Catalytic synthesis of benzimidazoles and organic carbamates using a polymer supported zinc catalyst through CO2 fixation. (30th August 2019)
- Record Type:
- Journal Article
- Title:
- Catalytic synthesis of benzimidazoles and organic carbamates using a polymer supported zinc catalyst through CO2 fixation. (30th August 2019)
- Main Title:
- Catalytic synthesis of benzimidazoles and organic carbamates using a polymer supported zinc catalyst through CO2 fixation
- Authors:
- Biswas, Imdadul Haque
Biswas, Surajit
Islam, Md Sarikul
Riyajuddin, Sk
Sarkar, Priyanka
Ghosh, Kaushik
Islam, Sk Manirul - Abstract:
- Abstract : Zinc metal is attached to the organically modified polystyrene and the obtained catalyst is well characterized. The catalyst is very efficient for the formation of benzimidazoles and organic carbamates through carbon dioxide fixation. Abstract : Utilization of carbon dioxide in chemical fixation for synthesis of fine chemicals like benzimidazoles, organic carbamates, etc. is in high demand in recent years as carbon dioxide is a cost effective, sustainable, and green renewable C1 source. In this article we present the design and synthesis of an organically modified polystyrene bound heterogeneous[PS-Zn(ii )-SALTETA] catalyst. The catalyst has been characterized thoroughly by Fourier transform infrared spectroscopy, atomic absorption spectroscopy, thermo gravimetric analysis, PXRD, SEM and EDAX studies. The catalyst was used for cyclization of o -phenylenediamines through insertion of carbon dioxide in order to produce benzimidazoles in the presence of dimethylamine borane (DMAB). The developed catalytic procedure is sustainable, economical and efficient owing to the utilization of ethanol/water as a biodegradable and environment friendly solvent system. Besides benzimidazole production the catalyst was also very active for manufacture of organic carbamates from anilines and n -butyl bromide under atmospheric CO2 pressure under solvent free conditions at room temperature and the catalytic protocol showed outstanding functional group tolerance. Moreover the catalystAbstract : Zinc metal is attached to the organically modified polystyrene and the obtained catalyst is well characterized. The catalyst is very efficient for the formation of benzimidazoles and organic carbamates through carbon dioxide fixation. Abstract : Utilization of carbon dioxide in chemical fixation for synthesis of fine chemicals like benzimidazoles, organic carbamates, etc. is in high demand in recent years as carbon dioxide is a cost effective, sustainable, and green renewable C1 source. In this article we present the design and synthesis of an organically modified polystyrene bound heterogeneous[PS-Zn(ii )-SALTETA] catalyst. The catalyst has been characterized thoroughly by Fourier transform infrared spectroscopy, atomic absorption spectroscopy, thermo gravimetric analysis, PXRD, SEM and EDAX studies. The catalyst was used for cyclization of o -phenylenediamines through insertion of carbon dioxide in order to produce benzimidazoles in the presence of dimethylamine borane (DMAB). The developed catalytic procedure is sustainable, economical and efficient owing to the utilization of ethanol/water as a biodegradable and environment friendly solvent system. Besides benzimidazole production the catalyst was also very active for manufacture of organic carbamates from anilines and n -butyl bromide under atmospheric CO2 pressure under solvent free conditions at room temperature and the catalytic protocol showed outstanding functional group tolerance. Moreover the catalyst is highly recyclable and reusable. … (more)
- Is Part Of:
- New journal of chemistry. Volume 43:Number 36(2019)
- Journal:
- New journal of chemistry
- Issue:
- Volume 43:Number 36(2019)
- Issue Display:
- Volume 43, Issue 36 (2019)
- Year:
- 2019
- Volume:
- 43
- Issue:
- 36
- Issue Sort Value:
- 2019-0043-0036-0000
- Page Start:
- 14643
- Page End:
- 14652
- Publication Date:
- 2019-08-30
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c9nj03015h ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11750.xml