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html/0/3/9/0395f1a8-44ec-4898-8dc5-c2d952c52993/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\3\9\0395f1a8-44ec-4898-8dc5-c2d952c52993\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Rouchal, M."/><meta name="DC.creator" content="Necas, M."/><meta name="DC.creator" content="Vicha, R."/><meta name="DC.date" content="2009-06-01"/><meta name="DC.identifier" content="doi:10.1107/S1600536809016596"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?bi2361"/><meta name="DC.language" content="en"/><meta name="DC.description" content="In the title compound, C26H30ClN5O.CHCl3, the purine molecule consists of essentially planar benzene and purine ring systems [maximum deviation 0.010 (4) A for both ring systems] forming a dihedral angle of 85.52 (9)degrees. Intermolecular N-H...N hydrogen bonds link adjacent molecules into centrosymmetric dimers. The structure also contains intermolecular C-H...O and C-H...N interactions. The benzene rings form offset face-to-face [pi]-[pi] stacking interactions with an interplanar distance of 3.541 (4) A and a centroid-to-centroid distance of 4.022 (4) A."/><meta name="DC.type" content="text"/><meta name="DC.title" content="(1-Adamantyl){4-[(2-chloro-9-isopropyl-9H-purin-6-yl)aminomethyl]phenyl}methanone trichloromethane solvate"/><meta name="DCTERMS.abstract" content="In the title compound, C26H30ClN5O.CHCl3, the purine molecule consists of essentially planar benzene and purine ring systems [maximum deviation 0.010 (4) A for both ring systems] forming a dihedral angle of 85.52 (9)degrees. Intermolecular N-H...N hydrogen bonds link adjacent molecules into centrosymmetric dimers. The structure also contains intermolecular C-H...O and C-H...N interactions. The benzene rings form offset face-to-face [pi]-[pi] stacking interactions with an interplanar distance of 3.541 (4) A and a centroid-to-centroid distance of 4.022 (4) A."/><meta name="prism.number" content="6"/><meta name="prism.volume" content="65"/><meta name="prism.publicationDate" content="2009-06-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="organic compounds"/><meta name="prism.startingPage" content="1268"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="1268"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
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+        xmlns:dc="http://purl.org/dc/elements/1.1/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?bi2361">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>(1-Adamantyl){4-[(2-chloro-9-isopropyl-9H-purin-6-yl)aminomethyl]phenyl}methanone trichloromethane solvate</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
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+--><title>(IUCr) (1-Adamantyl){4-[(2-chloro-9-isopropyl-9H-purin-6-yl)aminomethyl]phenyl}methanone trichloromethane solvate</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artbdy.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="bi2361hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="bi2361hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="bi2361bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="bi2361bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="bi2361bdy.html">CLICK HERE</a>
+</body></noframes></frameset></html>

html/0/3/9/0395f1a8-44ec-4898-8dc5-c2d952c52993/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/3/9/0395f1a8-44ec-4898-8dc5-c2d952c52993/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\3\9\0395f1a8-44ec-4898-8dc5-c2d952c52993\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">(1-Adamantyl){4-[(2-chloro-9-isopropyl-9H-purin-6-yl)aminomethyl]phenyl}methanone trichloromethane solvate</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536809016596</metadata></cml>

html/0/4/7/047d82f3-66c0-454d-83e6-b5bd730bb8c6/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\4\7\047d82f3-66c0-454d-83e6-b5bd730bb8c6\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Mohdaidin, S.M."/><meta name="DC.creator" content="Abdul Rahim, A.S."/><meta name="DC.creator" content="Osman, H."/><meta name="DC.creator" content="Kia, R."/><meta name="DC.creator" content="Fun, H.-K."/><meta name="DC.date" content="2008-08-01"/><meta name="DC.identifier" content="doi:10.1107/S160053680802206X"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2594"/><meta name="DC.language" content="en"/><meta name="DC.description" content="In the title compound, C13H18N2O4, intramolecular N-H...O, N-H...N and C-H...O (x 3) hydrogen bonds generate S(6) and S(5) ring motifs. There are two crystallographically independent molecules (A and B) in the asymmetric unit. The nitro group is coplanar with the benzene ring, with O-N-C-C torsion angles of -0.33 (13) and 0.93 (14)degrees in molecules A and B, respectively. In the crystal structure, neighbouring molecules are linked together by intermolecular C-H...O hydrogen bonds. In addition, the crystal structure is stabilized by [pi]-[pi] interactions with centroid-centroid distances ranging from 3.7853 (6) to 3.8625 (6) A."/><meta name="DC.type" content="text"/><meta name="DC.title" content="Ethyl 4-(tert-butylamino)-3-nitrobenzoate"/><meta name="DCTERMS.abstract" content="In the title compound, C13H18N2O4, intramolecular N-H...O, N-H...N and C-H...O (x 3) hydrogen bonds generate S(6) and S(5) ring motifs. There are two crystallographically independent molecules (A and B) in the asymmetric unit. The nitro group is coplanar with the benzene ring, with O-N-C-C torsion angles of -0.33 (13) and 0.93 (14)degrees in molecules A and B, respectively. In the crystal structure, neighbouring molecules are linked together by intermolecular C-H...O hydrogen bonds. In addition, the crystal structure is stabilized by [pi]-[pi] interactions with centroid-centroid distances ranging from 3.7853 (6) to 3.8625 (6) A."/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2594">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>Ethyl 4-(tert-butylamino)-3-nitrobenzoate</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) Ethyl 4-(tert-butylamino)-3-nitrobenzoate</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2594hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2594hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2594bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2594bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2594bdy.html">CLICK HERE</a>
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+var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www.");
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html/0/4/7/047d82f3-66c0-454d-83e6-b5bd730bb8c6/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/4/7/047d82f3-66c0-454d-83e6-b5bd730bb8c6/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/5/6/056633b1-a2a8-470f-9ca5-7e1177b48f1c/full.html

