4.5 Article

Schiff base complexes of methyltrioxorhenium (VII): Synthesis and catalytic application

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 739, Issue -, Pages 63-68

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2013.04.033

Keywords

Methyltrioxorhenium; Schiff-base; Epoxidation; UHP; Cyclooctene

Funding

  1. TUM Graduate School
  2. DFG [KU 1265/8-1]

Ask authors/readers for more resources

Schiff bases coordinate smoothly with methyltrioxorhenium (MTO) to yield the corresponding MTO-Schiff base adducts, which were characterized by IR, NMR and elemental analysis. The X-ray structure of one of the complexes was exemplary determined. The compounds were used as catalysts for cyclooctene epoxidation in ionic liquids with UHP (urea hydrogen peroxide adduct) as oxidant at room temperature. The results show that (N-salicylidene) aniline derived Schiff base complexes of MTO displayed higher catalytic activity and selectivity than di-nitrogen Schiff base complexes of MTO. No diol byproduct formation is observed. (C) 2013 Elsevier B. V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available