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    <title>NISCAIR Online Periodicals Repository Collection: IJC-A Vol.49A(01) [January 2010]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7147</link>
    <description />
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        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7192" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7191" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7190" />
        <rdf:li resource="http://nopr.niscair.res.in/handle/123456789/7189" />
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  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7192">
    <title>Undoped, single phase barite BaCrO&lt;sub&gt;4&lt;/sub&gt; photocatalyst for the degradation of methylene blue under visible light</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7192</link>
    <description>Title: Undoped, single phase barite BaCrO&lt;sub&gt;4&lt;/sub&gt; photocatalyst for the degradation of methylene blue under visible light
&lt;br/&gt;
&lt;br/&gt;Authors: Thakare, Sanjay R; Patil, S R; Choudhari, M D
&lt;br/&gt;
&lt;br/&gt;Abstract: The&lt;b&gt; &lt;/b&gt;photoassisted degradation of a phenothiazine dye, methylene blue, has been examined in aqueous dispersions under visible irradiation at wavelengths greater than 400 nm with BaCrO&lt;sub&gt;4&lt;/sub&gt; and bare TiO&lt;sub&gt;2&lt;/sub&gt;. Spectral changes during the photocatalytic degradation of methylene blue suggest that the de-methylation is an initiation process of photocatalysis reaction followed by ring opening and finally mineralisation into mineral acid and water. Comparative study shows that BaCrO&lt;sub&gt;4&lt;/sub&gt; is a better photocatalyst than bare TiO&lt;sub&gt;2 &lt;/sub&gt;under visible light irradiation. COD analysis suggests that the degradation of methylene blue is due to photocatalysis and not due to any other reason. Catalytic poisoning is observed for both the photocatalysts.&lt;b&gt;&lt;/b&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 54-58</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7191">
    <title>Chemoselective hydrogenation of crotonaldehyde to crotyl alcohol over Pt/Ce&lt;sub&gt;x&lt;/sub&gt;Sm&lt;sub&gt;1-x&lt;/sub&gt;O&lt;sub&gt;2-&lt;img src='/image/spc_char/delta1.gif' border=0&gt;&lt;/sub&gt; catalysts</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7191</link>
    <description>Title: Chemoselective hydrogenation of crotonaldehyde to crotyl alcohol over Pt/Ce&lt;sub&gt;x&lt;/sub&gt;Sm&lt;sub&gt;1-x&lt;/sub&gt;O&lt;sub&gt;2-&lt;img src='/image/spc_char/delta1.gif' border=0&gt;&lt;/sub&gt; catalysts
&lt;br/&gt;
&lt;br/&gt;Authors: Jin, Ling-Yun; Tao, Li-Ping; Liu, Xi-Jing; Xie, Guan-Qun; Lu, Ji-Qing; Luo, Meng-Fei
&lt;br/&gt;
&lt;br/&gt;Abstract: Pt/Ce&lt;sub&gt;x&lt;/sub&gt;Sm&lt;sub&gt;1-x&lt;/sub&gt;O&lt;sub&gt;2-&lt;/sub&gt;&lt;sub&gt;&lt;img src='/image/spc_char/delta1.gif' border=0&gt;&lt;/sub&gt; catalysts have been prepared with impregnation method using H&lt;sub&gt;2&lt;/sub&gt;PtCl&lt;sub&gt;6&lt;/sub&gt; as precursor. The selective vapor-phase hydrogenation of crotonaldehyde to crotyl alcohol over the catalysts has also been studied. It is found that introduction of Sm promotes the selective hydrogenation of C=O bond to crotyl alcohol due to formation of strong Lewis acidic sites. For Pt/Ce&lt;sub&gt;0.8&lt;/sub&gt;Sm&lt;sub&gt;0.2&lt;/sub&gt;O&lt;sub&gt;2-&lt;img src='/image/spc_char/delta1.gif' border=0&gt;&lt;/sub&gt; catalysts, with increasing reduction temperatures, the crotonaldehyde conversion decreases while the selectivity to crotyl alcohol increases. Also, during the reaction process there is carbon deposition on the catalyst surface, which results in decrease, both in the catalytic activity as well as selectivity.
