Schumacher, Maria and Goldfuss, Bernd ORCID: 0000-0002-1814-8818 (2015). Quantifying N-heterocyclic carbenes as umpolung catalysts in the benzoin reaction: balance between nucleophilicity and electrophilicity. New J. Chem., 39 (6). S. 4508 - 4519. CAMBRIDGE: ROYAL SOC CHEMISTRY. ISSN 1369-9261

Full text not available from this repository.

Abstract

Different types of N-heterocyclic carbenes, i.e. normal, reduced heteroatom stabilized, remote and abnormal carbenes, are computationally studied (THF-CPCM-B3LYP/6-311+G(d,p)//B3LYP/6-31G(d)) in the benzoin reaction to assess their characteristics as umpolung catalysts. Two general trends are apparent with an increasing number of nitrogen atoms in the heterocycles: (a) the tendency for the initial addition of the carbenes to the aldehyde decreases, due to decreased nucleophilicity; (b) during the umpolung step, the developing negative charge in the Breslow intermediates becomes better stabilized by conjugation with the adjacent, more electrophilic carbene carbon atoms. Relative to the starting reactants, the free energies for the intermediates and the transition structures decrease with more remote positions of the nitrogen atoms to the carbene carbon atoms. Among the normal N-heterocyclic carbenes oxazole-2-ylidene shows the lowest activation barrier for the rate determining umpolung step (E-a = 25.2 kcal mol(-1)) in the benzoin reaction. The comparison of all computed carbenes points to remote and abnormal pyridyl-3-ylidene as catalyst with the lowest activation energy (E-a = 24.0 kcal mol(-1)). This abnormal carbene exhibits the best balance between nucleophilic and electrophilic characteristics in the benzoin reaction.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Schumacher, MariaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Goldfuss, BerndUNSPECIFIEDorcid.org/0000-0002-1814-8818UNSPECIFIED
URN: urn:nbn:de:hbz:38-416456
DOI: 10.1039/c5nj00413f
Journal or Publication Title: New J. Chem.
Volume: 39
Number: 6
Page Range: S. 4508 - 4519
Date: 2015
Publisher: ROYAL SOC CHEMISTRY
Place of Publication: CAMBRIDGE
ISSN: 1369-9261
Language: English
Faculty: Faculty of Mathematics and Natural Sciences
Divisions: Faculty of Mathematics and Natural Sciences > Department of Chemistry > Institute of Organic Chemistry
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
REDUCED HETEROATOM STABILIZATION; DENSITY-FUNCTIONAL THEORY; ACTIVATED DOUBLE-BONDS; STABLE CARBENES; ELECTRONIC-PROPERTIES; CARBON-COMPOUNDS; AB-INITIO; ORGANOCATALYSTS; ALDEHYDES; CONDENSATIONMultiple languages
Chemistry, MultidisciplinaryMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/41645

Downloads

Downloads per month over past year

Altmetric

Export

Actions (login required)

View Item View Item