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Structural studies of several solvated potassium salts of tenatoprazole crystallizing as conglomerates
Despite the weak acidic character of tenatoprazole it is possible to crystallize, in strong alkaline media, different solvated salts of this active pharmaceutical ingredient. Among these solid phases, some potassium salts exhibiting non congruent solubilities, form stable conglomerates in equilibriu...
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Published in: | Journal of molecular structure 2009-11, Vol.936 (1), p.60-66 |
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creator | Tauvel, G. Sanselme, M. Coste-Leconte, S. Petit, S. Coquerel, G. |
description | Despite the weak acidic character of tenatoprazole it is possible to crystallize, in strong alkaline media, different solvated salts of this active pharmaceutical ingredient. Among these solid phases, some potassium salts exhibiting non congruent solubilities, form stable conglomerates in equilibrium with their mother liquors without detectable partial solid solutions between the enantiomers.
The crystal structures of the ethanol and the ethylene glycol stoichiometric solvates of potassium salts have been determined by single crystal X-ray diffraction, revealing that the solvent molecules play an important role in the crystal cohesion. They participate to the coordination polyhedra of the potassium cations and also contribute to strong periodic bond chains. Moreover, there is no direct link between the tenatoprazole anions and the potassium cations, so the solvent molecules act as electrostatic relays between ions of opposite charges. |
doi_str_mv | 10.1016/j.molstruc.2009.07.014 |
format | article |
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The crystal structures of the ethanol and the ethylene glycol stoichiometric solvates of potassium salts have been determined by single crystal X-ray diffraction, revealing that the solvent molecules play an important role in the crystal cohesion. They participate to the coordination polyhedra of the potassium cations and also contribute to strong periodic bond chains. Moreover, there is no direct link between the tenatoprazole anions and the potassium cations, so the solvent molecules act as electrostatic relays between ions of opposite charges.</description><identifier>ISSN: 0022-2860</identifier><identifier>EISSN: 1872-8014</identifier><identifier>EISSN: 0022-2860</identifier><identifier>DOI: 10.1016/j.molstruc.2009.07.014</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Chemical Sciences ; Chiral compound ; Conglomerate ; Cristallography ; Crystal structure ; Material chemistry ; Mixed solvate ; Organic chemistry ; Potassium salt ; Tenatoprazole</subject><ispartof>Journal of molecular structure, 2009-11, Vol.936 (1), p.60-66</ispartof><rights>2009 Elsevier B.V.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-cf2c40c74b898cd8a91047c2f2af051bf121639d23e3cc59ee31feba637f3b113</citedby><cites>FETCH-LOGICAL-c346t-cf2c40c74b898cd8a91047c2f2af051bf121639d23e3cc59ee31feba637f3b113</cites><orcidid>0000-0001-8977-8676</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://normandie-univ.hal.science/hal-01932937$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Tauvel, G.</creatorcontrib><creatorcontrib>Sanselme, M.</creatorcontrib><creatorcontrib>Coste-Leconte, S.</creatorcontrib><creatorcontrib>Petit, S.</creatorcontrib><creatorcontrib>Coquerel, G.</creatorcontrib><title>Structural studies of several solvated potassium salts of tenatoprazole crystallizing as conglomerates</title><title>Journal of molecular structure</title><description>Despite the weak acidic character of tenatoprazole it is possible to crystallize, in strong alkaline media, different solvated salts of this active pharmaceutical ingredient. Among these solid phases, some potassium salts exhibiting non congruent solubilities, form stable conglomerates in equilibrium with their mother liquors without detectable partial solid solutions between the enantiomers.
