نتایج جستجو برای: epoxidation of alkenes

تعداد نتایج: 21164396  

Journal: :Accounts of chemical research 2005
Kenneth S Suslick P Bhyrappa J-H Chou Margaret E Kosal Shirley Nakagaki Dennis W Smithenry Scott R Wilson

Metalloporphyrins are exceedingly useful building blocks for the design and synthesis of molecularly based solids. The use of hydrogen bonding or metal ion coordination provides a wide range of framework solids. Using various polyfunctionalized porphyrins, we have created porous solids that are thermally robust and that retain their internal porosity upon loss of solvates. Their pore dimensions...

Journal: :Journal of the American Chemical Society 2002
Revital Ben-Daniel Lev Weiner Ronny Neumann

A manganese(III)-substituted polyoxometalate of the "sandwich" structure, [MnIII2ZnW(ZnW9O34)2]10-, catalyzed the highly selective (>99.9%) epoxidation of alkenes, such as 1-octene, 2-octene, and cyclohexene with nitrous oxide. Reactions occurred in homogeneous media at 150 degrees C under 1 atm N2O. The epoxidation had a linear reaction profile; turnover frequencies of 0.5-1.4 h-1 were measure...

Journal: :Dalton transactions 2015
Ester Manrique Albert Poater Xavier Fontrodona Miquel Solà Montserrat Rodríguez Isabel Romero

We describe the synthesis of new manganese(ii) and manganese(iii) complexes containing the bidentate ligands 2-(3-pyrazolyl)pyridine, pypz-H, and 3(5)-(2-hydroxyphenyl)pyrazole, HOphpz-H, with formula [MnX2(pypz-H)2] (X = Cl(-), 1, CF3SO3(-), 2, OAc(-), 3 or NO3(-) (4)), [MnCl2(pypz-H)(H2O)2], 5, or [MnCl(Ophpz-H)2], 6. All the complexes have been characterized through analytical, spectroscopic...

Journal: :Archives of biochemistry and biophysics 1977
R T Ruettinger G R Griffith M J Coon

The w-hydroxylase of Pseudomonas oleovoruns, which catalyzes the hydroxylation of fatty acids and alkanes and the epoxidation of alkenes in the presence of a reduced pyridine nucleotide, a reductase, rubredoxin, and molecular oxygen, has been purified to electrophoretic homogeneity. Octane hydroxylation and octadiene epoxidation activities appear to remain at a constant ratio during the purific...

Journal: :Chemistry 2007
Lei Zhang Hendrikus C L Abbenhuis Gijsbert Gerritsen Nollaig Ní Bhriain Pieter C M M Magusin Brahim Mezari Wei Han Rutger A van Santen Qihua Yang Can Li

A novel interfacial hybrid epoxidation catalyst was designed with a new immobilization method for homogeneous catalysts by coating an inorganic support with an organic polymer film containing active sites. The titanium silsesquioxane (TiPOSS) complex, which contains a single-site titanium active center, was immobilized successfully by in-situ copolymerization on a mesoporous SBA-15-supported po...

Journal: :Molecules 2004
A L Baumstark P J Franklin P C Vasquez B S Crow

The mono-epoxidation of geraniol by dimethyldioxirane was carried out in various solvents. In all cases, the product ratios for the 2,3 and 6,7 mono-epoxides were in agreement with literature values. Kinetic studies were carried out at 23 degrees C in the following dried solvent systems: acetone (k(2) = 1.49 M(-1)s(-1)), carbon tetrachloride/acetone(9/1, k(2)=2.19 M(-1)s(-1)), and methanol/acet...

Journal: :Journal of bacteriology 1968
R Makula W R Finnerty

The utilization of 1-alkenes by Micrococcus cerificans was investigated with respect to characteristic fatty acid profiles resulting from growth at the expense of these substrates. Saturated fatty acids containing even numbers of carbon atoms were produced from 1-dodecene and 1-tetradecene. Unsaturated fatty acids related to the parent alkene were not detected. The fatty acid profile from 1-pen...

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