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<Article>
<Journal>
				<PublisherName>Semnan University Press</PublisherName>
				<JournalTitle>Applied Chemistry Today</JournalTitle>
				<Issn>2981-2437</Issn>
				<Volume>10</Volume>
				<Issue>36</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>09</Month>
					<Day>23</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Synthesis and Characterization of Azospiropyran Photochromic Dyes Based Para Nitro Aniline</ArticleTitle>
<VernacularTitle>Synthesis and Characterization of Azospiropyran Photochromic Dyes Based Para Nitro Aniline</VernacularTitle>
			<FirstPage>67</FirstPage>
			<LastPage>78</LastPage>
			<ELocationID EIdType="pii">2808</ELocationID>
			
<ELocationID EIdType="doi">10.22075/chem.2018.2637.</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>24</Day>
				</PubDate>
			</History>
		<Abstract>nitro-derived of azospiroptran has been synthesized by the reaction of Â Fischer&#039;s base with 5-((4-nitrophenyl)diazenyl) 2-hydroxyÂ  benzaldehyde. 5-((4-nitrophenyl)diazenyl) 2-hydroxyÂ  benzaldehyde was obtained from the diazocoupling reaction of para nitro aniline with 2-hydroxyÂ  benzaldehyde.With reduction NO2 group another-derived of azospiropyran was obtained. These compounds were characterized by IR and 1H,13C-NMR spectral studies. Investigating their photochromic properties Â Â showed an increasing rate of coloration reaction in the present of substitution NH2.</Abstract>
			<OtherAbstract Language="FA">nitro-derived of azospiroptran has been synthesized by the reaction of Â Fischer&#039;s base with 5-((4-nitrophenyl)diazenyl) 2-hydroxyÂ  benzaldehyde. 5-((4-nitrophenyl)diazenyl) 2-hydroxyÂ  benzaldehyde was obtained from the diazocoupling reaction of para nitro aniline with 2-hydroxyÂ  benzaldehyde.With reduction NO2 group another-derived of azospiropyran was obtained. These compounds were characterized by IR and 1H,13C-NMR spectral studies. Investigating their photochromic properties Â Â showed an increasing rate of coloration reaction in the present of substitution NH2.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Photochrom</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Azospiropyran</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Diazocoupling</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Merocyanine</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://chemistry.semnan.ac.ir/article_2808_d0010a6f34908640a4a6da2389772a78.pdf</ArchiveCopySource>
</Article>
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