全文获取类型
收费全文 | 788篇 |
免费 | 22篇 |
国内免费 | 2篇 |
专业分类
化学 | 529篇 |
晶体学 | 9篇 |
力学 | 10篇 |
数学 | 81篇 |
物理学 | 183篇 |
出版年
2023年 | 7篇 |
2022年 | 6篇 |
2021年 | 8篇 |
2020年 | 14篇 |
2019年 | 10篇 |
2018年 | 12篇 |
2016年 | 7篇 |
2015年 | 17篇 |
2014年 | 15篇 |
2013年 | 38篇 |
2012年 | 72篇 |
2011年 | 65篇 |
2010年 | 27篇 |
2009年 | 15篇 |
2008年 | 62篇 |
2007年 | 55篇 |
2006年 | 63篇 |
2005年 | 53篇 |
2004年 | 43篇 |
2003年 | 36篇 |
2002年 | 24篇 |
2000年 | 6篇 |
1998年 | 4篇 |
1997年 | 5篇 |
1996年 | 9篇 |
1995年 | 9篇 |
1994年 | 3篇 |
1993年 | 7篇 |
1992年 | 6篇 |
1991年 | 4篇 |
1990年 | 4篇 |
1989年 | 4篇 |
1988年 | 4篇 |
1987年 | 3篇 |
1985年 | 3篇 |
1984年 | 5篇 |
1983年 | 7篇 |
1982年 | 4篇 |
1980年 | 3篇 |
1979年 | 3篇 |
1977年 | 5篇 |
1976年 | 3篇 |
1974年 | 4篇 |
1961年 | 3篇 |
1960年 | 3篇 |
1941年 | 4篇 |
1939年 | 3篇 |
1937年 | 2篇 |
1936年 | 2篇 |
1907年 | 5篇 |
排序方式: 共有812条查询结果,搜索用时 15 毫秒
1.
Seth Sheeba Thavamani Murugesan Sudharsan Anitha Santhana Mariya Devarajan Suresh Arlin Jose Amali Sanniyasi Rajeswari Thomas Peter Amaladhas 《应用有机金属化学》2020,34(9):e5752
The catalytic activity of CeO2 and palladium nanoparticles supported fly ash zeolite (CeO2/Pd@FAZ) for Csp2-Csp2 bond formation was studied. CeO2/Pd@FAZ was characterized by FTIR, XRD, EDAX and TEM studies. In the Suzuki-Miyauracross-coupling reaction, biphenyl derivatives with excellent yields were obtained, and the reaction conditions were optimized. The catalytic activity was explored using a wide variety of diversely substituted aryl bromides and chlorides with aryl boronic acid under optimized reaction conditions. The recyclability of the catalyst was established for three cycles, with the conversion rate from 99 to 40%, which gained the advantage of heterogeneous catalysis. 相似文献
2.
Dr. Jiaqing Wang Weiyi Tan Dr. Guanying Li Difei Wu Hongjian He Jiashu Xu Meihui Yi Prof. Dr. Ye Zhang S. Ali Aghvami Prof. Dr. Seth Fraden Prof. Dr. Bing Xu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(66):15116-15120
Although lipids contribute to cancer drug resistance, it is challenging to target diverse range of lipids. Here, we show enzymatically inserting exceedingly simple synthetic lipids into membranes for increasing membrane tension and selectively inhibiting drug resistant cancer cells. The lipid, formed by conjugating dodecylamine to d -phosphotyrosine, self-assembles to form micelles. Enzymatic dephosphorylation of the micelles inserts the lipids into membranes and increases membrane tension. The micelles effectively inhibit a drug resistant glioblastoma cell (T98G) or a triple-negative breast cancer cell (HCC1937), without inducing acquired drug resistance. Moreover, the enzymatic reaction of the micelles promotes the accumulation of the lipids in the membranes of subcellular organelles (e.g., endoplasmic reticulum (ER), Golgi, and mitochondria), thus activating multiple regulated cell death pathways. This work, in which for the first time membrane tension is increased to inhibit cancer cells, illustrates a new and powerful supramolecular approach for antagonizing difficult drug targets. 相似文献
3.
