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851.
Haijing Liang Lixia Ma Changwei Li Qiang Peng Zhaoyan Wang Zhan-xin Zhang Lan Yu Huanxiang Liu Fengli An Weihua Xue 《Tetrahedron letters》2019,60(1):84-87
Glycosylation reactions are significant as they provide access to model compounds that are useful for elucidating biochemical pathways. Herein, we describe the development of glycosyl ortho-alkynylbenzoates as novel, bench-top stable, and readily available glycosyl donors. Glycosylation is promoted by inexpensive trimethylsilyl triflate (TMSOTf) in combination with N-iodosuccinimide (NIS) under mild reaction conditions; hence, the novel glycosyl donors are promising reagents for the synthesis of glycosides. 相似文献
852.
Lin-Lin Zhang Bing-Chao Da Shao-Hua Xiang Shuai Zhu Zi-Yun Yuan Zhen Guo Bin Tan 《Tetrahedron》2019,75(12):1689-1696
Quinones, precursors of aromatic structures, were firstly employed as the electrophiles for the organocatalytic Michael addition/cyclization cascade reaction with versatile 3-isothiocyanato oxindoles. Chiral bifunctional organocatalyst was appropriate for this enantioselective transformation to afford a variety of novel spirooxindoles, possessing a spirocyclic stereocenter adjacent to the aromatic ring, via asymmetric double arylation. These synthesized spirooxindoles are very difficult to access by the reported methods and were obtained in excellent chemical yields with excellent enantioselectivities. 相似文献
853.
A microwave-assisted base-free intramolecular cross dehydrogenative coupling (CDC) of 3-aniline substituted coumarins and quinolinones have been developed. A broad range of indolo[2,3-c]coumarins and indolo[2,3-c]quinolinones can be easily afforded in good to high yields (up to 93%) under palladium catalysis. The method is among the most straightforward and convenient ways to access these fused polyheterocycles. 相似文献
854.
The development of a facile strategy to construct stable hierarchal porous heterogeneous photocatalysts remains a great challenge for efficient CO_2 reduction. Additionally, hole-trapping sacrificial agents(e.g., triethanolamine, triethylamine, and methanol) are mostly necessary, which produce useless chemicals, and thus cause costs/environmental concerns. Therefore,utilizing oxidation ability of holes to develop an alternative photooxidation reaction to produce value-added chemicals, especially coupled with CO_2 photoreduction, is highly desirable. Here, an in situ partial phosphating method of In_2O_3 is reported for synthesizing In P–In_2O_3 p-n junction. A highly selective photooxidation of tetrahydroisoquinoline(THIQ) into value-added dihydroisoquinoline(DHIQ) is to replace the hole driven oxidation of typical sacrificial agents. Meanwhile, the photoelectrons of In P–In_2O_3 p-n junction can induce the efficient photoreduction of CO_2 to CO with high selectivity and stability. The evolution rates of DHIQ and CO are 2 and 3.8 times higher than those of the corresponding In_2O_3 n-type precursor, respectively. In situ irradiated X-ray photoelectron spectroscopy and electron spin resonance are utilized to confirm that the direct Z-scheme mechanism of In P–In_2O_3 p-n junction accelerate the efficient separation of photocarriers. 相似文献
855.
856.
Six mono/double‐layered 2D and three 3D coordination polymers were synthesized by a self‐assembly reaction of Zn (II) salts, organic dicarboxylic acids and L1/L2 ligands. These polymeric formulas are named as [Zn(L1)(C4H2O4)0.5 (H2O)]n·0.5n(C4H2O4)·2nH2O ( 1 ), [Zn2(L2)(C4H2O4)2]n·2nH2O ( 2 ), [Zn(L1)(m‐BDC)]n ( 3 ), [Zn2(L2)(m‐BDC)2]n·2nH2O ( 4 ), [Zn3(L1)2(p‐BDC)3(H2O)4]n·2nH2O ( 5 ), [Zn2(OH)(L2) (p‐BDC)1.5]n ( 6 ), [Zn2(L1)(p‐BDC)2]n·5nH2O ( 7 ), [Zn2(L2)(p‐BDC)2]n·3nH2O ( 8 ) and [Zn2(L1)(C4H4O4)1.5(H2O)]n·n(ClO4)·nH2O ( 9 ) [L1 = N,N′‐bis (pyridin‐4‐ylmethyl)propane‐1,2‐diamine, L2 = N,N′‐bis (pyridin‐3‐ylmethyl)propane‐1,2‐ diamine, m‐BDC2? = m‐benzene dicarboxylate, p‐BDC2? = p‐benzene dicarboxylate]. Meanwhile, these polymers have been characterized by elemental analysis, infrared, thermogravimetry (TG), photoluminescence, powder and single‐crystal X‐ray diffraction. Polymers 1–6 present mono‐ and double (4,4)‐layer motifs accomplished by L1/L2 ligands with diverse conformations and organic dicarboxylates, and the layer thickness locates in the range of 5.8–15.0 Å. In three 3D polymers, the L1 and L2 molecules adopt the same cis‐conformations and join adjacent Zn (II) cations together with p‐BDC2? or succinate, giving rise to different binodal (4,4)‐c nets with (4.52.83)(4.53.72) ( 7 ), pts ( 8 ) topology and twofold interpenetrated binodal (5,5)‐c nets with (32.44.52.62)(3.43.52.64) ( 9 ). Therefore, the diverse conformations of the two bis (pyridyl)‐propane‐1,2‐diamines and the feature of different organic dicarboxylate can effectively influence the architectures of these polymers. Powder X‐ray diffraction patterns demonstrate that these bulk solid polymers are pure phase. TG analyses indicate that these polymers have certain thermal stability. Luminescent investigation reveals that the emission maximum of these polymers varies from 402 to 449 nm in the solid state at room temperature. Moreover, 1 , 3 and 5–8 show average luminescence lifetimes from 8.81 to 16.30 ns. 相似文献
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