Hexa-aqua-nickel(II) bis-(3-carb-oxy-4-hy-droxy-benzene-sulfonate) dihydrate, [Ni(H(2)O)(6)][C(6)H(3)(CO(2)H)(OH)SO(3)](2)·2H(2)O, (I), crystallizes in the triclinic space group P with the nickel(II) aqua complexes on centers of inversion. The carboxyl-ate group is protonated and neither it nor the sulfonate group is involved in direct coordination to the metal ions. The structure consists of alternating layers of inorganic cations and organic anions linked by O-Hâ¯O hydrogen bonds that also include non-coordinated water mol-ecules of crystallization. The first-row divalent transition-metal salts of this anion are reported as both dihydrates and tetra-hydrates, with two distinct structures for the dihydrates that are both layered but differ in the hydrogen-bonding pattern. Compound (I) represents the second known example of one of these structures. Hexa-aqua-cobalt(II) bis-(3-carb-oxy-benzene-sulfonate) dihydrate, [Co(H(2)O)(6)][C(6)H(4)(CO(2)H)SO(3)](2)·2H(2)O, (II), also crystallizes in triclinic P with the cobalt(II) aqua complexes on centers of inversion. The structure is also built of alternating layers of complex cations and organic anions without direct coordination to the metal by the protonated carboxyl-ate or unprotonated sulfonate groups. A robust O-Hâ¯O hydrogen-bonding network involving primarily the coordin-ated and non-coordinated water mol-ecules and sulfonate groups directs the packing. This is the first reported example of a divalent transition-metal salt of the 3-carb-oxy-benzene-sulfonate anion.
Crystal structures of two new divalent transition-metal salts of carb-oxy-benzene-sulfonate anions.
阅读:15
作者:Bettinger Reuben T, Squattrito Philip J, Aulakh Darpandeep, Gianopoulos Christopher G
| 期刊: | Acta Crystallographica Section E: Crystallographic Communications | 影响因子: | 0.500 |
| 时间: | 2022 | 起止号: | 2022 Aug 31; 78(Pt 9):961-965 |
| doi: | 10.1107/S2056989022008295 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
