全文获取类型
收费全文 | 351篇 |
免费 | 6篇 |
专业分类
化学 | 269篇 |
晶体学 | 5篇 |
数学 | 2篇 |
物理学 | 81篇 |
出版年
2020年 | 5篇 |
2019年 | 4篇 |
2018年 | 1篇 |
2017年 | 1篇 |
2016年 | 3篇 |
2015年 | 3篇 |
2014年 | 3篇 |
2013年 | 12篇 |
2012年 | 8篇 |
2011年 | 13篇 |
2010年 | 5篇 |
2009年 | 3篇 |
2008年 | 18篇 |
2007年 | 25篇 |
2006年 | 30篇 |
2005年 | 32篇 |
2004年 | 25篇 |
2003年 | 21篇 |
2002年 | 12篇 |
2001年 | 6篇 |
2000年 | 5篇 |
1999年 | 2篇 |
1998年 | 3篇 |
1997年 | 2篇 |
1996年 | 5篇 |
1995年 | 5篇 |
1994年 | 10篇 |
1993年 | 7篇 |
1992年 | 4篇 |
1991年 | 6篇 |
1990年 | 7篇 |
1989年 | 5篇 |
1988年 | 11篇 |
1987年 | 8篇 |
1986年 | 8篇 |
1985年 | 2篇 |
1984年 | 10篇 |
1983年 | 3篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1979年 | 2篇 |
1978年 | 4篇 |
1976年 | 1篇 |
1975年 | 2篇 |
1974年 | 3篇 |
1973年 | 4篇 |
1972年 | 1篇 |
1971年 | 1篇 |
1968年 | 1篇 |
1907年 | 3篇 |
排序方式: 共有357条查询结果,搜索用时 15 毫秒
1.
2.
3.
4.
Martin Christlieb Hannah J. Claughton Andrew R. Cowley Julia M. Heslop Jonathan R. Dilworth 《Transition Metal Chemistry》2006,31(1):88-92
During the condensation of 4-methyl-4-phenyl-3-thiosemicarbazide (3) with 2,3-butanedione an unexpected by-product, 8a-methyl-6,8a-dihydro-8-methyl-2-[N-methyl-N-phenylamino]-5H-1,3,4-thiadiazolo[3,2-d][1,2,4]triazine-5-thione, (5) was obtained in addition to the desired bis(thiosemicarbazone) (4). An X-ray crystal structure was obtained and is presented together with a proposed mechanism for its formation. A brief investigation
of the coordination chemistry of bicycle (5) was carried out. The formation of cyclic compounds during the synthesis of analogues with extended backbones is also described. 相似文献
5.
6.
7.
Frampton MJ Akdas H Cowley AR Rogers JE Slagle JE Fleitz PA Drobizhev M Rebane A Anderson HL 《Organic letters》2005,7(24):5365-5368
[structure: see text] A vinylene-linked porphyrin dimer, with no substituents at the beta-positions, has been synthesized by CuI/CsF promoted Stille coupling. In the crystal structure of this dimer, the C(2)H(2) bridge is twisted by 45 degrees relative to the plane of the porphyrins. The absorption, emission spectra, and electrochemistry reveal substantial porphyrin-porphyrin pi-conjugation. The triplet excited-state absorption spectrum of this dimer makes it suitable for reverse saturable absorption at 710-900 nm. 相似文献
8.
Cowley AH 《Chemical communications (Cambridge, England)》2004,(21):2369-2375
Donor-acceptor bonding between group 13 elements seems counter-intuitive because one normally thinks of e.g. boron and aluminium compounds as classical Lewis acids. Indeed, many such compounds have achieved industrial prominence in this regard. Recently, however, it has become possible to stabilize these and other group 13 elements in the +1 oxidation state as opposed to the archetypical +3 oxidation state. Moreover, it turns out that in the +1 oxidation state these species are excellent donors--hence the formation of these unprecedented donor-acceptor bonds. The discovery of such bonds has led, albeit indirectly, to the development of triple-decker main group cations. This aspect is also covered in the review. 相似文献
9.
[reaction: see text] The partial reduction of electron-deficient 2,5-disubstituted pyrroles has been developed into a flexible procedure that gives control of relative stereochemistry by variation of the reduction conditions. After the reaction, the pyrroline products were dihydroxylated at C-3,4 to give either the cis or trans isomers; this flexibility means that a variety of polyhydroxylated pyrrolidines can be prepared in a short sequence. Finally, this method was applied to a synthesis of the naturally occurring glycosidase inhibitor DMDP. 相似文献
10.