TY - JOUR
T1 - Cycloaddition of carbon dioxide and epoxides using pentaerythritol and halides as dual catalyst system
AU - Wilhelm, Michael E.
AU - Anthofer, Michael H.
AU - Cokoja, Mirza
AU - Markovits, Iulius I.E.
AU - Herrmann, Wolfgang A.
AU - Kühn, Fritz E.
PY - 2014/5
Y1 - 2014/5
N2 - The combination of pentaerythritol with nucleophilic halide salts such as nBu4NI is used as a dual catalyst system for the cycloaddition of carbon dioxide (CO2) with a broad range of organic epoxides yielding the respective cyclic carbonates. Due to synergistic effects of the organocatalysts, excellent yields and selectivities could be achieved under mild reaction conditions. Moreover, the nontoxic, cost-efficient, and readily available system is easily recyclable without significant loss of reactivity, representing an exceptional sustainable approach for the fixation of CO 2. Doubleteam: The combination of pentaerytrithol with tetrabutylammonium iodide leads to an efficient catalytic system for the cycloaddition of carbon dioxide (CO2) with various epoxides to cyclic carbonates. The nontoxic, metalfree, and cost-efficient dual catalysts, as well as the easy recyclability result in an exceptional sustainable organocatalytic approach for the fixation of carbon dioxide.
AB - The combination of pentaerythritol with nucleophilic halide salts such as nBu4NI is used as a dual catalyst system for the cycloaddition of carbon dioxide (CO2) with a broad range of organic epoxides yielding the respective cyclic carbonates. Due to synergistic effects of the organocatalysts, excellent yields and selectivities could be achieved under mild reaction conditions. Moreover, the nontoxic, cost-efficient, and readily available system is easily recyclable without significant loss of reactivity, representing an exceptional sustainable approach for the fixation of CO 2. Doubleteam: The combination of pentaerytrithol with tetrabutylammonium iodide leads to an efficient catalytic system for the cycloaddition of carbon dioxide (CO2) with various epoxides to cyclic carbonates. The nontoxic, metalfree, and cost-efficient dual catalysts, as well as the easy recyclability result in an exceptional sustainable organocatalytic approach for the fixation of carbon dioxide.
KW - carbon dioxide fixation
KW - cooperative effects
KW - cycloaddition
KW - green chemistry
KW - organocatalysis
UR - http://www.scopus.com/inward/record.url?scp=84901023049&partnerID=8YFLogxK
U2 - 10.1002/cssc.201301273
DO - 10.1002/cssc.201301273
M3 - Article
C2 - 24664547
AN - SCOPUS:84901023049
SN - 1864-5631
VL - 7
SP - 1357
EP - 1360
JO - ChemSusChem
JF - ChemSusChem
IS - 5
ER -