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            <name>Title</name>
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                <text>Articles</text>
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    <name>Article</name>
    <description>Faculty Publications -Articles</description>
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      <name>Dublin Core</name>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>Crystal structures of 1,7-bis(furyl)-4-(1,3-dithiolan-2-ylidene)-1, 6-heptadiene-3,5-dione and 1,7-bis(thienyl)-4-(1,3-dithiolan- 2-ylidene)-1,6-heptadiene-3,5-dione</text>
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              <text>1,7-Bis(thienyl)-4-(1,3-dithiolan-2-ylidene)-1; 17-Bis(furyl)- 4-(1,3-dithiolan-2-ylidene)-1,6- heptadiene-3,5-dione; Crystal structure</text>
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              <text>The title compounds (bis(alkenoyl) ketene dithioacetals) were prepared starting from the cyclic acyl ketene dithioacetal and aromatic aldehydes. These compounds were characterized by IR, 1H NMR, mass spectral studies and X-ray crystal structure analysis. The bis(furyl) ketene dithioacetal crystallized in the space group P1? with unit cell dimensions a = 7.7626(12) , b = 9.0217(13) , c = 26.827(5) , ? = 86.271(14), ? = 87.643(14), ? = 66.286(11) and the structure was refined to an R-factor of 0.0528 while bis(thienyl) ketene dithioacetal crystallized in the space group P21/c with unit cell dimensions a = 10.2433(9) , b = 10.4142(6) , c = 18.0973(18) , ? = 106.0 and the structure was refined to an R-factor of 0.0446. The ketenedithioacetal functionality present between the carbonyl groups prevents the possibility of keto-enol tautomerization in these compounds. In both the crystal structures, the crystal packing is stabilized by C-H?O hydrogen bonds as well as van der Waals interactions.  Springer Science+Business Media, LLC 2011.</text>
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          <name>Creator</name>
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              <text>Bubbly S.G.; Gudennavar S.B.; Viswam D.; Sudarsanakumar C.</text>
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              <text>Journal of Chemical Crystallography, Vol-41, No. 9, pp. 1310-1316.</text>
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          <name>Date</name>
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              <text>2011-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1007/s10870-011-0095-6" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1007/s10870-011-0095-6&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-80055020894&amp;amp;doi=10.1007%2Fs10870-011-0095-6&amp;amp;partnerID=40&amp;amp;md5=9a614542b595bd59f9a6d41087b51646" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-80055020894&amp;amp;doi=10.1007%2fs10870-011-0095-6&amp;amp;partnerID=40&amp;amp;md5=9a614542b595bd59f9a6d41087b51646&lt;/a&gt;</text>
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              <text>Restricted Access</text>
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          <description>A related resource</description>
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              <text>ISSN: 10741542</text>
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              <text>Online</text>
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              <text>English</text>
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          <name>Type</name>
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              <text>Article</text>
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              <text>Bubbly S.G., Department of Physics, Christ University, Bangalore 560 029, Karnataka, Hosur Road, India; Gudennavar S.B., Department of Physics, Christ University, Bangalore 560 029, Karnataka, Hosur Road, India; Viswam D., Department of Chemistry, Sree Narayana College, Cherthala 688 524, Kerala, India; Sudarsanakumar C., School of Pure and Applied Physics, Mahatma Gandhi University, Kottayam 686 560, Kerala, India</text>
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