1995
DOI: 10.1016/0379-6779(94)02296-b
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Selective elimination in dialkoxy-PPV precursors yielding polymers with isolated tetraalkoxy-stilbene units

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Cited by 3 publications
(1 citation statement)
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“…244,245 Mono-and dialkoxy-substituted PPVs can be prepared by a sulfonium precursor route as described for the synthesis of PPV (1). 87,232,240,[246][247][248][249][250] Delmotte et al 251 have studied the synthesis of poly(2,5-diethoxy-1,4-phenylene vinylene) (21) by the sulfonium precursor route and found that partial elimination of the sulfonium groups occurred when >1 equiv of base was used. This elimination was found to be selective for short conjugated fragments, yielding only tetraethoxystilbene units even when up to 35% of leaving groups had been eliminated.…”
Section: Alkoxy- Thioalkyl- and Alkylamino-substituted Ppvsmentioning
confidence: 99%
“…244,245 Mono-and dialkoxy-substituted PPVs can be prepared by a sulfonium precursor route as described for the synthesis of PPV (1). 87,232,240,[246][247][248][249][250] Delmotte et al 251 have studied the synthesis of poly(2,5-diethoxy-1,4-phenylene vinylene) (21) by the sulfonium precursor route and found that partial elimination of the sulfonium groups occurred when >1 equiv of base was used. This elimination was found to be selective for short conjugated fragments, yielding only tetraethoxystilbene units even when up to 35% of leaving groups had been eliminated.…”
Section: Alkoxy- Thioalkyl- and Alkylamino-substituted Ppvsmentioning
confidence: 99%