Browse by author
Lookup NU author(s): Dr Simon DohertyORCiD,
Dr Julian Knight,
Dr Rakesh Rath,
Emeritus Professor William McFarlane,
Dr Ross Harrington,
Emeritus Professor Bill CleggORCiD
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The palladium-catalyzed Buchwald-Hartwig aryl amination between 2,2′- diaminobiphenyl and 2 equiv of 2-(2′-bromophenyl)oxazoline has been used to prepare a new class of tetradentate bis(amino-oxazoline). The reaction between 2,2′- diaminobiphenyl and 1 equiv of 2-(2′-bromophenyl) oxazoline is highly selective for monoarylation, and the resulting products have been reacted in a second arylation to afford unsymmetrically substituted bis(amino-oxazolines). These new diamido/donors belong to the tropos class of ligand and exist as an equilibrium mixture of S,aS,S- and S,aR,S- diastereoisomers, which interconvert by rotation about the biaryl axis. Variable-temperature 1H NMR studies and line-shape analysis of simulated spectra gave ΔH‡ and ΔS ‡ values of 51.5-57 kJ mol-1 and -25.9 to -57.0 J mol-1 K-1, respectively, for diastereointerconversion. Interestingly, reaction of one of the symmetrical bis(amino-oxazoline) with [Cu(MeCN)4][PF6] results in dynamic resolution to afford diastereopure (S,aS,S)-[Cu(L)][PF6], which has a highly unusual sawhorse geometry at copper with the two oxazolines occupying trans coordination sites and two weak interactions to the nitrogen atoms of the secondary amino groups. 1H and 13C NMR spectra of this copper complex are entirely consistent with a single C2- symmetric diastereoisomer in solution that shows no sign of diastereointerconversion even after standing for one week. © 2006 American Chemical Society.
Author(s): Doherty S, Knight JG, Smyth CH, Sore NT, Rath RK, McFarlane W, Harrington RW, Clegg W
Publication type: Article
Publication status: Published
ISSN (print): 0276-7333
ISSN (electronic): 1520-6041
Publisher: American Chemical Society
Altmetrics provided by Altmetric