全文获取类型
收费全文 | 309篇 |
免费 | 6篇 |
国内免费 | 4篇 |
专业分类
化学 | 288篇 |
晶体学 | 3篇 |
力学 | 1篇 |
数学 | 9篇 |
物理学 | 18篇 |
出版年
2022年 | 4篇 |
2021年 | 1篇 |
2020年 | 6篇 |
2018年 | 1篇 |
2017年 | 3篇 |
2016年 | 4篇 |
2015年 | 7篇 |
2014年 | 7篇 |
2013年 | 28篇 |
2012年 | 9篇 |
2011年 | 23篇 |
2010年 | 6篇 |
2009年 | 14篇 |
2008年 | 19篇 |
2007年 | 14篇 |
2006年 | 12篇 |
2005年 | 17篇 |
2004年 | 16篇 |
2003年 | 11篇 |
2002年 | 21篇 |
2001年 | 9篇 |
2000年 | 10篇 |
1999年 | 3篇 |
1998年 | 3篇 |
1997年 | 4篇 |
1996年 | 3篇 |
1995年 | 5篇 |
1994年 | 7篇 |
1993年 | 9篇 |
1992年 | 2篇 |
1991年 | 6篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1986年 | 3篇 |
1985年 | 2篇 |
1984年 | 1篇 |
1983年 | 2篇 |
1982年 | 3篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1978年 | 1篇 |
1977年 | 4篇 |
1976年 | 2篇 |
1975年 | 4篇 |
1974年 | 3篇 |
1973年 | 2篇 |
1967年 | 1篇 |
排序方式: 共有319条查询结果,搜索用时 15 毫秒
1.
2.
3.
J. P. S. Farinha J. M. G. Martinho H. Xu M. A. Winnik R. P. Quirk 《Journal of Polymer Science.Polymer Physics》1994,32(9):1635-1642
Cyclization of a polystyrene chain (Mn = 10,600; Mw/Mn = 1.09) both ends labeled with 4-(1-pyrenyl)butanoamide groups was studied in cyclohexane between 25 and 95°C. The amide groups (peptide bonds) at both ends can form an intrachain hydrogen bond between the amide hydrogen at one chain end and the carbonyl oxygen at the other. The presence of two sets of conformers, random coils, and chains cyclized through hydrogen bonding, complicates the data analysis. The pyrene excimer kinetics of this polymer is well described by a model composed of two monomers (hydrogen bonded and nonbonded chains) and one excimer, in equilibrium. The cyclization rate constant for hydrogen-bonded chains is larger than the one for nonhydrogen-bonded chains. The pyrene excimer binding energy (ca. 1.6 kcal/mol) is lower than the published value for nonhydrogen-bonded chains (~ 9 kcal/mol), suggesting that intrachain hydrogen bonding hinders the stabilization of the excimer. © 1994 John Wiley & Sons, Inc. 相似文献
4.
5.
Kujawa P Moraille P Sanchez J Badia A Winnik FM 《Journal of the American Chemical Society》2005,127(25):9224-9234
The layer-by-layer growth of multilayer assemblies of two polysaccharides, the polyanion hyaluronan (HA) and the polycation chitosan (CH), was investigated using atomic force microscopy (AFM) and surface plasmon resonance (SPR) spectroscopy, with primary emphasis on the effect of the polysaccharide molecular weights on the film thickness and surface morphology. The HA/CH multilayers exhibit an exponential increase of the optical film thickness with the number of deposited bilayers. We show that the multilayer thickness at a given stage depends on the size of both CH, the diffusing polyelectrolyte, and HA, the non-diffusing species. Assemblies (12 bilayers) of high molecular weight polysaccharides (HA, 360,000; CH, 160,000) were twice as thick (approximately 900 nm vs approximately 450 nm) as those obtained with low molecular weight polymers (HA, 30,000; CH, 31,000), as assessed by AFM scratch tests. The exponential growth rate is the same for the high and low molecular weight pairs; the larger film thicknesses observed by SPR and by AFM arising from an earlier onset of the steep exponential growth phase in the case of the high molecular weight pair. In all cases, isolated islets form during the deposition of the first CH layer onto the underlying HA. Upon further film growth, individual islets coalesce into larger vermiculate features. The transition from distinct islands to vermiculate structures depends on the molecular weights of the polysaccharides and the lower molecular weight construct presents larger worm-like surface domains than the high molecular weight pair. 相似文献
6.
