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81.
Nemoto Rei Wang Li Ikoma Toshiyuki Tanaka Junzo Senna Mamoru 《Journal of nanoparticle research》2004,6(2):259-265
Hydroxyapatite (HAp) nanocrystals were prepared at room temperature by a coprecipitation method from Ca(OH)2 and H3PO4, in the presence of chemically disintegrated silk fibroin (SF). Adsorbed amounts of cations on SF and crystallinity of HAp in the composite were increased by the chemical disintegration of SF higher order structure. Preferential alignment of c-axis of HAp crystallites along the longitudinal direction of ca. 150nm SF fibril was observed. These changes due to disintegration of SF were discussed in terms of the chemical interaction between HAp and SF. The resulted composite with preferential alignment of HAp nanocrystals is a good candidate as a starting material for bone substitutes. 相似文献
82.
Mamoru Kobayashi Kentaro Uchino Takashi Ishizone 《Journal of polymer science. Part A, Polymer chemistry》2005,43(18):4126-4135
Well‐defined end‐functionalized polystyrene, poly(α‐methylstyrene), and polyisoprene with polymerizable aziridine groups were synthesized by the termination reactions of the anionic living polymers of styrene, α‐methylstyrene, and isoprene with 1‐[2‐(4‐chlorobutoxy)ethyl]aziridine in tetrahydrofuran at ?78 °C. The resulting polymers possessed the predicted molecular weights and narrow molecular weight distributions (weight‐average molecular weight/number‐average molecular weight < 1.1) as well as aziridine terminal moieties. The cationic ring‐opening polymerization of the ω‐monofunctionalized polystyrene having an aziridinyl group with Et3OBF4 gave the polymacromonomer, whereas the α,ω‐difunctional polystyrene underwent crosslinking reactions to afford an insoluble gel. Crosslinking products were similarly obtained by the reaction of the α,ω‐diaziridinyl polystyrene with poly(acrylic acid)‐co‐poly(butyl acrylate). © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4126–4135, 2005 相似文献
83.
Keisuke Yoshiki Hiroki Azuma Kazuhiko Yoshioka Mamoru Hashimoto Tsutomu Araki 《Optical Review》2005,12(5):415-419
We have investigated the fluorescence lifetime properties of 8 calcium ion probes, calcium-green-1, calcium green-2, calcium
green-5N, calcium orange, oregon green 488 BAPTA-6F, fluo-3, fluo-4, and fluo-5N. We found that the decay time of calcium
green-5N varied more sensitively with calcium concentration than calcium green-1 which was known to be a highly sensitive
probe. We have also found that the center of observable range of calcium concentration by fluorescence lifetime measurement
is lower than that by fluorescence intensity measurement. 相似文献
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87.
Xestospongin A,B,C and D represent a new class of macrocyclic 1-oxaquinolizidines, have been isolated from Australian sponge . The structure of xestospongin C has been determined by X-ray analysis. 相似文献
88.
89.
This paper provides a characterization of the storage needs of a quadtree when used as an index to access large volumes of 2-dimensional data. It is shown that the page occupancy for data in random order approaches 33%. A precise mathematical analysis that involves a modicum of hypergeometric functions and dilogarithms, together with some computer algebra is presented.A brief survey of the analysis of storage usage in tree structures is included. The 33% ratio for quadtrees is to be compared to the figures for binary search trees (50%), tries (69%), and quadtries (46%).The research of this author was done while visiting INRIA, Rocquencourt, France under support from the Ministry of Education of Japanese Government.Work of this author was supported in part by the Basic Research Action of the E.C. under contract No. 3075 (Project ALCOM). 相似文献
90.
Hiromu Saito Mamoru Takahashi Takashi Inoue 《Journal of Polymer Science.Polymer Physics》1988,26(8):1761-1768
Orientation relaxation of dissimilar chains in the molten miscible blends, poly(methyl methacrylate)/poly(vinylidene fluoride) and poly(methyl methacrylate)/poly(vinylidene fluoride-co-trifluoroethylene), were investigated by measuring (1) the change of infrared dichroic ratio with time after the uniaxial stretching of film specimens, (2) the shear stress relaxation spectrum, and (3) birefringence relaxation in shear. The dissimilar polymers showed an identical time variation of the normalized Hermans orientation function. The blend showed a relaxation spectrum with a single characteristic relaxation time τc, depending on the blend composition. The birefringence relaxed monotonically, remaining positive. These results suggest that the dissimilar polymers do not relax independently but cooperatively. This behavior may be induced by a constraint due to the specific interactions between the dissimilar polymers, e.g., weak hydrogen bonding. For the cooperative chain relaxation, a third power relationship was found; τc/τe vprop; (M/Me),3 where τe and Me are the relaxation time and molecular weight of entanglement strand, respectively, and M is the number average molecular weight in the blend. 相似文献