Theoretical insights into CO2 hydrogenation to methanol by a Mn–PNP complex. Issue 8 (21st March 2019)
- Record Type:
- Journal Article
- Title:
- Theoretical insights into CO2 hydrogenation to methanol by a Mn–PNP complex. Issue 8 (21st March 2019)
- Main Title:
- Theoretical insights into CO2 hydrogenation to methanol by a Mn–PNP complex
- Authors:
- Mandal, Shyama Charan
Rawat, Kuber Singh
Nandi, Surajit
Pathak, Biswarup - Abstract:
- Abstract : Unravelling the role of an amide intermediate in co-catalyst-based sequential CO2 hydrogenation reaction to methanol. Abstract : DFT and microkinetic modelling studies have been carried out to explore the reaction mechanism of newly reported CO2 hydrogenation reaction to methanol. The catalytic activity of PNP-based Mn(i ), Fe(ii ) and Ru(ii ) homogeneous complexes for CO2 hydrogenation to methanol has been explored. The hydrogenation occurs in the presence of a morpholine co-catalyst via a formamide intermediate. DFT calculations performed on the demonstrative reaction pathway allow us to suggest a complete reaction mechanism. The present study reports the multistep transformation of CO2 to methanol. We propose that following initial CO2 hydrogenation to HCOOH by metal catalysts, amidation of HCOOH to N -formylmorpholine occurs in the presence of morpholine, which further undergoes hydrogenation reaction for the formation of methanol by metal catalysts. The highly exergonic nature of the amidation step increases the overall rate of the reaction. Remarkably, the N -formylmorpholine hydrogenation step may follow two different pathways (CO vs. C–N bond hydrogenation) and both the pathways involve comparable reaction free energy barriers for hydrogenation, i.e., both the considered reaction mechanisms are competitive in nature. Furthermore, our microkinetic modelling results agree well with previous experimental studies, which confirm that the proposed reactionAbstract : Unravelling the role of an amide intermediate in co-catalyst-based sequential CO2 hydrogenation reaction to methanol. Abstract : DFT and microkinetic modelling studies have been carried out to explore the reaction mechanism of newly reported CO2 hydrogenation reaction to methanol. The catalytic activity of PNP-based Mn(i ), Fe(ii ) and Ru(ii ) homogeneous complexes for CO2 hydrogenation to methanol has been explored. The hydrogenation occurs in the presence of a morpholine co-catalyst via a formamide intermediate. DFT calculations performed on the demonstrative reaction pathway allow us to suggest a complete reaction mechanism. The present study reports the multistep transformation of CO2 to methanol. We propose that following initial CO2 hydrogenation to HCOOH by metal catalysts, amidation of HCOOH to N -formylmorpholine occurs in the presence of morpholine, which further undergoes hydrogenation reaction for the formation of methanol by metal catalysts. The highly exergonic nature of the amidation step increases the overall rate of the reaction. Remarkably, the N -formylmorpholine hydrogenation step may follow two different pathways (CO vs. C–N bond hydrogenation) and both the pathways involve comparable reaction free energy barriers for hydrogenation, i.e., both the considered reaction mechanisms are competitive in nature. Furthermore, our microkinetic modelling results agree well with previous experimental studies, which confirm that the proposed reaction mechanism is the most plausible reaction mechanism for CO2 hydrogenation to methanol. … (more)
- Is Part Of:
- Catalysis science & technology. Volume 9:Issue 8(2019)
- Journal:
- Catalysis science & technology
- Issue:
- Volume 9:Issue 8(2019)
- Issue Display:
- Volume 9, Issue 8 (2019)
- Year:
- 2019
- Volume:
- 9
- Issue:
- 8
- Issue Sort Value:
- 2019-0009-0008-0000
- Page Start:
- 1867
- Page End:
- 1878
- Publication Date:
- 2019-03-21
- Subjects:
- Catalysis -- Periodicals
541.395 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/CY ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cy00114j ↗
- Languages:
- English
- ISSNs:
- 2044-4753
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3090.943100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9849.xml