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首页> 外文期刊>Macromolecular chemistry and physics >Syntheses of poly(dimethyl)-co-(4,7,10,13-tetraoxatetradecylmethylsilanes). An evaluation of the use of C8K versus Na in the preparation of polysilanes
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Syntheses of poly(dimethyl)-co-(4,7,10,13-tetraoxatetradecylmethylsilanes). An evaluation of the use of C8K versus Na in the preparation of polysilanes

机译:Syntheses of poly(dimethyl)-co-(4,7,10,13-tetraoxatetradecylmethylsilanes). An evaluation of the use of C8K versus Na in the preparation of polysilanes

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摘要

Full Paper: To evaluate the use of C8K versus Na as the reducing agent in the preparation of polysilanes, the homopolymers poly(4,7,10,13-tetraoxatetradecylmethyl-silanes) 1 and poly(dimethylsilane) 5 as well as the copolymers poly(dimethyl)-co-(4,7,10,13-tetraoxatetradecyl-methylsilane) 2-4 were synthesized from 4,7,10,13-tetraoxatetradecylmethyldichlorosilane (6) and/or dimethyldichlorosilane (7). C8K in comparison to Na gave an increased yields and enhanced purity, when used with polar monomers, such as 6, that persumably intercalate not graphite. In the presence of increasing amounts of apolar 7 both a decrease in yield as well as purity is observed in the C8K based copolymerizations. In contrast, the type of monomer does not affect the results of the Na based copolymerizations. Whereas at ambient temperatures the introduction of dimethylsiline units in 2-4, causes minor changes in the polysilane optical properties, as compared to 1, at low temperatures differences are discernible both in solution and the solid state (thin film) in the case of 4(Na). Apparently, the incorporated dimethylsilane moieties reduce the mean free energy of defect formulation E, i.e. at these low temperatures the silicon backbone adopts a more extended confirmation as reflected by the occurrence of an additional "abrupt" transition. References: 25

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