Two pillared-layer metal–organic frameworks based on the pinwheel trinuclear carboxylate-clusters of Zn(ii) and Co(ii): synthesis, crystal structures, magnetic study, and Lewis acid catalysis. Issue 5 (16th January 2023)
- Record Type:
- Journal Article
- Title:
- Two pillared-layer metal–organic frameworks based on the pinwheel trinuclear carboxylate-clusters of Zn(ii) and Co(ii): synthesis, crystal structures, magnetic study, and Lewis acid catalysis. Issue 5 (16th January 2023)
- Main Title:
- Two pillared-layer metal–organic frameworks based on the pinwheel trinuclear carboxylate-clusters of Zn(ii) and Co(ii): synthesis, crystal structures, magnetic study, and Lewis acid catalysis
- Authors:
- Das, Moyna
Jaswal, Vishakha
Bhambri, Himanshi
Das, Prasenjit
Maity, Suvendu
Ghosh, Prasanta
Mandal, Sanjay K.
Sarkar, Madhushree - Abstract:
- Abstract : Zn-MOF and Co-MOF have 3D pillared-layer structure based on pinwheel trinuclear metal-carboxylate clusters. Zn-MOF is efficient catalyst for Knoevenagel condensation reaction while Co-MOF have shown magnetic properties due to the trimeric Co(ii ). Abstract : Using a dicarboxylic acid, [1, 1′-biphenyl]-4, 4′-dicarboxylic acid (H2 L1 ) and an exobidentate ligand, (1 E, 1′ E )- N, N ′-(1, 4-phenylene)bis(1-(pyridin-4-yl)methanimine) (L2 ), two 3D interpenetrated networks, {[Zn3 (L1 )3 (L2 )]·9H2 O} n (Zn-MOF ) and {[Co3 (L1 )3 (L2 )(DMF)]·0.5DMF} n (Co-MOF ), have been prepared in good yields. The crystal structure analysis of Zn-MOF and Co-MOF revealed that both have a 3D pillared-layer structure based on pinwheel trinuclear metal–carboxylate clusters as secondary building units (SBUs). Furthermore, the structures also exhibited three-fold interpenetration. Although the overall networks in Zn-MOF and Co-MOF showed significant resemblances, there are marked differences in their crystal structures, which are associated with the coordination environment of the metal centre and the binding modes of the carboxylates. Gas adsorption studies (N2 at 77 K and 1 bar) indicated that Co-MOF is more porous than Zn-MOF . Magnetic measurements on Co-MOF indicate a significant antiferromagnetic interaction (45 K to 303 K) between trimeric Co(ii ) S = 3/2 spins through syn – syn carboxylato bridges. Both MOFs were studied for the Lewis acid catalyzed Knoevenagel condensationAbstract : Zn-MOF and Co-MOF have 3D pillared-layer structure based on pinwheel trinuclear metal-carboxylate clusters. Zn-MOF is efficient catalyst for Knoevenagel condensation reaction while Co-MOF have shown magnetic properties due to the trimeric Co(ii ). Abstract : Using a dicarboxylic acid, [1, 1′-biphenyl]-4, 4′-dicarboxylic acid (H2 L1 ) and an exobidentate ligand, (1 E, 1′ E )- N, N ′-(1, 4-phenylene)bis(1-(pyridin-4-yl)methanimine) (L2 ), two 3D interpenetrated networks, {[Zn3 (L1 )3 (L2 )]·9H2 O} n (Zn-MOF ) and {[Co3 (L1 )3 (L2 )(DMF)]·0.5DMF} n (Co-MOF ), have been prepared in good yields. The crystal structure analysis of Zn-MOF and Co-MOF revealed that both have a 3D pillared-layer structure based on pinwheel trinuclear metal–carboxylate clusters as secondary building units (SBUs). Furthermore, the structures also exhibited three-fold interpenetration. Although the overall networks in Zn-MOF and Co-MOF showed significant resemblances, there are marked differences in their crystal structures, which are associated with the coordination environment of the metal centre and the binding modes of the carboxylates. Gas adsorption studies (N2 at 77 K and 1 bar) indicated that Co-MOF is more porous than Zn-MOF . Magnetic measurements on Co-MOF indicate a significant antiferromagnetic interaction (45 K to 303 K) between trimeric Co(ii ) S = 3/2 spins through syn – syn carboxylato bridges. Both MOFs were studied for the Lewis acid catalyzed Knoevenagel condensation reactions between benzaldehydes and malononitrile with an active methylene group, where Zn-MOF was found to be a better catalyst than Co-MOF . This was supported by the Monte Carlo simulations indicating the better substrate binding ability of Zn-MOF than Co-MOF . … (more)
- Is Part Of:
- Dalton transactions. Volume 52:Issue 5(2023)
- Journal:
- Dalton transactions
- Issue:
- Volume 52:Issue 5(2023)
- Issue Display:
- Volume 52, Issue 5 (2023)
- Year:
- 2023
- Volume:
- 52
- Issue:
- 5
- Issue Sort Value:
- 2023-0052-0005-0000
- Page Start:
- 1449
- Page End:
- 1460
- Publication Date:
- 2023-01-16
- 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/d2dt04106e ↗
- 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:
- 25503.xml