全文获取类型
收费全文 | 96篇 |
免费 | 3篇 |
专业分类
化学 | 38篇 |
晶体学 | 1篇 |
数学 | 5篇 |
物理学 | 55篇 |
出版年
2023年 | 1篇 |
2021年 | 2篇 |
2020年 | 3篇 |
2019年 | 1篇 |
2016年 | 4篇 |
2015年 | 1篇 |
2014年 | 2篇 |
2013年 | 5篇 |
2012年 | 2篇 |
2011年 | 8篇 |
2010年 | 1篇 |
2009年 | 2篇 |
2008年 | 4篇 |
2007年 | 3篇 |
2006年 | 1篇 |
2005年 | 2篇 |
2004年 | 2篇 |
2003年 | 1篇 |
2002年 | 3篇 |
2001年 | 3篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1996年 | 3篇 |
1995年 | 1篇 |
1993年 | 4篇 |
1992年 | 4篇 |
1991年 | 3篇 |
1990年 | 5篇 |
1989年 | 6篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1983年 | 1篇 |
1982年 | 4篇 |
1980年 | 2篇 |
1979年 | 2篇 |
1976年 | 1篇 |
1975年 | 2篇 |
1973年 | 1篇 |
排序方式: 共有99条查询结果,搜索用时 15 毫秒
1.
2.
3.
4.
5.
The thiols Cp2M(SH)2, where M = Ti and Zr, react to form the complexes Cp2MS5 when treated with mono- and di-sulfur transfer reagents. Treatment of Cp2MCl2 with Li2S2 and sulfur gave Cp2MS5, M = Ti, Zr and Hf, in better yield. The new Zr and Hf complexes have a six-membered MS5 ring in a chair conformation similar to the previously observed for M = Ti. Variable temperature NMR studies show that the barriers to MS5 ring inversion decrease in the order Ti > Hf > Zr. 相似文献
6.
7.
8.
Abstract A series of condensation polymer intermediates, which included several new compositions, was prepared from 5-t-butyl-m-xylene (I) so that the effect of the bulky t-butyl group on polymer properties could be determined. Compound (I) was oxidized with nitric acid to obtain 5-t-butyl-isophthalic acid (II), which was converted successively to the diacid chloride, the diamide, the dinitrile, and finally to 5-t-butyl-m-xylene-α,α′-diamine (VI); the overall yield was 80%. The dimethyl ester of (II) was prepared and converted to 5-t-butyl-m-xylene-α,α′-diol (VIII), a new composition, in 79.5% overall yield; the diphenyl ester was also prepared. The sodium salt of (II) was catalytically reduced to obtain 5-t-butyl-1,3-cyclohexanedicarboxylic acid (IIa) in 95% yield. (IIa) was converted successively to the diacid chloride, the diamide, the dinitrile, and finally to 5-t-butyl-1,3-cyclohexanebis(methylamine) (VIa), a new composition; the overall yield was 37%. (IIa) was also converted to the dimethyl ester and finally to 5-t-butyl-1,3-cyclohexanedimethanol (VIIIa), a new composition; the overall yield was 64%. Condensation polymers were prepared from the intermediates (II), (IIa), (VI), (VIa), (VIII), and (VIIIa). These polymers had higher glass transition temperatures (Tg) than corresponding polymers containing no t-butyl groups. This general effect of the t-butyl group to increase the Tg value of the polymer was noted in all polymers prepared, regardless of whether the intermediate carrying the t-butyl group was a diacid, a diol, or a diamine, or whether the polymer was a polyamide, a polyester, or a polyurethane. 相似文献
9.
Kyle M. McCall Bogdan M. Benin Michael Wörle Thomas Vonderach Detlef Günther Maksym V. Kovalenko 《Helvetica chimica acta》2021,104(1):e2000206
Inorganic, lead-free metal halides are widely sought after following the rise of the halide perovskites as outstanding optoelectronic materials, due to their enhanced stability and reduced toxicity. Herein, we report on the solvothermal synthesis of Rb7Sb3Br16, which exhibits a 0D structure comprised of [SbBr6]3− octahedra and edge-sharing bioctahedra [Sb2Br10]4− dimers that order into layers along the c-axis. This all-inorganic material is air-stable and exhibits weak orange photoluminescence (PL) at room temperature. Low-temperature PL and PL excitation (PLE) measurements reveal the presence of two distinct emission bands that originate from these structural units, with the high-energy emission quenching as temperature rises beyond 150 K. We are also able to obtain Rb7Bi3Br16 and Rb7Bi3I16 which both crystallize in orthorhombic symmetry, with Rb7Bi3Br16 presenting weak low-temperature luminescence while Rb7Bi3I16 is non-luminescent. This work expands the library of emissive inorganic metal halides and provides further evidence for the efficacy of low-dimensional Sb−X luminescent centers based on octahedral and edge-sharing [Sb2X10]4− dimers. 相似文献
10.
Marcel Aebli Bogdan M. Benin Kyle M. McCall Viktoriia Morad Debora Thöny Hansjörg Grützmacher Maksym V. Kovalenko 《Helvetica chimica acta》2020,103(7):e2000080
Inorganic lead halide perovskites have gained immense scientific interest for optoelectronic applications. In this work, we present a one-dimensional polymorph of cesium lead bromide (δ-CsPbBr3) synthesized through a simple anion-exchange reaction, wherein distorted edge-sharing PbBr6 octahedra form 1D chains isolated by Cs ions. δ-CsPbBr3 was characterized by Raman spectroscopy, X-ray diffraction, 207Pb and 133Cs solid-state NMR, and by optical emission and absorption spectroscopies. This non-perovskite material irreversibly transforms into the well-known three-dimensional perovskite phase (γ-CsPbBr3) upon heating to above 151 °C. The indirect bandgap was determined by absorption measurements and calculation to be 2.9 eV. δ-CsPbBr3 exhibits broadband yellow photoluminescence with a quantum yield of 3.2 %±0.2 % at room temperature and 95 %±5 % at 77 K, and this emission is attributed to the recombination of self-trapped excitons. This study emphasizes that the metastable δ-CsPbBr3 may be a persistent, concomitant phase in Cs−Pb-Br-containing materials systems, such as those used in solar cells and LEDs, and it showcases the characterization tools used for its detection. 相似文献