting chains, all except 4, interacted antiferromagnetically among each other, and especially in 1, 5, 7, and 8, the magnetic behaviors characteristic to canted two-dimensional (2D) antiferromagnets with T(c) = 5.6, 4.0, 4.0, and 6.2 K, respectively, were observed. All complexes showed slow magnetic relaxations affected by the interchain antiferromagnetic interaction. The effective activation barriers, Δ(eff)/k(B), for the reorientation of the magnetism for all complexes except 4 were estimated to be 25-39 K in the presence of a direct current (dc) field. 相似文献
82.
A nonporous crystalline solid consisting of an organoarsenic platinum(II) complex, i.e., a mononuclear diiodoplatinum(II) complex trans-PtI(2)(cis-DHDAtBu)(2) (1) with cis-1,4-dihydro-1,4-dimethyl-2,3,5,6-tetrakis(tert-butoxycarbonyl)-1,4-diarsinine (cis-DHDAtBu), shows on-off solid-state luminescence switching through reversible solvent vapor uptake and escape. The on-off switching of solid-state luminescence was achieved without changing the structure or electronic state of the organoarsenic platinum(II) complex. 相似文献
83.
The reactions of N‐([1]benzofuro[3,2‐d]pyrimidin‐4‐yl)formamidines with hydroxylamine hydrochloride gave rearranged cyclization products via ring cleavage of the pyrimidine component accompanied by a ring closure of the 1,2,4‐oxadiazole to give N‐[2‐([1,2,4]oxadiazol‐5‐yl)[1]benzofuran‐3‐yl)formamide oximes. N‐([1]Benzothieno[3,2‐d]pyrimidin‐4‐yl)formamidines and N‐(pyrido[2,3‐d]pyrimidin‐4‐yl)formamidines with hydroxylamine hydrochloride gave similar results. 相似文献
84.
Hironobu Kunieda Hamidul Kabir Kenji Aramaki Kazuki Shigeta 《Journal of Molecular Liquids》2001,90(1-3):157-166
Cloud temperatures, phase behavior, and the structures of liquid crystals were investigated in the aqueous systems of homogenous hexaethylene glycol dodecyl ether(C12EO6) and mixed C12EO4-C12EO8, C12EO2-EO8, C12EO2-C12EO8, and C12EO0-C12EO8 In the mixed surfactant systems, the average polyoxyethylene- (EO-) chain lengths are kept constants, the same as C12EO6. The change in cloud temperatures is small in all the systems, whereas the phase behavior is successively changed with increasing the difference in EO-chain length in the mixture. Lamellar liquid crystal is developed in the phase diagrams and it intrudes in the two-phase region above the cloud temperature. Hence, the phase pattern of the present mixed surfactant systems resembles that of C12EO5 system, but both cloud point and W+L region appear at much higher temperature. Hence, the Hydrophile-Lipophile Balance of the surfactant is not largely changed by mixing the surfactants but the SAXS results show that the surfactant molecules are more tightly packed in the hexagonal and lamellar phases by mixing. It is considered that when surfactants of different EO-chain lengths are mixed, the considerable reduction in repulsion between the hydrophilic moieties takes place and the surfactant molecules are more tightly packed. 相似文献
85.
H. Nagao K. Kinugawa Y. Shigeta K. Ohta K. Yamaguchi 《Journal of Molecular Liquids》2001,90(1-3):63-68
We investigate quantum spin dynamics of spin network systems in a liquid and in a molecular cluster with external magnetic field and discuss the importance of topological spin structures in relation to the quantum computing and quantum mechanical dimensions of the nuclear and the electron spins. 相似文献
86.
Kensuke Naka Shinsuke Inagi Yoshiki Chujo 《Macromolecular rapid communications》2006,27(24):2113-2117
Summary: The first π‐conjugated poly(thioketene dimer) was synthesized via the homopolymerization of a silylthioketene dimer by a chemical oxidation‐reduction process. The polymerization of trimethylsilylthioketene dimer in the presence of FeCl3 (in CHCl3 at 70 °C for 24 h) gave the corresponding doped poly(thioketene dimer). After treatment of the doped polymer with an aqueous solution of ammonia, the neutral poly(thioketene dimer) was obtained with an incidental desilylation. The polymer obtained was soluble in DMF and DMSO. From gel permeation chromatographic analysis (DMF, polystyrene standards), the number‐average molecular weight of the polymer was found to be 7 460. The polymer showed low oxidation potentials derived from the thioketene dimer unit. An effective extension of the π‐conjugation was observed in the polymer.
87.
Tolerance bioaccumulation and biotransformation of arsenic compounds by a freshwater prawn (Macrobrachium rosenbergii) were investigated. M. rosenbergii was exposed to 10, 20, 30 and 35 μg As cm−3 of disodium arsenate [abbreviated as As(V)], 25, 50, 100 and 120 μg As cm−3 of methylarsonic acid (MMAA), or 100,200, 300 and 350 μg As cm−3 of dimethylarsinic acid (DMAA). Tolerances (50% lethal concentration: LC50) of the prawn against As(V), MMAA, and DMAA were 30, 100, and 300 μg As cm−3, respectively. The prawn accumulated arsenic compounds directly from aqueous phase and biotransformed them in part. Both methylation and demethylation of the arsenicals were observed in vivo. Highly methylated and less toxic arsenicals were less accumulated in M. rosenbergii. 相似文献
88.
89.
Dr. Goki Hirata Prof. Yoichi Kobayashi Dr. Ryuma Sato Prof. Yasuteru Shigeta Dr. Nobuhiro Yasuda Prof. Hiromitsu Maeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(37):8797-8804
Heteroleptic PtII complexes comprising π-extended dipyrrins and 2-phenylquinoline were prepared. Single-crystal X-ray analysis disclosed the stepped conformations of two ligand moieties in these PtII complexes. The enantiomers could be separated by HPLC and their configurations were determined from CD spectroscopy results and TD-DFT calculations. Transient absorption measurements revealed excited-state dynamics characterized by fast intersystem crossing and microsecond-order triplet-state lifetimes. 相似文献
90.
Yuri Sato Hiroaki Imoto Kensuke Naka 《Journal of polymer science. Part A, Polymer chemistry》2020,58(10):1456-1462
Cage silsesquioxane, denoted as polyhedral oligomeric silsesquioxane (POSS) has high crystallinity to readily cause aggregation when it is induced into polymer side chain. In this work, side-opened POSS was employed to construct a bifunctional monomer for cyclopolymerization. The collapsed symmetry of the POSS core effectively reduced the crystallinity to realize homogeneous films, while a traditional POSS homopolymer formed turbid and brittle films. The obtained film showed high transparency and thermal stability. 相似文献