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排序方式: 共有100条查询结果,搜索用时 15 毫秒
1.
Anju Goyal Aditya Sharma Jasanpreet Kaur Sapna Kumari Madhukar Garg Rakesh K. Sindhu Md. Habibur Rahman Muhammad Furqan Akhtar Priti Tagde Agnieszka Najda Barbara Banach-Albiska Katarzyna Masternak Ibtesam S. Alanazi Hanan R. H. Mohamed Attalla F. El-kott Muddaser Shah Mousa O. Germoush Hamdan S. Al-malky Salman H. Abukhuwayjah Ahmed E. Altyar Simona G. Bungau Mohamed M. Abdel-Daim 《Molecules (Basel, Switzerland)》2022,27(3)
2.
The adiabatic Shinnar–Le Roux (SLR) algorithm for radiofrequency (RF) pulse design enables systematic control of pulse parameters such as bandwidth, RF energy distribution and duration. Some applications, such as diffusion-weighted imaging (DWI) at high magnetic fields, would benefit from RF pulses that can provide greater B1 insensitivity while adhering to echo time and specific absorption rate (SAR) limits. In this study, the adiabatic SLR algorithm was employed to generate 6-ms and 4-ms 180° semi-adiabatic RF pulses which were used to replace the refocusing pulses in a twice-refocused spin echo (TRSE) diffusion-weighted echo planar imaging (DW-EPI) sequence to create two versions of a twice-refocused adiabatic spin echo (TRASE) sequence. The two versions were designed for different trade-offs between adiabaticity and echo time. Since a pair of identical refocusing pulses is applied, the quadratic phase imposed by the first is unwound by the second, preserving the linear phase created by the excitation pulse. In vivo images of the human brain obtained at 7 Testa (7 T) demonstrate that both versions of the TRASE sequence developed in this study achieve more homogeneous signal in the diffusion-weighted images than the conventional TRSE sequence. Semi-adiabatic SLR pulses offer a more B1-insensitive solution for diffusion preparation at 7 T, while operating within SAR constraints. This method may be coupled with any EPI readout trajectory and parallel imaging scheme to provide more uniform coverage for diffusion tensor imaging at 7 T and 3 T. 相似文献
3.
Doiphode Vidya Vairale Priti Sharma Vidhika Waghmare Ashish Punde Ashvini Shinde Pratibha Shah Shruti Pandharkar Subhash Hase Yogesh Aher Rahul Nair Shruthi Jadkar Vijaya Bade Bharat Prasad Mohit Rondiya Sachin Jadkar Sandesh 《Journal of Solid State Electrochemistry》2021,25(6):1835-1846
Journal of Solid State Electrochemistry - Herein, we report the synthesis of ZnO nanorod films onto FTO (fluorine-doped tin oxide) substrates using the solution-processed electrodeposition method.... 相似文献
4.
Oximes of ketones and aldehydes are efficiently deprotected with glyoxylic acid in an aqueous medium at room temperature. Oximes can be cleaved selectively in the presence of a TBDMS group. This method is high yielding, fast, clean, safe, cost effective, and therefore very suitable for practical organic synthesis. 相似文献
5.
Vijaya Kabra Suneeta Ojha Priti Kaushik Arpana Meel 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2337-2344
Eight novel amidothiophosphates have been successfully achieved using cycloiminium salts of pyridine as the starting material. Phosphorylation was done using phosphorus trichloride, and the resulting functionalized iminohalophosphines in situ were further oxidized and substituted through sulfur and a suitable secondary amine (alkyl, alicyclic, and aryl). The reactions were carried out in a dry nitrogen atmosphere. The synthesized products were characterized using different spectroscopic techniques (1H and 31P NMR). The pyridine nucleus incorporating a phosphoryl group is highly bioactive. Hence, the synthesized organothiophosphates should be potential pesticidal molecules. 相似文献
6.
Priti Kumar Roy Sumit Nandi Mithun Kumar Ghosh 《Journal of mathematical chemistry》2013,51(10):2704-2717
Double substrate enzyme kinetics has a leading role for product quantification and optimization in different chemical and biochemical sectors. Mathematical approach for controlling these reactions in different stages by suitable parameters adds a new dimension in this interdisciplinary field of research. Applying control theoretic approach in the reversible backward stages of double substrate enzymatic model, time economization with regard to product formation is significant. In this article, we formulate a double substrate mathematical model of enzymatic dynamical reaction system with control measures with a view to observe the effect of changes of these measures with respect to the concentration of substrates, enzyme, complexes and finally product. Here, Pontryagin Minimum Principle is used for observing the effect of control measures in the system dynamics with the help of Hamiltonian. We compare the relevant numerical solutions for the substrates, enzyme, complexes and product concentration profile for a specified time interval with respect to control factors. 相似文献
7.
V G Adlakha 《The Journal of the Operational Research Society》1999,50(2):177-182
We present an alternate linear algorithm for finding the minimum flow in (s, t)-planar networks using a new concept of minimal removable sets developed here. The iterative nature of the algorithm facilitates the adjustment of solutions for systems in developmental stages. The minimum flow algorithm presented here requires O(|V|) time, where V denotes the set of vertices. The minimum flow problem arises in many transportation and communication systems. 相似文献
8.
Baijayantimala Swain Abrar Khan Priti Singh Vaibhav S. Marde Andrea Angeli Krishna Kartheek Chinchilli Venkata Madhavi Yaddanapudi Simone Carradori Claudiu T. Supuran Mohammed Arifuddin 《Molecules (Basel, Switzerland)》2022,27(22)
A novel series of twenty-five rhodamine-linked benzenesulfonamide derivatives (7a–u and 9a–d) were synthesized and screened for their inhibitory action against four physiologically relevant human (h) carbonic anhydrase (CA) isoforms, namely hCA I, hCA II, hCA IX, and hCA XII. All the synthesized molecules showed good to excellent inhibition against all the tested isoforms in the nanomolar range due to the presence of the sulfonamide as a zinc binding group. The target compounds were developed from indol-3-ylchalcone-linked benzenesulfonamide where the indol-3-ylchalcone moiety was replaced with rhodanine-linked aldehydes or isatins to improve the inhibition. Interestingly, the molecules were slightly more selective towards hCA IX and XII compared to hCA I and II. The most potent and efficient ones against hCA I were 7h (KI 22.4 nM) and 9d (KI 35.8 nM) compared to the standard drug AAZ (KI 250.0 nM), whereas in case of hCA II inhibition, the derivatives containing the isatin nucleus as a tail were preferred. Collectively, all compounds were endowed with better inhibition against hCA IX compared to AAZ (KI 25.8 nM) as well as strong potency against hCA XII. Finally, these newly synthesized molecules could be taken as potential leads for the development of isoform selective hCA IX and XII inhibitors. 相似文献
9.
Several amino acid ester hydrochlorides were reacted with ammonium formate to give N-formyl amino acid esters in good yields. 相似文献
10.
A short and efficient enantioselective synthesis of sulfobacin A has been achieved using the Sharpless asymmetric dihydroxylation and the regiospecific nucleophilic opening of a cyclic sulfate as the key steps. 相似文献