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Spatial Recognition Within Terpenes: Redox and H-bond Promoted Linkage Isomerizations and the Selective Binding of Complex Alkenes.

Authors :
Dakermanji SJ
Westendorff KS
Pert EK
Wilson KB
Myers JT
Wilde JH
Dickie DA
Welch KD
Harman WD
Source :
Organometallics [Organometallics] 2020 May 26; Vol. 39 (10), pp. 1961-1975. Date of Electronic Publication: 2020 Apr 27.
Publication Year :
2020

Abstract

A method for the resolution of η <superscript>2</superscript> -alkene-complex isomers of the type MoTp(NO)(DMAP)( η <superscript>2</superscript> -alkene) and WTp(NO)(PMe <subscript>3</subscript> )( η <superscript>2</superscript> -alkene) (where Tp = hydridotris(pyrazolyl)-borate and DMAP = 4-(dimethylamino)pyridine) has been explored. Alkene and polyene compounds form as a mixture of kinetically trapped isomers. For both types of complexes, it was found that addition of either a fluorinated alcohol or one-electron oxidant reduces the number of isomers in solution. Accelerated ligand exchange was also observed, although these reactions were accompanied by significant decomposition.<br />Competing Interests: Notes The authors declare no competing financial interest.

Details

Language :
English
ISSN :
0276-7333
Volume :
39
Issue :
10
Database :
MEDLINE
Journal :
Organometallics
Publication Type :
Academic Journal
Accession number :
33456102
Full Text :
https://doi.org/10.1021/acs.organomet.0c00151