+<?xml version="1.0" encoding="UTF-8"?>
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+                        <dc:title>Bis([mu]-naphthalene-1,8-dicarboxylato)bis[aqua(2,2'-bipyridine)zinc(II)] tetrahydrate</dc:title>
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+--><title>(IUCr) Bis([mu]-naphthalene-1,8-dicarboxylato)bis[aqua(2,2'-bipyridine)zinc(II)] tetrahydrate</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2661hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2661hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2661bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2661bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
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html/0/5/6/056633b1-a2a8-470f-9ca5-7e1177b48f1c/opsin.xml

Empty file added.

html/0/5/6/056633b1-a2a8-470f-9ca5-7e1177b48f1c/title.xml

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html/0/6/3/063dff97-fa77-458e-b7f0-efaf2838404c/full.html

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+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
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+--><title>(IUCr) N-(1-Acetyl-r-7,c-9-diphenyl-4,8-dithia-1,2-diazaspiro[5.4]dec-2-en-3-yl)acetamide</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2527hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2527hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2527bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2527bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2527bdy.html">CLICK HERE</a>
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html/0/6/3/063dff97-fa77-458e-b7f0-efaf2838404c/opsin.xml

Empty file added.

html/0/6/3/063dff97-fa77-458e-b7f0-efaf2838404c/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/6/8/0685ff4d-2caa-42d2-b4af-e5d77ea37961/full.html

+<?xml version="1.0" encoding="UTF-8"?>
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+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\6\8\0685ff4d-2caa-42d2-b4af-e5d77ea37961\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Zheng, L.-M."/><meta name="DC.creator" content="Wei, X."/><meta name="DC.creator" content="Peng, X.-R."/><meta name="DC.creator" content="Zeng, J.-P."/><meta name="DC.creator" content="Zhang, Y.-Q."/><meta name="DC.date" content="2008-11-01"/><meta name="DC.identifier" content="doi:10.1107/S1600536808032406"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2638"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The molecules of the title compound, C15H16N2O4, are linked via N-H...O hydrogen bonds, forming undulating one-dimensional chains. Adjacent chains are linked by weak C-H...[pi] interactions, forming a three-dimensional network."/><meta name="DC.type" content="text"/><meta name="DC.title" content="4-[3-(4-Nitrophenoxy)propoxy]aniline"/><meta name="DCTERMS.abstract" content="The molecules of the title compound, C15H16N2O4, are linked via N-H...O hydrogen bonds, forming undulating one-dimensional chains. Adjacent chains are linked by weak C-H...[pi] interactions, forming a three-dimensional network."/><meta name="prism.number" content="11"/><meta name="prism.volume" content="64"/><meta name="prism.publicationDate" content="2008-11-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="organic compounds"/><meta name="prism.startingPage" content="2110"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="2110"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
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+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
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+--><title>(IUCr) 4-[3-(4-Nitrophenoxy)propoxy]aniline</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artbdy.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2638hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2638hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2638bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2638bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
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html/0/6/8/0685ff4d-2caa-42d2-b4af-e5d77ea37961/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/6/8/0685ff4d-2caa-42d2-b4af-e5d77ea37961/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\6\8\0685ff4d-2caa-42d2-b4af-e5d77ea37961\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">4-[3-(4-Nitrophenoxy)propoxy]aniline</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536808032406</metadata></cml>

