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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Semnan University Press</PublisherName>
				<JournalTitle>Applied Chemistry Today</JournalTitle>
				<Issn>2981-2437</Issn>
				<Volume>5</Volume>
				<Issue>14</Issue>
				<PubDate PubStatus="epublish">
					<Year>2010</Year>
					<Month>03</Month>
					<Day>21</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Synthesis, Characterization and electrochemical Studies of a series of polypyridile Ruthenium complexes</ArticleTitle>
<VernacularTitle>Synthesis, Characterization and electrochemical Studies of a series of polypyridile Ruthenium complexes</VernacularTitle>
			<FirstPage>61</FirstPage>
			<LastPage>74</LastPage>
			<ELocationID EIdType="pii">570</ELocationID>
			
<ELocationID EIdType="doi">10.22075/chem.2017.570</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Davar</FirstName>
					<LastName>Boghaei</LastName>
<Affiliation></Affiliation>

</Author>
<Author>
					<FirstName>Mehdi</FirstName>
					<LastName>Behzad</LastName>
<Affiliation></Affiliation>
<Identifier Source="ORCID">0000-0001-5957-0778</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2017</Year>
					<Month>01</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>In this study, we report the synthesis and characterization of two new polypyridile Ruthenium Complexes, [Ru(Tttp)(opda-H2)Cl]PF6 and [Ru(Tttp)(en)(H2O)](PF6)2.3/2CH3CN. Complexes were characherized by 1HNMR, 13CNMR, IR and UV-Vis spectroscopies, Mass spectroscopy and elemental analysis. 1HNMR studies show that in [Ru(Tttp)(opda-H2)Cl]PF6 , orthophenylenediamine is coordinated as (bqdi) or (s-bqdi) by loosing two hydrogen atoms, one from each amino groups. Electrochemiccal studies also show a redox potential at 1.55 V Vs. NHE which is duo to either RuII(bqdi)/RuIII(bqdi) or RuIII(s-bqdi)/RuIV(sbqdi) Reactions. Besides, another peak at -0.924 V is observed which due to either RuII(bqdi)/RuII(s-bqdi) or RuIII(s-bqdi)/RuII(s-bqdi). In the case of [Ru(Tttp)(en)(H2O)](PF6)2.3/2CH3CN, despite the usual coordination of chloro atom, a water molecule is coordinated. Electrochemical studies also reveal a redox peak at 1.66 Vs. NHE which is due to RuII/RuIV(O) redox reaction.</Abstract>
			<OtherAbstract Language="FA">In this study, we report the synthesis and characterization of two new polypyridile Ruthenium Complexes, [Ru(Tttp)(opda-H2)Cl]PF6 and [Ru(Tttp)(en)(H2O)](PF6)2.3/2CH3CN. Complexes were characherized by 1HNMR, 13CNMR, IR and UV-Vis spectroscopies, Mass spectroscopy and elemental analysis. 1HNMR studies show that in [Ru(Tttp)(opda-H2)Cl]PF6 , orthophenylenediamine is coordinated as (bqdi) or (s-bqdi) by loosing two hydrogen atoms, one from each amino groups. Electrochemiccal studies also show a redox potential at 1.55 V Vs. NHE which is duo to either RuII(bqdi)/RuIII(bqdi) or RuIII(s-bqdi)/RuIV(sbqdi) Reactions. Besides, another peak at -0.924 V is observed which due to either RuII(bqdi)/RuII(s-bqdi) or RuIII(s-bqdi)/RuII(s-bqdi). In the case of [Ru(Tttp)(en)(H2O)](PF6)2.3/2CH3CN, despite the usual coordination of chloro atom, a water molecule is coordinated. Electrochemical studies also reveal a redox peak at 1.66 Vs. NHE which is due to RuII/RuIV(O) redox reaction.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Ruthenium Complexes</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Amine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">electrochemistry</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://chemistry.semnan.ac.ir/article_570_a86c450b76fb8c371afead6410d55534.pdf</ArchiveCopySource>
</Article>
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