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151.
Lin Jiacheng Li Qianqian Zeng Xiaodong Chen Ziyang Ding Qihang Li Yang Zhou Hui Meng Xianli Chen Deliang Deng Zixin Hong Xuechuan Xiao Yuling 《中国科学:化学(英文版)》2020,63(6):766-770
Osteosarcoma is the most common primary malignant tumor of bone, particularly among children and adolescents. Advances in imaging, surgical techniques, and implants have dramatically reduced the need for amputation in the past three decades.Recently, in vivo fluorescence imaging in the second near-infrared window(NIR-II, 1,000–1,700 nm) shows impressive advantages of deeper tissue penetration and higher spatial resolution, which makes it a promising tool for the early diagnosis and post-operative observation of Osteosarcoma. To the best of our knowledge, this paper is the first time to develop a novel NIR-II fluorescence probe conjugated with an osteosarcoma targeted oligopeptide for molecular tumor imaging in a xenograft orthotopic osteosarcoma mouse model. 相似文献
152.
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154.
Ji-Ben Meng Mei-Qen Shen Xiao-Hong Wang Chen-Heng Kao Ru-Ji Wang Hong-Gen Wang Teruo Matsuura 《Journal of heterocyclic chemistry》1991,28(6):1481-1484
A number of fluorescent 3-aryl-1-methylquinolinones 3 were synthesized by the regiospecific photocoupling reaction of 3-halo-1-methylquinolinones 1 with aromatic and heteroaromatic compounds 2 . An unusual photocoupling product 4 was obtained in the photolysis of 3-iodo-1-methylquinolinone in the presence of benzene. The structure of 4 was unequivocally established by an X-ray crystallographic analysis. 相似文献
155.
A new highly sensitive and selective chromogenic reagent, 2-(2,5-disulfonic-4-methoxyphenylazo)-7-(2-hydroxyl-5-carboxylphenylazo)-1,8-dihydroxynaphthalene-3,6-disulfonic
acid (1), was synthesized and applied to the spectrophotometric determination of trace thorium. In 5 mL of a 6 M perchloric acid
medium, which greatly increases the selectivity, thorium reacts with 1 to form a 1: 2 green complex, having a sensitive absorption peak at 670 nm. Under optimal conditions, Beer’s law is obeyed
over the range from 0 to 0.8 μg/mL Th(IV) and the apparent molar absorptivity is 2.09 × 105 L/mol cm. It is found that, uranium(VI), Ti(IV), heavy rare earths, and most of other common metal ions do not interfere.
The method has been tested on the determination of thorium in food samples with satisfactory results.
The text was submitted by the authors in English. 相似文献
156.
乌江流域沉积岩风化过程中稀土元素的富集与释放 总被引:1,自引:0,他引:1
以乌江流域石灰岩、白云质灰岩、白云岩、硅质岩、页岩和砂岩等沉积岩的13条风化剖面为对象,运用R型分层聚类分析和质量平衡计算方法,研究了这些岩石风化过程中稀土元素(REE)的富集与释放及其对植物生长和河水REE分布的影响,目的是为河水物质来源研究和为农业生产提供依据。结果表明:(1)乌江流域石灰土中REE的富集程度显著高于各自母岩、黄壤、上陆壳(UCC)、中国土壤(CS)和世界土壤(WS);(2)沉积岩风化过程中REE的富集特征和机制可能与母岩中REE分布特征以及风化剖面中有机质、铁(氢)氧化物和粘土矿物的吸附有关;(3)沉积岩风化过程中释放的REE可为植物吸收利用;(4)石灰岩等沉积岩风化过程中REE和F。等元素的释放对河水溶解态REE的分布有重要影响。 相似文献
157.
The atom transfer radical polymerization(ARP)of (-)-menthyl methacrylatc((-)-MnMA) mediated by CuCl/bipyridine and ethy1 2-bromopropionate or 1-phenylethyl bromide in THF system has been studied.The dependence of the specific rotation on molecular weight and the CD of Poly((-)-MnMA) thus obatined was investigated. 相似文献
158.
氟阴离子在有机合成中的应用:Ⅱ.无水氟化钾催化乙酐与苯甲醛的Perkin反应 总被引:4,自引:0,他引:4
用无水醋酸盐催化苯甲醛与乙酐的Perkin反应,一般反应时间较长,产率最高为55—60%.用三乙胺、吡啶和无水碳酸钾等作催化剂,产率也无明显提高.近年来氟阴离子在有机合成中的应用迅速发展,我们曾用无水氟化钾催化成功地实施了丙二酸二乙酯与苯甲醛的Knoevenagel缩合,并研讨了该反应的微环境效应.本工作首次用无水氟 相似文献
159.
Ren Xiaoming Wu Peiheng Zhang Wenwei Meng Qingjin Chen Xiaoyuan 《Transition Metal Chemistry》2002,27(4):394-397
Ion-pair complexes consisting of the [Fe(mnt)2]– anion and [RBzPy]+ cations [R = NO2
(1) or Cl (2)] have been prepared and characterized by elemental analysis and i.r. spectroscopy. The single crystal structure of (1) shows that the [Fe(mnt)2]– anions are dimeric, and that the coordination geometry of each Fe atom is square pyramidal. The most significant structural feature of (1) is that anions and cations form completely separate columns and – interactions occur within the cation columns. Thermal variations of
m
T for the complexes indicated antiferromagnetic coupling within the dimer. 相似文献
160.
Two new charge-transfer hybrids with one or two ferrocenyl units covalently attached to a hexamolybdate cluster through an extended pi-conjugated bridge have been prepared using Pd-catalyzed coupling reactions on monoiodo- or diiodo-functionalized cluster substrates in over 60% yields. These hybrids have been characterized by (1)H NMR, FTIR, electrospray ionization mass spectrometry, and X-ray diffraction. The electronic spectra of these hybrids show a broad absorption tail extending beyond 550 nm, indicating the existence of charge-transfer transition from the ferrocenyl donor to the cluster acceptor. The observation of the clear charge-transfer transition indicates the contribution of charge-transfer resonance to the ground state in both 2a and 2b even though the donor-acceptor separation distance of 11.29 A is rather long, signaling a through-bond charge-transfer nature made possible by the organic pi-conjugated bridge. Cyclic voltammetry studies reveal a one-electron oxidation wave and a one-electron reduction wave for the hybrid with one ferrocenyl unit. For the one with two ferrocenyl units, a lower reduction potential and a two-electron oxidation wave are observed, indicating negligible electronic interactions between the two ferrocenyl units. 相似文献