English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/19708
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:


Preparation of half-sandwich alkyl−titanium(IV) complexes stabilized by a cyclopentadienyl ligand with a pendant phosphine tether and their use in the catalytic hydroamination of aliphatic and aromatic alkynes

AuthorsBuil, María L. ; Esteruelas, Miguel A. ; López, Ana M. ; Mateo, A. Concepción
Issue DateJul-2006
PublisherAmerican Chemical Society
CitationOrganometallics 25(17): 4079-4089 (2006)
AbstractComplex CpPTiCl3 (1; CpP = C5H4CH2CH2PPh2) reacts with 3.0, 2.0, and 1.0 equiv of MeMgCl to give CpPTiMe3 (2), CpPTiMe2Cl (3), and CpPTiMeCl2 (4). In solution the P-donor substituent of the cyclopentadienyl ligand is involved in a coordination−dissociation equilibrium (ΔH° = 7.7 ± 0.1 kcal·mol-1 and ΔS° = 36.9 ± 0.4 cal·mol-1·K-1 for 2, ΔH° = 6.0 ± 0.2 kcal·mol-1 and ΔS° = 22.3 ± 0.6 cal·mol-1·K-1 for 3, and ΔH° = 6.1 ± 0.2 kcal·mol-1 and ΔS° = 24.4 ± 1 cal·mol-1·K-1 for 4). The reaction of 1 with 3.0 equiv of PhCH2MgCl affords CpPTi(CH2Ph)3 (5), containing a free phosphine pendant group between −90 and 20 °C. In contrast to 5, the PPh2 group of {(2,6-iPr2C6H3)NH}CpPTi{N(2,6-iPr2C6H3)} (7), which is formed from the reaction of 2 with 2,6-diisopropylaniline, remains coordinated to the titanium atom between 60 and −60 °C. Complex 2 is an efficient catalyst precursor for the regioselective hydroamination of aliphatic (1-octyne and cyclohexylacetylene) and aromatic (phenylacetylene and 1-phenylpropyne) alkynes with aromatic (2,6-dimethylaniline and 2,6-diisopropylaniline) and aliphatic (tert-butylamine, dodecylamine, and cyclohexylamine) amines. The reactions give imines or imine−enamine mixtures, which are reduced to the corresponding secondary amines. The Markovnikov or anti-Markovnikov nature of the obtained products depends on the aliphatic or aromatic character of both the alkyne and the amine. Markovnikov products with regioselectivities of 100% are formed from the reactions between aliphatic alkynes and aromatic amines, while anti-Markovnikov derivatives with regioselectivies of 100% are obtained from the reactions of aromatic alkynes with all the studied amines and from the reactions of the aliphatic alkynes with tert-butylamine and dodecylamine. The reaction of 1-octyne and cyclohexylacetylene with cyclohexylamine gives mixtures of both types of products. Some considerations about the mechanism of the catalysis are also presented.
Description11 pages, 5 schemes, 2 tables, 1 figure.
Publisher version (URL)http://dx.doi.org/10.1021/om060370h
Appears in Collections:(ICMA) Artículos
Files in This Item:
There are no files associated with this item.
Show full item record
Review this work

Related articles:

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.