TOWARDS ORGANOMETALLIC ZEOLITES - SPONTANEOUS SELF-ASSEMBLY OF ET3SNCN CUCN AND (NBU4N)CN TO SUPRAMOLECULAR [(NBU4N)(ET3SN)2CU(CN)4]

Citation
Ak. Brimah et al., TOWARDS ORGANOMETALLIC ZEOLITES - SPONTANEOUS SELF-ASSEMBLY OF ET3SNCN CUCN AND (NBU4N)CN TO SUPRAMOLECULAR [(NBU4N)(ET3SN)2CU(CN)4], Journal of organometallic chemistry, 475(1-2), 1994, pp. 85-94
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
0022328X
Volume
475
Issue
1-2
Year of publication
1994
Pages
85 - 94
Database
ISI
SICI code
0022-328X(1994)475:1-2<85:TOZ-SS>2.0.ZU;2-R
Abstract
Spontaneous self-assembly of Et3Sn+-, nBu4N+- and [Cu(CN)4]3- ions in H2O affords white, crystalline [(nBu4N)(ET3Sn)2-Cu(CN)4]infinity (7). A single-crystal X-ray study has confirmed the formation of a negative ly charged, three-dimensional host framework with wide and parallel, i nterior channels occupied by well-ordered nBu4N+ guest cations. 7: Tet ragonal I-lattice, I4(3)22; a, b = 14.360(2), c = 40.003(6) angstrom; cell volume = 8249(2) angstrom3, Z = 8; wR2 = 0.1145; wR2' (all data) = 0.1355. The title compound has, moreover, been characterized by IR/R aman (nu(CN)) and MAS solid-state NMR spectroscopy (C-13, Sn-119). The NMR features are consistent with requirements based on the asymmetric unit. Even modest variations of the organic groups belonging to the 3 D-framework, and of the template, R4N+, respectively, have been shown to afford 'derailed' assemblies of distinctly different stoichiometrie s, and/or spectroscopic properties, from [(R4N)(R'3Sn)2Cu(CN)4].