全文获取类型
收费全文 | 94篇 |
免费 | 4篇 |
国内免费 | 15篇 |
专业分类
化学 | 73篇 |
力学 | 6篇 |
综合类 | 2篇 |
数学 | 14篇 |
物理学 | 18篇 |
出版年
2023年 | 2篇 |
2022年 | 1篇 |
2021年 | 5篇 |
2020年 | 3篇 |
2019年 | 1篇 |
2016年 | 1篇 |
2015年 | 6篇 |
2014年 | 3篇 |
2013年 | 4篇 |
2012年 | 13篇 |
2011年 | 5篇 |
2010年 | 2篇 |
2009年 | 5篇 |
2008年 | 13篇 |
2007年 | 9篇 |
2006年 | 6篇 |
2005年 | 2篇 |
2004年 | 1篇 |
2003年 | 2篇 |
2001年 | 1篇 |
2000年 | 1篇 |
1999年 | 2篇 |
1996年 | 1篇 |
1994年 | 3篇 |
1993年 | 6篇 |
1989年 | 7篇 |
1988年 | 2篇 |
1987年 | 3篇 |
1986年 | 2篇 |
1985年 | 1篇 |
排序方式: 共有113条查询结果,搜索用时 31 毫秒
1.
The present paper determines the form of automorphisms of $\[{E_2}(R)\]$ and $\[G{E_2}(R)\]$ over commutative rings provided 2, 3 and 5 are units. 相似文献
2.
3.
4.
5.
我们用Fe_2(SO_4)_3·xH_2O为催化剂,对2-甲基-2-已醇脱水生成烯烃反应的溶剂化能力及其动力学做了研究,测定了20种不同溶剂中的反应速率常数和以丙至辛6种直链醇为溶剂于不同温度下反应的速率常数,确定了溶剂化能力与溶剂介电常数之间的线性关系。这方面工作尚未见报道。 相似文献
6.
溶胶凝胶分配理论是在分子水平上表征交联网络结构的有效工具。由Flory等建立和发展起来的这一理论,由于引用了溶胶相无分子内环化反应的假定,特别是在理论推导中将分子内交联反应与分子间的链增长反应对两相分配的贡献未能加以区别,致使理论与实验不符。本文充分考虑了经典理论的这些缺欠,建立了更为符合客观实际的理论模型。同时,用十分简便的方法推导了反应溶胶分数,溶胶反应程度,分子内和分子间总反应程度等量宏观联系的参数方程组。以聚酯为模型化合物的实验研究与本文所得理论结果基本相符。 相似文献
7.
Yukun Li Leela Christian‐Tabak Vivien Li Fong Fuan Jiong Zou Chong Cheng 《Journal of polymer science. Part A, Polymer chemistry》2014,52(22):3250-3259
Amphiphilic double‐brush copolymers (DBCs) with each graft site quantitatively carrying both a hydrophilic poly(ethylene oxide) (PEO) graft and a hydrophobic polystyrene (PSt) graft are synthesized by sequential reversible addition‐fragmentation chain transfer (RAFT) polymerization and ring‐opening metathesis polymerization (ROMP). These DBCs are used as both surfactants and polyfunctional RAFT agents in the radical polymerization of St in aqueous dispersed media. Miniemulsions with narrowly dispersed St‐based nanodroplets are readily obtained after ultrasonication of the reaction mixtures. Without the presence of crosslinker, chain‐extension polymerization of St from the DBCs yields well‐defined polymeric latexes with narrow size distributions. However, with the presence of divinylbenzene (DVB) as the crosslinker, vesicular polymeric nanoparticles are formed as the major product. Such crosslinking‐induced change in morphology of the resulting latex nanomaterials may be ascribed to the increase of interfacial curvature in the heterophase systems during crosslinking polymerization. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3250–3259 相似文献
8.
9.
10.
Dr. Fuan Wang Ron Orbach Prof. Itamar Willner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(50):16030-16036
The Cu2+‐dependent ligation DNAzyme is implemented as a biocatalyst for the colorimetric or chemiluminescence detection of Cu2+ ions, Hg2+ ions, or cocaine. These sensing platforms are based on the structural tailoring of the sequence of the Cu2+‐dependent ligation DNAzyme for specific analytes. The tethering of a subunit of the hemin/G‐quadruplex DNAzyme to the ligation DNAzyme sequence, and the incorporation of an imidazole‐functionalized nucleic‐acid sequence, which acts as a co‐substrate for the ligation DNAzyme that is tethered to the complementary hemin/G‐quadruplex subunit. In the presence of different analytes, Cu2+ ions, Hg2+ ions, or cocaine, the pretailored Cu2+‐dependent ligation DNAzyme sequence stimulates the respective ligation process by combining the imidazole‐functionalized co‐substrate with the ligation DNAzyme sequence. These reactions lead to the self‐assembly of stable hemin/G‐quadruplex DNAzyme nanostructures that enable the colorimetric analysis of the substrate through the DNAzyme‐catalyzed oxidation of 2,2′‐azinobis(3‐ethylbenzothiazoline‐6‐sulfonic acid), ABTS2?, by H2O2 into the colored product ABTS.?, or the chemiluminescence detection of the substrate through the DNAzyme‐catalyzed oxidation of luminol by H2O2. The detection limits for the sensing of Cu2+ ions, Hg2+ ions, and cocaine correspond to 1 nM , 10 nM and 2.5 μM , respectively. These different sensing platforms also reveal impressive selectivities. 相似文献