“…In addition, the diffraction peaks shown at 2 θ = 11°, 23°, 35°, 53°, and 63° are related to hydrotalcite‐like structure. [ 59,62–64 ] These XRD results revealed the successful immobilization of PCE cobalt complex on γ ‐Fe 2 O 3 @Cu 3 Al‐LDH NPs to produce γ ‐Fe 2 O 3 @Cu 3 Al‐LDH/PCE‐Co nanocomposite. In addition, the exact similarity between the XRD pattern of the recycled catalyst (Figure 2b) and that of the authentic catalyst (Figure 2a) confirms that the crystalline nature the catalyst remains intact after the reaction.…”
A magnetically separable cobalt complex of macrocyclic pseudo-crown ether (PCE) immobilized on magnetic Cu/Al-layered double hydroxide (γ-Fe 2 O 3 @Cu 3 Al-layered double hydroxide (LDH)/PCE-Co) was readily fabricated using a simple four-step postsynthetic modification strategy. This newly prepared nanocomposite was characterized by different chemo-physical approaches, including Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), inductively coupled plasma optical emission spectroscopy (ICP-OES), vibrating sample magnetometer (VSM), X-ray diffraction (XRD), nitrogen adsorptiondesorption isotherms, energy-dispersive X-ray spectroscopy (EDX), and elemental mapping. The catalytic performance of these nanoparticles (NPs) was explored in the synthesis of diverse 1H-chromeno[2,3-b]pyridine-3-carbonitrile derivatives via one-pot three-component reactions under green reaction conditions. Environmentally benign reaction conditions, simple separation, high yields of the reactions, versatility, easy magnetic separation, and reusability for several runs without significant loss of catalytic performance are the key advantages that make this protocol an ideal alternative method for the synthesis of chromene derivatives.
“…In addition, the diffraction peaks shown at 2 θ = 11°, 23°, 35°, 53°, and 63° are related to hydrotalcite‐like structure. [ 59,62–64 ] These XRD results revealed the successful immobilization of PCE cobalt complex on γ ‐Fe 2 O 3 @Cu 3 Al‐LDH NPs to produce γ ‐Fe 2 O 3 @Cu 3 Al‐LDH/PCE‐Co nanocomposite. In addition, the exact similarity between the XRD pattern of the recycled catalyst (Figure 2b) and that of the authentic catalyst (Figure 2a) confirms that the crystalline nature the catalyst remains intact after the reaction.…”
A magnetically separable cobalt complex of macrocyclic pseudo-crown ether (PCE) immobilized on magnetic Cu/Al-layered double hydroxide (γ-Fe 2 O 3 @Cu 3 Al-layered double hydroxide (LDH)/PCE-Co) was readily fabricated using a simple four-step postsynthetic modification strategy. This newly prepared nanocomposite was characterized by different chemo-physical approaches, including Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), inductively coupled plasma optical emission spectroscopy (ICP-OES), vibrating sample magnetometer (VSM), X-ray diffraction (XRD), nitrogen adsorptiondesorption isotherms, energy-dispersive X-ray spectroscopy (EDX), and elemental mapping. The catalytic performance of these nanoparticles (NPs) was explored in the synthesis of diverse 1H-chromeno[2,3-b]pyridine-3-carbonitrile derivatives via one-pot three-component reactions under green reaction conditions. Environmentally benign reaction conditions, simple separation, high yields of the reactions, versatility, easy magnetic separation, and reusability for several runs without significant loss of catalytic performance are the key advantages that make this protocol an ideal alternative method for the synthesis of chromene derivatives.