&lt;br/&gt;
&lt;br/&gt;Page(s): 49-53</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7190">
    <title>Synthesis and novel fluorescence phenomenon of terbium(III) complex with N, N′, N″-tris (2-benzimidazolmethyl) amine</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7190</link>
    <description>Title: Synthesis and novel fluorescence phenomenon of terbium(III) complex with N, N′, N″-tris (2-benzimidazolmethyl) amine
&lt;br/&gt;
&lt;br/&gt;Authors: Yang, Tianlin; Gao, Min; Qin, Wenwu; Yang, Jinhui
&lt;br/&gt;
&lt;br/&gt;Abstract: A benzimidazole ligand with a tripodal structure, N, N′, N″-tris (2-benzimidazolmethyl) amine, and its terbium (Ⅲ) complex has been synthesized. The complex has been characterized by element analysis, IR spectra, mass spectra, thermal analysis and molar conductivity. The terbium ion is found to coordinate with the nitrogen atoms（=N-）of imidazole ring and the bridgehead nitrogen atom. The fluorescence properties of the complex in aqueous solutions have been studied. Under excitation of UV light, the complex exhibits characteristic fluorescence of terbium ion. The luminescence of terbium complex in aqueous solutions is strongly enhanced by H&lt;sup&gt;+&lt;/sup&gt; concentration. This phenomenon makes the new complex favorable for use in fluorescence switches and sensors. The mechanism of the fluorescence enhancement by protonation of the nitrogen atoms（-NH-）of imidazole ring is due to the suppressed photoinduced electron transfer fluorescence quenching on addition of acid.
&lt;br/&gt;
&lt;br/&gt;Page(s): 45-48</description>
  </item>
  <item rdf:about="http://nopr.niscair.res.in/handle/123456789/7189">
    <title>Synthesis and crystal structure of a triprotonated decavanadate, [(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;)(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;3&lt;/sub&gt;N]&lt;sub&gt;3&lt;/sub&gt;[H&lt;sub&gt;3&lt;/sub&gt;V&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;28&lt;/sub&gt;].3H&lt;sub&gt;2&lt;/sub&gt;O</title>
    <link>http://nopr.niscair.res.in/handle/123456789/7189</link>
    <description>Title: Synthesis and crystal structure of a triprotonated decavanadate, [(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;)(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;3&lt;/sub&gt;N]&lt;sub&gt;3&lt;/sub&gt;[H&lt;sub&gt;3&lt;/sub&gt;V&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;28&lt;/sub&gt;].3H&lt;sub&gt;2&lt;/sub&gt;O
&lt;br/&gt;
&lt;br/&gt;Authors: Dewan, Anindita; Kakati, Dilip K; Das, Birinchi K
&lt;br/&gt;
&lt;br/&gt;Abstract: The title compound, [(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;)(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;3&lt;/sub&gt;N]&lt;sub&gt;3&lt;/sub&gt;[H&lt;sub&gt;3&lt;/sub&gt;V&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;28&lt;/sub&gt;].3H&lt;sub&gt;2&lt;/sub&gt;O, has been obtained by treating V&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;5 &lt;/sub&gt;with H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; in presence of benzyltrimethylammonium chloride and characterised. The crystal structure of the compound has been determined. The protonation sites on the cage surface of the decavanadate [H&lt;sub&gt;3&lt;/sub&gt;V&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;28&lt;/sub&gt;]&lt;sup&gt;3-&lt;/sup&gt; anion have been clearly identified. Intermolecular O-H...O hydrogen bonds involving the surface protons leads to the formation of an unprecedented zigzag chain of the [H&lt;sub&gt;3&lt;/sub&gt;V&lt;sub&gt;10&lt;/sub&gt;O&lt;sub&gt;28&lt;/sub&gt;]&lt;sup&gt;3-&lt;/sup&gt; anions.
&lt;br/&gt;
&lt;br/&gt;Page(s): 39-44</description>
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