Publication Type Journal Article
Title Synthesis of inexpensive chiral half-sandwich nickel N-heterocyclic carbene complexes: X-ray diffraction study of the D-menthyl-functionalized complex [Ni(iPr(2)Ph-NHC-CH(2)OMent)ClCp]
Authors Mansuy Rocquin Vincent Ritleng Sonia Barroso Ana M. Martins Michael J. Chetcuti
Groups IOARC
Journal JOURNAL OF ORGANOMETALLIC CHEMISTRY
Year 2016
Month April
Volume 808
Number
Pages 57-62
Abstract The imidazolium salts, 1-(2,4,6-trimethylphenyl)-3-[(1R,2S,5R)-(-)-menthoxymethyl] imidazolium chloride (Mes-NHC-CH(2)OMent center dot HCl) (1a) and 1-(2,6-diisopropylphenyl)-3-[(1R, 2S, 5R)-(-)-menthoxymethyl] imidazolium chloride (iPr(2)Ph-NHC-CH(2)OMent center dot HCl) (1b), are readily accessible from inexpensive (1R,2S,5R)-(-)-menthol. They react with nickelocene to give two new chiral nickel-N-heterocyclic carbene (NHC) complexes, [Ni(Mes-NHC-CH(2)OMent)ClCp] (2a) and [Ni(iPr(2)Ph-NHC-CH(2)OMent)ClCp] (2b), in good yields. The new complexes were fully characterized by standard spectroscopic techniques and by a single crystal X-ray diffraction study on complex 2b. Complex 2b crystallizes in the chiral spacegroup P1, with two independent molecules in the unit cell, which are slightly different from each other. Preliminary studies show that these complexes are effective catalysts for the hydrosilylation of ketones. However no chiral induction was observed. (C) 2016 Elsevier B.V. All rights reserved.
DOI http://dx.doi.org/10.1016/j.jorganchem.2016.02.018
ISBN
Publisher ELSEVIER SCIENCE SA
Book Title
ISSN 0022-328X
EISSN 1872-8561
Conference Name
Bibtex ID ISI:000372056500007
Observations
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