Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
155 0 |
SM ISO690:2012 FONARI, Marina, SIMONOV, Yurii A., BOTOSHANSKY, Mark, GANIN, Eduard, YAVOLOVSKII, Arkadii. The hydrogen-bonded adduct 7,16-diazonia-18-crown-6-4-amino-benzensulfonate-water (1/2/2). In: Acta Crystallographica Section C: Crystal Structure Communications, 2003, vol. 59, pp. 88-90. ISSN 0108-2701. DOI: https://doi.org/10.1107/S010827010300129X |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Acta Crystallographica Section C: Crystal Structure Communications | |
Volumul 59 / 2003 / ISSN 0108-2701 /ISSNe 1600-5759 | |
|
|
DOI:https://doi.org/10.1107/S010827010300129X | |
Pag. 88-90 | |
Descarcă PDF | |
Rezumat | |
In the title hydrated adduct, 1,4,10,13-tetraoxa-7,16-diazonia-cyclooctadecane bis(4-aminobenzenesulfonate) dihydrate, C12H28N2O42+ ·2C6H6NO3S- ·2H2O, formed between 7,16-diaza-18-crown-6 and the dihydrate of 4-aminobenzenesulfonic acid, the macrocyclic cations lie across centres of inversion in the orthorhombic space group Pbca. The anions alone form zigzag chains, and the cations and anions together form sheets that are linked via water molecules and anions to form a three-dimensional grid. |
|
Cuvinte-cheie hydration, Hydrogen bonds, Molecules, Positive ions, Supramolecular chemistry |
|
|
Cerif XML Export
<?xml version='1.0' encoding='utf-8'?> <CERIF xmlns='urn:xmlns:org:eurocris:cerif-1.5-1' xsi:schemaLocation='urn:xmlns:org:eurocris:cerif-1.5-1 http://www.eurocris.org/Uploads/Web%20pages/CERIF-1.5/CERIF_1.5_1.xsd' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' release='1.5' date='2012-10-07' sourceDatabase='Output Profile'> <cfResPubl> <cfResPublId>ibn-ResPubl-190064</cfResPublId> <cfResPublDate>2003-02-01</cfResPublDate> <cfStartPage>88</cfStartPage> <cfISSN>0108-2701</cfISSN> <cfURI>https://ibn.idsi.md/ro/vizualizare_articol/190064</cfURI> <cfTitle cfLangCode='EN' cfTrans='o'>The hydrogen-bonded adduct 7,16-diazonia-18-crown-6-4-amino-benzensulfonate-water (1/2/2)</cfTitle> <cfKeyw cfLangCode='EN' cfTrans='o'>hydration; Hydrogen bonds; Molecules; Positive ions; Supramolecular chemistry</cfKeyw> <cfAbstr cfLangCode='EN' cfTrans='o'><p>In the title hydrated adduct, 1,4,10,13-tetraoxa-7,16-diazonia-cyclooctadecane bis(4-aminobenzenesulfonate) dihydrate, C<sub>12</sub>H<sub>28</sub>N<sub>2</sub>O<sub>4</sub><sup>2+</sup> ·2C<sub>6</sub>H<sub>6</sub>NO<sub>3</sub>S<sup>-</sup> ·2H<sub>2</sub>O, formed between 7,16-diaza-18-crown-6 and the dihydrate of 4-aminobenzenesulfonic acid, the macrocyclic cations lie across centres of inversion in the orthorhombic space group Pbca. The anions alone form zigzag chains, and the cations and anions together form sheets that are linked via water molecules and anions to form a three-dimensional grid.</p></cfAbstr> <cfResPubl_Class> <cfClassId>eda2d9e9-34c5-11e1-b86c-0800200c9a66</cfClassId> <cfClassSchemeId>759af938-34ae-11e1-b86c-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfResPubl_Class> <cfResPubl_Class> <cfClassId>e601872f-4b7e-4d88-929f-7df027b226c9</cfClassId> <cfClassSchemeId>40e90e2f-446d-460a-98e5-5dce57550c48</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfResPubl_Class> <cfPers_ResPubl> <cfPersId>ibn-person-106536</cfPersId> <cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId> <cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfPers_ResPubl> <cfPers_ResPubl> <cfPersId