Copper doped K-birnessite as an efficient catalyst for the synthesis of 2-aryl benzimidazoles

被引:1
|
作者
Bilge Eren
Huseyin Gumus
机构
[1] Bilecik Seyh Edebali University,Department of Chemistry, Faculty of Science and Arts
关键词
Benzimidazole; Birnessite; Cu doped birnessite; XRD;
D O I
暂无
中图分类号
学科分类号
摘要
In this study, an efficient and highly selective synthesis of 2-aryl benzimidazoles from the reaction of o-phenylenediamine and aromatic aldehydes in the presence of birnessite type copper doped manganese oxide (BCM) is reported. BCM was synthesized by the one-step hydrothermal method. Recycling of BCM up to five runs was investigated with appreciable yield and selectivity of the products. The best overall yields and selectivities were obtained in methanol. The crystal structure and thermal stability of BCM are characterized by using XRD, IR and thermal analysis techniques. The acid sites of BCM were investigated by IR using pyridine as a molecular probe. The improved catalytic activity observed in the BCM catalyst was associated to a high lattice oxygen mobility and availability due to the formation of Cu–O–Mn bridges.
引用
收藏
页码:571 / 582
页数:11
相关论文
共 50 条
  • [1] Copper doped K-birnessite as an efficient catalyst for the synthesis of 2-aryl benzimidazoles
    Eren, Bilge
    Gumus, Huseyin
    REACTION KINETICS MECHANISMS AND CATALYSIS, 2015, 114 (02) : 571 - 582
  • [2] Magnetic Ionic Liquid [bmim][FeCl4] as an Efficient Catalyst for the Synthesis of 2-Aryl Benzimidazoles and 2-Aryl Benzothiazoles Derivatives
    Sayyahi, Soheil
    Shabani, Sara
    Ghasemi, Sara
    Azin, Atena
    Hasani, Seyyed Morteza
    ORIENTAL JOURNAL OF CHEMISTRY, 2015, 31 (03) : 1773 - 1778
  • [3] AN EFFICIENT AND MILD SYNTHESIS OF 2-ARYL BENZIMIDAZOLES IN AQUEOUS MEDIA
    Sonar, Jayant P.
    Pardeshi, Sandeep D.
    Pawar, Shivaji S.
    Thore, Shivaji N.
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY, 2012, 21 (04) : 315 - 318
  • [4] Cobalt ferrite magnetic nanoparticles as highly efficient catalyst for the mechanochemical synthesis of 2-aryl benzimidazoles
    Borade, Ravikumar M.
    Kale, Swati B.
    Tekale, Sunil U.
    Jadhav, K. M.
    Pawar, Rajendra P.
    CATALYSIS COMMUNICATIONS, 2021, 159 (159)
  • [5] A simple and efficient mechanochemical route for the synthesis of 2-aryl benzothiazoles and substituted benzimidazoles
    Banerjee, Mainak
    Chatterjee, Amrita
    Kumar, Vikash
    Bhutia, Zigmee T.
    Khandare, Dipratn G.
    Majik, Mahesh S.
    Roy, Biswajit Gopal
    RSC ADVANCES, 2014, 4 (74) : 39606 - 39611
  • [6] Simple, Efficient, and Applicable Route for Synthesis of 2-Aryl(Heteroaryl)-Benzimidazoles at Room Temperature Using Copper Nanoparticles on Activated Carbon as a Reusable Heterogeneous Catalyst
    Hashem Sharghi
    Reza Khalifeh
    Seyed Gholamhossein Mansouri
    Mahdi Aberi
    Mohammad Mehdi Eskandari
    Catalysis Letters, 2011, 141 : 1845 - 1850
  • [7] Simple, Efficient, and Applicable Route for Synthesis of 2-Aryl(Heteroaryl)-Benzimidazoles at Room Temperature Using Copper Nanoparticles on Activated Carbon as a Reusable Heterogeneous Catalyst
    Sharghi, Hashem
    Khalifeh, Reza
    Mansouri, Seyed Gholamhossein
    Aberi, Mahdi
    Eskandari, Mohammad Mehdi
    CATALYSIS LETTERS, 2011, 141 (12) : 1845 - 1850
  • [8] Biogenic Ag-nanoparticles as heterogeneous catalyst for synthesis of 2-aryl benzimidazoles at room temperature
    Saikia, Eramoni
    Chetia, Bolin
    INDIAN JOURNAL OF CHEMISTRY SECTION A-INORGANIC BIO-INORGANIC PHYSICAL THEORETICAL & ANALYTICAL CHEMISTRY, 2016, 55 (05): : 537 - 543
  • [9] Xanthan Sulfuric Acid: An Efficient Bio-supported and Recyclable Solid Acid Catalyst for the Synthesis of 2-Aryl Thiadiazolo Benzimidazoles
    Kuarm, B. Suresh
    Janardan, B.
    Crooks, Peter A.
    Rajitha, B.
    CHINESE JOURNAL OF CHEMISTRY, 2012, 30 (04) : 947 - 950
  • [10] Synthesis and Antifungal Activity of Substituted 2-Aryl Benzimidazoles Derivatives
    Huang, Daye
    Qiu, Fang
    Zhang, Zhigang
    Shi, Liqiao
    Cao, Chunxia
    Ke, Shaoyong
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2019, 56 (09) : 2494 - 2498