Heterobimetallic metallation studies of N, N-dimethylphenylethylamine (DMPEA): benzylic C–H bond cleavage/dimethylamino capture or intact DMPEA complex12. Issue 12 (26th February 2015)
- Record Type:
- Journal Article
- Title:
- Heterobimetallic metallation studies of N, N-dimethylphenylethylamine (DMPEA): benzylic C–H bond cleavage/dimethylamino capture or intact DMPEA complex12. Issue 12 (26th February 2015)
- Main Title:
- Heterobimetallic metallation studies of N, N-dimethylphenylethylamine (DMPEA): benzylic C–H bond cleavage/dimethylamino capture or intact DMPEA complex12
- Authors:
- Kennedy, Alan R.
Mulvey, Robert E.
Ramsay, Donna L.
Robertson, Stuart D. - Abstract:
- Abstract : The cleave and capture capacity of various bimetallic amido–alkyl mixtures is illustrated through reaction with the deprotonation sensitive N, N -dimethylphenylethylamine. Abstract : Reaction of the sodium monoamido-bisalkylzincate [(TMEDA)Na(TMP)(Bu t )Zn(Bu t )] (TMEDA is N, N, N ′, N ′-tetramethylethylenediamine; TMP is 2, 2, 6, 6-tetramethylpiperidide) and the related lithium zincate [(PMDETA)Li(TMP)Zn(Bu t )2 ] (PMDETA is N, N, N ′, N ′′, N ′′-pentamethyldiethylenetriamine) with the sensitive bio-relevant scaffold N, N -dimethylphenylethylamine, DMPEA, afforded the crystalline complexes [(TMEDA)Na(TMP)(NMe2 )Zn(Bu t )] and [(PMDETA)Li(NMe2 )Zn(Bu t )2 ], respectively, both of which have been characterized by NMR spectroscopic and X-ray crystallographic studies. Made by reaction of a LiTMP–(TMP)Al(Bu i )2 mixture with DMPEA, a third dimethylamino-containing crystalline complex, the aluminate [(THF)Li(TMP)(NMe2 )Al(Bu i )2 ] has been similarly characterized. All three complexes can be regarded as products of cleave and capture chemistry whereby metallation at the benzylic position of DMPEA has led to a β-elimination of an anionic Me2 N fragment that has been captured by a charge balancing cationic heterobimetallic entity. While a metallated intermediate prior to the elimination has proved elusive in all of these reactions, DMPEA has been captured fully intact in the novel Lewis acid–Lewis base crystalline complex [DMPEA·Li(TMP)Zn(Me)2 ], which has also beenAbstract : The cleave and capture capacity of various bimetallic amido–alkyl mixtures is illustrated through reaction with the deprotonation sensitive N, N -dimethylphenylethylamine. Abstract : Reaction of the sodium monoamido-bisalkylzincate [(TMEDA)Na(TMP)(Bu t )Zn(Bu t )] (TMEDA is N, N, N ′, N ′-tetramethylethylenediamine; TMP is 2, 2, 6, 6-tetramethylpiperidide) and the related lithium zincate [(PMDETA)Li(TMP)Zn(Bu t )2 ] (PMDETA is N, N, N ′, N ′′, N ′′-pentamethyldiethylenetriamine) with the sensitive bio-relevant scaffold N, N -dimethylphenylethylamine, DMPEA, afforded the crystalline complexes [(TMEDA)Na(TMP)(NMe2 )Zn(Bu t )] and [(PMDETA)Li(NMe2 )Zn(Bu t )2 ], respectively, both of which have been characterized by NMR spectroscopic and X-ray crystallographic studies. Made by reaction of a LiTMP–(TMP)Al(Bu i )2 mixture with DMPEA, a third dimethylamino-containing crystalline complex, the aluminate [(THF)Li(TMP)(NMe2 )Al(Bu i )2 ] has been similarly characterized. All three complexes can be regarded as products of cleave and capture chemistry whereby metallation at the benzylic position of DMPEA has led to a β-elimination of an anionic Me2 N fragment that has been captured by a charge balancing cationic heterobimetallic entity. While a metallated intermediate prior to the elimination has proved elusive in all of these reactions, DMPEA has been captured fully intact in the novel Lewis acid–Lewis base crystalline complex [DMPEA·Li(TMP)Zn(Me)2 ], which has also been characterized by the aforementioned techniques. … (more)
- Is Part Of:
- Dalton transactions. Volume 44:Issue 12(2015)
- Journal:
- Dalton transactions
- Issue:
- Volume 44:Issue 12(2015)
- Issue Display:
- Volume 44, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 44
- Issue:
- 12
- Issue Sort Value:
- 2015-0044-0012-0000
- Page Start:
- 5875
- Page End:
- 5887
- Publication Date:
- 2015-02-26
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5dt00247h ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9480.xml