html/0/7/0/07087a7f-0d6f-4852-a38a-0ae0b475b7fb/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\7\0\07087a7f-0d6f-4852-a38a-0ae0b475b7fb\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="Copyright (c) 2008 International Union of Crystallography"/><meta name="DC.creator" content="Cao, L."/><meta name="DC.creator" content="Englert, U."/><meta name="DC.creator" content="Li, Q."/><meta name="DC.date" content="2008-02-01"/><meta name="DC.copyright" content="Copyright (c) 2008 International Union of Crystallography"/><meta name="DC.identifier" content="doi:10.1107/S1600536808001360"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2533"/><meta name="DC.language" content="en"/><meta name="DC.description" content="In the title compound, (C5H5ClN)2[NiCl4], the dianion lies on a twofold rotation axis. Two cations are linked to each anion by classical N-H...Cl hydrogen bonds, and short Cl...Cl contacts and Cl...[pi] stacking interactions [with distances of 3.376 (2) and 3.684 (2) A, respectively] extend this pattern into a chain. The [NiCl4]2- anion shows significant deviation from ideal tetrahedral geometry."/><meta name="DC.type" content="text"/><meta name="DC.title" content="Bis(4-chloropyridinium) tetrachloridonickelate(II)"/><meta name="DCTERMS.abstract" content="In the title compound, (C5H5ClN)2[NiCl4], the dianion lies on a twofold rotation axis. Two cations are linked to each anion by classical N-H...Cl hydrogen bonds, and short Cl...Cl contacts and Cl...[pi] stacking interactions [with distances of 3.376 (2) and 3.684 (2) A, respectively] extend this pattern into a chain. The [NiCl4]2- anion shows significant deviation from ideal tetrahedral geometry."/><meta name="keywords" lang="en" content=""/><meta name="copyright" content="Copyright (c) 2008 International Union of Crystallography"/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><title>(IUCr) Bis(4-chloropyridinium) tetrachloridonickelate(II)</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2533hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2533hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2533bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2533bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2533bdy.html">CLICK HERE</a>
+
+        
+    <script type="text/javascript">
+var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www.");
+document.write(unescape("%3Cscript src='" + gaJsHost + "google-analytics.com/ga.js' type='text/javascript'%3E%3C/script%3E"));
+</script>
+<script type="text/javascript">
+var pageTracker = _gat._getTracker("UA-187984-1");
+pageTracker._trackPageview();
+</script>
+</body></noframes></frameset></html>

html/0/7/0/07087a7f-0d6f-4852-a38a-0ae0b475b7fb/opsin.xml

Empty file added.

html/0/7/0/07087a7f-0d6f-4852-a38a-0ae0b475b7fb/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\7\0\07087a7f-0d6f-4852-a38a-0ae0b475b7fb\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">Bis(4-chloropyridinium) tetrachloridonickelate(II)</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536808001360</metadata></cml>

html/0/7/c/07cfa3c6-8eeb-476c-bed3-d276aa658467/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\7\c\07cfa3c6-8eeb-476c-bed3-d276aa658467\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Li, Y.-F."/><meta name="DC.creator" content="Jian, F.-F."/><meta name="DC.date" content="2008-09-01"/><meta name="DC.identifier" content="doi:10.1107/S1600536808025142"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2604"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The title compound, C12H16N2S, was prepared by the reaction of with phenyl isothiocyanate and piperidine. In the crystal structure, the molecule exhibits intermolecular N-H...S hydrogen bonds and weak intramolecular C-H...S and C-H...N hydrogen-bonding interactions."/><meta name="DC.type" content="text"/><meta name="DC.title" content="N-Phenylpiperidine-1-carbothioamide"/><meta name="DCTERMS.abstract" content="The title compound, C12H16N2S, was prepared by the reaction of with phenyl isothiocyanate and piperidine. In the crystal structure, the molecule exhibits intermolecular N-H...S hydrogen bonds and weak intramolecular C-H...S and C-H...N hydrogen-bonding interactions."/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
+        xmlns:dc="http://purl.org/dc/elements/1.1/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2604">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>N-Phenylpiperidine-1-carbothioamide</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) N-Phenylpiperidine-1-carbothioamide</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2604hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2604hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2604bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2604bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2604bdy.html">CLICK HERE</a>
+
+        
+    <script type="text/javascript">
+var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www.");
+document.write(unescape("%3Cscript src='" + gaJsHost + "google-analytics.com/ga.js' type='text/javascript'%3E%3C/script%3E"));
+</script>
+<script type="text/javascript">
+var pageTracker = _gat._getTracker("UA-187984-1");
+pageTracker._trackPageview();
+</script>
+</body></noframes></frameset></html>

