Chandrasekhar, Vadapalli ; Gopal, Kandasamy ; Singh, Puja ; Narayanan, Ramakirushnan Suriya ; Duthie, Andrew (2009) Self-assembly of organostannoxanes: formation of gels in aromatic solvents Organometallics, 28 (15). pp. 4593-4601. ISSN 0276-7333
Full text not available from this repository.
Official URL: http://pubs.acs.org/doi/abs/10.1021/om900474a
Related URL: http://dx.doi.org/10.1021/om900474a
Abstract
Organostannoxane drums [n-BuSn(O)O2C-C6H4-4-OR]6 [R = -CH3 (1); -C9H19 (2); -C11H23 (3)] and [n-BuSn(O)O2C-C6H3-3,5-(OR)2]6 [R = -CH3 (4); -C9H19 (5)] were synthesized by the reaction of n-BuSn(O)(OH) with the corresponding carboxylic acid in a 1:1 stoichiometry. Analogous reactions involving [n-Bu2SnO]n in a 1:1 stoichiometry afforded the diorganostannoxane ladders {[n-Bu2SnO2C-C6H4-4-OR]2O}2 [R = -CH3 (6); -C9H19 (7); -C11H23 (8)] and {[n-Bu2SnO2C-C6H3-3,5-(OR)2]2O}2 [R = -CH3 (9) and -C9H19 (10)]. Compounds 1-10 could also be prepared by a solventless methodology, which involved grinding the reactants together in a mortar and pestle at room temperature. Compounds 1-10 exhibit gelation behavior in aromatic solvents. In contrast, in aliphatic solvents gelation behavior was not observed. Among the organostannoxanes reported here, 2, 3, 5, and 8 were found to be extremely efficient gelators based on their critical gelation concentration values. The microstructure of the organometallic gels, investigated by optical and scanning electron microscopy, reveals the presence of cross-linked network structures. The gels formed from 2and 3 can be converted into xerogels by removal of solvent. The latter can be reconverted into the original gels by treatment with aromatic solvents.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 8945 |
Deposited On: | 28 Oct 2010 10:29 |
Last Modified: | 28 Oct 2010 10:29 |
Repository Staff Only: item control page