echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Chemicals Industry > Chemical Technology > Preparation of N, O ligand chelating resin

    Preparation of N, O ligand chelating resin

    • Last Update: 2022-01-01
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Amino carboxylic acids are the most important series of such resins, and iminodiacetate (IDA) resins are the most important commercial chelating resins


    ① Introducing ligands such as styrene iminodiacetic acid type chelating resins on the polymer carrier through polymer reaction is prepared by introducing functional groups into the polystyrene matrix obtained by styrene-divinylbenzene copolymerization


    Synthesis of iminodiacetic acid resin:

    Synthesis of O-hydroxybenzyl iminodiacetic acid:

    ②Polymerization reaction of vinyl monomers containing amino carboxylic acid First synthesize the vinyl monomers containing amino carboxylic acid, and then carry out the polymerization reaction


    In addition, styrene-based IDA resins can be synthesized from chloromethylated intermediates or aminated products (weakly basic anion exchange resins with primary amino groups) as starting materials


    Hydrophobic chloromethyl cross-linked polystyrene is difficult to react with water-soluble nucleophilic amino carboxylic acid, so it is impossible to use such reagents for amination and directly obtain IDA resin


    Acrylic and other polycondensation polyamine resins and meta- or para-phenylene diamines can also be used to prepare IDA resins


    When preparing IDA resin by the above-mentioned various methods, the chlorocarboxylic acid used can be β-chloropropionic acid, γ-chlorobutyric acid, etc.


    There are other methods for preparing imine carboxylic acid resins, but styrene-based IDA is still the most important


    8-Hydroxyquinoline resin is also N, O coordination and integration agent, and there are many synthetic methods


    Firstly, 8-hydroxyquinoline is chloromethylated, and then reacted with primary amine resin at 100°C for 10 hours to obtain spherical chelating resin:

    Using 5-chloromethyl-8 quinoline, under the catalysis of SnCl 4 and macroporous cross-linked polystyrene for Friedel-Crafts reaction, 8-hydroxyquinoline resin can also be obtained


    Schiff base is also a large class of N, O chelating resins


    The structure of the chelate formed with Cu 2+ is:

    The structure of the Schiff base resin synthesized by the condensation of 2,6-diamino-p-cresol and glyoxal is

    The chelate structure formed with Cu 2+ is similar to the above integrant


    Related link: Condensation type anion exchange resin

     

     

    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Related Articles

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.