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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Institute for Color Science and Technology (ICST)</PublisherName>
				<JournalTitle>Progress in Color, Colorants and Coatings</JournalTitle>
				<Issn>2008-2134</Issn>
				<Volume>5</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>03</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Synthesis and characterization of some novel linear azo-azomethine compounds based on 1-bromo, 4-4-4-nitrophenylazo phenoxy butane</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>23</FirstPage>
			<LastPage>33</LastPage>
			<ELocationID EIdType="pii">75793</ELocationID>
			
<ELocationID EIdType="doi">10.30509/pccc.2012.75793</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>A.</FirstName>
					<LastName>Mohammadi</LastName>
<Affiliation>Department of Chemistry,Faculty of Sciences, University of Guilan</Affiliation>

</Author>
<Author>
					<FirstName>M.R.</FirstName>
					<LastName>Yazdanbakhsh</LastName>
<Affiliation>Department of Chemistry, Faculty of Sciences, University of Guilan, Rasht, Iran,</Affiliation>

</Author>
<Author>
					<FirstName>N.</FirstName>
					<LastName>Mahmoodi</LastName>
<Affiliation>Department of Chemistry, University of Guilan</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>11</Month>
					<Day>30</Day>
				</PubDate>
			</History>
		<Abstract>The reaction of some carbocyclic and heterocyclic Schiff bases with the synthesized 1-bromo, 4-[4-(4-nitrophenylazo) phenoxy] butane and formation of novel linear azo-azomethine compounds in good to excellent yields were investigated. The compounds were fully characterized by UV-Vis, FT-IR, 1H NMR spectroscopic techniques and elemental analysis. Effects of various solvents on their visible absorption spectra at a concentration of 10-5-10-6 M were estimated. The color of the dyes is discussed with respect to the substituent therein. Introduction of an electron-withdrawing group into the para-position of azomethines produces bathochromic shift of the absorption peak in all solvents. The key features of these reactions are, in turn, their operational simplicity, mild reaction conditions and easily-accessed starting materials.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Azo dye</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Schiff</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Base</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Azo</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">azomethine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Substituent effect</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Absorption spectra</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://pccc.icrc.ac.ir/article_75793_6bb61a2cc1da4e46915515e573990a0c.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