html/0/7/c/07cfa3c6-8eeb-476c-bed3-d276aa658467/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\7\c\07cfa3c6-8eeb-476c-bed3-d276aa658467\opsin.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><molecule id="m1" xmlns:cmlDict="http://www.xml-cml.org/dictionary/cml/" xmlns:nameDict="http://www.xml-cml.org/schema/foo"><name dictRef="nameDict:unknown">N-Phenylpiperidine-1-carbothioamide</name><atomArray><atom id="a1" elementType="C" hydrogenCount="0"><label value="1" dictRef="cmlDict:locant"/></atom><atom id="a2" elementType="C"><label value="2" dictRef="cmlDict:locant"/></atom><atom id="a3" elementType="C"><label value="3" dictRef="cmlDict:locant"/></atom><atom id="a4" elementType="C"><label value="4" dictRef="cmlDict:locant"/></atom><atom id="a5" elementType="C"><label value="5" dictRef="cmlDict:locant"/></atom><atom id="a6" elementType="C"><label value="6" dictRef="cmlDict:locant"/></atom><atom id="a18" elementType="H"/><atom id="a19" elementType="H"/><atom id="a20" elementType="H"/><atom id="a21" elementType="H"/><atom id="a22" elementType="H"/><atom id="a7" elementType="N" hydrogenCount="0"><label value="1" dictRef="cmlDict:locant"/></atom><atom id="a8" elementType="C"><label value="2" dictRef="cmlDict:locant"/></atom><atom id="a9" elementType="C"><label value="3" dictRef="cmlDict:locant"/></atom><atom id="a10" elementType="C"><label value="4" dictRef="cmlDict:locant"/></atom><atom id="a11" elementType="C"><label value="5" dictRef="cmlDict:locant"/></atom><atom id="a12" elementType="C"><label value="6" dictRef="cmlDict:locant"/></atom><atom id="a14" elementType="S" hydrogenCount="0"><label value="S" dictRef="cmlDict:locant"/></atom><atom id="a15" elementType="N"><label value="N" dictRef="cmlDict:locant"/></atom><atom id="a16" elementType="C" hydrogenCount="0"><label value="X" dictRef="cmlDict:locant"/></atom><atom id="a23" elementType="H"/><atom id="a24" elementType="H"/><atom id="a25" elementType="H"/><atom id="a26" elementType="H"/><atom id="a27" elementType="H"/><atom id="a28" elementType="H"/><atom id="a29" elementType="H"/><atom id="a30" elementType="H"/><atom id="a31" elementType="H"/><atom id="a32" elementType="H"/><atom id="a33" elementType="H"/></atomArray><bondArray><bond id="a1_a2" atomRefs2="a1 a2" order="D"/><bond id="a2_a3" atomRefs2="a2 a3" order="S"/><bond id="a3_a4" atomRefs2="a3 a4" order="D"/><bond id="a4_a5" atomRefs2="a4 a5" order="S"/><bond id="a5_a6" atomRefs2="a5 a6" order="D"/><bond id="a6_a1" atomRefs2="a6 a1" order="S"/><bond id="a2_a18" atomRefs2="a2 a18" order="S"/><bond id="a3_a19" atomRefs2="a3 a19" order="S"/><bond id="a4_a20" atomRefs2="a4 a20" order="S"/><bond id="a5_a21" atomRefs2="a5 a21" order="S"/><bond id="a6_a22" atomRefs2="a6 a22" order="S"/><bond id="a7_a8" atomRefs2="a7 a8" order="S"/><bond id="a8_a9" atomRefs2="a8 a9" order="S"/><bond id="a9_a10" atomRefs2="a9 a10" order="S"/><bond id="a10_a11" atomRefs2="a10 a11" order="S"/><bond id="a11_a12" atomRefs2="a11 a12" order="S"/><bond id="a12_a7" atomRefs2="a12 a7" order="S"/><bond id="a14_a16" atomRefs2="a14 a16" order="D"/><bond id="a15_a16" atomRefs2="a15 a16" order="S"/><bond id="a7_a16" atomRefs2="a7 a16" order="S"/><bond id="a8_a23" atomRefs2="a8 a23" order="S"/><bond id="a8_a24" atomRefs2="a8 a24" order="S"/><bond id="a9_a25" atomRefs2="a9 a25" order="S"/><bond id="a9_a26" atomRefs2="a9 a26" order="S"/><bond id="a10_a27" atomRefs2="a10 a27" order="S"/><bond id="a10_a28" atomRefs2="a10 a28" order="S"/><bond id="a11_a29" atomRefs2="a11 a29" order="S"/><bond id="a11_a30" atomRefs2="a11 a30" order="S"/><bond id="a12_a31" atomRefs2="a12 a31" order="S"/><bond id="a12_a32" atomRefs2="a12 a32" order="S"/><bond id="a15_a33" atomRefs2="a15 a33" order="S"/><bond id="a1_a15" atomRefs2="a1 a15" order="S"/></bondArray></molecule></cml>

html/0/7/c/07cfa3c6-8eeb-476c-bed3-d276aa658467/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\7\c\07cfa3c6-8eeb-476c-bed3-d276aa658467\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">N-Phenylpiperidine-1-carbothioamide</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536808025142</metadata></cml>

