全文获取类型
收费全文 | 71篇 |
免费 | 0篇 |
专业分类
化学 | 19篇 |
晶体学 | 1篇 |
数学 | 44篇 |
物理学 | 7篇 |
出版年
2019年 | 1篇 |
2013年 | 2篇 |
2012年 | 1篇 |
2011年 | 3篇 |
2010年 | 3篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2007年 | 1篇 |
2006年 | 3篇 |
2005年 | 2篇 |
2004年 | 1篇 |
1996年 | 1篇 |
1993年 | 3篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1988年 | 1篇 |
1986年 | 1篇 |
1977年 | 1篇 |
1958年 | 1篇 |
1957年 | 3篇 |
1956年 | 1篇 |
1948年 | 4篇 |
1947年 | 5篇 |
1946年 | 2篇 |
1945年 | 7篇 |
1943年 | 1篇 |
1942年 | 2篇 |
1941年 | 1篇 |
1940年 | 3篇 |
1939年 | 2篇 |
1938年 | 1篇 |
1937年 | 4篇 |
1936年 | 1篇 |
1935年 | 1篇 |
排序方式: 共有71条查询结果,搜索用时 15 毫秒
21.
The coordination chemistry of platinum(II) with a series of thiosemicarbazones {R(H)C2=N3‐N2(H)‐C1(=S)‐N1H2, R = 2‐hydroxyphenyl, H2stsc; pyrrole, H2ptsc; phenyl, Hbtsc} is described. Reactions of trans‐PtCl2(PPh3)2 precursor with H2stsc (or H2ptsc) in 1 : 1 molar ratio in the presence of Et3N base yielded complexes, [Pt(η3‐ O, N3, S‐stsc)(PPh3)] ( 1 ) and [Pt(η3‐ N4, N3, S‐ptsc)(PPh3)] ( 2 ), respectively. Further, trans‐PtCl2(PPh3)2 and Hbtsc in 1 : 2 (M : L) molar ratio yielded a different compound, [Pt(η2‐ N3, S‐btsc)(η1‐S‐btsc)(PPh3)] ( 3 ). Complex 1 involved deprotonation of hydrazinic (‐N2H‐) and hydroxyl (‐OH) groups, and stsc2? is coordinating via O, N3, S donor atoms, while complex 2 involved deprotonation of hydrazinic (‐N2H‐) and ‐N4H groups and ptsc2? is probably coordinating via N4, N3, S donor atoms. Reaction of PdCl2(PPh3)2 with Hbtsc‐Me {C6H5(CH3)C2=N3‐N2(H)‐C1(=S)‐N1H2} yielded a cyclometallated complex [Pd(η3‐C, N3, S‐btsc‐Me)(PPh3)] ( 4 ). These complexes have been characterized with the help of analytical data, spectroscopic techniques {IR, NMR (1H, 31P), U.V} and single crystal X‐ray crystallography ( 1 , 3 and 4 ). The effects of substituents at C2 carbon of thiosemicarbazones on their dentacy and cyclometallation are emphasized. 相似文献
22.
Abstract
Direct reductive amination of 1,3-diphenyl-1H-pyrazole-4-carbaldehyde and 3-(4-methylphenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde with various substituted aromatic amines using NaBH4 in the presence of I2 as reducing agent is described. The reaction has been carried out in anhydrous methanol under neutral conditions at room temperature. The structure of newly synthesized diphenyl pyrazolylmethylanilines was established on the basis of IR, 1H, 13C NMR, and mass spectral data. All diphenyl pyrazolylmethylaniline derivatives were tested in vitro for their antifungal and antibacterial activity against different strains of fungi and bacteria. Most of the compound exhibited considerable antifungal activity but poor antibacterial activity against the test strains. 相似文献23.
Prof. Dr. Tarlok S. Lobana Poonam Kumari Gagandeep Bawa Geeta Hundal Ray J. Butcher Francisco J. Fernandez Jerry P. Jasinski James A. Golen 《无机化学与普通化学杂志》2012,638(5):804-810
Complexes of pyrrole‐2‐carbaldehyde thiosemicarbazones, [(C4H4N4)(H)C2=N3–N2(H)–C1(=S)–N1HR; R = Ph, H2L1; Me, H2L2; H, H2L3] with nickel(II) and palladium(II) are described. The reaction of nickel(II) acetate with H2L1 in methanol in 1:1 molar ratio yielded a complex of composition, [Ni(κ2‐N3,S‐HL1)2] ( 1 ). Likewise reaction of NiCl2 with H2L2 in 1:1 molar ratio in acetonitrile in the presence of triethylamine base followed by the addition of pyridine did not yield the anticipated [Ni(κ3‐N4,N3,S‐L2)(py)] complex, moreover a bis‐square‐planar complex, [Ni(κ2‐N3,S‐HL2)2] ( 2 ) was formed. However, in the presence of bipyridine (bipy), it yielded the addition product, [Ni(κ2‐N3,S‐HL2)2(κ2‐N, N‐bipy)] ( 3 ). Reaction of PdCl2(κ2‐P, P–PPh2–CH2–PPh2) with H2L3 in toluene in the presence of triethylamine has yielded a complex of stoichiometry, [Pd(κ3‐N4,N3,S–L3)(κ1‐P–PPh2–CH2–P(O)Ph2] ( 4 ). The ligands (HL1)– and (HL2)– are chelating to NiII metal atom as anions binding through N3,S‐donor atoms with pendant pyrrole groups, and (L3)2– is chelating to the PdII metal atom as dianion through N4,N3,S‐donor atoms (pyrrole is N4‐bonded). Fourth site in 4 is bonded to one P‐donor atom of PPh2–CH2–P(O)Ph2, whose pendant –PPh2 group involves auto oxidation to –P(O)PPh2 during reaction. These complexes were characterized using analytical data, IR, NMR (1H, 31P) spectroscopy and X‐ray crystallography. Complexes 1 , 2 , and 4 have square‐planar arrangement, whereas complex 3 is octahedral. 相似文献
24.
25.
26.
27.
28.
29.
30.