Cu-NPs@COF: A potential heterogeneous catalyst for CO2 fixation to produce 2-oxazolidinones as well as benzimidazoles under moderate reaction conditions

2020 ◽  
Vol 40 ◽  
pp. 101180 ◽  
Author(s):  
Resmin Khatun ◽  
Surajit Biswas ◽  
Imdadul Haque Biswas ◽  
Sk Riyajuddin ◽  
Najirul Haque ◽  
...  
Keyword(s):  
Heterogeneous Catalyst ◽  
Co2 Fixation ◽  
Reaction Conditions ◽  
Moderate Reaction

Efficient synthesis of pyrido[2,3-d]pyrimidine-7-carboxylic acids catalyzed by a TiO2/SiO2 nanocomposite in aqueous media at room temperature

2018 ◽  
Vol 73 (9) ◽  
pp. 641-645 ◽  
Author(s):  
Sepehr Sadegh-Samiei ◽  
Shahrzad Abdolmohammadi
Keyword(s):  
Heterogeneous Catalyst ◽  
Carboxylic Acids ◽  
Room Temperature ◽  
Aqueous Media ◽  
Reaction Times ◽  
Molar Ratio ◽  
Efficient Synthesis ◽  
Reaction Conditions ◽  
Moderate Reaction ◽  
Recyclable Heterogeneous Catalyst

AbstractA novel and efficient synthesis of eight 5-aryl-1,3-dimethyl-2,4-dioxo-1,2,3,4,5,8-hexahydropyrido[2,3-d]pyrimidine-7-carboxylic acids using a TiO2/SiO2 nanocomposite with a molar ratio of 1:1 as a recyclable heterogeneous catalyst is described. The desired products, five of which are new, are formed in short reaction times (2–3 h) with high to excellent yields (94%–98%) under very moderate reaction conditions (room temperature, aqueous media).

scholarly journals Design of bifunctional quaternary phosphonium salt catalysts for CO2 fixation reaction with epoxides under mild conditions

2016 ◽  
Vol 18 (17) ◽  
pp. 4611-4615 ◽  
Author(s):  
Shiyao Liu ◽  
Naoki Suematsu ◽  
Keiji Maruoka ◽  
Seiji Shirakawa
Keyword(s):  
Co2 Fixation ◽  
Phosphonium Salt ◽  
Cyclic Carbonates ◽  
Efficient Synthesis ◽  
Reaction Conditions ◽  
Mild Conditions ◽  
Phosphonium Iodide ◽  
Fixation Reaction ◽  
Quaternary Phosphonium Salt

An efficient synthesis of cyclic carbonates from epoxides and CO2 under mild reaction conditions was achieved via the use of a designed bifunctional quaternary phosphonium iodide catalyst.

scholarly journals Conversion of CO2 into Chloropropene Carbonate Catalyzed by Iron (II) Phthalocyanine Hypercrosslinked Porous Organic Polymer

Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4598
Author(s):  
Eva M. Maya ◽  
Antonio Valverde-González ◽  
Marta Iglesias
Keyword(s):  
Heterogeneous Catalyst ◽  
Direct Synthesis ◽  
Cyclic Carbonate ◽  
Organic Polymer ◽  
Iron Loading ◽  
Reaction Conditions ◽  
Porous Organic Polymer ◽  
Commercial Iron ◽  
Excellent Stability ◽  
Efficient Heterogeneous Catalyst

Commercial iron (II) phthalocyanine (FePc) was knitted with biphenyl using a Friedel–Crafts reaction to yield a micro-meso porous organic polymer (FePc-POP) with a specific surface area of 427 m2/g and 5.42% of iron loading. This strategy allowed for the direct synthesis of a heterogeneous catalyst from an iron containing monomer. The catalytic system, formed by the knitted polymer containing FePc and DMAP (4-dimethylamino pyridine) as base, results in an efficient heterogeneous catalyst in the cycloaddition of CO2 to epichlorohydrin to selectively obtain the corresponding cyclic carbonate. Thus, a TON (mmol substrate converted/mmol catalysts used) value of 2700 was reached in 3 h under mild reaction conditions (solvent free, 90 °C, 3 bar of CO2). The catalyst does not exhibit leaching during the reactions, which was attributed to the excellent stability of the metal in the macrocycle.

Copper-catalyzed synthesis of 2-aminophenyl benzothiazoles: a novel approach

2018 ◽  
Vol 16 (37) ◽  
pp. 8267-8272 ◽  
Author(s):  
S. N. Murthy Boddapati ◽  
Chandra Mohan Kurmarayuni ◽  
Baby Ramana Mutchu ◽  
Ramana Tamminana ◽  
Hari Babu Bollikolla
Keyword(s):  
Nucleophilic Substitution ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Reaction Conditions ◽  
Moderate Reaction ◽  
Cross Coupling Reactions ◽  
Novel Approach

Substituted 2-aminophenyl benzothiazoles have been constructed from thiourea via copper-catalyzed desulfurization/nucleophilic substitution followed by domino intra- and intermolecular C–N cross-coupling reactions under moderate reaction conditions.

scholarly journals Air-stable, recyclable, and time-efficient diphenylphosphinite cellulose-supported palladium nanoparticles as a catalyst for Suzuki–Miyaura reactions

2011 ◽  
Vol 7 ◽  
pp. 378-385 ◽  
Author(s):  
Qingwei Du ◽  
Yiqun Li
Keyword(s):  
Heterogeneous Catalyst ◽  
Palladium Nanoparticles ◽  
Palladium Complex ◽  
Complex Cell ◽  
Reaction Conditions ◽  
Highly Efficient ◽  
Excellent Yield ◽  
Simple Filtration ◽  
Supported Palladium ◽  
Efficient Heterogeneous Catalyst

A diphenylphosphinite cellulose palladium complex (Cell–OPPh2–Pd0) was found to be a highly efficient heterogeneous catalyst for the Suzuki–Miyaura reaction. The products were obtained in good to excellent yield under mild reaction conditions. Moreover, the catalyst could be easily recovered by simple filtration and reused for at least 6 cycles without losing its activity.

Oxidation of Higher Alkanes at Moderate Reaction Conditions with Ozone in Presence of Mesoporous Materials

2008 ◽  
Vol 11 (3) ◽  
Author(s):  
V. S. R. Rajasekhar Pullabhotla ◽  
S. B. Jonnalagadda
Keyword(s):  
Carboxylic Acids ◽  
Mesoporous Materials ◽  
Molecular Sieves ◽  
Mesoporous Molecular Sieves ◽  
Reaction Products ◽  
Reaction Conditions ◽  
Moderate Reaction ◽  
Product Molecule ◽  
Relative Selectivity ◽  
Mcm 41

AbstractThe scope of mesoporous molecular sieves, Al-MCM-41, as catalysts in the ozone initiated fuctionalisation of higher n-alkanes at 20 ± 1 °C and ~1 atm conditions is investigated. Oxygen is introduced into carbonaceous site in the product molecule forming 2-, 3- and 4- keto- isomers as main products and carboxylic acids as minor products. The % conversion, reaction products and selectivity for the catalysed reactions are compared. In presence of catalysts, the relative selectivity towards 4-ketone is increased.

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