Synthesis, Immobilization and Catalytic Activity of a Copper(II) Complex with a Chiral Bis(oxazoline)

Molecules

Liliana Carneiro²  Ana R. Silva²  Peter S. Shuttleworth¹  Vitaly Budarin³ 

[1] Departamento de Física de Polímeros, Elastámeros y Applicaciones Energéticas, Instituto de Ciencia e Tecnología de Polímeros, CSIC, Madrid 28006, Spain;Department of Chemistry, CICECO, University of Aveiro, Aveiro 3810-193, Portugal;Green Chemistry Centre of Excellence, Department of Chemistry, University of York, York YO10 5DD, UK

关键词: copper(II);    bis(oxazoline);    homogeneous catalysis;    heterogeneous catalysis;    asymmetric catalysis;   

DOI  :  10.3390/molecules190811988

来源: mdpi

【 摘 要 】

A chiral bis(oxazoline) bearing CH₂OH groups was synthesized from a commercial bis(oxazoline) and characterized by ¹H- and ¹³C-NMR, high resolution ESI-mass spectrometry and FTIR. The corresponding copper(II) complex was immobilized onto the surface of a mesoporous carbonaceous material (Starbon^® 700) in which the double bonds had been activated via conventional bromination. The materials were characterized by elemental analysis, ICP-OES, XPS, thermogravimetry and nitrogen adsorption at 77 K. The new copper(II) bis(oxazoline) was tested both in the homogeneous phase and once immobilized onto a carbonaceous support for the kinetic resolution of hydrobenzoin. Both were active, enantioselective and selective in the mono-benzoylation of hydrobenzoin, but better enantioselectivities were obtained in the homogeneous phase. The heterogeneous catalyst could be separated from the reaction media at the end of the reaction and reused in another catalytic cycle, but with loss of product yield and enantioselectivity.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.