Kinetics of Cyclooctene Epoxidation with tert ‐Butyl Hydroperoxide in the Presence of [MoO 2 X 2 L]‐Type Catalysts (L = Bidentate Lewis Base)-Reference-Cited by-同舟云学术

Kinetics of Cyclooctene Epoxidation with tert ‐Butyl Hydroperoxide in the Presence of [MoO 2 X 2 L]‐Type Catalysts (L = Bidentate Lewis Base)

Published:2005-04-28 Issue:9 Volume:2005 Page:1716-1723
ISSN:1434-1948
Container-title:European Journal of Inorganic Chemistry
language:en
Short-container-title:Eur. J. Inorg. Chem.

Author:

Al‐Ajlouni Ahmad¹,Valente Anabela A.²,Nunes Carla D.²,Pillinger Martyn²,Santos Ana M.³⁴,Zhao Jin³,Romão Carlos C.⁴,Gonçalves Isabel S.²,Kühn Fritz E.³

Affiliation:

1. Department of Applied Chemical Science, Jordan University of Science and Technology, 22110 Irbid, Jordan

2. Department of Chemistry, CICECO, University of Aveiro, Campus de Santiago, 3810–193 Aveiro, Portugal Fax: +351‐234‐370‐084

3. Anorganisch‐chemisches Institut der Technischen Universität München, Lichtenbergstr. 4, 85747 Garching, Germany

4. Instituto de Tecnologia Química e Biológica da Universidade Nova de Lisboa, Quinta do Marquês, EAN, Apt. 127, 2781‐901 Oeiras, Portugal

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.200400852

Reference60 articles.

2. Chemistry of molybdenum. Part 7. Reactivity of terminal oxo-ligands in cis-[MoO2(acda)2](Hacda = 2-aminocyclopent-1-ene-1-carbodithioic acid) toward proton- and electron-donor reagents. Synthesis, redox chemistry and spectroscopic characterisation of neutral seven-co-ordinate catecholato and aryldiazenido compounds of molybdenum

3. Model compounds for the active sites of oxo-transfer molybdoenzymes. Synthesis, structural characterization, and electrochemical properties of [NH4]2[MoO2{O2CC(S)Ph2}2]

4. Formation of bis[bis(3,5-di-tert-butylcatecholato)oxomolybdenum(VI)] and related stable molybdenum-catechol complexes

5. Model for the active sites of oxo-transfer molybdoenzymes: reactivity, kinetics, and catalysis

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