نتایج جستجو برای: ethylene epoxidation

تعداد نتایج: 30626  

2005
Didik Prasetyoko Zainab Ramli Hadi Nur

Titanosilicalite-1 (TS-1) in combination with sulfated zirconia efficiently catalyzes the epoxidation of 1-octene with aqueous hydrogen peroxide. The presence of both octahedral zirconium and sulfate species in the catalysts enhances the epoxidation rates.

Journal: :Dalton transactions 2014
Junkuo Gao Linlu Bai Qian Zhang Yongxin Li Ganguly Rakesh Jong-Min Lee Yanhui Yang Qichun Zhang

A new hexaprismane Co(II)6(μ3-OH)6 cluster-based three-dimensional coordination polymer ({Co(μ3-OH)(HCOO)0.72(CH3COO)0.28}n, Co6-CP) was successfully synthesized and characterized with single-crystal XRD, IR spectra, TGA spectra and elemental analysis. Co6-CP was used as an effective heterogeneous catalyst for the aerobic epoxidation of various alkenes. For the catalytic epoxidation of trans-st...

2014
Jiangnan Peng April L. Risinger Jing Li Susan L. Mooberry

The taccalonolides are microtubule stabilizers isolated from plants of the genus Tacca. Taccalonolide AF is 231 times more potent than the major metabolite taccalonolide A and differs only by the oxidation of the C-22,23 double bond in A to an epoxy group in AF. In the current study, 10 other rare natural taccalonolides were epoxidized and in each case epoxidation improved potency. The epoxidat...

   Mo-doped SnO2 nanoparticles were prepared using hydrothermal method. The average grain size obtained by varying calcinations temperature from 160 to 500 oC showed the different sizes. Prepared materials characterized by X-Ray diffraction (XRD) and scanning electron microscopy (SEM). Also the FTIR and the UV–Vis absorptive spectra have been carried out. Mo- doped SnO...

Journal: :Plant physiology 2002
Heiko Mewes Michael Richter

A treatment of the diatom Phaeodactylum tricornutum with high light (HL) in the visible range led to the conversion of diadinoxanthin (Dd) to diatoxanthin (Dt). In a following treatment with HL plus supplementary ultraviolet (UV)-B, the Dt was rapidly epoxidized to Dd. Photosynthesis of the cells was inhibited under HL + UV-B. This is accounted for by direct damage by UV-B and damage because of...

2013
Lilian R. Graser Sophie Jürgens Michael E. Wilhelm Mirza Cokoja Wolfgang A. Herrmann Fritz E. Kühn

Polyoxomolybdates were generated in situ by treating a carboxylic acid-functionalized ionic liquid with an aqueous solution of sodium molybdate. This reaction mixture was applied in the catalytic epoxidation of olefins using hydrogen peroxide as oxidant. The influence of acid and catalyst concentration as well as of the reaction temperature was investigated. The system showed a good performance...

2013
Chi-Ming Che Wing-Yiu Yu

Dioxoruthenium(VI) porphyrins including those containing chiral porphyrinato ligands can be readily prepared by oxidation of [RuII(Por)(CO)(MeOH)] with PhIO or metachloroperoxybenzoic acid. Similar reactions with PhINTs gave [Ru(Por)(NTs)2] isolated as air stable solids at room temperature. The [Ru(Por)O2] complexes are competent oxidants for epoxidation of alkenes with high selectivities. Enan...

Journal: :The Biochemical journal 1986
H Iwahashi Y Negoro A Ikeda H Morishita R Kido

Chlorogenic acid (3-O-caffeoylquinic acid) inhibited haematin- and haemoglobin-catalysed retinoic acid 5,6-epoxidation. Some other phenol compounds (caffeic acid and 4-hydroxy-3-methoxybenzoic acid) also showed inhibitory effects on the haematin- and haemoglobin-catalysed epoxidation, but salicylic acid did not. Of the above compounds, caffeic acid and chlorogenic acid were potent inhibitors co...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 1999
daryoush mohajer mojtaba bagherzadeh

the epoxidation of olefins with tetra n-butylammonium periodate, n-bu4/nio4, is catalyzed by six different tetrakis (4-substituted phenyl) porphyrinatomanganese(iii) acetate, mn(t4-xpp)oac, complexes in the presence of imidazole as an axial ligand with low to high yields and complete selectivity at room temperature. while the electronic effects of the highly electron-withdrawing no2 substituent...

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