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991.
Tadashi Inoue Takayuki Onogi Kunihiro Osaki 《Journal of Polymer Science.Polymer Physics》2000,38(7):954-964
The dynamic birefringence and the dynamic viscoelasticity of an oligostyrene, A1000, whose molecular weight (Mw = 1050) was comparable to the Kuhn segment size, MK, were examined near and above the glass‐transition temperature in order to characterize polymeric features of very short chains with M ∼ MK. The complex shear modulus, G*(ω), was similar to that for supercooled liquids: No polymeric modes such as the Rouse mode were detected at low frequencies of viscoelastic spectrum. On the other hand, the strain‐optical coefficient was found to be negative in the terminal flow zone and positive in the glassy zone. Because the negative birefringence of polystyrene is originated by polymeric modes associated with chain orientation, the present results indicate that polymeric modes exist and become dominant for birefringence in the terminal flow. The data were analyzed using a modified stress‐optical rule: The modulus and the strain‐optical ratio were separated into polymeric (rubbery) and glassy components. The total modulus, G*(ω), was mostly due to the glassy component, GG*(ω), resulting in the positive birefringence. GG*(ω) for A1000 agreed with that for high M polystyrenes when compared at a comparable reduced frequency scale. The polymeric component, GR*(ω), giving rise to the negative birefringence was lower than GG*(ω) over the whole frequency range but its contribution to the birefringence exceeded that of the glassy component at low frequencies because of the larger optical anisotropy and longer characteristic relaxation time of the former. The limiting modulus of GR* at high frequencies was about 3 times lower than that for high M polystyrenes, indicating that the main‐chain orientation of the oligostyrene on instantaneous deformation was reduced compared with that of high M polystyrenes. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 954–964, 2000 相似文献
992.
Haruo Nishida Fumio Sanda Takeshi Endo Takeshi Nakahara Takayuki Ogata Koshi Kusumoto 《Journal of polymer science. Part A, Polymer chemistry》2000,38(1):68-73
Polyaddition of bifunctional spiro orthoesters (SOEs) with bifunctional acid chlorides was examined to develop zero‐shrinkage polymerization. The polyaddition afforded the corresponding polyether‐esters by repeating the addition reaction accompanying the double ring‐opening isomerization of the SOE moiety in a manner similar to the reaction of monofunctional SOEs with acid chlorides. The polyaddition accompanied a slight shrinkage or expansion in volume. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 68–73, 2000 相似文献
993.
Si-Si Liu Fei Jin Yi-Shi Liu Yoshiko Murakami Yukihiko Sugita Takayuki Kato Xiao-Dong Gao Taroh Kinoshita Motoyuki Hattori Morihisa Fujita 《Molecules (Basel, Switzerland)》2021,26(18)
Glycosylphosphatidylinositol (GPI) anchor modification is a posttranslational modification of proteins that has been conserved in eukaryotes. The biosynthesis and transfer of GPI to proteins are carried out in the endoplasmic reticulum. Attachment of GPI to proteins is mediated by the GPI-transamidase (GPI-TA) complex, which recognizes and cleaves the C-terminal GPI attachment signal of precursor proteins. Then, GPI is transferred to the newly exposed C-terminus of the proteins. GPI-TA consists of five subunits: PIGK, GPAA1, PIGT, PIGS, and PIGU, and the absence of any subunit leads to the loss of activity. Here, we analyzed functionally important residues of the five subunits of GPI-TA by comparing conserved sequences among homologous proteins. In addition, we optimized the purification method for analyzing the structure of GPI-TA. Using purified GPI-TA, preliminary single particle images were obtained. Our results provide guidance for the structural and functional analysis of GPI-TA. 相似文献
994.
微纳米材料及其结构的界面强度的实验研究 总被引:4,自引:2,他引:2
介绍了近年来微纳米材料强度实验测试研究方面的最新进展,重点综述了可用于微纳米材料及其结构中界面强度测试的实验系统、测试方法及结果.主要内容包括:测试微纳米薄膜界面端分层裂纹启裂的夹层悬臂梁方法,测试纳米岛/衬底间界面结合强度的改进AFM (atomic force microscopy)方法, 测试裂纹沿界面扩展的预裂纹法,可实现纳米薄膜界面裂纹原位观察的实验测试方法,测试薄膜在疲劳、蠕变条件下界面裂纹扩展的改进4点弯曲法等.除了总结分析测试结果,还讨论了上述实验方法的优缺点和适用范围,并指出了微纳米材料界面强度实验研究方面的一些挑战与难点,最后提出了若干需要继续研究的课题. 相似文献
995.
Tomoaki Kawaguchi Koji Tagawa Fumiyo Senda Takayuki Matsunaga Hiromi Kitano 《Journal of colloid and interface science》1999,210(2):290
Amphiphiles which carry many pendent galactose residues as side chains were prepared by telomerization of 2-methacryloyloxyethyl β-D-galactopyranoside (MEGal) or 3-(2-methacryloyl aminoethylthio)propylD-galactopyranoside (MEPGal, α:β = 3.9:1) using a lipophilic radical initiator. The galactose-carrying amphiphiles (DP (degree of polymerization) = 15) incorporated in liposomes were recognized by a lectin fromRicinus communis(RCA120), which was proven by the increase in turbidity of the liposome suspension after mixing with the lectin. The recognition was largely affected by the distance between the galactose residues and the polymer main chain, and the surface density of the amphiphile in the liposomes. The liposomes containing these galactolipids were not taken up by mouse peritoneal macrophages, probably due to a steric hindrance of polymer main chains from the uptake of D-galactose receptors on the macrophages. 相似文献
996.
Hiroyuki Hamazaki Takayuki Abe Hidefumi Yamakawa Tomoyuki Yokota Shiro Shigeta Hiroshi Takaku 《Helvetica chimica acta》2002,85(7):2183-2194
We have demonstrated that a new type of circular dumbbell RNA/DNA chimeric oligonucleotide (CDRDON) with two closed nucleotide or alkyl loop structures (hexa‐ethylene glycol) inhibits influenza virus A replication in MDCK cells. The enzymatic synthesis of circular dumbbell RNA/DNA chimeric oligonucleotides was achieved by enzymatically ligating a self‐complementary phosphorylated oligonucleotide with T4‐RNA ligase. The CDRDON‐Al, with two closed alkyl loop structures, showed higher nuclease resistance, hybridization, and cellular uptake than the anti‐S‐ODN and the CDRDON, with two closed nucleotide hairpin‐loop structures. The circular dumbbell RNA/DNA chimeric oligonucleotide (CDRDON‐Al‐PB2‐as), containing an AUG initiation‐codon sequence as the target of PB2, showed highly inhibitory effects on influenza A virus RNA expression. The limited toxicity of unmodified phosphodiester oligonucleotides and the sequence‐specific binding to target mRNA indicate that circular dumbbell RNA/DNA chimeric phosphodiester oligonucleotides can be used with intact cells, and may prevent viral replication in culture. 相似文献
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