{"title":"两个异构体Ba5Mg4C54O48H114和Pb5Mg4C54O48H114","authors":"Jan Fábry, Erika Samolová, Michal Dušek","doi":"10.1515/zkri-2021-2074","DOIUrl":null,"url":null,"abstract":"Abstract There are reported two related structures of Ba5Mg4C54O48H114 (dodeca(aqua-6κ3O,7κ3O,8κ3O,9κ3O)-tris(μ2-propanoato-1:6κ2O,1κO′)-tris(μ-propanoato-2:7κ2O,2κO′-tris(μ-propanoato-3:8κ2O,3κO′)-tris(μ-propanoato-4:9κ2O,4κO′)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)-pentabarium tetramagnesium), (I), and Pb5Mg4C54O48H114 (dodeca(aqua-1κ3O,2κ3O,3κ3O,4κ3O)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5 κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)tetramagnesium lead(II) tris(propanoato-κ2O,O′)plumbate(II)), (II). The title structures are compositional isomers which crystallize in the same space group type. The structure of (I) comprises molecules with symmetry 4 ‾ 3 m $\\overline{4}3m$ . The structure (II) comprises the complex cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ with the symmetry 4 ‾ 3 m $\\overline{4}3m$ and four anions [tris(propanoato-κ2O,O′)plumbate(II)]−, [Pb(C3H5O2)3]− , with 3m symmetry. The central cations Ba12+ and Pb12+ in (I) and in the cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ of the structure (II), respectively, have similar structural features which are comparable to the environment of the Ba2+ cation in BaCa2(C3H5O2)6 [Stadnicka, K. & Glazer, A. M. (1980). Acta Cryst. B36, 2977–2985]. The molecules in (I) and the ions in (II) are interconnected by Owater‒H⋯Opropanoate hydrogen bonds of a moderate strength. The ethyl chains are disordered which is common in propanoates. However, there are unprecedented features in the title structures: 1) The central atom Pb12+ is the first known example of a Pb2+ cation which is surrounded by six carboxylates in a bidentate bridging mode, i.e. by 12 oxygens. 2) The anion [tris(propanoato-κ2O,O′)plumbate(II)]− has a constitution with unusually prominent stereochemical activity of the 6s2 electron pair of the cation Pb2+ completing the coordination to the tetrahedral one. Thus, its formula can be expressed as [Pb[ψ−4t](C3H5O2)3]−. 3) In both title structures, there are propanoate molecules with disordered carboxylate oxygens.","PeriodicalId":23855,"journal":{"name":"Zeitschrift für Kristallographie - Crystalline Materials","volume":"53 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two isomers Ba5Mg4C54O48H114 and Pb5Mg4C54O48H114\",\"authors\":\"Jan Fábry, Erika Samolová, Michal Dušek\",\"doi\":\"10.1515/zkri-2021-2074\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract There are reported two related structures of Ba5Mg4C54O48H114 (dodeca(aqua-6κ3O,7κ3O,8κ3O,9κ3O)-tris(μ2-propanoato-1:6κ2O,1κO′)-tris(μ-propanoato-2:7κ2O,2κO′-tris(μ-propanoato-3:8κ2O,3κO′)-tris(μ-propanoato-4:9κ2O,4κO′)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)-pentabarium tetramagnesium), (I), and Pb5Mg4C54O48H114 (dodeca(aqua-1κ3O,2κ3O,3κ3O,4κ3O)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5 κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)tetramagnesium lead(II) tris(propanoato-κ2O,O′)plumbate(II)), (II). The title structures are compositional isomers which crystallize in the same space group type. The structure of (I) comprises molecules with symmetry 4 ‾ 3 m $\\\\overline{4}3m$ . The structure (II) comprises the complex cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ with the symmetry 4 ‾ 3 m $\\\\overline{4}3m$ and four anions [tris(propanoato-κ2O,O′)plumbate(II)]−, [Pb(C3H5O2)3]− , with 3m symmetry. The central cations Ba12+ and Pb12+ in (I) and in the cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ of the structure (II), respectively, have similar structural features which are comparable to the environment of the Ba2+ cation in BaCa2(C3H5O2)6 [Stadnicka, K. & Glazer, A. M. (1980). Acta Cryst. B36, 2977–2985]. The molecules in (I) and the ions in (II) are interconnected by Owater‒H⋯Opropanoate hydrogen bonds of a moderate strength. The ethyl chains are disordered which is common in propanoates. However, there are unprecedented features in the title structures: 1) The central atom Pb12+ is the first known example of a Pb2+ cation which is surrounded by six carboxylates in a bidentate bridging mode, i.e. by 12 oxygens. 2) The anion [tris(propanoato-κ2O,O′)plumbate(II)]− has a constitution with unusually prominent stereochemical activity of the 6s2 electron pair of the cation Pb2+ completing the coordination to the tetrahedral one. Thus, its formula can be expressed as [Pb[ψ−4t](C3H5O2)3]−. 3) In both title structures, there are propanoate molecules with disordered carboxylate oxygens.\",\"PeriodicalId\":23855,\"journal\":{\"name\":\"Zeitschrift für Kristallographie - Crystalline Materials\",\"volume\":\"53 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-08-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift für Kristallographie - Crystalline Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/zkri-2021-2074\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Kristallographie - Crystalline Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/zkri-2021-2074","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Abstract There are reported two related structures of Ba5Mg4C54O48H114 (dodeca(aqua-6κ3O,7κ3O,8κ3O,9κ3O)-tris(μ2-propanoato-1:6κ2O,1κO′)-tris(μ-propanoato-2:7κ2O,2κO′-tris(μ-propanoato-3:8κ2O,3κO′)-tris(μ-propanoato-4:9κ2O,4κO′)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)-pentabarium tetramagnesium), (I), and Pb5Mg4C54O48H114 (dodeca(aqua-1κ3O,2κ3O,3κ3O,4κ3O)-hexakis(μ3-propanoato-1:5κ2O,2:5κ2O′;1:5κ2O,3:5κ2O′;1:5 κ2O,4:5κ2O′;2:5κ2O,3:5κ2O′;2:5κ2O,4:5κ2O′;3:5κ2O,4:5κ2O′)tetramagnesium lead(II) tris(propanoato-κ2O,O′)plumbate(II)), (II). The title structures are compositional isomers which crystallize in the same space group type. The structure of (I) comprises molecules with symmetry 4 ‾ 3 m $\overline{4}3m$ . The structure (II) comprises the complex cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ with the symmetry 4 ‾ 3 m $\overline{4}3m$ and four anions [tris(propanoato-κ2O,O′)plumbate(II)]−, [Pb(C3H5O2)3]− , with 3m symmetry. The central cations Ba12+ and Pb12+ in (I) and in the cation {Pb(C3H5O2)6[Mg(H2O)3]4}4+ of the structure (II), respectively, have similar structural features which are comparable to the environment of the Ba2+ cation in BaCa2(C3H5O2)6 [Stadnicka, K. & Glazer, A. M. (1980). Acta Cryst. B36, 2977–2985]. The molecules in (I) and the ions in (II) are interconnected by Owater‒H⋯Opropanoate hydrogen bonds of a moderate strength. The ethyl chains are disordered which is common in propanoates. However, there are unprecedented features in the title structures: 1) The central atom Pb12+ is the first known example of a Pb2+ cation which is surrounded by six carboxylates in a bidentate bridging mode, i.e. by 12 oxygens. 2) The anion [tris(propanoato-κ2O,O′)plumbate(II)]− has a constitution with unusually prominent stereochemical activity of the 6s2 electron pair of the cation Pb2+ completing the coordination to the tetrahedral one. Thus, its formula can be expressed as [Pb[ψ−4t](C3H5O2)3]−. 3) In both title structures, there are propanoate molecules with disordered carboxylate oxygens.