Designed pincer ligand supported Co(ii)-based catalysts for dehydrogenative activation of alcohols: Studies on N-alkylation of amines, α-alkylation of ketones and synthesis of quinolines. Issue 24 (2nd June 2021)
- Record Type:
- Journal Article
- Title:
- Designed pincer ligand supported Co(ii)-based catalysts for dehydrogenative activation of alcohols: Studies on N-alkylation of amines, α-alkylation of ketones and synthesis of quinolines. Issue 24 (2nd June 2021)
- Main Title:
- Designed pincer ligand supported Co(ii)-based catalysts for dehydrogenative activation of alcohols: Studies on N-alkylation of amines, α-alkylation of ketones and synthesis of quinolines
- Authors:
- Singh, Anshu
Maji, Ankur
Joshi, Mayank
Choudhury, Angshuman R.
Ghosh, Kaushik - Abstract:
- Abstract : Base-metal Co-based catalysts Co1, Co2 and Co3 supported by pincer ligands were utilized for dehydrogenative activation of alcohols giving rise to N -alkylation of amines, α-alkylation of ketones and synthesis of quinolines. Abstract : Base-metal catalysts Co1, Co2 and Co3 were synthesized from designed pincer ligands L 1, L 2 and L 3 having NNN donor atoms respectively. Co1, Co2 and Co3 were characterized by IR, UV–Vis. and ESI-MS spectroscopic studies. Single crystal X-ray diffraction studies were investigated to authenticate the molecular structures of Co1 and Co3 . Catalysts Co1, Co2 and Co3 were utilized to study the dehydrogenative activation of alcohols for N -alkylation of amines, α-alkylation of ketones and synthesis of quinolines. Under optimized reaction conditions, a broad range of substrates including alcohols, anilines and ketones were exploited. A series of control experiments for N -alkylation of amines, α-alkylation of ketones and synthesis of quinolines were examined to understand the reaction pathway. ESI-MS spectral studies were investigated to characterize cobalt-alkoxide and cobalt-hydride intermediates. Reduction of styrene by evolved hydrogen gas during the reaction was investigated to authenticate the dehydrogenative nature of the catalysts. Probable reaction pathways were proposed for N -alkylation of amines, α-alkylation of ketones and synthesis of quinolines on the basis of control experiments and detection of reaction intermediates.
- Is Part Of:
- Dalton transactions. Volume 50:Issue 24(2021)
- Journal:
- Dalton transactions
- Issue:
- Volume 50:Issue 24(2021)
- Issue Display:
- Volume 50, Issue 24 (2021)
- Year:
- 2021
- Volume:
- 50
- Issue:
- 24
- Issue Sort Value:
- 2021-0050-0024-0000
- Page Start:
- 8567
- Page End:
- 8587
- Publication Date:
- 2021-06-02
- 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/d0dt03748f ↗
- 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:
- 17345.xml