全文获取类型
收费全文 | 871篇 |
免费 | 23篇 |
国内免费 | 1篇 |
专业分类
化学 | 796篇 |
晶体学 | 4篇 |
力学 | 4篇 |
数学 | 16篇 |
物理学 | 75篇 |
出版年
2023年 | 5篇 |
2022年 | 5篇 |
2021年 | 7篇 |
2020年 | 11篇 |
2019年 | 13篇 |
2018年 | 8篇 |
2017年 | 11篇 |
2016年 | 12篇 |
2015年 | 8篇 |
2014年 | 31篇 |
2013年 | 69篇 |
2012年 | 54篇 |
2011年 | 67篇 |
2010年 | 27篇 |
2009年 | 40篇 |
2008年 | 70篇 |
2007年 | 44篇 |
2006年 | 55篇 |
2005年 | 55篇 |
2004年 | 54篇 |
2003年 | 42篇 |
2002年 | 50篇 |
2001年 | 13篇 |
2000年 | 11篇 |
1999年 | 9篇 |
1998年 | 11篇 |
1997年 | 6篇 |
1996年 | 4篇 |
1995年 | 6篇 |
1994年 | 6篇 |
1993年 | 13篇 |
1992年 | 6篇 |
1990年 | 2篇 |
1988年 | 1篇 |
1987年 | 2篇 |
1986年 | 5篇 |
1985年 | 5篇 |
1984年 | 5篇 |
1983年 | 7篇 |
1982年 | 9篇 |
1981年 | 4篇 |
1980年 | 3篇 |
1979年 | 9篇 |
1978年 | 6篇 |
1977年 | 2篇 |
1976年 | 6篇 |
1975年 | 1篇 |
1967年 | 1篇 |
1966年 | 1篇 |
1962年 | 1篇 |
排序方式: 共有895条查询结果,搜索用时 15 毫秒
151.
Excitation and emission spectra of polyethylene terephthalate and polyethylene 2,6‐naphthalate films
Isuke Ouchi Ryo Miyamura Makoto Sakaguchi Shuuhei Hosaka Masahiko Kitagawa 《先进技术聚合物》1999,10(3):195-198
With excitation by the light of the wavelengths longer than 320 nm, fluorescence spectra of polyethylene terephthalate (PET) films had somewhat different shapes from those excited below 300 nm through the intrinsic absorption of PET molecules. Also, in the measurements taken with a polarizer in front of the receiving monochoromator but none before the sample, the intensity ratio of parallel (to the draw axis of the film) and perpendicular components of the emission spectra was different if excited above 320 nm or below 300 nm. Discussion was made about the first step of pumping photon energy at the wavelengths above 320 nm. Fluorescence spectra of polyethylene 2,6‐naphthalate films showed a mirror image of their absorption spectra, consisting of one broad band having the same polarization as their absorption spectra. Their fluorescence occurred from the lowest excited level, conforming to the Kasha law. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献
152.
K. Kanai T. Nishi T. Iwahashi Y. Ouchi K. Seki Y. Harada S. Shin 《Journal of Electron Spectroscopy and Related Phenomena》2009,174(1-3):110
Electronic structures of ionic liquids formed by 1-buthyl-3-alkylimidazolium ion [Cnmim]+ (n = 4 and 8) with various inorganic and organic anions have been investigated by ultraviolet photoemission, X-ray photoemission, inverse photoemission and soft X-ray emission spectroscopies (SXES). The comparison of the calculated density of states with the observed spectra revealed that the molecular orbital energies of these ionic liquids are significantly affected by the electrostatic Madelung potential among the ions. The SXES results clearly show that the both highest occupied and lowest unoccupied states of [C4mim]+PF6− are derived from the cation as a result of strong Madelung potential. On the other hand, the SXES results show the valence electronic structures of ionic liquids with larger anion molecules, [Cnmim]+Tf2N− and [Cnmim]+OTf− are contributed from the both cation and anion. 相似文献
153.
154.
Y. Morisaki K. Saito H. Imoto K. Suzuki Y. Ouchi Y. Chujo 《Polymer Science Series A》2009,51(11-12):1218-1228
Anionic polymerization of triphenylmethyl methacrylate was performed by using P-chiral bisphosphine initiators. According to the optical rotation analysis and circular dichroism measurements, the polymer obtained by using the initiator (S,S)-1,2-bis(boranato(tert-butyl)methylphosphino) ethane exhibited one-handed helical conformation induced by the chirality of phosphorus atoms in the polymer terminal. The enantiomer (R,R)-1,2-bis(boranato(tert-butyl)methylphosphino) ethane gave the opposite one-handed helical polymer. Optically active bisphosphine (S,S)-1,2-bis(boranatomethylphenylphosphino) ethane was employed for the helix-sense-selective polymerization of triphenylmethyl methacrylate in order to obtain the polymer with the same helix sense as the polymer obtained from the initiator (S,S)-1,2-ethane bis(t-butylm-ethylphosphineborane). Further, removal of the coordinated boranes and complexation with platinum(II) on the chiral phosphorus atoms were carried out in order to yield the corresponding polymer-platinum(II) complex without loss of its chiral higher-ordered structure. 相似文献
155.
156.