“…The morphologies of Zn 0.75 CrAl- x and Zn 0.75 CrAl- x -c are examined with the SEM technique. Figure a,c shows that both samples Zn 0.75 CrAl-6 and Zn 0.75 CrAl-9 before calcination are composed of platelet-like agglomerated crystals, which represent the characteristics of layered clay materials. , Compared to Zn 0.75 CrAl-9, the structure of Zn 0.75 CrAl-6 becomes fluffier, which makes it have a larger external surface area . After calcination at 460 °C, the hydrotalcite structure collapses and both the samples become flocculent (Figure b,d)…”
Cr-doped ZnAl mixed oxide catalysts (Zn0.75CrAl-x-c) were obtained via calcining the Zn0.75CrAl-x hydrotalcite precursors and were
applied in the selective
oxidation of 5-hydroxymethylfurfural (5-HMF) to 2,5-furandicarboxylic
acid (FDCA). Cr doping significantly enhanced the catalytic activity.
A 95.1% 5-HMF conversion with an 88.1% FDCA selectivity was achieved
over the Zn0.75CrAl-6-c catalyst at 130 °C under 0.6
MPa oxygen for 4 h. The good performance was associated with the high
specific surface area and high oxygen vacancy concentration. Moreover,
the Zn0.75CrAl-6-c catalyst was used for five cycles without
a significant activity loss indicating excellent stability.
“…The selective oxidation of styrene is an important transformation in the fine chemical industry because the oxidation products (benzaldehyde, benzoic acid, and styrene epoxide) are critical chemical intermediates to synthesize some value-added fine and bulk chemicals, such as perfumes, pharmaceuticals, dyes, and the rubber auxiliary and fine chemicals industry. − A number of transition-metal catalysts have been developed for the oxidation of styrene to benzaldehyde or styrene epoxide, − but relatively very few studies had their focus on acid compounds as the main product. Besides, current research is aimed at obtaining only one desired product, − although there are also a few reports on the adjustment of the main products of styrene oxidation to obtain benzaldehyde and styrene epoxide. − Likewise, there are few reports on control of the selectivity of benzaldehyde and benzoic acid by adjusting the variable factors, i.e., reaction temperature, initial volume ratio of the solvent, and catalyst amount .…”
Section: Introductionmentioning
confidence: 99%
“…Besides, current research is aimed at obtaining only one desired product, − although there are also a few reports on the adjustment of the main products of styrene oxidation to obtain benzaldehyde and styrene epoxide. − Likewise, there are few reports on control of the selectivity of benzaldehyde and benzoic acid by adjusting the variable factors, i.e., reaction temperature, initial volume ratio of the solvent, and catalyst amount . However, some of these reported methods still suffered from precious metal catalysis, ,− poor selectivity and conversion, ,− and the use of a large amount of volatile organic solvents. ,,,,,, Considering the economic and environmental facts, the selective oxidation of styrene to benzaldehyde and benzoic acid, respectively, by controlling the reaction conditions using a heterogeneous catalyst might be a desirable process.…”
A nanosized
Cu3(BTC)2 (HKUST-1; BTC = 1,3,5-benzenetricarboxylate)
catalyst with a size range of 10–20 nm was synthesized with
2-methylimidazole (2-MI) as an effective competitive ligand and Lewis
base to tune its morphology and improve its catalytic performance
simultaneously. On the one hand, the addition of 2-MI can accelerate
deprotonation of the bridging ligand H3BTC, thereby accelerating
the rapid nucleation of crystals, which leads to a rapid decrease
of the solution supersaturation and inhibits further growth of the
nucleated small crystal, resulting in nanosized HKUST-1 crystals.
On the other hand, the uncoordinated 2-MI in nano-HKUST-1 can improve
the catalytic performance of the crystal because of its basicity.
Further catalytic experiments demonstrate that nano-HKUST-1 showed
high catalytic activity compared with bulk HKUST-1 in the controllable
oxidation of styrene under solvent-free conditions. More importantly,
both benzaldehydes and benzoic acids were successfully obtained via
a facile variation of the reaction temperature or time. The benzaldehydes
can be produced in 78% gas chromatographic yield after 9 h at 50 °C
or 72% after 50 min at 80 °C, while benzoic acids can be obtained
in moderate-to-good yield after 6 h at 80 °C. Notably, nano-HKUST-1
could be expediently recycled in four cycles without significantly
affecting the yield of the desired product.
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