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971.
SynthesisandCrystalStructureof1,5-Bis(1'-phenyl-3'-methyl-5'-pyrazolone-4')-1-(4'-aminobutand-1'-imino)-5-pentaneone¥YangLu-Q... 相似文献
972.
CrystalandMolecularStructureof3,4-diphenyl-5-ethyl-5-methyl-1,3,4-diazaphospholidin-2-thione-4-oxide¥FengKe-Sheng;ChenRu-Yu(I... 相似文献
973.
含N-苯甲酰皮考林酰肼的钒酰、镍及锰配合物的合成和晶体结构 总被引:2,自引:0,他引:2
合成了3个含N-苯甲酰皮考林酰肼(简写为HL)的钒、镍和锰配合物[VO_2L](1,C_(13)H_(10)N_3O_4V,M_r=323.18),[NiL_2]·0.5CH_3OH(2,C_(26.5)H_(22)N_6NiO_(4.5),Mr=555.21)和[MnL_2]·0.5CH_3OH(3,C_(26.5)H_(22)MnN_6O_(4.5),Mr=551.44)。配合物1属三斜晶系,空间群为P1,a=0.71241(3)nm,b=0.89625(6)nm,c=1.11706(6)nm,α=94.715(2)°,β=102.053(2)°,γ=112.375(3)°,V=0.63461(7)nm~3,Z=2,F(000)=328,μ(MoKα)=0.802mm~(-1),R=0.0290,wR=0.0816;配合物2属单斜晶系,空间群为C2/c,a=2.5875(1)nm,b=1.4868(1)nm,c=1.8353(1)nm,β=134.470(4)°,V=5.2081(5)nm~3,Z=8,F(000)=2368,μ(MoKα)=0.795mm~(-1),R=0.0459,wR=0.1330;配合物3属单斜晶系,空间群为C2/c,a=2.60113(3)nm,b=1.45231(4)nm,c=1.92903(1)nm,β=132.824(1)°,V=5.3448(2)nm~3,Z=8,F(000)=2344,μ(MoKα)=0.543mm~(-1),R=0.0457,wR=0.1325。在配合物1中,钒(V)原子具有畸变的N_2O_3四角锥配位构型,晶体内每两个分子通过分子间氢键作用形成缔合分子对。在配合物2和配合物3中,镍(Ⅱ)原子和锰(Ⅱ)原子具有扭曲的N_4O_2八面体配位构型,晶体通过分子间氢键作用形成一维的无限链状结构。红外光谱表明,配体在形成配合物后,ν(C=O)和ν(C=N)红移。电 相似文献
974.
在用琥珀酸二异辛酯磺酸钠(AOT)构建的具有长程有序结构的层状溶致液晶内, 用不同方式导入预制的亲油或亲水贵金属纳米粒子, 可得到纳米粒子分布在不同介观空间内的无机/有机杂合体. 依据小角X射线散射和偏光显微镜结果, 通过分析掺杂纳米粒子与液晶模板的相互作用, 对掺杂前后体系结构的变化及制得杂合体的稳定性进行了表征. 结果表明, 除考虑掺杂粒子与层状模板空间的匹配外, 体系中静电斥力、范德华引力和Helfrich涨落力之间的平衡是维持液晶结构稳定的基本条件. 相似文献
975.
