CCCXXXIV.—The nature of the supposed dimethiodide of trimethylene sulphide

Bennett, G. M.; Hock, Alfred Louis

doi:10.1039/jr9270002496

Cited by 14 publications

(3 citation statements)

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“…Interaction with methyl iodide gives crystalline 1:2 adducts which are likewise used in many instances for the characterization of thietanes (6,8,9,16,26,27,35). According to Bennet and Hock (9), these adducts represent sulfonium salts of open-chain sulfides, where one iodine atom is linked by an ionic bond.…”

Section: Addition Compoundsmentioning

confidence: 99%

Thietanes

Sander¹

1966

Chem. Rev.

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Section: Addition Compoundsmentioning

confidence: 99%

Thietanes

Sander¹

1966

Chem. Rev.

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“…Received August 4,1952 This note will serve to record the preparation and properties of some previously undescribed alkyl esters of isodehydroacetic acid. The esters were obtained by reaction of isodehydroacetic acid chloride with the alcohol.…”

Section: Bauermentioning

confidence: 99%

Reactions of Trimethylene Sulfide with Chlorine and Bromine

Stewart¹,

Burnside²

1953

J. Am. Chem. Soc.

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“…This unusual easy cleavage from a carbon atom of a primary hydroxyl group was first found by Bennett and Hock [98,99] in the self condensation of 2-mercaptoethanol:…”

Section: Polysulfides From Condensation Of Poly (Thiodiglycols)mentioning

confidence: 53%

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

Kishore

Ganesh

Polymer Synthesis/Polymer Engineering

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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.

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CCCXXXIV.—The nature of the supposed dimethiodide of trimethylene sulphide

Cited by 14 publications

References 0 publications

Thietanes

Thietanes

Reactions of Trimethylene Sulfide with Chlorine and Bromine

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

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