html/0/8/6/086b1f52-4d1f-437a-821f-b1609d5a2578/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\6\086b1f52-4d1f-437a-821f-b1609d5a2578\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Esterhuysen, C."/><meta name="DC.creator" content="Retief, L."/><meta name="DC.creator" content="Kruger, G.J."/><meta name="DC.creator" content="Cronje, S."/><meta name="DC.creator" content="Raubenheimer, H.G."/><meta name="DC.date" content="2009-02-01"/><meta name="DC.identifier" content="doi:10.1107/S1600536808042621"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2691"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The title compound, [CrZr(C5H5)2(C2H3O)Cl(CO)5], consists of two metal centres, with a (pentacarbonylchromium)oxymethylcarbene group coordinating as a monodentate ligand to the zirconocene chloride. [pi]-Delocalization through the Zr-O-C=Cr unit is indicated by a short Zr-O distance [2.041 (3) A] and a nearly linear Zr-O-C angle [170.5 (3)degrees]. Molecules are aligned with their molecular planes (through Zr, Cl, carbene and Cr) parallel to the ab plane. C-H...Cl interactions result in zigzag chains of molecules propagating parallel to the b axis."/><meta name="DC.type" content="text"/><meta name="DC.title" content="Pentacarbonyl-2[kappa]5C-chlorido-1[kappa]Cl-bis[1([eta]5)-cyclopentadienyl]([mu]-1-oxidoethylene-1:2[kappa]2O:C)chromium(0)zirconium(IV)"/><meta name="DCTERMS.abstract" content="The title compound, [CrZr(C5H5)2(C2H3O)Cl(CO)5], consists of two metal centres, with a (pentacarbonylchromium)oxymethylcarbene group coordinating as a monodentate ligand to the zirconocene chloride. [pi]-Delocalization through the Zr-O-C=Cr unit is indicated by a short Zr-O distance [2.041 (3) A] and a nearly linear Zr-O-C angle [170.5 (3)degrees]. Molecules are aligned with their molecular planes (through Zr, Cl, carbene and Cr) parallel to the ab plane. C-H...Cl interactions result in zigzag chains of molecules propagating parallel to the b axis."/><meta name="prism.number" content="2"/><meta name="prism.volume" content="65"/><meta name="prism.publicationDate" content="2009-02-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="metal-organic compounds"/><meta name="prism.startingPage" content="125"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="125"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2691">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>Pentacarbonyl-2[kappa]5C-chlorido-1[kappa]Cl-bis[1([eta]5)-cyclopentadienyl]([mu]-1-oxidoethylene-1:2[kappa]2O:C)chromium(0)zirconium(IV)</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) Pentacarbonyl-2[kappa]5C-chlorido-1[kappa]Cl-bis[1([eta]5)-cyclopentadienyl]([mu]-1-oxidoethylene-1:2[kappa]2O:C)chromium(0)zirconium(IV)</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artbdy.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2691hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2691hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2691bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2691bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2691bdy.html">CLICK HERE</a>
+</body></noframes></frameset></html>

html/0/8/6/086b1f52-4d1f-437a-821f-b1609d5a2578/opsin.xml

Empty file added.

html/0/8/6/086b1f52-4d1f-437a-821f-b1609d5a2578/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\6\086b1f52-4d1f-437a-821f-b1609d5a2578\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">Pentacarbonyl-2[kappa]5C-chlorido-1[kappa]Cl-bis[1([eta]5)-cyclopentadienyl]([mu]-1-oxidoethylene-1:2[kappa]2O:C)chromium(0)zirconium(IV)</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536808042621</metadata></cml>

html/0/8/a/08ad15b0-58a1-45a7-bc76-20be2264b15d/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\a\08ad15b0-58a1-45a7-bc76-20be2264b15d\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Fun, H.-K."/><meta name="DC.creator" content="Kia, R."/><meta name="DC.creator" content="Kargar, H."/><meta name="DC.date" content="2008-10-01"/><meta name="DC.identifier" content="doi:10.1107/S160053680802816X"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2626"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The crystal structure of the title Schiff base compound, C19H20Br2N2O2, contains two crystallographically independent molecules (A and B) in the asymmetric unit, with similar conformations. Intramolecular O-H...N (x 4) and C-H...N (x 5) hydrogen bonds form six- and five-membered rings, producing S(6) and S(5) ring motifs, respectively. One of the N atoms in molecule A acts as a trifurcated acceptor, the rest of the N atoms being bifurcated acceptors. The dihedral angles between the benzene rings in molecules A and B are 47.83 (17) and 61.11 (17)degrees, respectively. The molecular conformation is stabilized by intramolecular O-H...N and C-H...N hydrogen bonds. The short distances between the centroids of the benzene rings [3.7799 (19)-3.890 (2) A] indicate the existence of [pi]-[pi] interactions. In addition, the crystal structure is further stabilized by an intermolecular C-H...O hydrogen bond, C-H...[pi] interactions, and short intermolecular Br...Br and Br...O contacts [3.4786 (5) and 3.149 (3) A, respectively]."/><meta name="DC.type" content="text"/><meta name="DC.title" content="N,N'-Bis(5-bromo-2-hydroxybenzylidene)-2,2-dimethylpropane-1,3-diamine"/><meta name="DCTERMS.abstract" content="The crystal structure of the title Schiff base compound, C19H20Br2N2O2, contains two crystallographically independent molecules (A and B) in the asymmetric unit, with similar conformations. Intramolecular O-H...N (x 4) and C-H...N (x 5) hydrogen bonds form six- and five-membered rings, producing S(6) and S(5) ring motifs, respectively. One of the N atoms in molecule A acts as a trifurcated acceptor, the rest of the N atoms being bifurcated acceptors. The dihedral angles between the benzene rings in molecules A and B are 47.83 (17) and 61.11 (17)degrees, respectively. The molecular conformation is stabilized by intramolecular O-H...N and C-H...N hydrogen bonds. The short distances between the centroids of the benzene rings [3.7799 (19)-3.890 (2) A] indicate the existence of [pi]-[pi] interactions. In addition, the crystal structure is further stabilized by an intermolecular C-H...O hydrogen bond, C-H...[pi] interactions, and short intermolecular Br...Br and Br...O contacts [3.4786 (5) and 3.149 (3) A, respectively]."/><meta name="prism.number" content="10"/><meta name="prism.volume" content="64"/><meta name="prism.publicationDate" content="2008-10-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="organic compounds"/><meta name="prism.startingPage" content="1895"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="1896"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
+        xmlns:dc="http://purl.org/dc/elements/1.1/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2626">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>N,N'-Bis(5-bromo-2-hydroxybenzylidene)-2,2-dimethylpropane-1,3-diamine</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) N,N'-Bis(5-bromo-2-hydroxybenzylidene)-2,2-dimethylpropane-1,3-diamine</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artbdy.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2626hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2626hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2626bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2626bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2626bdy.html">CLICK HERE</a>
+</body></noframes></frameset></html>