Robert Glaum 《无机化学与普通化学杂志》1992,616(10):46-52
Contributions on the Thermal Behaviour of Anhydrous Phosphates. IX. Synthesis and Crystal Structure of Cr6(P2O7)4. A Pyrophosphate Containing Di- and Trivalent Chromium Cr6(P2O7)4 (Cr22+Cr43+(P2O7)4) can be obtained reducing CrPO4 by phosphorus (950°C, 48 h, 100 mg iodine as mineralizer). By means of chemical transport reactions (transport agent iodine; 1050 → 950°C) the compound has been separated from its neighbour phases (Cr2P2O7, CrP3O9) and crystallized (greenish, transparent crystals; edge length up to 0.3 mm). The crystal structure of Cr6(P2O7)4 (Spcgrp.: P-1; z = 1; a = 4.7128(8) Å, b = 12.667(3) Å, c = 7.843(2) Å, α = 89.65(2)°, β = 92.02(2)°, γ = 90.37(2) has been solved and refined from single crystal data (2713 unique reflections, 194 parameter, R = 0.035). Cr2+ is surrounded by six oxygen atoms which occupy the corners of an elongated octahedron (4 × dCr? O ≈? 2.04 Å; 2 × dCr? O ≈? 2.62 Å). The Cr3+ ions are also coordinated octahedraly (1.930 Å ≤ dCr? O ≤ 2.061 Å). The crystallographically independent pyrophosphate groups show nearly eclipsed conformation. The bridging angles (P? O? P) are 136.5° and 138.9° respectively. 相似文献
976.
Chun-Kiu Kwok Thomas C. W. Mak 《Journal of inclusion phenomena and macrocyclic chemistry》1988,6(5):461-471
N,N-DicyclohexylpiperazineN,N-dioxide octahydrate, C16H46N2O10,M
r=426.55, monoclinic, space groupC2/m (No. 12),a=12.961(4),b=11.533(4),c=7.907(1) Å, =98.37(2)o,V=1169.3(6) Å3,Z=2. The structure was solved by the direct method and refined toR=0.045 for 1192 observed MoK
reflections. TheN,N-dioxide molecule occupies a site of symmetry 2/m. The piperazine ring takes the chair form with the two N–O bonds oriented axially in atrans configuration. Hydrogen bonding between the water molecules, as well as between theN-oxide groups and water molecules, gives rise to a puckered layer composed of edge-sharing four-membered, five-membered, six-membered, and eight-membered rings. Adjacent layers are cross-linked by theN,N-dicyclohexylpiperazine moieties lying between them, thereby generating a sandwich structure consolidated by covalent and hydrogen bonding.
Supplementary Data relating to this article are deposited with the British Library as Supplementary Publication No. SUP 82062 (8 pages). 相似文献
977.
Ryo HorikoshiTomoyuki Mochida Hiroshi Moriyama 《Journal of solid state chemistry》2002,164(2):320-325
A series of ionic 4-(4′-pyridylthio)-1-methylpyridinium salts with different counteranions (1, I−; 2, BF−4; 3, PF−6; and 4, OTf−, where OTf=trifluoromethanesulfonate) have been prepared. Structural analysis reveals that the cation exhibits a variety of stacking structures dependent on the anion. Compound 1 crystallizes in space group P21/n (#14), with a=10.764(3) Å, b=9.601(5) Å, c=13.105(3) Å, β=108.35(2), V=1285.4(8) Å3, and Z=4. In this compound, each cation moiety is stacked in a helical arrangement along the c-axis. Compound 2, which is isomorphous to 1, has space group P21/n (#14), with a=11.647(2) Å, b=9.203(3) Å, c=13.232(2) Å, β=108.42(2), V=1345.6(5) Å3, and Z=4. Compound 3 crystallizes in space group P21/n (#14), with a=8.06(1) Å, b=17.43(1) Å, c=10.30(1) Å, β=103.0(1), V=1410(3) Å3, and Z=4. In this salt, the cation molecules assume a head-to-tail stacking arrangement, forming a polar pseudo 1-D chain. Compound 4 crystallizes in space group Pb? (#2), with a=7.585(4) Å, b=15.443(7) Å, c=6.775(4) Å, α=99.33(4), β=108.35(2)o, γ=98.37(4), V=756.6(7) Å3, and Z=2. The structure of 4 consists of a columnar stacking of pyridine moieties, with the cation moieties surrounded by the counteranions. Calculations show that the 4-(4′-pyridylthio)-1-methylpyridinium cation may be a good building block for second harmonic generation (SHG) materials, even though salts 1-4 crystallized in centrosymmetric structures and were SHG inactive. 相似文献
978.
