Abstract:Six novel Co(ii) coordination polymers, namely, [CoL(OH)(HO)]·10.5HO (1), [CoL(3-abpt)]·4HO (2), [CoL(4-azpy)(HO)(EtOH)] (3), [CoL(4,4'-bipy)(HO)(MeCN)] (4), [CoL(4,4'-bipy)] (5), and [CoL(OH)(ina)(HO)] (6) (HL = 2,2'-phosphinico-dibenzoic acid, 3-abpt = 4-amino-3,5-bis(3-pyridyl)-1,2,4-triazole, 4-azpy = 4,4'-azobispyridine, 4,4'-bipy = 4,4'-bipyridine, Hina = isonicotinic acid), have been hydrothermally synthesized and their magnetic properties have been characterized. The L anion displays six types of coord… Show more
“…The large Co–O–Co angles and long Co···Co separations for Co1 and Co3 atoms and for Co2 and Co3 atoms cause the antiferromagnetic interactions between these two pairs of Co(II) centers, while the small Co–O–Co angles and short Co···Co separations determine the ferromagnetic exchanges between Co1 and Co2 atoms (Figure S10). − Therefore, the cluster and framework display an overall antiferromagnetic behavior, and the similar magnetic properties were also reported in a cluster-based complex, [Co II 5 (N 3 ) 2 ( N - n -bda) 2 (bae) 2 (bza·SMe) 2 ]·1.5H 2 O …”
Utilizing the oxygen-bridged 5,5′-oxidiisophthalic
acid (H4L) linker, one Co(II)-based 3D porous MOF {[Co5(L)2(OH)2(OH2)2(H2O)4]·2DMF·H2O}
n
(1) with pentanuclear [Co5(μ3-OH)2(μ2-OH2)2]8+ cluster was prepared. The glassy
carbon electrode was modified by 1, and the obtained
electrode revealed electrocatalytic performance for glucose oxidation.
The porous MOF matrix is beneficial for dispersing Ag nanoparticles
evenly in the interior cages or channels, so Ag@1 composite
composed of both Ag nanoparticles and MOF was further prepared through
deposition-reduction method to enhance electrocatalytic activity.
The result demonstrates that the glucose oxidation by Ag@1 was greatly increased with low detection limit (1.32 μM) and
good selectivity and sensitivity (0.135 μA μM–1), which promote the application of MOF-template porous composites
as advanced electrochemical sensor materials. Furthermore, 1 shows an interesting magnetic spin-glass slow dynamics for the existing
of peculiar pentanuclear Co(II) clusters.
“…The large Co–O–Co angles and long Co···Co separations for Co1 and Co3 atoms and for Co2 and Co3 atoms cause the antiferromagnetic interactions between these two pairs of Co(II) centers, while the small Co–O–Co angles and short Co···Co separations determine the ferromagnetic exchanges between Co1 and Co2 atoms (Figure S10). − Therefore, the cluster and framework display an overall antiferromagnetic behavior, and the similar magnetic properties were also reported in a cluster-based complex, [Co II 5 (N 3 ) 2 ( N - n -bda) 2 (bae) 2 (bza·SMe) 2 ]·1.5H 2 O …”
Utilizing the oxygen-bridged 5,5′-oxidiisophthalic
acid (H4L) linker, one Co(II)-based 3D porous MOF {[Co5(L)2(OH)2(OH2)2(H2O)4]·2DMF·H2O}
n
(1) with pentanuclear [Co5(μ3-OH)2(μ2-OH2)2]8+ cluster was prepared. The glassy
carbon electrode was modified by 1, and the obtained
electrode revealed electrocatalytic performance for glucose oxidation.
The porous MOF matrix is beneficial for dispersing Ag nanoparticles
evenly in the interior cages or channels, so Ag@1 composite
composed of both Ag nanoparticles and MOF was further prepared through
deposition-reduction method to enhance electrocatalytic activity.
The result demonstrates that the glucose oxidation by Ag@1 was greatly increased with low detection limit (1.32 μM) and
good selectivity and sensitivity (0.135 μA μM–1), which promote the application of MOF-template porous composites
as advanced electrochemical sensor materials. Furthermore, 1 shows an interesting magnetic spin-glass slow dynamics for the existing
of peculiar pentanuclear Co(II) clusters.
“…Only one hydrogen atom was observed and modelled for water ligand O11W (Fig. 1) [24]. Also, the bond angles around the Co 2+ ions in the complexes are in the range 72.1(5) to 180.00 (11) which is in good agreement with literature [25].…”
A luminescent Cobalt(II) co-crystal [Co13(PDC)16(H2O)24.7H2O] 1 (where H2PDC = 2,6pyridinedicarboxylic acid) have been prepared by oven-heating and slow evaporation of solvent. Single crystal X-ray diffraction (SCXRD) analysis revealed that 1 is a mixture of complexes that crystallizes in the triclinic space group P-1 and the geometry around the Co(II) ions is octahedral. The structure is extensively imbued with hydrogen bonding that helps in stabilizing the complex. Thermogravimetric analysis indicates that 1 is thermally stable up to 364 ο C. The luminescence properties of 1 revealed a strong emission centered at 437 nm (λex = 345 nm) assigned to ligand to metal charge transfer (LMCT). The luminescence sensing of 1 towards volatile organic molecules were also examined. However, 1 displayed a turn off towards methanol compared to other molecules with high quenching efficiency and low limit of detection (3.5 x 10 -4 vol%). The results show excellent selectively and high sensitivity.Powder X-ray diffraction studies revealed that the structural integrity of the complex was maintained after exposure to methanol vapour. Theoretical studies also revealed small binding energy (-413.2 au) and low energy gap (1.19) for 1-CH3OH adduct.
“…Rational design and construction of cobalt complexes has garnered remarkable attention in the field of molecular materials owing to their potential applications in biochemistry, catalysis, electrochemistry, hydrogen production and magnetism [3][4][5].…”
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