html/0/8/a/08ad15b0-58a1-45a7-bc76-20be2264b15d/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/8/a/08ad15b0-58a1-45a7-bc76-20be2264b15d/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\a\08ad15b0-58a1-45a7-bc76-20be2264b15d\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">N,N'-Bis(5-bromo-2-hydroxybenzylidene)-2,2-dimethylpropane-1,3-diamine</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S160053680802816X</metadata></cml>

html/0/8/f/08f4079b-0105-472a-9cf7-36723992e422/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\f\08f4079b-0105-472a-9cf7-36723992e422\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Kong, L."/><meta name="DC.creator" content="Qiao, Y."/><meta name="DC.creator" content="Zhang, J.-D."/><meta name="DC.creator" content="Ju, X.-P."/><meta name="DC.date" content="2008-12-01"/><meta name="DC.identifier" content="doi:10.1107/S1600536808038270"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?bi2310"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The title compound, C8H9N3S, contains two molecules in the asymmetric unit. One molecule is close to being planar (r.m.s. deviation from the mean plane = 0.06 A for the non-H atoms), while the other exhibits a dihedral angle of 21.7 (1)degrees between the benzene ring and the mean plane of the thiosemicarbazone unit. Intermolecular N-H...S hydrogen bonds link the molecules into layers parallel to the (010) plane."/><meta name="DC.type" content="text"/><meta name="DC.title" content="Benzaldehyde thiosemicarbazone"/><meta name="DCTERMS.abstract" content="The title compound, C8H9N3S, contains two molecules in the asymmetric unit. One molecule is close to being planar (r.m.s. deviation from the mean plane = 0.06 A for the non-H atoms), while the other exhibits a dihedral angle of 21.7 (1)degrees between the benzene ring and the mean plane of the thiosemicarbazone unit. Intermolecular N-H...S hydrogen bonds link the molecules into layers parallel to the (010) plane."/><meta name="prism.number" content="12"/><meta name="prism.volume" content="64"/><meta name="prism.publicationDate" content="2008-12-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="organic compounds"/><meta name="prism.startingPage" content="2412"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="2412"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
+        xmlns:dc="http://purl.org/dc/elements/1.1/"
+        xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?bi2310">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>Benzaldehyde thiosemicarbazone</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) Benzaldehyde thiosemicarbazone</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="bi2310hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="bi2310hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="bi2310bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="bi2310bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="bi2310bdy.html">CLICK HERE</a>
+</body></noframes></frameset></html>

html/0/8/f/08f4079b-0105-472a-9cf7-36723992e422/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/8/f/08f4079b-0105-472a-9cf7-36723992e422/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\8\f\08f4079b-0105-472a-9cf7-36723992e422\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">Benzaldehyde thiosemicarbazone</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S1600536808038270</metadata></cml>