Synthesis of 8‐Aminoquinolines by Using Carbamate Reagents: Facile Installation and Deprotection of Practical Amidating Groups 下载免费PDF全文
Hye Kyung Kim Prof. Dr. Seth R. Marder Prof. Dr. Sukbok Chang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(48):17200-17204
Described herein is the development of practical routes to 8‐aminoquinolines by using readily installable and easily deprotectable amidating reagents. Two scalable procedures were optimized under RhIII‐catalyzed conditions: i) the use of pre‐generated chlorocarbamates and ii) a two‐step one‐pot process that directly employs carbamates. Both approaches are highly convenient for the gram‐scale synthesis of 8‐aminoquinolines under mild conditions. Facile deprotection of the synthetically versatile amidating groups was achieved under the Pd‐catalyzed transfer hydrogenation conditions with simultaneous deoxygenation of quinoline N‐oxides, thus yielding 8‐aminoquinolines in excellent overall efficiency. 相似文献
4.
Contrasting Response of Two Dipolar Fluorescence Probes in a Leucine‐Based Organogel and Its Implications 下载免费PDF全文
Sivalingam Soumya Sudipta Seth Sneha Paul Prof. Dr. Anunay Samanta 《Chemphyschem》2015,16(11):2440-2446
The microenvironments of a leucine‐based organogel are probed by monitoring the fluorescence behavior of coumarin 153 (C153) and 4‐aminophthalimide (AP). The steady‐state data reveals distinctly different locations of the two molecules in the gel. Whereas AP resides close to the hydroxyl moieties of the gelator and engages in hydrogen‐bonding interactions, C153 is found in bulk‐toluene‐like regions. In contrast to C153, AP exhibits excitation‐wavelength‐dependent emission, indicating that the environments of the hydrogen‐bonded AP molecules are not all identical. A two‐component fluorescence decay of AP in gel, unlike C153, supports this model. A time‐resolved fluorescence anisotropy study of the rotational motion of the molecules also reveals the strong association of only AP with the gelator. That AP influences the critical gelation concentration implies its direct involvement in the gel‐formation process. The results highlight the importance of guest–gelator interactions in gels containing guest molecules. 相似文献
5.
Effect of Controlled Deposition of ZnS Shell on the Photostability of CdTe Quantum Dots as Studied by Conventional Fluorescence and FCS Techniques
下载免费PDF全文
The effect of one and two monolayers of ZnS shells on the photostability of CdTe quantum dots (QDs) in aqueous and nonaqueous media has been studied by monitoring the fluorescence behavior of the QDs under ensemble and single‐molecule conditions. ZnS capping of the CdTe QDs leads to significant enhancement of the fluorescence brightness of these QDs. Considerable enhancement of the photostability of the shell‐protected QDs, including the suppression of photoactivation, is also observed. Fluorescence correlation spectroscopy measurements reveal an increase in the number of particles undergoing reversible fluorescent on–off transitions in the volume under observation with increasing excitation power; this effect is found to be more pronounced in the case of core‐only QDs than for core–shell QDs. 相似文献
6.
Functionalization of the bio-relevant heterocycles 2-arylbenzo[d]oxazole and 2-arylbenzo[d]thiazole has been achieved through Ru(II)-catalyzed alkenylation with unactivated olefins leading to selective formation of the mono-alkenylated products. This approach has a broad substrate scope with respect to the coupling partners, affords high yields, and works for gram scale synthesis using a readily available Ru-based catalyst. Mechanistic studies reveal a C−H activation pathway for the dehydrogenative coupling leading to the alkenylation. However, the results of the ESI-MS-guided deuterium kinetic isotope effect studies indicate that the C−H activation stage may not be the rate-determining step of the reaction. The use of a radical scavenging agent such as TEMPO did not show any detrimental effect on the reaction outcome, eliminating the possibility of the involvement of a free-radical pathway. 相似文献
7.
8.
9.
Mandal Prashanta Kumar Seth Gauri Shanker Sarkar Subharthi Chamkha Ali 《Journal of Thermal Analysis and Calorimetry》2021,143(3):1901-1916
Journal of Thermal Analysis and Calorimetry - Numerical simulation of a non-linear mathematical model governing an arbitrarily oblique slip flow of a nanofluid, with suspended carbon nanotubes in... 相似文献
10.