>ibn-person-1070</cfPersId> <cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId> <cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfPers_ResPubl> <cfPers_ResPubl> <cfPersId>ibn-person-15513</cfPersId> <cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId> <cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfPers_ResPubl> <cfPers_ResPubl> <cfPersId>ibn-person-77037</cfPersId> <cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId> <cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfPers_ResPubl> <cfPers_ResPubl> <cfPersId>ibn-person-22084</cfPersId> <cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId> <cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> </cfPers_ResPubl> <cfFedId> <cfFedIdId>ibn-doi-190064</cfFedIdId> <cfFedId>10.1107/S010827010300129X</cfFedId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFedId_Class> <cfClassId>31d222b4-11e0-434b-b5ae-088119c51189</cfClassId> <cfClassSchemeId>bccb3266-689d-4740-a039-c96594b4d916</cfClassSchemeId> </cfFedId_Class> <cfFedId_Srv> <cfSrvId>5123451</cfSrvId> <cfClassId>eda2b2e2-34c5-11e1-b86c-0800200c9a66</cfClassId> <cfClassSchemeId>5a270628-f593-4ff4-a44a-95660c76e182</cfClassSchemeId> </cfFedId_Srv> </cfFedId> </cfResPubl> <cfPers> <cfPersId>ibn-Pers-106536</cfPersId> <cfPersName_Pers> <cfPersNameId>ibn-PersName-106536-3</cfPersNameId> <cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId> <cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFamilyNames>Fonari</cfFamilyNames> <cfFirstNames>Marina</cfFirstNames> </cfPersName_Pers> </cfPers> <cfPers> <cfPersId>ibn-Pers-1070</cfPersId> <cfPersName_Pers> <cfPersNameId>ibn-PersName-1070-3</cfPersNameId> <cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId> <cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFamilyNames>Simonov</cfFamilyNames> <cfFirstNames>Yurii A.</cfFirstNames> <cfFamilyNames>Симонов</cfFamilyNames> <cfFirstNames>Юрий</cfFirstNames> </cfPersName_Pers> </cfPers> <cfPers> <cfPersId>ibn-Pers-15513</cfPersId> <cfPersName_Pers> <cfPersNameId>ibn-PersName-15513-3</cfPersNameId> <cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId> <cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFamilyNames>Botoshansky</cfFamilyNames> <cfFirstNames>Mark</cfFirstNames> <cfFamilyNames>Ботошанский</cfFamilyNames> <cfFirstNames>М</cfFirstNames> </cfPersName_Pers> </cfPers> <cfPers> <cfPersId>ibn-Pers-77037</cfPersId> <cfPersName_Pers> <cfPersNameId>ibn-PersName-77037-3</cfPersNameId> <cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId> <cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFamilyNames>Ганин</cfFamilyNames> <cfFirstNames>Эдуард</cfFirstNames> </cfPersName_Pers> </cfPers> <cfPers> <cfPersId>ibn-Pers-22084</cfPersId> <cfPersName_Pers> <cfPersNameId>ibn-PersName-22084-3</cfPersNameId> <cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId> <cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId> <cfStartDate>2003-02-01T24:00:00</cfStartDate> <cfFamilyNames>Yavolovskii</cfFamilyNames> <cfFirstNames>Arkadii</cfFirstNames> </cfPersName_Pers> </cfPers> <cfSrv> <cfSrvId>5123451</cfSrvId> <cfName cfLangCode='en' cfTrans='o'>CrossRef DOI prefix service</cfName> <cfDescr cfLangCode='en' cfTrans='o'>The service of issuing DOI prefixes to publishers</cfDescr> <cfKeyw cfLangCode='en' cfTrans='o'>persistent identifier; Digital Object Identifier</cfKeyw> </cfSrv> </CERIF>