Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Markus Dugal"'
Autor:
Gopinathan Sankar, Sang-Ok Lee, Kenneth D. M. Harris, Markus Dugal, Simon J. Kitchin, John Meurig Thomas
Publikováno v:
The Journal of Physical Chemistry B. 106:1322-1326
Acetaldehyde is shown to undergo a reversible Bronsted acid-catalyzed cyclotrimerization reaction, with 100% selectivity, at ambient temperature within the zeolite host material ferrierite. It is shown by in situ solid-state 13C NMR spectroscopy and
Autor:
Markus Dugal, Sang-Ok Lee, John Meurig Thomas, Gopinathan Sankar, Simon J. Kitchin, Kenneth D. M. Harris
Publikováno v:
Catalysis Letters. 73:91-94
The solid-acid (Bronsted)-catalyzed cyclo-dimerization of 3-hydroxy-3-methylbutan-2-one (HMB) over a synthetic ferrierite molecular sieve is reported. HMB is a stable liquid at ambient temperatures but in acidic solutions it readily undergoes reactio
Publikováno v:
ResearcherID
A critical dependance upon molecular constraints is found for the aerial, free radical, shape-selective oxidation of cyclohexane (see picture). The oxidation occurs at the FeIII sites inside the framework of FeAlPO molecular-sieve catalysts. Oxidatio
Publikováno v:
Angewandte Chemie. 112:2399-2402
Autor:
Manfred T. Reetz, Markus Dugal
Publikováno v:
Catalysis Letters. 58:207-212
The fluoride-catalysed hydrolysis of mixtures of CH3Si(OCH3)3 and Mg(OC2H5)2 in the presence of preformed nanosized R4N+Br−-stabilised Pd colloids results in the formation of micro/mesoporous hydrophobic sol–gel materials in which the Pd clusters
Autor:
Markus Dugal
Publikováno v:
Kirk-Othmer Encyclopedia of Chemical Technology
Nitrobenzene is a pale yellow to yellowish brown liquid with a boiling point of 207–212°C, depending on its purity. It is a very toxic substance with a maximum allowable concentration (PEL) of 1 ppm. The commercial production of nitrobenzene invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5fcc46948243e674110b53303a40f28
https://doi.org/10.1002/0471238961.1409201801041109.a01.pub2
https://doi.org/10.1002/0471238961.1409201801041109.a01.pub2