全文获取类型
收费全文 | 535篇 |
免费 | 128篇 |
国内免费 | 100篇 |
专业分类
化学 | 716篇 |
晶体学 | 7篇 |
综合类 | 1篇 |
物理学 | 39篇 |
出版年
2024年 | 1篇 |
2023年 | 3篇 |
2022年 | 11篇 |
2021年 | 25篇 |
2020年 | 29篇 |
2019年 | 28篇 |
2018年 | 13篇 |
2017年 | 17篇 |
2016年 | 43篇 |
2015年 | 40篇 |
2014年 | 33篇 |
2013年 | 46篇 |
2012年 | 35篇 |
2011年 | 51篇 |
2010年 | 34篇 |
2009年 | 37篇 |
2008年 | 39篇 |
2007年 | 38篇 |
2006年 | 38篇 |
2005年 | 40篇 |
2004年 | 27篇 |
2003年 | 25篇 |
2002年 | 9篇 |
2001年 | 13篇 |
2000年 | 14篇 |
1999年 | 12篇 |
1998年 | 4篇 |
1997年 | 13篇 |
1996年 | 10篇 |
1995年 | 12篇 |
1994年 | 7篇 |
1993年 | 1篇 |
1992年 | 11篇 |
1991年 | 2篇 |
1988年 | 1篇 |
1987年 | 1篇 |
排序方式: 共有763条查询结果,搜索用时 453 毫秒
71.
《Angewandte Chemie (International ed. in English)》2017,56(7):1914-1918
Our new, simple, and accurate colorimetric method is based on diarylethenes (DAEs) for the rapid detection of a wide range of primary and secondary amines. The probes consist of aldehyde‐ or ketone‐substituted diarylethenes, which undergo an amine‐induced decoloration reaction, selectively to give the ring‐closed isomer. Thus, these probes can be activated at the desired moment by light irradiation, with a sensitivity that allows the detection of amines at concentrations as low as 10−6 m in solution. In addition, the practical immobilization of DAEs on paper makes it possible to detect biogenic amines, such as cadaverine, in the gas phase above a threshold of 12 ppbv within 30 seconds. 相似文献
72.
Saleh A. Ahmed Ziad Moussa Shaya Y. Al‐Raqa Saleh N. Alamry 《Journal of Physical Organic Chemistry》2009,22(6):593-606
Multi‐addressable photophysical properties of new synthesized photochromic materials based on photochromic dihydroindolizine system (DHI) covalently linked to N‐acyl‐11 aminoundecanoic acid (AUDA) or to its sodium salt or to its ester, through an amidic or urethane linkage have been studied. The DHI skeleton in these compounds is substituted in both the fluorene part (region A) or in the heterocyclic base (region B) with the gelling moieties. These molecules have been designed to respond to their environment. Interestingly, they are shown to act as efficient gelators for polar organic fluids, water and obviously they exhibit a thermosensitive answer as low molecular mass organogelators. In these fluids, the aggregative properties are totally suppressed upon conversion to neutral carboxylic species. The gels of these carboxylate sodium salts are shown to be markedly affected by light irradiation. Supramolecular gelating assemblies can be disrupted by the photoinduced ring opening of the DHI subunit, so that the macroscopic flowing property is recovered. Upon a further thermal treatment, the system is reversibly converted back to the supramolecular network. Controlled gelation could be achieved using temperature, light, or acidity as external stimuli. These new synthesized photochromic gels with their multi‐addressable properties will find their applications as super photoresponsive materials. Developing and tuning of the photophysical properties of the synthesized compounds by the amide and urethane substituents in the 4‐position of the fluorene and pyridazine regions have been achieved. The absorption maxima (λmax) and the half‐lives (t1/2) of the colored betaines were detected in all cases using UV/VIS spectrophotometric measurements. Irradiation of DHI 12‐20 in CH2Cl2 or in acetonitrile solutions at ambient temperature with polychromatic light leads to the formation of red to red‐violet colored betaines 12 ′ ‐20 ′. The kinetics of the bleaching process of betaines 12 ′ ‐20 ′ to DHIs 12‐20 were found to take place in the second range (96‐218 s) and fit well the first order thermal back reaction. Some of these DHIs showed a photostability higher than that of the standard one. These interesting photophysical properties will help this family of compounds to find useful applications. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
73.
