Ward, Benjamin David  ORCID: https://orcid.org/0000-0003-1406-5940, Risler, H., Weitershaus, K., Bellemin-Laponnaz, S., Wadepohl, H. and Gade, L. H.
      2006.
      
      2-Aminopyrrolines: New chiral amidinate ligands with a rigid well-defined molecular structure and their coordination to Ti-IV.
      Inorganic Chemistry -American Chemical Society-
      45
      
        (19)
      
      , pp. 7777-7787.
      
      10.1021/ic060809y
    
  
  
       
       
     
         | 
      
Abstract
The use of an amino-oxazolinate (NNox = κ2-2,6-dimethylphenylamido-4(S)-isopropyloxazoline) as a chiral analogue to amidinate ligands in the chemistry of titanium was found to lead to undesired side reactions. The reaction of 2,6-dimethylphenylamido-4(S)-isopropyloxazoline with [Ti(NMe2)4] afforded the bis(amidinato) complex [Ti(NNox)2(NMe2)2] (2) which was thermally converted to the ring-opened decomposition products [Ti(NNox){κ3-N(2,6-C6H3Me2)C(NMe2)NC(iPr)CH2O}(NMe2)] (3) and [Ti{κ3-N(2,6-C6H3Me2)C(NMe2)-NC(iPr)CH2O}2] (4). The NMR spectra of 4 recorded at low temperature displayed two sets of resonances corresponding to two symmetric isomers in a 2:5 ratio, the probable geometries of which were established by ONIOM (QM/MM) simulations. To suppress ring opening of the oxazolines, their oxygen atom was formally replaced by a CH2 group in the synthesis of a series of amino-pyrroline protioligands 2-RN(H)(5-C4H5NR‘) (HNRNR‘). Their reaction with [Ti(NMe2)4] gave the thermally stable complexes [Ti(NRNR‘)2(NMe2)2], of which three derivatives were characterized by X-ray diffraction. They are stereochemically dynamic and undergo reversible ligand rearrangements in solution, for which the activation parameters were determined by variable-temperature 1H NMR spectroscopy.
| Item Type: | Article | 
|---|---|
| Date Type: | Publication | 
| Status: | Published | 
| Schools: | Schools > Chemistry | 
| Subjects: | Q Science > QD Chemistry | 
| Publisher: | American Chemical Society | 
| ISSN: | 0020-1669 | 
| Last Modified: | 18 Oct 2022 12:24 | 
| URI: | https://orca.cardiff.ac.uk/id/eprint/9722 | 
Citation Data
Cited 37 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
![]()  | 
              Edit Item | 

							



 Altmetric
 Altmetric