623-04-1Relevant articles and documents
Development of Efficient Copper-Based MOF-Derived Catalysts for the Reduction of Aromatic Nitro Compounds
Karahan, ?zlem,Bi?er, Emre,Ta?demir, Adnan,Yürüm, Alp,Gürsel, Selmiye Alkan
, p. 1073 - 1079 (2018)
Two copper-based Cu3(btc)2 and Cu(Im)2 metal–organic frameworks are synthesized and annealed to form nanoporous Cu/Cu2O@C and Cu@N-C nanoparticles for utilization as catalysts in the reduction reaction of aromatic nitro compounds to aromatic amines. All synthesized MOF compounds and MOF-derived nanoparticles are characterized using XRD, Raman spectroscopy, TGA, SEM-EDX, and XPS methods. Also, the pore-size distribution and surface area of the MOF-derived Cu/Cu2O@C and Cu@N-C nanoparticles are characterized by the BJH and BET methods. After characterization, the catalysts Cu/Cu2O@C and Cu@N-C are catalytically tested for the reduction reactions of various aromatic nitro compounds chemically by monitoring with a UV/Vis spectrometer. Both catalysts exhibit remarkable results compared with those in the literature. Also, the Cu/Cu2O@C catalyst shows better results than the Cu@N-C catalyst.
The X-ray Structure of 4-Aminobenzyl alcohol (4-Aminophenylmethanol)
Aitken, R. Alan,Davidson, Lewis,Slawin, Alexandra M. Z.
, p. 8 - 13 (2020)
A second polymorph of 4-aminobenzyl alcohol [orthorhombic, a = 8.95051(15), b = 5.8248(1), c = 12.1645(2) ?, space group Pna21] shows a “herringbone” structure with stacks of hydrogen-bonded molecules when viewed down the b-axis. Graphical Abst
Design of Stimuli-Responsive Dynamic Covalent Delivery Systems for Volatile Compounds (Part 1): Controlled Hydrolysis of Micellar Amphiphilic Imines in Water
Lutz, Eric,Moulin, Emilie,Tchakalova, Vera,Benczédi, Daniel,Herrmann, Andreas,Giuseppone, Nicolas
supporting information, p. 13457 - 13467 (2021/08/09)
Despite their intrinsic hydrolysable character, imine bonds can become remarkably stable in water when self-assembled in amphiphilic micellar structures. In this work, we systematically studied some of these structures and the influence of various parameters that can be used to take control of their hydrolysis, including pH, concentration, the position of the imine function in the amphiphilic structure, relative lengths of the linked hydrophilic and hydrophobic moieties. Thermodynamic and kinetic data led us to the rational design of stable imines in water, partly based on the location of the imine function within the hydrophobic part of the amphiphile and on a predictable quantitative term that we define as the total hydrophilic–lipophilic balance (HLB). In addition, we show that such stable systems are also stimuli-responsive and therefore, of potential interest in trapping and releasing micellar components on demand.
Reductive Knoevenagel Condensation with the Zn-AcOH System
Ivanov, Konstantin L.,Melnikov, Mikhail Ya.,Budynina, Ekaterina M.
, p. 1285 - 1291 (2020/11/13)
An efficient gram-scale one-pot approach to 2-substituted malonates and related structures is developed, starting from commercially available aldehydes and active methylene compounds. The technique combines Knoevenagel condensation with the reduction of the C=C bond in the resulting activated alkenes with the Zn-AcOH system. The relative ease with which the C=C bond reduction occurs can be traced to the accepting abilities of the substituents in the intermediate arylidene malonates.
