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101.
Hirokazu Nishimura 《International Journal of Theoretical Physics》1999,38(2):653-663
We present a basic theory of differential formsin synthetic differential supergeometry. Exteriordifferential calculus is developed, and Cartan's threemagic formulas as well as a variant of de Rham's theorem are established. 相似文献
102.
The efficiency of microwave irradiation at low temperature for glycosylations is described. Although oligosaccharide synthesis usually requires reactive donors for glycosylations, which have leaving groups on the anomer positions, i.e., trichloroacetoimidates, halogenates, thioalkyl glycosides, etc., the suitable donors in our microwave supported synthesis of Lewis X oligosaccharide were very stable acetate derivatives. Regarding glycosylation with a fucosyl acetate donor and a glucosamine acceptor, microwave irradiation with simultaneous cooling improved yields. Moreover, further synthesis to Lewis X derivatives was achieved only with microwave irradiation at low temperatures. Without microwave irradiation, we could only obtain byproducts and none of the designed product at any reaction temperature. 相似文献
103.
Ling-yan Li Hui Gu Yong-jun Tian Toshiyuki Nishimura Joachim Bill 《Journal of Non》2009,355(48-49):2390-2395
Inner pore channels were commonly found in precursor-derived Si–C–N ceramics. After annealing in air at 1420 °C, their oxidation structures were investigated by analytical TEM. A carbon-rich ring was frequently observed under the silica layer inside the pore channels, which consisted of graphite-like clusters in size of 20–30 nm. Origin of such interfacial structure is due to the excessive free-carbon in the amorphous Si–C–N matrix that had survived the oxidation process. This graphitic interface could further improve the oxidation resistance of the SiO2 over-layer. This novel interfacial structure was also found by annealing in N2, reaffirming the effect of composition of Si–C–N matrix. 相似文献
104.
Koji Kita Sho Suzuki Tomonori Nishimura Akira Toriumi 《Applied Surface Science》2008,254(19):6100-6105
Two approaches to control high-k/Ge interface qualities were investigated. The first approach was using high-k materials that are intimate with Ge. These Ge-intimate high-k materials should have moderate reactivity with Ge to form an amorphized interface that will reduce the interface defects and will suppress the GeO desorption at the interface. The second approach was modifying the annealing processes by using a cap layer to block GeO out-diffusion. We found that Si works as the cap layer very efficiently. By combining those two approaches, we achieved fairly good high-k/Ge metal-insulator-semiconductor (MIS) characteristics with LaYO3 as the Ge-intimate high-k material, and a NiSiX electrode as the cap layer. These results provide us an important guide for controlling the high-k/Ge interface properties. 相似文献
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108.
Tsuyoshi Nishimura 《Journal of Graph Theory》1989,13(1):63-69
We show that if r ? 1 is an odd integer and G is a graph with |V(G)| even such that k(G) ? (r + 1)2/2 and (r + 1)2α(G) ? 4rk(G), then G has an r-factor; if r ? 2 is even and G is a graph with k(G) ? r(r + 2)/2 and (r + 2)α(G) ? 4k(G), then G has an r-factor (where k(G) and α(G) denote the connectivity and the independence number of G, respectively). 相似文献
109.
Prof. Dr. Yoshihiko Yamamoto Kei-ichiro Nishimura Dr. Shota Mori Dr. Masatoshi Shibuya 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(20):5586-5589
In the presence of a cationic Ru catalyst, 1,6-diynes bearing a terminal styryl moiety underwent [2+2+2] cyclization to produce dehydrobiphenylenes fused with a five-membered ring. Although the cycloadducts were unstable toward purification, their one-pot iodine-mediated ring expansion successfully afforded unprecedented bridged ketone products containing a benzo-fused bicyclo[3.2.1] framework. 相似文献
110.
A variety of 2-azabicyclo[2.1.0]pentanes were synthesized by the intramolecular nucleophilic substitution of cyclopropylmagnesium carbenoids with magnesium anilide. The 1-chlorocyclopropyl p-tolyl sulfoxides possessing an N-aryl-substituted aminomethyl group were prepared from dichloromethyl p-tolyl sulfoxide, α,β-unsaturated carboxylic acid esters, and anilines in four steps. The deprotonation of the amine with t-BuMgCl followed by sulfoxide/magnesium exchange of the sulfoxides with i-PrMgCl led to the generation of the cyclopropylmagnesium carbenoids possessing a magnesium anilide moiety. Subsequent intramolecular nucleophilic substitution of the cyclopropylmagnesium carbenoids occurred in a 4-exo-tet manner to give the 2-azabicyclo[2.1.0]pentanes. The optically active 2-azabicyclo[2.1.0]pentane was synthesized using a p-tolylsulfinyl group as a chiral auxiliary. 相似文献