新型多孔双金属 H 键催化剂在通过乙烯基异构体协同氧化法制备生物指甲花基吡唑并[3,4-b]喹啉中的应用

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-11-07 DOI:10.1016/j.mcat.2024.114628
Milad Mohammadi Rasooll , Hassan Sepehrmansourie , Mohammad Ali Zolfigol , Mojtaba Hosseinifard , Seyedeh Latifeh Hosseini , Yanlong Gu
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引用次数: 0

摘要

双金属有机框架(bimetallic-MOFs)因其可调的孔隙、强度和高催化性能而被认为是很有前途的催化剂。本文设计、合成并表征了一种基于铁(Fe)和钴(Co)金属的双金属-MOF。然后,用异氰酸苯酯对合成的双金属-MOF 进行后修饰,以生成易产生氢键催化活性的脲分子。为确定合成催化剂的结构,使用了各种技术,如 SEM、XRD、BET/BJH、FT-IR、TGA/DTA、EDX 和元素图谱。在多组分反应中,MIL-88B(Fe2/Co)-UR 可作为 H 键催化剂,通过具有药用特性的适当部分生成吡唑并[3,4-b]喹啉类化合物。使用 MIL-88B(Fe2/Co)-UR 作为 H 键催化剂的特点是效率高、反应时间短和催化剂可重复使用。
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Application of a new porous bimetallic H-bond catalyst in the preparation of biological henna-based pyrazolo[3,4-b]quinolines via a cooperative vinylogous anomeric based oxidation
Bimetallic organic frameworks (bimetallic-MOFs) are considered promising catalysts due to their tunable pores, strength, and high catalytic performance. Here, a bimetallic-MOF-based on iron (Fe) and cobalt (Co) metals was designed, synthesized and characterized. Next, the synthesized bimetallic-MOFs were post-modified with phenyl isocyanate to create urea moieties that are susceptible to hydrogen bonding (H-bond) catalytic activities. Various techniques such as SEM, XRD, BET/BJH, FT-IR, TGA/DTA, EDX and elemental-mapping were used to approve the structure of the synthesized catalyst. MIL-88B(Fe2/Co)-UR acts as an H-bond catalyst in the multi-component reaction to form pyrazolo[3,4-b]quinolines via appropriate sections with medicinal properties. The features of using MIL-88B(Fe2/Co)-UR as an H-bond catalyst are increased efficiency, decreased reaction time and reusability of the catalyst.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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