Boron based intramolecular heterocyclic frustrated Lewis pairs as organocatalysts for CO2 adsorption and activation

被引:14
|
作者
Faizan, Mohmmad [1 ]
Pawar, Ravinder [1 ]
机构
[1] Natl Inst Technol Warangal NITW, Dept Chem, Warangal 506004, Telangana, India
关键词
atoms in molecule (AIM) theory; density functional theory (DFT); frustrated Lewis pairs (FLP); intramolecular frustrated Lewis pairs (IFLP); natural bond orbitals (NBO); CARBON-DIOXIDE BINDING; EFFICIENT CYCLOADDITION; METHANOL SYNTHESIS; PROTON-TRANSFER; HYDROGENATION; REDUCTION; CATALYSTS; EPOXIDES; NANOPARTICLES; COMPLEX;
D O I
10.1002/jcc.26949
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The massive increase in the amount of carbon dioxide (CO2) in the atmosphere has led to serious environmental problems. One of the best ways to tackle this problem is the CO2 capture and its utilization as a C1 carbon source for the production of industrially valuable chemicals. But the thermodynamic stability of the CO2 molecule poses a great challenge in its transformation. Since the last two decades, various metal-based and organic catalysts have been developed for the adsorption and activation of CO2. Among all the catalysts the Frustrated Lewis pairs (FLPs) have been shown great potential in CO2 capture and conversion. Thus, in the present work, Intramolecular Frustrated Lewis pairs (IFLP) based on N-Heterocycles with boron group functionalization at the alpha-position to N has been theoretically investigated for CO2 activation. Thorough orbital analysis has been carried out to investigate the reactivity of the proposed catalytic systems. The result shows that the considered IFLPs are capable of activating CO2 with minimum energy requirements. The CO2 activation energy range between 8 and 14 kcal/mol. The non-polar solvent was found to be the suitable medium for the reaction. Also, the reversibility of the adducts formed with the IFLPs can be controlled by appropriate substitution at B atom in the IFLPs.
引用
收藏
页码:1474 / 1483
页数:10
相关论文
共 50 条
  • [1] Implications of CO2 Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+ Frustrated Lewis Pairs
    von Wolff, N.
    Lefevre, G.
    Berthet, J. -C.
    Thuery, P.
    Cantat, T.
    ACS CATALYSIS, 2016, 6 (07): : 4526 - 4535
  • [2] Homogeneous and Heterogeneous Frustrated Lewis Pairs for the Activation and Transformation of CO2
    Du, Tao
    Zhang, Peng
    Jiao, Zhen
    Zhou, Jiancheng
    Ding, Yuxiao
    CHEMISTRY-AN ASIAN JOURNAL, 2024, 19 (12)
  • [3] Activation of Small Molecules and Hydrogenation of CO2 Catalyzed by Frustrated Lewis Pairs
    Pal, Ranita
    Ghara, Manas
    Chattaraj, Pratim Kumar
    CATALYSTS, 2022, 12 (02)
  • [4] Borane derivatives of five-membered N-heterocyclic rings as frustrated Lewis pairs: activation of CO2
    Ferrer, Maxime
    Alkorta, Ibon
    Oliva-Enrich, Josep M.
    Elguero, Jose
    STRUCTURAL CHEMISTRY, 2023, 34 (04) : 1591 - 1601
  • [5] Borane derivatives of five-membered N-heterocyclic rings as frustrated Lewis pairs: activation of CO2
    Maxime Ferrer
    Ibon Alkorta
    Josep M. Oliva-Enrich
    José Elguero
    Structural Chemistry, 2023, 34 : 1591 - 1601
  • [6] Advances in CO2 activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions
    Khan, Md. Nasim
    van Ingen, Yara
    Boruah, Tribani
    Mclauchlan, Adam
    Wirth, Thomas
    Melen, Rebecca L.
    CHEMICAL SCIENCE, 2023, 14 (47) : 13661 - 13695
  • [7] Small Molecule Activation with Intramolecular "Inverse" Frustrated Lewis Pairs
    Manankandayalage, Chamila
    Unruh, Daniel K.
    Krempner, Clemens
    CHEMISTRY-A EUROPEAN JOURNAL, 2021, 27 (20) : 6263 - 6273
  • [8] Stoichiometric Reduction of CO2 to CO by Aluminum-Based Frustrated Lewis Pairs
    Menard, Gabriel
    Stephan, Douglas W.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (36) : 8396 - 8399
  • [9] Microfluidic Studies of CO2 Sequestration by Frustrated Lewis Pairs
    Voicu, Dan
    Abolhasani, Milad
    Choueiri, Rachelle
    Lestari, Gabriella
    Seiler, Caroline
    Menard, Gabriel
    Greener, Jesse
    Guenther, Axel
    Stephan, Douglas W.
    Kumacheva, Eugenia
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (10) : 3875 - 3880
  • [10] Advances in "frustrated Lewis pairs" hydrogenations and CO2 reduction
    Stephan, Douglas W.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245