Deprotonation of Mn2(μ-H)(μ-PR2)(CO)8 (R = Ph Cy) for Synthesis of Heteronuclear Manganese-Gold Clusters with Mn2Aun Cores (n = 1–3) The dimanganese complexes Mn2(μ-H)(μ-PR2)(CO)8 (R = Ph, Cy) have been deprotonated with 1,8-diazabicyclo[5.4.0]undec-7-en (DBU) in tetrahydrofuran solution at 20°C to give the anions [Mn2(μ-PR2)(CO)8]?, which were isolated as tetraethylammonium salts. Both dimanganese complexes and the related anions were measured by cyclic voltammetry. The treatment of the aforementioned dimanganese complexes in thf solution with Lir' (R =Me, Ph) and subsequently with PPh3AuCl gave at 20°C three types of products: Mn2(μ-PR2(CO)8(AuPPh3),Mn2(μ-PR2)(μ-C(R′)O)(CO)6-(AuPPh3)2 and Mn2(μ-PR2)(CO)6(AuPPh3)3. The newly prepared substances were characterized by means of IR-, UV/VIS, 31P NMR data. The results of single X-ray analyses showed for the three-membered metal ring compound Mn2(μ-PPh2)(CO)8(AuPPh3) an uni-fold bridged σ(Mn? Mn) bond length of 306.7(3) pm, the metallatetrahedron complex Mn2(μ-PPh3)(μ-C(Ph)O(CO)6(AuPPh3)2 a twofold bridged σ(Mn? Mn) bond length of 300.6(4) pm and the trigonal-bipyramidal cluster Mn2(μ-Pph2)(CO)6(AuPPh3)3 an uni-fold bridged π(Mn? Mn) bond length of 274.7(3) pm. The Mn? Au bonds of these substances are accompanyied by semi-bridging CO ligands which are signified through short Au…C contact lengths in the range of 251 to 270 pm. In the substance with the Mn2Au2 metallatetrahedron core exists, additionally, such a contact with the acylic C atom of C(Ph)O bridging group of 263.4(18) pm. Such contact lengths were compared for corresponding dimanganese and dirhenium complexes. 相似文献
979.
H. Schumann F. H. Grlitz F. E. Hahn J. Pickardt Changtao Qian Zuowei Xie 《无机化学与普通化学杂志》1992,609(3):131-138
The partial hydrolysis of [O(CH2CH2C5H4)2]Y(C5H4CH3) 1 , [O(CH2CH2C5H4)2]Y(C5H5) 3 , and [O(CH2CH2C5H4)2]Ho(C5H4CH3) 5 results in the formation of [O(CH2CH2CH2C5H4)2Y(μ-OH)2]2 2 , (C5H5)3Y(OH2) 9 and (MeC5H4)3Ho(OH2) 11 . The new compounds have been characterized by elemental analyses, IR and NMR spectra. The X-ray structural analyses shows 2 to be monoclinic, space group P21/n with a = 1146.0(3), b= 1046.6(3), c = 1514.9(3) pm, β = 94.83(2)°. The molecular structure shows bridging hydroxyl groups with a mean distance Y? O = 223.8(3) pm. 11 crystallizes in the cubic space group 14 3d with a = 1847.9(3)pm with Z = 16 molecules per unit cell. The molecules posses symmetry C3-3, the coordination is trigonal pyramidal with three methylcyclopentadienyl anions and one water molecule as ligands. The distance Ho? O is 231 pm. 相似文献
980.
直链醇链长对层状液晶结构与稳定性的影响 总被引:8,自引:4,他引:8
作为助表面活性剂,直链醇在层状溶致液晶的制备中是非常重要的。本文以层状液晶的相行为和小角度X射线衍射测量,研究了直链醇链长对层状液晶结构与稳定的影响。 相似文献