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    <name>Article</name>
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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>Role of supramolecular interactions in crystal packing of Strandberg-type cluster-based hybrid solids</text>
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          <name>Subject</name>
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              <text>electrochemical behavior; Phosphomolybdate; Strandberg-type; supramolecular interactions</text>
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              <text>Abstract: Two new Strandberg-type cluster-based phosphomolybdates {H-2a3mp}5[{PO3(OH)}{PO4}Mo5O15], 1 and {H-2a4mp}5[{PO3(OH)}{PO4}Mo5O15]6H2O, 2 have been crystallized via solvent evaporation technique using 2-amino-3-methylpyridine (2a3mp) and 2-amino-4-methylpyridine (2a4mp) respectively. The solids were characterized using single-crystal X-ray diffraction, powder X-ray diffraction, fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy and cyclic voltammetry. The solid 1 crystallized in monoclinic system with space group P21/c, a = 8.394(1), b = 27.398(6), c = 21.521(4)  ? = 97.68(3), Z = 4. The solid 2 crystallized in triclinic system with space group P-1, a = 11.728(1), b = 14.234(1), c = 19.589(1)  ? = 68.906(3), ? = 89.454(3), ? = 66.559(3), Z = 2. The solids 1 and 2 formed a supramolecular framework stabilized by hydrogen bonding interaction between cluster anions and organic moieties. CH? interactions between the organic moieties reinforced the crystal packing in 1 and 2. While crystal packing effects resulted in the formation of solvent-accessible voids in 1; aggregation of lattice water molecules in 2 facilitated the formation of pentameric water cluster. In addition, electrochemical behavior of 1 and 2 has also been investigated. Graphic abstract: Two new Strandberg-type cluster based phosphomolybdates, 1 and 2 have been crystallized via solvent evaporation technique using 2-amino-3-methylpyridine and 2-amino-4-methylpyridine. Detailed structural analysis revealed the role of supramolecular interactions in the crystal packing of these solids. In addition, electrochemical behavior of 1 and 2 has also been investigated.[Figure not available: see fulltext.]  2020, Indian Academy of Sciences.</text>
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          <name>Creator</name>
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              <text>Joseph J.; Winson C.; Singh B.; Jose J.; Thomas J.</text>
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              <text>Journal of Chemical Sciences, Vol-132, No. 1</text>
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              <text>Springer</text>
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          <name>Date</name>
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              <text>2020-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1007/s12039-020-01826-w" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1007/s12039-020-01826-w&lt;/a&gt;
&lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85092164214&amp;amp;doi=10.1007%2Fs12039-020-01826-w&amp;amp;partnerID=40&amp;amp;md5=c667747bb8e41f49d3d82bd4f5d93532" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/inward/record.uri?eid=2-s2.0-85092164214&amp;amp;doi=10.1007%2fs12039-020-01826-w&amp;amp;partnerID=40&amp;amp;md5=c667747bb8e41f49d3d82bd4f5d93532&lt;/a&gt;</text>
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              <text>ISSN: 9743626; CODEN: JCSBB</text>
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          <name>Format</name>
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              <text>Online</text>
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          <name>Language</name>
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              <text>English</text>
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              <text>Joseph J., Centre for Sustainability Science, Research &amp;amp; PG Department of Chemistry, St. Thomas College (Autonomous), Thrissur, 680 001, Kerala, India; Winson C., Centre for Sustainability Science, Research &amp;amp; PG Department of Chemistry, St. Thomas College (Autonomous), Thrissur, 680 001, Kerala, India; Singh B., Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110 016, India; Jose J., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560 029, India; Thomas J., Centre for Sustainability Science, Research &amp;amp; PG Department of Chemistry, St. Thomas College (Autonomous), Thrissur, 680 001, Kerala, India</text>
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