Poly-organic semiconductors with straight through conjugation

Losev, Yu. P.; Isakovich, V.N.; Paushkin, Ya. M.; Loseva, L. P.; Ksenofontov, M. A.; Volod'ko, L. V.

doi:10.1016/0032-3950(80)90393-7

Cited by 1 publication

(2 citation statements)

References 0 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Paushkin et al [185][186][187][188][189][190][191][192][193] have done extensive studies on poly(amine sulfides). Cross-linked polyethylene, on heating at 150 °C for 75 h in air in the presence of poly(aniline disulfide), lost only 5% of the crosslinked phase in comparison to 100% in the absence of poly(aniline disulfide) [185]:…”

Section: Polysulfides From Sulfur Monochloridementioning

confidence: 99%

“…The mechanism is the formation of weakly active S radicals, consequently leading to slowing down of the reaction. Poly(arylamine disulfides) were also found to have efficiently catalyzed the dehydration of diacetone alcohol [187,188] and l-phenyl cyclohexanol [189,190] respectively. Since poly(arylamine disulfides) are paramagnetic, their electrical and magnetic properties such as electrical conductivity (~) and concentration of ferromagnetic species (N) respectively were also investigated [191,192].…”

Section: Polysulfides From Sulfur Monochloridementioning

confidence: 99%

See 1 more Smart Citation

Polymers containing disulfide, tetrasulfide, diselenide and ditelluride linkages in the main chain

Kishore

Ganesh

Polymer Synthesis/Polymer Engineering

View full text Add to dashboard Cite

The present review articulates the syntheses and properties of industrially important disulfide and tetrasulfide polymers. The diselenide and ditelluride polymers have also been reviewed, for the first time, so that a comprehensive view on the polymers containing group VIA elements can be obtained. The latter two polymers are gaining considerable current attention due to their semi-conducting properties. The emphasis has been made to sift through the developments in the last ten years or so to get the latest flavour in these rapidly developing polymers. We have also attempted to bring to the fore several contradicting results, like, for example, the crystallinity of ditelluride polymers, to clear the mist in such reports. We hope that this review will help those working in the field to assess the progress achieved in this area and that it may also provide useful orientation for those who wish to become involved.

show abstract

Section: Polysulfides From Sulfur Monochloridementioning

confidence: 99%

Section: Polysulfides From Sulfur Monochloridementioning

confidence: 99%