Author:
Bromley MK,Gason SJ,Jhingran AG,Looney MG,Solomon DH
Abstract
Spiro orthocarbonates ( SOCs ) have been widely studied, particularly as monomers which on polymerization undergo minimal shrinkage. Of particular interest has been the dimethylidene SOC because, unlike the parent SOC, it is amenable to free-radical polymerization. The incorporation of other hetero atoms, particularly sulfur, into the bicyclic structure offers the potential of polymers with improved refractive indices and mechanical properties. However, whilst literature methods are available for the spiro tetrathioorthocarbonates ( STOCs ),3 the synthesis of a methylidene derivative has not been reported. In this communication we report the synthesis of 3,9-dimethylidene-1,5,7,11-tetra-thiaspiro[5.5] undecane (DMSTOC) (1).
Cited by
11 articles.
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1. ChemInform Abstract: Synthetic Routes to 3,9-Dimethylidene-1,5,7,11-tetrathiaspiro(5.5) undecane.;ChemInform;2010-08-04
2. Dichlorodiphenoxymethane;Acta Crystallographica Section E Structure Reports Online;2008-01-04
3. 1,3-Dioxins, Oxathiins, Dithiins, and their Benzo Derivatives;Comprehensive Heterocyclic Chemistry III;2008
4. Tricoordinated Stabilized Cations, Anions, and Radicals, +CX1X2X3, −CX1X2X3, and CX1X2X3;Comprehensive Organic Functional Group Transformations II;2005
5. Functions Containing Halogens and Any Other Elements;Comprehensive Organic Functional Group Transformations II;2005