Quasi-HKUST as Tandem Catalyst for Direct Imine Formation under Green Approach

: Copper based metal-organic framework (Cu 3 (BTC) 2 (H 2 O) 3 ] n ·nH 2 OMeOH (HKUST) has been submitted to under controlled conditions to thermolysis under air atmosphere at different temperatures ranging from 100 to 300 °C. This treatment produces the partial removal of ligands, as well as, the generation of structural defects and additional porosity in a controlled way. The resulting defective materials,The resulting defective materials denoted according to the literature as quasi MOFs, were subsequently employed as heterogeneous tandem catalysts in the one pot synthesis of N-benzylideneaniline from aniline and benzyl alcohol in open air as terminal oxidant at 70 °C under base-and dehydrating agent-free conditions. The Q-HKUST catalysts calcined at 240 °C and 260 °C (QH-240 and QH-260, respectively) was the most efficient in the series, can efficiently promotinge imine synthesis, in particular QH-240 within 1h by forming water as the only by-product. Data from Knoevenagel condensation of malononitrile shows that in QH-240 the distances of Cu ions in HKUST cavities are preserved, increasing the Knoevenagel activity, but a strong rearrangement takes place at 300 o C or above. The unsaturated copper active sites with simultaneous presence of micro-and mesopores in QH-240 tandem catalyst are responsible for this excellent catalytic performance. The effective parameters on catalytic activity of QH-240 including deligandation temperature, the amount of catalyst, the ratio of reactants, and reaction temperature as well as the stability and recyclability of the catalyst were also investigated. The possible mechanism used by QH-240 follows alcohol aerobic oxidation and subsequent anaerobic condensation of aldehyde intermediate with aniline.

[1]  H. García,et al.  Metal-Organic Framework Derived Bimetallic Materials for Electrochemical Energy Storage. , 2020, Angewandte Chemie.

[2]  Shaobin Wang,et al.  Quasi-MOF derivative-based electrode for efficient electro-Fenton oxidation. , 2020, Journal of hazardous materials.

[3]  Xiao Xiao,et al.  Synthesis of “Quasi-Ce-MOF” Electrocatalysts for Enhanced Urea Oxidation Reaction Performance , 2020 .

[4]  J. Gascón,et al.  Metal-Organic Frameworks in Heterogeneous Catalysis: Recent Progress, New Trends, and Future Perspectives. , 2020, Chemical reviews.

[5]  Ying-Ying Zhang,et al.  A Ni3(OH)(COO)6 −based MOF from C3 symmetric ligands: Structure and heterogeneous catalytic activities in one-pot synthesis of imine , 2019, Microporous and Mesoporous Materials.

[6]  H. García,et al.  Mixed-Metal MOFs: Unique Opportunities in Metal-organic Framework Functionality and Design. , 2019, Angewandte Chemie.

[7]  R. Luque,et al.  Functional metal–organic frameworks for catalytic applications , 2019, Coordination Chemistry Reviews.

[8]  B. Martín‐Matute,et al.  Metal-Organic Frameworks as Catalysts for Organic Synthesis: A Critical Perspective. , 2019, Journal of the American Chemical Society.

[9]  Longlong Fan,et al.  Partial deligandation of M/Ce-BTC nanorods (M = Au, Cu, au-cu) with “Quasi-MOF” structures towards improving catalytic activity and stability , 2019, Applied Catalysis A: General.

[10]  Xintao Wu,et al.  Pore surface engineering of metal–organic frameworks for heterogeneous catalysis , 2018, Coordination Chemistry Reviews.

[11]  Xinquan Hu,et al.  Direct synthesis of imines by 9-azabicyclo-[3,3,1]nonan-N-oxyl/KOH-catalyzed aerobic oxidative coupling of alcohols and amines , 2017, Chinese Chemical Letters.

[12]  Xiaoxiao Ma,et al.  MnO2/graphene oxide: A highly efficient catalyst for imine synthesis from alcohols and amines , 2017 .

[13]  A. Morsali,et al.  High organic sulfur removal performance of a cobalt based metal-organic framework. , 2017, Journal of hazardous materials.