Yasunobu Kotani Haruka Yasuda Dr. Kenji Higashiguchi Prof. Kenji Matsuda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(43):11158-11166
An amphiphilic rectangular-shaped photochromic diarylethene bearing two hydrophobic alkyl chains and two hydrophilic tri(ethylene glycol) chains was synthesized, and its photoinduced morphological transformation in water was investigated. Two unexpected phenomena were revealed in the course of the experiments: a re-entrant photoinduced macroscopic morphological transformation and temperature-dependent kinetic products of supramolecular assembly. When the pure closed-ring isomer was dispersed in water, a re-entrant photoinduced morphological transformation, that is, a photoinduced transition from the hydrated phase to the dehydrated phase and then back to the hydrated phase, was observed by optical microscopy upon irradiation with green light at 20 °C; this was interpreted by the V-shaped phase diagram of the LCST transition. The aqueous assembly of the pure closed-ring isomer was controlled by changing the temperature; specifically, rapid cooling to 15 and 5 °C gave J and H aggregates, respectively, as the kinetic products. The thermodynamic product at both temperatures was a mixture of mostly H aggregate with a small amount of J aggregate. This behavior was rationalized by the temperature-dependent potential energy surface of the supramolecular assembly. 相似文献
74.
Structural Effects in Visible‐Light‐Responsive Metal–Organic Frameworks Incorporating ortho‐Fluoroazobenzenes
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Dr. Sonia Castellanos Dr. Alexis Goulet‐Hanssens Fangli Zhao Alla Dikhtiarenko Alexey Pustovarenko Prof. Stefan Hecht Prof. Jorge Gascon Prof. Freek Kapteijn Dr. David Bléger 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(2):746-752
The ability to control the interplay of materials with low‐energy photons is important as visible light offers several appealing features compared to ultraviolet radiation (less damaging, more selective, predominant in the solar spectrum, possibility to increase the penetration depth). Two different metal–organic frameworks (MOFs) were synthesized from the same linker bearing all‐visible ortho‐fluoroazobenzene photoswitches as pendant groups. The MOFs exhibit different architectures that strongly influence the ability of the azobenzenes to isomerize inside the voids. The framework built with Al‐based nodes has congested 1D channels that preclude efficient isomerization. As a result, local light–heat conversion can be used to alter the CO2 adsorption capacity of the material on exposure to green light. The second framework, built with Zr nodes, provides enough room for the photoswitches to isomerize, which leads to a unique bistable photochromic MOF that readily responds to blue and green light. The superiority of green over UV irradiation was additionally demonstrated by reflectance spectroscopy and analysis of digested samples. This material offers promising perspectives for liquid‐phase applications such as light‐controlled catalysis and adsorptive separation. 相似文献
75.
Alexandru Vlasceanu Dr. Søren L. Broman Anne S. Hansen Anders B. Skov Prof. Dr. Martina Cacciarini Prof. Dr. Anders Kadziola Prof. Dr. Henrik G. Kjaergaard Prof. Dr. Kurt V. Mikkelsen Prof. Dr. Mogens Brøndsted Nielsen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(31):10796-10800
The conversion and efficient storage of solar energy is recognized to hold significant potential with regard to future energy solutions. Molecular solar thermal batteries based on photochromic systems exemplify one possible technology able to harness and apply this potential. Herein is described the synthesis of a macrocycle based on a dimer of the dihydroazulene/vinylheptafulvene (DHA/VHF) photo/thermal couple. By taking advantage of conformational strain, this DHA–DHA macrocycle presents an improved ability to absorb and store incident light energy in chemical bonds (VHF–VHF). A stepwise energy release over two sequential ring‐closing reactions (VHF→DHA) combines the advantages of an initially fast discharge, hypothetically addressing immediate energy consumption needs, followed by a slow process for consistent, long‐term use. This exemplifies another step forward in the molecular engineering and design of functional organic materials towards solar thermal energy storage and release. 相似文献
76.