Surface passivation of luminescent colloidal quantum dots with poly(dimethylaminoethyl methacrylate) through a ligand exchange process 总被引:1,自引:0,他引:1
Wang XS Dykstra TE Salvador MR Manners I Scholes GD Winnik MA 《Journal of the American Chemical Society》2004,126(25):7784-7785
Polydimethylaminoethyl methacrylate (PDMAEMA) was used as a multidentate ligand to modify the surface of CdSe/ZnS core-shell colloidal quantum dots in toluene with trioctylphosphine oxide (TOPO) as the surface ligand. Adsorption of PDMAEMA was accompanied by release of TOPO. The process is free of agglomeration, and the modified nanocrystals become soluble in methanol. The photoluminescence properties are well-preserved in either toluene or methanol. 相似文献
7.
聚丙烯表面的生物相容性修饰: 表面氨基放大还原胺化接枝磷酰胆碱 总被引:5,自引:0,他引:5
在氨气氛中对聚丙烯薄膜表面进行等离子处理, 获得了不同浓度的表面氨基. 表面氨基的数量经1,6-己二异氰酸酯键合三(2-氨乙基)胺可成倍增加. 用还原胺化法将磷酰胆碱醛共价接枝到表面氨基上获得了磷酰胆碱改性的聚丙烯薄膜. X射线光电子能谱(XPS)测定结果表明, 接枝磷酰胆碱基团的表面覆盖率可达20%~40%. 衰减全反射傅立叶变换红外(ATR-FTIR)和动态接触角测定结果也都说明磷酸胆碱基团被成功地接枝于聚丙烯表面. 还原胺化法结合等离子处理及表面氨基放大技术, 有望成为获取新型生物材料的一种有效途径. 相似文献
8.
9.
Jung Kwon Oh Jun Wu Mitchell A. Winnik Gary P. Craun Jude Rademacher Rajeev Farwaha 《Journal of polymer science. Part A, Polymer chemistry》2002,40(17):3001-3011
We describe the synthesis and characterization of three new polymerizable benzophenone derivatives [2‐acryloxy‐5‐methyl benzophenone ( 8 ), 4′‐dimethylamino‐2‐acryloxy‐5‐methyl benzophenone ( 9 ), and 4′‐dimethylamino‐2‐(β‐acryloxyethyl)oxy‐5‐methyl benzophenone ( 10 )]. We show that these monomers can successfully be incorporated into vinyl acetate (VAc) copolymer latex particles. These particles were prepared by semicontinuous emulsion polymerization and mini‐emulsion polymerization of VAc with butylacrylate (BA) for VAc/BA = 4/1 by weight. The two monomers 9 and 10 bearing the 4′‐dimethylamino group satisfy the important spectroscopic criteria required of a dye to serve as an acceptor chromophore for nonradiative energy transfer from phenanthrene (Phe) as the donor. Their UV absorption spectra suggest significant overlap with the emission spectrum of Phe, which can be incorporated into P(VAc‐co‐BA) latex through copolymerization with 9‐acryloxymethyl Phe ( 2 ). In addition, these chromophores provide a window in their absorption spectra for excitation of the Phe chromophore at 300 nm. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3001–3011, 2002 相似文献
10.
Jean-Charles Boutonnet Francoise Rose-Munch Eric Rose Gilles Precigoux 《Journal of organometallic chemistry》1985,284(2):C25-C30
The complex CpV(CO)3THF has been prepared in THF solution (i) photochemically from CpV(CO)4, and (ii) from [CpV(H)(CO)3]?/[Ph3C]+ at low temperatures. THF is replaced by [CpV(H)(CO)3]? to form [{CpV(CO)3}2-μ-H]?, and by various ligands L with C, η2-CC, Sn, N, O, S, Se or Te functionality to yield CpV(CO)3L and cis-[CpV(CO)2LL] (LL = bipy, o-phen, tolane). The δ (51V) values range over ca. 1400 ppm and allow the assignment of distinct coordination modes for ambidentate ligands. The temperature gradient is ca. +1.2 ppm/deg. For [CpV(SnCl3)(CO)3]? (δ ?1340 ppm rel. to VOCl3), 1J(51V-117,119Sn) is 900 Hz. The isotope effect on introducing 12CO for 13CO in CpV(CO)4 is ?0.48(2) ppm; 1J(51V-13C) 107 Hz. 相似文献