[14]  Yu‐Bin Dong,et al.  Dual Heterogeneous Catalyst Pd-Au@Mn(II)-MOF for One-Pot Tandem Synthesis of Imines from Alcohols and Amines. , 2017, Inorganic chemistry.

[15]  Abdullah M. Asiri,et al.  Metal-Organic Frameworks as Catalysts for Oxidation Reactions. , 2016, Chemistry.

[16]  Shuang Gao,et al.  Recent Advances in Aerobic Oxidation of Alcohols and Amines to Imines , 2015 .

[17]  K. Tomishige,et al.  Redox properties of CeO2 at low temperature: the direct synthesis of imines from alcohol and amine. , 2015, Angewandte Chemie.

[18]  S. Stahl,et al.  Practical Aerobic Oxidations of Alcohols and Amines with Homogeneous Copper/TEMPO and Related Catalyst Systems , 2014 .

[19]  Jiaqing Wang,et al.  Common metal of copper(0) as an efficient catalyst for preparation of nitriles and imines by controlling additives. , 2014, Chemical communications.

[20]  G. Seo,et al.  CO2 cycloaddition of styrene oxide over MOF catalysts , 2013 .

[21]  J. Čejka,et al.  Metal Organic Frameworks as Solid Catalysts in Condensation Reactions of Carbonyl Groups , 2013 .

[22]  J. Čejka,et al.  Comparison of the catalytic activity of MOFs and zeolites in Knoevenagel condensation , 2013 .

[23]  Xiaochun Yu,et al.  General, Green, and Scalable Synthesis of Imines from Alcohols and Amines by a Mild and Efficient Copper‐Catalyzed Aerobic Oxidative Reaction in Open Air at Room Temperature , 2012 .

[24]  M. Yus,et al.  Straightforward Synthesis of Aromatic Imines from Alcohols and Amines or Nitroarenes Using an Impregnated Copper Catalyst , 2012 .

[25]  Yugen Zhang,et al.  Copper-catalyzed highly efficient aerobic oxidative synthesis of imines from alcohols and amines , 2012 .

[26]  Lan Jiang,et al.  Direct and mild palladium-catalyzed aerobic oxidative synthesis of imines from alcohols and amines under ambient conditions. , 2011, Chemical communications.

[27]  Francesca M. Kerton,et al.  Simple copper/TEMPO catalyzed aerobic dehydrogenation of benzylic amines and anilines. , 2012, Organic & biomolecular chemistry.

[28]  Lan Jiang,et al.  Direct and mild palladium-catalyzed aerobic oxidative synthesis of imines from alcohols and amines under ambient conditions. , 2011, Chemical communications.

[29]  R. Patil,et al.  Copper‐Catalyzed Aerobic Oxidation of Amines to Imines under Neat Conditions with Low Catalyst Loading , 2011 .

[30]  H. García,et al.  Aerobic Oxidation of Benzylic Alcohols Catalyzed by Metal−Organic Frameworks Assisted by TEMPO , 2011 .

[31]  H. García,et al.  Aerobic Oxidation of Benzyl Amines to Benzyl Imines Catalyzed by Metal–Organic Framework Solids , 2010 .

[32]  Kangnian Fan,et al.  Gold supported on hydroxyapatite as a versatile multifunctional catalyst for the direct tandem synthesis of imines and oximes. , 2009, Angewandte Chemie.

[33]  Ranjit Kumar,et al.  Tandem catalysis: Direct catalytic synthesis of imines from alcohols using manganese octahedral molecular sieves , 2008 .

[34]  K. Jørgensen,et al.  One-pot organocatalytic domino Michael-aldol and intramolecular SN2 reactions. Asymmetric synthesis of highly functionalized epoxycyclohexanone derivatives. , 2006, Journal of the American Chemical Society.

[35]  Robert Raja,et al.  Design of a green one-step catalytic production of e-caprolactam (precursor of nylon-6) , 2005 .

[36]  Hong-yu Zhang,et al.  Activated Carbon Supported Ruthenium Nanoparticles Catalyzed Synthesis of Imines from Aerobic Oxidation of Alcohols with Amines , 2016, Catalysis Letters.