A novel asymmetrical diarylethene with a (formyloxyethoxy)ethyl‐linked naphthalimide unit was synthesized, and its photochromic and fluorescence properties were systematically investigated in both solution and a poly(metyl methacrylate) film. The diarylethene showed significant photochromism and notable fluorescence switching properties upon irradiation with ultraviolet/visible light. Compared with the parent diarylethene, introduction of the naphthalimide moiety was effective to increase the molar absorption coefficient, the fluorescence quantum yield, and fluorescent modulation efficiency of the diarylethene. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
77.
The emission spectra of pure cellulose samples of various origins were monitored during several heating/cooling cycles. During heating the emission intensity decreased due to the greater probability for internal conversion at higher temperatures. Cooling resulted in an emission recovery that was nearly reversible over several heating/cooling cycles, provided that the final 0temperature was sufficiently low. The change in the relative emission yield with temperature showed two regimes, both with linear decreases but different slopes, suggesting different mechanisms for the internal conversion in these regions. Heating to temperatures higher than 160°C for filter papers and higher than 145°C for microcrystalline cellulose initiated reactions that caused changes in the emission spectra typical of thermal degradation. If the samples were heated beyond these threshold temperatures the emission recovery on cooling after the first heat treatment occurred to a much higher intensity level than that observed initially, indicating the formation of a multitude of new chromophores due to thermal reactions. Exposure of the samples to IR radiation caused a slow increase in the emission intensity for almost 600h. 相似文献
78.
Xiao-Fan Jiang Dr. Song-De Han Dr. A-Ni Wang Dr. Jie Pan Prof. Dr. Guo-Ming Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(4):1410-1415
The intermarriage of neutral and tripodal imidazole ligand, tris(4-(1H-imidazol-1-yl)phenyl)amine (TIPA), with zinc phosphite yields two hybrid phosphites, [Zn2(HPO3)2(TIPA)]⋅2 H2O ( 1 ) and [Zn3(HPO3)3(TIPA)]⋅6 H2O ( 2 ). Compound 1 has a hybrid sheet with neutral zinc-phosphite chains as supramolecular building blocks (SBBs), whereas 2 exhibits a 3D hybrid architecture with other neutral zincophosphite chains as supramolecular building blocks. The structural discrepancy between 1 and 2 is mainly due to the distinct linkage modes between organic TIPA ligands and inorganic zincophosphite chains. Interestingly, compounds 1 and 2 feature fast photochromism in response to UV light irradiation under ambient conditions. The discrepancy of photochromic performance between 1 and 2 is mainly due to the different geometrical configuration of the TIPA ligand. Different to majority of reported hybrid photochromic compounds driven by photochromic active units, the photochromism in 1 and 2 is derived from the electron transfer (ET) between phosphite and non-photochromic triimidazole-derivative ligand TIPA. Compared with the widely explored nonphotochromic polypyridine-derivative as electron acceptors (EAs), our work provides a new EA model for the design of hybrid photochromic materials based on the ligand-to-ligand ET mechanism. A multiple anti-counterfeiting application based on 1 and 2 was investigated. 相似文献
79.
Alexander Ryabchun Alexey Bobrovsky Alexey Medvedev Valery Shibaev 《Journal of polymer science. Part A, Polymer chemistry》2011,49(3):625-633
A series of novel crown ether‐containing photochromic comb‐shaped liquid crystalline polyacrylates with different macromolecular structure of side groups were synthesized and investigated. Phase behavior, optical and photo‐optical properties of thin spin‐coated films of these polymers were studied. A special attention was paid to a comparative study of the photo‐orientation phenomena occurring in the polymer films under a polarized light action. It was shown that complex formation with the potassium ions results in the decrease in degree of the photoinduced order that can be used for the creation of new materials for sensor devices. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献