html/0/9/4/0943e378-591b-4bbb-be9a-9ce4b942c63f/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
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+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\9\4\0943e378-591b-4bbb-be9a-9ce4b942c63f\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/dc/elements/1.1/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><link rel="schema.prism" href="http://prismstandard.org/namespaces/1.2/basic/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Wang, H.-M."/><meta name="DC.creator" content="Chen, L.-L."/><meta name="DC.creator" content="Hu, T."/><meta name="DC.creator" content="Zeng, X.-H."/><meta name="DC.date" content="2008-12-01"/><meta name="DC.identifier" content="doi:10.1107/S160053680803732X"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2674"/><meta name="DC.language" content="en"/><meta name="DC.description" content="In the title compound, C19H19BrN2O2S, the central thienopyrimidine ring system is essentially planar, with a maximum displacement of 0.068 (3) A. The attached cyclohexene ring adopts a half-chair conformation. The molecular conformation and crystal packing are stabilized by three intramolecular C-H...O hydrogen bonds and two C-H...[pi] interactions."/><meta name="DC.type" content="text"/><meta name="DC.title" content="2-(4-Bromophenoxy)-3-isopropyl-5,6,7,8-tetrahydro-1-benzothieno[2,3-d]pyrimidin-4(3H)-one"/><meta name="DCTERMS.abstract" content="In the title compound, C19H19BrN2O2S, the central thienopyrimidine ring system is essentially planar, with a maximum displacement of 0.068 (3) A. The attached cyclohexene ring adopts a half-chair conformation. The molecular conformation and crystal packing are stabilized by three intramolecular C-H...O hydrogen bonds and two C-H...[pi] interactions."/><meta name="prism.number" content="12"/><meta name="prism.volume" content="64"/><meta name="prism.publicationDate" content="2008-12-01"/><meta name="prism.publicationName" content="Acta Crystallographica Section E: Structure Reports Online"/><meta name="prism.issn" content="1600-5368"/><meta name="prism.section" content="organic compounds"/><meta name="prism.startingPage" content="2404"/><meta name="prism.rightsAgent" content="med@iucr.org"/><meta name="prism.endingPage" content="2404"/><meta name="prism.eissn" content="1600-5368"/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2674">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>2-(4-Bromophenoxy)-3-isopropyl-5,6,7,8-tetrahydro-1-benzothieno[2,3-d]pyrimidin-4(3H)-one</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
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+        </rdf:RDF>
+--><title>(IUCr) 2-(4-Bromophenoxy)-3-isopropyl-5,6,7,8-tetrahydro-1-benzothieno[2,3-d]pyrimidin-4(3H)-one</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2674hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2674hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2674bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2674bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
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html/0/9/4/0943e378-591b-4bbb-be9a-9ce4b942c63f/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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html/0/9/4/0943e378-591b-4bbb-be9a-9ce4b942c63f/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\9\4\0943e378-591b-4bbb-be9a-9ce4b942c63f\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">2-(4-Bromophenoxy)-3-isopropyl-5,6,7,8-tetrahydro-1-benzothieno[2,3-d]pyrimidin-4(3H)-one</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S160053680803732X</metadata></cml>

html/0/a/4/0a44803e-44eb-43dc-9f57-9ddd44129d63/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\a\4\0a44803e-44eb-43dc-9f57-9ddd44129d63\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Wei, L.-H."/><meta name="DC.date" content="2008-04-01"/><meta name="DC.identifier" content="doi:10.1107/S160053680800737X"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2551"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The title complex, {[Ni(C7H7N4O2)]OH}n, has been prepared through hydrothermal synthesis. The asymmetric unit contains one [Ni(TH)]+ cation (TH is the theophylline anion) and one hydroxide anion. The Ni2+ ion is coordinated by two N atoms from two neighboring theophylline anions. The alternating linkage of the Ni2+ cation and theophylline anion results in a one-dimensional chain along the [010] direction. Intermolecular O-H...O hydrogen bonds are present n the crystal structure."/><meta name="DC.type" content="text"/><meta name="DC.title" content="catena-Poly[[nickel(II)-[mu]-1,3-dimethyl-2,6-dioxo-7H-purinato-[kappa]2N7:N9] hydroxide]"/><meta name="DCTERMS.abstract" content="The title complex, {[Ni(C7H7N4O2)]OH}n, has been prepared through hydrothermal synthesis. The asymmetric unit contains one [Ni(TH)]+ cation (TH is the theophylline anion) and one hydroxide anion. The Ni2+ ion is coordinated by two N atoms from two neighboring theophylline anions. The alternating linkage of the Ni2+ cation and theophylline anion results in a one-dimensional chain along the [010] direction. Intermolecular O-H...O hydrogen bonds are present n the crystal structure."/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
+        <rdf:RDF xmlns="http://web.resource.org/cc/"
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2551">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>catena-Poly[[nickel(II)-[mu]-1,3-dimethyl-2,6-dioxo-7H-purinato-[kappa]2N7:N9] hydroxide]</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) catena-Poly[[nickel(II)-[mu]-1,3-dimethyl-2,6-dioxo-7H-purinato-[kappa]2N7:N9] hydroxide]</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2551hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2551hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2551bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2551bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2551bdy.html">CLICK HERE</a>
+
+        
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html/0/a/4/0a44803e-44eb-43dc-9f57-9ddd44129d63/opsin.xml

Empty file added.