The crystal structures of the ethanol and the ethylene glycol stoichiometric solvates of potassium salts have been determined by single crystal X-ray diffraction, revealing that the solvent molecules play an important role in the crystal cohesion. They participate to the coordination polyhedra of the potassium cations and also contribute to strong periodic bond chains. Moreover, there is no direct link between the tenatoprazole anions and the potassium cations, so the solvent molecules act as electrostatic relays between ions of opposite charges.</description><subject>Chemical Sciences</subject><subject>Chiral compound</subject><subject>Conglomerate</subject><subject>Cristallography</subject><subject>Crystal structure</subject><subject>Material chemistry</subject><subject>Mixed solvate</subject><subject>Organic chemistry</subject><subject>Potassium salt</subject><subject>Tenatoprazole</subject><issn>0022-2860</issn><issn>1872-8014</issn><issn>0022-2860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkE9LAzEUxIMoWKtfQfbqYdeXZLt_bpaiVih4UM8hm32pKdmmJOlC_fTuturV0xuG-Q28IeSWQkaBFvebrHM2RL9XGQOoMygzoPkZmdCqZGk16HMyAWAsZVUBl-QqhA0A0AGeEP02gnHvpU1C3LcGQ-J0ErDHo-VsLyO2yc5FGYLZd0mQNh4zEbcyup2XX85iovwhRGmt-TLbdSJDotx2bV031EQM1-RCSxvw5udOycfT4_tima5en18W81WqeF7EVGmmclBl3lR1pdpK1hTyUjHNpIYZbTRltOB1yzhypWY1IqcaG1nwUvOGUj4ld6feT2nFzptO-oNw0ojlfCVGD2jNWc3LfswWp6zyLgSP-g-gIMZlxUb8LivGZQWUA58P4MMJxOGT3qAXQRncKmyNRxVF68x_Fd8aiYji</recordid><startdate>20091112</startdate><enddate>20091112</enddate><creator>Tauvel, G.</creator><creator>Sanselme, M.</creator><creator>Coste-Leconte, S.</creator><creator>Petit, S.</creator><creator>Coquerel, G.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-8977-8676</orcidid></search><sort><creationdate>20091112</creationdate><title>Structural studies of several solvated potassium salts of tenatoprazole crystallizing as conglomerates</title><author>Tauvel, G. ; Sanselme, M. ; Coste-Leconte, S. ; Petit, S. ; Coquerel, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-cf2c40c74b898cd8a91047c2f2af051bf121639d23e3cc59ee31feba637f3b113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Chemical Sciences</topic><topic>Chiral compound</topic><topic>Conglomerate</topic><topic>Cristallography</topic><topic>Crystal structure</topic><topic>Material chemistry</topic><topic>Mixed solvate</topic><topic>Organic chemistry</topic><topic>Potassium salt</topic><topic>Tenatoprazole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tauvel, G.</creatorcontrib><creatorcontrib>Sanselme, M.</creatorcontrib><creatorcontrib>Coste-Leconte, S.</creatorcontrib><creatorcontrib>Petit, S.</creatorcontrib><creatorcontrib>Coquerel, G.</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of molecular structure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tauvel, G.</au><au>Sanselme, M.</au><au>Coste-Leconte, S.</au><au>Petit, S.</au><au>Coquerel, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural studies of several solvated potassium salts of tenatoprazole crystallizing as conglomerates</atitle><jtitle>Journal of molecular structure</jtitle><date>2009-11-12</date><risdate>2009</risdate><volume>936</volume><issue>1</issue><spage>60</spage><epage>66</epage><pages>60-66</pages><issn>0022-2860</issn><eissn>1872-8014</eissn><eissn>0022-2860</eissn><abstract>Despite the weak acidic character of tenatoprazole it is possible to crystallize, in strong alkaline media, different solvated salts of this active pharmaceutical ingredient. Among these solid phases, some potassium salts exhibiting non congruent solubilities, form stable conglomerates in equilibrium with their mother liquors without detectable partial solid solutions between the enantiomers.
The crystal structures of the ethanol and the ethylene glycol stoichiometric solvates of potassium salts have been determined by single crystal X-ray diffraction, revealing that the solvent molecules play an important role in the crystal cohesion. They participate to the coordination polyhedra of the potassium cations and also contribute to strong periodic bond chains. Moreover, there is no direct link between the tenatoprazole anions and the potassium cations, so the solvent molecules act as electrostatic relays between ions of opposite charges.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.molstruc.2009.07.014</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8977-8676</orcidid></addata></record> |
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subjects | Chemical Sciences Chiral compound Conglomerate Cristallography Crystal structure Material chemistry Mixed solvate Organic chemistry Potassium salt Tenatoprazole |
title | Structural studies of several solvated potassium salts of tenatoprazole crystallizing as conglomerates |
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