Premium
Methyltrioxorhenium Catalysis in Nonconventional Solvents: A Great Catalyst in a Safe Reaction Medium
Author(s) -
Crucianelli Marcello,
Saladino Raffaele,
De Angelis Francesco
Publication year - 2010
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201000022
Subject(s) - catalysis , green chemistry , chemistry , reagent , selectivity , ionic liquid , hydrogen peroxide , stoichiometry , solvent , organic chemistry , combinatorial chemistry
The requirement that chemical processes are sustainabable, reflected in waste reduction and the use of safe reagents and reaction conditions, is becoming even more stringent as a result of pressure by society and governments to preserve the environment and protect human health. Catalysis offers numerous benefits related to green chemistry, including lowered energetic reaction requirements; catalytic, rather than stoichiometric, amounts of materials; increased selectivity; lowered consumption of processing and separation agents; and, in many cases, the use of less‐toxic compounds. Our research group has for a long time been studying methyltrioxorhenium in the oxyfunctionalization of different substrates, by using H 2 O 2 or its urea‐hydrogen peroxide complex as the primary oxidant. In this Review paper we aim to provide a full literature account on the catalytic activity and selectivity of methyltrioxorhenium in the oxyfunctionalization reaction, either in nonconventional solvents or under solvent‐free conditions, with a particular emphasis on the use of ionic liquids as green reaction media.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom