全文获取类型
收费全文 | 204篇 |
免费 | 10篇 |
国内免费 | 1篇 |
专业分类
化学 | 182篇 |
力学 | 2篇 |
数学 | 21篇 |
物理学 | 10篇 |
出版年
2023年 | 1篇 |
2022年 | 3篇 |
2021年 | 6篇 |
2020年 | 2篇 |
2019年 | 2篇 |
2018年 | 1篇 |
2016年 | 2篇 |
2015年 | 5篇 |
2014年 | 3篇 |
2013年 | 7篇 |
2012年 | 9篇 |
2011年 | 21篇 |
2010年 | 5篇 |
2009年 | 9篇 |
2008年 | 17篇 |
2007年 | 12篇 |
2006年 | 12篇 |
2005年 | 11篇 |
2004年 | 6篇 |
2003年 | 3篇 |
2002年 | 5篇 |
2001年 | 7篇 |
2000年 | 5篇 |
1999年 | 4篇 |
1998年 | 5篇 |
1997年 | 1篇 |
1996年 | 4篇 |
1995年 | 2篇 |
1993年 | 5篇 |
1992年 | 3篇 |
1991年 | 3篇 |
1990年 | 2篇 |
1989年 | 4篇 |
1988年 | 3篇 |
1987年 | 1篇 |
1986年 | 4篇 |
1985年 | 3篇 |
1984年 | 3篇 |
1982年 | 1篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1978年 | 5篇 |
1976年 | 2篇 |
1975年 | 1篇 |
1973年 | 1篇 |
1967年 | 2篇 |
排序方式: 共有215条查询结果,搜索用时 0 毫秒
41.
42.
Clegg W Dale SH Graham DV Harrington RW Hevia E Hogg LM Kennedy AR Mulvey RE 《Chemical communications (Cambridge, England)》2007,(16):1641-1643
The first sodium-magnesium and sodium-zinc ketimido complexes display contrasting inverse crown ring and pseudo-cubane structures respectively, while a sodium-zinc heterotrianionic alkide-alkoxide-amide adopts a third type of structure with a stepped ladder motif. 相似文献
43.
44.
Jonathan G. MacLellan Alan R. Kennedy Robert E. Mulvey 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(8):m302-m303
A `missing' member of the inverse crown ether family, namely μ4‐oxo‐tetrakis(μ‐2,2,6,6‐tetramethylpiperidinido)dimagnesium(II)disodium(I), [Na2Mg2O(C9H18N)4], has been synthesized by blocking the alternative aromatic metallation route via the use of sterically hindered 1,3,5‐mesitylene as a solvent. [Na2Mg2O(NR2)4] (NR2 is 2,2,6,6‐tetramethylpiperidinide) is shown to form a cationic planar eight‐membered ring with alternating metal and N atoms, which captures at its core an oxide guest that lies on an inversion centre [principal dimensions: Na—O = 2.2405 (11) Å, Na—N = 2.445 (3) and 2.572 (3) Å, Mg—O = 1.8673 (9) Å, and Mg—N = 2.032 (2) and 2.063 (2) Å]. 相似文献
45.
46.
Pablo Alborés Dr. Luca M. Carrella William Clegg Prof. Pablo García‐Álvarez Dr. Alan R. Kennedy Dr. Jan Klett Dr. Robert E. Mulvey Prof. Eva Rentschler Prof. Dr. Luca Russo Dr. 《Angewandte Chemie (International ed. in English)》2009,48(18):3193-3193
Chromation and ferration are the latest additions to the concept of alkali‐metal‐mediated metalation, as described by J. Klett, R. E. Mulvey, and co‐workers in their Communication on page 3317 ff. While the more electropositive sodium is essential for the reaction, it is the less electropositive chromium or iron that actually performs deprotonation of benzene. This novel reactivity can be likened to a game of chess in which the queen (Na) holds the king in check, while the knight (Cr, Fe) scores checkm(etal)ate.
47.
Clegg W Dale SH Drummond AM Hevia E Honeyman GW Mulvey RE 《Journal of the American Chemical Society》2006,128(23):7434-7435
The new concept of alkali-metal-mediated zincation (AMMZ), formally a zinc-hydrogen exchange reaction but one that requires the participation of an alkali metal, is applied here to the alkyl aryl ether anisole, an important molecule for studying directed ortho-metalation (DoM) chemistry. Treating one molar equivalent of anisole with the lithium dialkyl-TMP zincate reagent [THF.Li(mu-TMP)(mu-tBu)Zn(tBu)] (1) in hexane solution affords the mono-ortho-zincated complex [THF.Li(mu-TMP)(mu-o-C6H4OMe)Zn(tBu)] (2), which establishes that 1 functions as an alkyl base although previously it was regarded as an amido (TMP) base in other DoM applications. Treating two molar equivalents of anisole with 1, and increasing the reaction time, affords the bis-ortho-zincated complex [THF.Li(mu-TMP)(mu-o-C6H4OMe)Zn(o-C6H4OMe)] (3), which establishes that 1 can also function as a dual alkyl base. Omitting THF and rerunning the reaction with one or two molar equivalents of anisole affords [Ph(Me)O.Li(mu-TMP)(mu-o-C6H4OMe)Zn(tBu)] (4), which remarkably contains a combination of neutral and ortho-deprotonated anisole ligands. On isolating crystalline 4 from solution and adding THF, it converts to 2 and then to 3 on further stirring of the solution, as determined by NMR studies. This fact, along with other observations, would suggest that a complex-induced proximity effect does not need to be invoked to explain the observed zincation of anisole. The crystal structures of 2-4 are presented, as are their 1H, 13C, and 7Li NMR spectra recorded in C6D6 solution. 相似文献
48.
Alberto Hernn‐Gmez Emma Herd Eva Hevia Alan R. Kennedy Paul Knochel Konrad Koszinowski Sophia M. Manolikakes Robert E. Mulvey Christoph Schnegelsberg 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(10):2744-2748
The pivalates RZnOPiv⋅Mg(OPiv)X⋅n LiCl (OPiv=pivalate; R=aryl; X=Cl, Br, I) stand out amongst salt‐supported organometallic reagents, because apart from their effectiveness in Negishi cross‐coupling reactions, they show more resistance to attack by moist air than conventional organometallic compounds. Herein a combination of synthesis, coupling applications, X‐ray crystallographic studies, NMR (including DOSY) studies, and ESI mass spectrometric studies provide details of these pivalate reagents in their own right. A p‐tolyl case system shows that in [D8]THF solution these reagents exist as separated Me(p‐C6H4)ZnCl and Mg(OPiv)2 species. Air exposure tests and X‐ray crystallographic studies indicate that Mg(OPiv)2 enhances the air stability of aryl zinc species by sequestering H2O contaminants. Coupling reactions of Me(p‐C6H4)ZnX (where X=different salts) with 4‐bromoanisole highlight the importance of the presence of Mg(OPiv)2. Insight into the role of LiCl in these multicomponent mixtures is provided by the molecular structure of [(THF)2Li2(Cl)2(OPiv)2Zn]. 相似文献
49.
50.