Effects of substituants in stilbene upon its reactivity in radical polymerizations
β Scribed by John C. Bevington; Stephen W. Breuer; Thomas N. Huckerby
- Publisher
- Springer
- Year
- 1984
- Tongue
- English
- Weight
- 194 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0170-0839
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π SIMILAR VOLUMES
## Abstract The substituent effect on the antimony atom in organostibineβmediated degenerative transfer living radical polymerization has been studied. 2βDiphenylstibanylβ2βmethylpropionitrile (**1a**) was synthesized as an organostibine chain transfer agent (CTA), and its effect was compared with
Persistent radical cations were produced electrochemically from the parent hydrocarbons 9,lO-diphenylanthracene (DPA), 9-phenylanthracene (9-PA), 9,l O-dimethylanthracene (DMA), rubrene (Ru), triphenylene (TP), 1,3,6&tetraphenylpyrene (TPP), and perylene (P). The stabilities of these cations in the