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1.
S Ponnusamy 《Proceedings Mathematical Sciences》1994,104(2):397-411
Denote byS
* (⌕), (0≤⌕<1), the family consisting of functionsf(z)=z+a
2z2+...+anzn+... that are analytic and starlike of order ⌕, in the unit disc ⋎z⋎<1. In the present article among other things, with very
simple conditions on μ, ⌕ andh(z) we prove the f’(z) (f(z)/z)μ−1<h(z) implies f∈S*(⌕). Our results in this direction then admit new applications in the study of univalent functions. In many cases these results
considerably extend the earlier works of Miller and Mocanu [6] and others. 相似文献
2.
[reaction: see text] A novel and powerful reagent system R(3)Al-R'(3)SiOTf for the one-pot alkylation-silylation reaction of epoxides was discovered, and the reactions of various epoxides with the new reagent system have been demonstrated to occur stereospecifically giving rise to the corresponding alkylation-silylation products in excellent yields. 相似文献
3.
4.
N. Rajeswari R. Nagarathinam S. Viswanathan H. Kothandaraman E. Ponnusamy 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(12):1585-1610
New polymaleamides were synthesized by ring-opening polyaddition of N,N'-biphenylbismaleimide (BPBMI) to the aliphatic diamines 1,4-diaminobutane, 1,6-diaminohexane, 1,8-diaminooctane, piperazine, and 2,5-dimethylpiperazine in m-cresol. The appropriate model compound was also prepared. These polymers are completely soluble in concentrated sulfuric acid as well as in m-cresol and are found to be insoluble in common organic solvents. The identities of BPBMI, the model compound, and the polymaleamides were confirmed by elemental analysis and IR spectroscopy. These polymaleamides were found to have inherent viscosities in the range 0.10–0.14 dL/g. Their IR spectra reveal the retention of cis-geometry about the C=C bonds in BPBMI and in the polymaleamides. The thermal degradation behavior of the polymaleamides was studied by thermogravimetric analysis, differential scanning calorimetry, and mass spectrometry. Fragmentation schemes for the polymaleamides are proposed. 相似文献
5.
The O-glycosidation reaction of 1-O-acetyl-2,3-dideoxy-DL-pent-2-enopyran - 4 -ulose catalysed by the environmentally accepted and inexpensive industrial catalyst Montmorillonite K-10 clay with variety of alcohols in high yield is reported. 相似文献
6.
Arunkumar Ammasi Shanavas Shajahan Acevedo Roberto Anbarasan Ponnusamy Munusamy 《Structural chemistry》2020,31(3):1029-1042
Structural Chemistry - A new series of triphenylamine (TPA)-based organic dyes (A1-A4) are characterized and implemented as photosensitizers for dye-sensitized solar cells (DSSCs). In the... 相似文献
7.
In this paper we characterize John domains in terms of John domain decomposition property. In addition, we also show that
a domain D in ℔
n
is a John domain if and only if D\P is a John domain, where P is a subset of D containing finitely many points of D. The best possibility and an application of the second result are also discussed. 相似文献
8.
Ponnusamy Sami Kandasamy Venkateshwari Natarajan Mariselvi Arunachalam Sarathi Kasi Rajasekaran 《Transition Metal Chemistry》2010,35(2):137-142
l-cysteine undergoes facile electron transfer with heteropoly 10-tungstodivanadophosphate,
[ \textPV\textV \textV\textV \textW 1 0 \textO 4 0 ]5 - , \left[ {{\text{PV}}^{\text{V}} {\text{V}}^{\text{V}} {\text{W}}_{ 1 0} {\text{O}}_{ 4 0} } \right]^{5 - } , at ambient temperature in aqueous acid medium. The stoichiometric ratio of [cysteine]/[oxidant] is 2.0. The products of the
reaction are cystine and two electron-reduced heteropoly blue, [PVIVVIVW10O40]7−. The rates of the electron transfer reaction were measured spectrophotometrically in acetate–acetic acid buffers at 25 °C.
The orders of the reaction with respect to both [cysteine] and [oxidant] are unity, and the reaction exhibits simple second-order
kinetics at constant pH. The pH-rate profile indicates the participation of deprotonated cysteine in the reaction. The reaction
proceeds through an outer-sphere mechanism. For the dianion −SCH2CH(NH3
+)COO−, the rate constant for the cross electron transfer reaction is 96 M−1s−1 at 25 °C. The self-exchange rate constant for the
- \textSCH2 \textCH( \textNH3 + )\textCOO - \mathord