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<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>8</Volume>
<Issue>3</Issue>
<PubDate PubStatus="epublish">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>Silica-anchored Cu(I) aminothiophenol complex: An efficient heterogeneous catalyst for synthesis of 1,4-disubstituted 1,2,3-triazoles in water</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi"></ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Mohammad</FirstName>
<LastName>Bakherad</LastName>
<Affiliation>Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Ali</FirstName>
<LastName>Keivanloo</LastName>
<Affiliation>Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Amir Hossein</FirstName>
<LastName>Amin</LastName>
<Affiliation>Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Pooya</FirstName>
<LastName>Ghmari</LastName>
<Affiliation>Faculty of Chemistry, Shahrood University of Technology, Shahrood, Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</History>
<Abstract>An efficient method has been developed for synthesis of 1,4-disubstituted 1,2,3-triazoles using the silica-anchored Cu(I) aminothiophenol complex [SiO2-AT-Cu(I)] as a novel heterogeneous catalyst. The prepared catalyst is characterized by the FT-IR spectroscopy, and TGA, SEM, and ICP techniques. Terminal alkynes react with aroyl bromides and sodium azide in the presence of CuI anchored on silica in water at 80°C. The reactions exclusively generate the corresponding regiospecific 1,4-disubstituted 1,2,3-triazoles in good yields. The attractive features of this method are the simple procedure, clean reaction, use of a reusable catalyst, easy workup, and performing a click reaction in water. Moreover, the catalyst can be removed from the reaction mixture by means of simple filtration, and used again for up to five runs without a remarkable loss in its activity.</Abstract>
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<Object Type="keyword">
<Param Name="value">3-triazole</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Aroyl bromide</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Click reaction</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Silica-supported</Param>
</Object>
</ObjectList>
</Article>
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