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<Article>
<Journal>
				<PublisherName>Iranian Nanotechnology Society</PublisherName>
				<JournalTitle>International Journal of Nanoscience and Nanotechnology</JournalTitle>
				<Issn>1735-7004</Issn>
				<Volume>13</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2017</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>One-Pot Facile Synthesis of New 1, 2, 4-‎Triazolidine Derivatives Using Sodium ‎Borohydride and Fe3O4 Magnetic ‎Nanoparticles (MNPs)‎</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>347</FirstPage>
			<LastPage>357</LastPage>
			<ELocationID EIdType="pii">28653</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>N.</FirstName>
					<LastName>Nami</LastName>
<Affiliation>Department of Chemistry, Qaemshahr Branch, Islamic Azad University, Qaemshahr, Iran.‎</Affiliation>
<Identifier Source="ORCID">0000-0003-2656-3410</Identifier>

</Author>
<Author>
					<FirstName>S.</FirstName>
					<LastName>Lale Mohammadi</LastName>
<Affiliation>Department of Chemistry, Qaemshahr Branch, Islamic Azad University, Qaemshahr, Iran.‎</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>11</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>&lt;em&gt;   One-pot reaction of aldehydes with thiosemicarbazide was performed using NaBH&lt;sub&gt;4 &lt;/sub&gt;and Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; magnetic nanoparticles (MNPs).&lt;/em&gt; &lt;em&gt;The reaction mixture of thiosemicarbazide and carbonyl compounds was stirred under reflux condition in the present of Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; MNPs and NaBH&lt;sub&gt;4&lt;/sub&gt;&lt;/em&gt;.&lt;em&gt;The optimum amount of Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; MNPs was 5 mol% in ethanol.&lt;/em&gt; &lt;em&gt;The precipitate was appeared immediately to obtain 1,2,4-triazolidine. The reflux continued 20 min after addition of NaBH&lt;sub&gt;4&lt;/sub&gt; to complete the reaction. 1,2,4-triazolidines were obtained in good to excellent yields.&lt;/em&gt; &lt;em&gt;All products were identiﬁed by GC-Mass, NMR, FT-IR spectra and physical data with those of authentic samples. The magnetically recoverable iron oxide nanoparticles are found to be efficient for synthesis of 1,2,4-triazolidine derivatives. &lt;/em&gt;&lt;em&gt;The Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4 &lt;/sub&gt;MNPs were simply recovered by external magnetic field and exhibited exceptionally &lt;em&gt;high&lt;/em&gt; catalytic activity in green chemistry and enhanced reaction speed without pollution. Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4 &lt;/sub&gt;MNPs could be successfully recovered and reuse. This method is easier and less expensive than the other methods.&lt;/em&gt;</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Fe3O4 magnetic nanoparticles</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Thiosemicarbazone</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">2</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">4-triazolidine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NaBH4.‎</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.ijnnonline.net/article_28653_638c1a4f003b46aad4aa5cf3f424d215.pdf</ArchiveCopySource>
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