Solid-state structures of group 1 and group 2 metal 1,5-naphthalenedisulfonates: systematic investigation of lamellar three-dimensional networks constructed by metal arenedisulfonate

Citation
Jw. Cai et al., Solid-state structures of group 1 and group 2 metal 1,5-naphthalenedisulfonates: systematic investigation of lamellar three-dimensional networks constructed by metal arenedisulfonate, ACT CRYST B, 57, 2001, pp. 520-530
Citations number
34
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE
ISSN journal
0108-7681 → ACNP
Volume
57
Year of publication
2001
Part
4
Pages
520 - 530
Database
ISI
SICI code
0108-7681(200108)57:<520:SSOG1A>2.0.ZU;2-C
Abstract
Seven Group 1 and Group 2 1,5-naphthalenedisulfonates (1,5-nds) have been s ynthesized and structurally characterized by single-crystal X-ray diffracti on, IR spectroscopy and thermal gravimetric analysis. For Group I metal com plexes, with M = Li+ (1), Na+ (2) and K+ (3). all crystallize in the same s pace group (P2(1)/c) with the same composition, [M-2(1,5-nds)(H2O)(2)]. The y adopt similar three-dimensional packing arrangements with the metal-sulfo nate inorganic layers pillared by naphthalene rings. However, the coordinat ion behavior of three metal cations toward the SO 3 group and water molecul e are different, resulting in different architectures for the inorganic por tion. For Group 2 complexes with M = Mg2+ (4), Ca2+ (5), Sr2+ (6) and Ba2(7), Mg2+ shows no direct coordination by the SO3- group while Ca2+ is coor dinated by four SO3- groups and a two-dimensional network is formed. Comple xes (6) and (7) are isostructural, adopting the same three-dimensional, ino rganic-organic pillared framework as seen for (1)-(3). The coordination beh avior of the metal cations in these structures neatly illustrates the incre ase in coordination strength with decreasing charge/radius ratio for Group 1 and Group 2 metal cations with large organic anions.