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	<Journal> 

	<PublisherName>International Science Community Association</PublisherName>

	<JournalTitle>Research Journal of Chemical Sciences</JournalTitle> 

	<Issn>2231 - 606X</Issn>

	<Volume>1</Volume>

	<Issue>9</Issue>

	<PubDate PubStatus="ppublish"> 

	<Year>2011</Year> 

	<Month>December</Month> 

	<Day>18</Day> 

	</PubDate>

	</Journal>



	<ArticleTitle>Synthesis, Structural Investigations and Antifungal Studies on Symmetrically Substituted Metal (II) Octa-1- (3-chlorophenyl) Methanimine Phthalocyanine</ArticleTitle> 


	<FirstPage>29</FirstPage>

	<LastPage>36</LastPage>



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		<FirstName>Eruola</FirstName>

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		<LastName>A.O.</LastName>

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		<Affiliation>University of Agriculture, Abeokuta, NIGERIA </Affiliation>

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		<FirstName>Ufoegbune</FirstName>

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		<LastName>G.C.</LastName>

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		<Affiliation> Yaba College of Technology, Lagos State, NIGERIA</Affiliation>

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		<LastName>Eruola</LastName>

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		<FirstName>Abhulimen</FirstName>

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		<FirstName>Glossman-Mitnik</FirstName>

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		<LastName>D.</LastName>

		<Suffix>1</Suffix>

		<Affiliation>NANOCOSMOS Virtual Lab - Centro de Investigación en Materiales Avanzados, S.C., M. de Cervantes 120,  Complejo Industrial Chihuahua, Chihuahua, Chih. 31109, MEXICO </Affiliation>

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		<FirstName>Heda</FirstName>

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		<LastName>L.C.</LastName>

		<Suffix>1</Suffix>

		<Affiliation>Research Laboratory, S. D. Govt. College, Beawar, 305901, Rajasthan, INDIA </Affiliation>

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		<FirstName>Sharma</FirstName>

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		<LastName>Pramod B.</LastName>

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		<FirstName>Gordillo-Delgadoa</FirstName>

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		<LastName>F.</LastName>

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		<Affiliation>Laboratorio de Optoelectrónica, Universidad del Quindío Apdo. Postal 2639 Armenia, COLOMBIA </Affiliation>

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		<FirstName>Marinb</FirstName>

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		<LastName>E.</LastName>

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		<Affiliation> Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada del I.P.N, Unidad Legaria. 694, Col. Irrigación, D.F, MÉXICO</Affiliation>

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		<FirstName>CortÃ©s-HernÃ¡ndez</FirstName>

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		<LastName>D.M.</LastName>

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		<FirstName>Shrivastava</FirstName>

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		<LastName>Shikha</LastName>

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		<Affiliation>Govt. V.Y.T. P.G. Autonomous Collage, Durg, C.G., INDIA </Affiliation>

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		<FirstName>Dwivedi</FirstName>

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		<LastName>Sushma</LastName>

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		<FirstName>Fasiulla</FirstName>

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		<LastName>K.R.</LastName>

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		<Affiliation>Dept. of Chemistry, Manipal Institute of Technology, Manipal, Udupi Dist. –576104, Karnataka, INDIA </Affiliation>

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		<FirstName>Reddy</FirstName>

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		<LastName>Venugopala</LastName>

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		<Affiliation> Dept. of Studies in Industrial Chemistry, Sahyadri Science College, Shimoga -577201 Shimoga Dist., Karnataka, INDIA </Affiliation>

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		<FirstName>Keshavayya</FirstName>

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		<LastName>J.</LastName>

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		<Affiliation> Dept. of Studies in Chemistry, Kuvempu University, Janna Sahyadri, Shankaragatta-577451, Shimoga Dist., Karnataka, INDIA </Affiliation>

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		<FirstName>Moinuddin Khan</FirstName>

		<MiddleName> </MiddleName>

		<LastName>M.H.</LastName>

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		<Affiliation>  Dept. of Chemistry, JNNC of Engineering, Shimoga. Dist., Karnataka, INDIA </Affiliation>

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		<LastName>Anitha</LastName>

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		<LastName>Vittala</LastName>

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	<PublicationType>Research Paper</PublicationType>


	<History>  
	<PubDate PubStatus="received">
	<Year>2011</Year>
	<Month>8</Month>
	<Day>18</Day>
	</PubDate>
	<PubDate PubStatus="accepted">										
	<Year>2011</Year> 
	<Month>December</Month>									
	<Day>18</Day> 
	</PubDate>

	</History>
	<Abstract> Metallophthalocyanine (M = Cu, Co, Ni, Zn) carrying eight (3-chlorophenyl) methanimine groups at peripheral positions were synthesized by an efficient simple and novel method. The precursor octaamino metal (II) phthalocyanines were synthesized by the reduction of the corresponding nitro metal phthalocyanines. The dark green octa-1-(3- chlorophenyl) methanimine phthalocyanine derivatives were characterized by elemental analysis, magnetic susceptibility, electronic, IR and powder X-ray diffraction studies to check the purity, structural integrity and crystalline properties of the complexes. Magnetic susceptibility studies on Co (II) and Cu (II) octa-1-(3-chlorophenyl) methanimine phthalocyanine complexes exhibit a variation of the magnetic moments as a function of field strength indicating the presence of inters molecular co-operative effect. The title complexes were screened for antifungal activity. </Abstract>

	<CopyrightInformation>Copyright@ International Science Community Association</CopyrightInformation>

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