Toshinari Kawada Yuko Yoneda Kensaku Shimizu Chiori Itoh 《Monatshefte für Chemie / Chemical Monthly》2009,18(1):1257-1260
Abstract
The stereospecific synthesis of a chitosan derivative repeating 2-azido-3,6-di-O-benzyl-2-deoxy-β-d-glucopyranosyl-(1 → 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-d-glucopyranose, which has two distinguishing faces, was achieved by polycondensation of the sole starting disaccharide, trichloroacetimidoyl 2-azido-3,6-di-O-benzyl-2-deoxy-β-d-glucopyranosyl-(1 → 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-d-glucopyranoside in a short and efficient way. 相似文献157.
Yuko Hasegawa Shuhei Saitou Sayaka Tamaki Hirofumi Yajima Makoto Tadokoro 《Helvetica chimica acta》2009,92(11):2565-2575
The UV, excitation, and luminescence spectra of tris(pivaloyltrifluoroacetonato)europium(III) ([Eu(pta)3]; Hpta=1,1,1‐trifluoro‐5,5‐dimethylhexane‐2,4‐dione=HA) were measured in the presence of bis(salicylidene)trimethylenediamine (H2saltn), bis[5‐(tert‐butyl)salicylidene]trimethylenediamine (H2(tBu)saltn), or bis(salicylidene)cyclohexane‐1,2‐diyldiamine (H2salchn), and the corresponding ZnII complexes [ZnB] (B=Schiff base). The excitation and luminescence spectra of the solution containing [Eu(pta)3] and [Zn(salchn)] exhibited much stronger intensities than those of solutions containing the other [ZnB] complexes. The introduction of a tBu group into the Schiff base was not effective in sensitizing the luminescence of [Eu(pta)3]. The luminescence spectrum of [ZnB] showed a band around 450 nm. The intensity decreased in the presence of [Eu(pta)3], reflecting complexation between [Eu(pta)3] and [ZnB]. On the basis of the change in intensity against the concentration of [ZnB], stability constants were determined for [Eu(pta)3Zn(saltn)], [Eu(pta)3Zn{(tBu)saltn}], and [Eu(pta)3Zn(salchn)] as 4.13, 4.9 and 5.56, respectively (log , where =[[Eu(pta)3ZnB]]([[Eu(pta)3]][[ZnB]])?1). The quantum yields of these binuclear complexes were determined as 0.15, 0.11, and 0.035, although [Eu(pta)3Zn(salchn)] revealed the strongest luminescence at 613 nm. The results of X‐ray diffraction analysis for [Eu(pta)3Zn(saltn)] showed that ZnII had a coordination number of five and was bridged with EuIII by three donor O‐atoms, i.e., two from the salicylidene moieties and one from the ketonato group pta. 相似文献
158.
Kanji Miyabe Yuko Matsumoto Yusuke Niwa Nobuho Ando Georges Guiochon 《Journal of chromatography. A》2009,1216(47):8319-8330
It has been shown previously that most columns are not radially homogeneous but exhibit radial distributions of the mobile phase flow velocity and the local efficiency. Both distributions are best approximated by fourth-order polynomial, with the velocity in the column center being maximum for most packed columns and minimum for monolithic columns. These distributions may be an important source of tailing of elution peaks. The numerical calculation of elution peaks shows how peak tailing is related to the characteristics of these two distributions. An approach is proposed that permits estimations of the true efficiency and of the degree of column radial heterogeneity by inversing this calculation and using the tailing profiles of the elution peaks that are experimentally measured. This method was applied in two concrete cases of tailing peak profiles that had been previously reported and were analyzed by applying this new inverse approach. The results obtained prove its validity and demonstrate that this numerical method is effective for deriving the true column efficiency from experimental tailing profiles. 相似文献
159.
Matsuo Y Muramatsu A Kamikawa Y Kato T Nakamura E 《Journal of the American Chemical Society》2006,128(30):9586-9587
A series of conical molecules featuring a [60]fullerene/ferrocene hybrid and five aralkyl side chains (Fe[C60{C6H4-(OCO-C6H3-(OR)2-3,4)-4}5]Cp) have been synthesized and examined for their structural and electrochemical properties as well as their ability to form supramolecular structures in crystals and liquid crystals. When the R group on the side is a methyl group, the compound forms crystals in which the dipolar conical molecules are stacked head-to-tail to form a columnar structure. When the R group is as long as a C18H38 group, the compound forms liquid crystals. Oxidation of the liquid crystalline compound by an aminium salt [(4-BrC6H4)3N][SbCl6] produces the corresponding paramagnetic Fe(III) compound that also exhibits liquid crystalline properties. 相似文献
160.
Li T Tsuda Y Minoura K In Y Ishida T Lazarus LH Okada Y 《Chemical & pharmaceutical bulletin》2006,54(6):873-877
Six phenylalanine analogues containing 2'-methyl-, 2',6'-dimethyl-, 2'-ethyl-6'-methyl-, 2'-isopropyl-6'-methyl-, 2',4',6'-trimethyl-, and 3',5'-dimethyl-L-phenylalanine were synthesized enantioselectively through asymmetric hydrogenation of acetamidoacrylate derivatives. Enzymatic digestion and X-ray analysis supported the L-configuration of the phenylalanine derivatives obtained. 相似文献