html/0/a/4/0a44803e-44eb-43dc-9f57-9ddd44129d63/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
+<cml fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\a\4\0a44803e-44eb-43dc-9f57-9ddd44129d63\title.xml" xmlns="http://www.xml-cml.org/schema" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><metadata dictRef="cmlx:title">catena-Poly[[nickel(II)-[mu]-1,3-dimethyl-2,6-dioxo-7H-purinato-[kappa]2N7:N9] hydroxide]</metadata><metadata dictRef="cmlx:doi">doi:10.1107/S160053680800737X</metadata></cml>

html/0/a/b/0abd4ddd-ce52-4338-8bb6-899524b573f0/full.html

+<?xml version="1.0" encoding="UTF-8"?>
+<!-- To achieve the required appearance in current browsers we have to use some markup that 
+does not conform to this DOCTYPE  where this occurs it will be followed by a comment with explanation-->
+<html version="-//W3C//DTD HTML 4.01 Transitional//EN" cmlx:fileId="C:\Users\pm286\workspace\crystaleyeTestData\html\0\a\b\0abd4ddd-ce52-4338-8bb6-899524b573f0\full.html" xmlns="http://www.w3.org/1999/xhtml" xmlns:cmlx="http://www.xml-cml.org/schema/cmlx"><head><link rel="schema.DC" href="http://purl.org/DC/elements/1.0/"/><link rel="schema.DCTERMS" href="http://purl.org/dc/terms/"/><meta name="DC.source" content="urn:issn:1600-5368"/><meta name="DC.rights" content="http://creativecommons.org/licenses/by/2.0/uk"/><meta name="DC.creator" content="Tang, C.-B."/><meta name="DC.date" content="2008-08-01"/><meta name="DC.identifier" content="doi:10.1107/S160053680801965X"/><meta name="DC.publisher" content="International Union of Crystallography"/><meta name="DC.link" content="http://scripts.iucr.org/cgi-bin/paper?at2583"/><meta name="DC.language" content="en"/><meta name="DC.description" content="The title Schiff base compound, C14H9Br2ClN2O2.CH4O, was derived from the condensation reaction of 3,5-dibromosalicylaldehyde with 2-chlorobenzohydrazide. The dihedral angle between the two benzene rings is 48.2 (2)degrees. In the crystal structure, molecules are linked through O-H...O and N-H...O intermolecular hydrogen bonds, forming layers parallel to the bc plane. There is also an O-H...N intramolecular hydrogen bond."/><meta name="DC.type" content="text"/><meta name="DC.title" content="2-Chloro-N'-(3,5-dibromo-2-hydroxybenzylidene)benzohydrazide methanol solvate"/><meta name="DCTERMS.abstract" content="The title Schiff base compound, C14H9Br2ClN2O2.CH4O, was derived from the condensation reaction of 3,5-dibromosalicylaldehyde with 2-chlorobenzohydrazide. The dihedral angle between the two benzene rings is 48.2 (2)degrees. In the crystal structure, molecules are linked through O-H...O and N-H...O intermolecular hydrogen bonds, forming layers parallel to the bc plane. There is also an O-H...N intramolecular hydrogen bond."/><meta name="keywords" lang="en" content=""/><meta name="ROBOTS" content="NOARCHIVE,NOINDEX"/><!--
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+                <Work rdf:about="http://scripts.iucr.org/cgi-bin/paper?at2583">
+                        <license rdf:resource="http://creativecommons.org/licenses/by/2.0/uk/" />
+                        <dc:title>2-Chloro-N'-(3,5-dibromo-2-hydroxybenzylidene)benzohydrazide methanol solvate</dc:title>
+                </Work>
+        <License rdf:about="http://creativecommons.org/licenses/by/2.0/uk/">
+          <permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
+          <permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Notice"/>
+          <requires rdf:resource="http://creativecommons.org/ns#Attribution"/>
+          <permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
+        </License>
+        </rdf:RDF>
+--><title>(IUCr) 2-Chloro-N'-(3,5-dibromo-2-hydroxybenzylidene)benzohydrazide methanol solvate</title><link rel="stylesheet" type="text/css" href="/style/global.css"/><link rel="stylesheet" type="text/css" href="/style/artindex.css"/><link rel="SHORTCUT ICON" href="http://journals.iucr.org/favicon.ico"/></head><frameset rows="82,*" border="0" scrolling="auto"><!-- Valid <frameset rows="82,*" > --><frame frameborder="1" scrolling="auto" src="at2583hdr.html" border="0" marginheight="3"/><!-- Valid <frameset  src="at2583hdr.html" frameborder="0" scrolling="auto" marginheight="3" / > > --><frame frameborder="1" scrolling="auto" src="at2583bdy.html" border="0" name="iucr_body"/><!-- Valid <frameset  src="at2583bdy.html" frameborder="0"  name="iucr_body" />  --><noframes><body>
+Because your browser cannot handle the frames used to structure this article, you must <a shape="rect" href="at2583bdy.html">CLICK HERE</a>
+
+        
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+var gaJsHost = (("https:" == document.location.protocol) ? "https://ssl." : "http://www.");
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html/0/a/b/0abd4ddd-ce52-4338-8bb6-899524b573f0/opsin.xml

+<?xml version="1.0" encoding="UTF-8"?>
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a36" order="S"/></bondArray></molecule></molecule></cml>

html/0/a/b/0abd4ddd-ce52-4338-8bb6-899524b573f0/title.xml

+<?xml version="1.0" encoding="UTF-8"?>
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