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1,2,3-Selenadiazoles as precursors to cyclopentadienylcobalt dithiolenes and 1,4-dithiins: molecular structures of bis(cycloocteno)-1,4-dithiin and bis(cycloocteno)-1,4-diselenin

✍ Scribed by Michael R. J. Dorrity; Ann Lavery; John F. Malone; Christopher P. Morley; Richard R. Vaughan


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
397 KB
Volume
3
Category
Article
ISSN
1042-7163

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✦ Synopsis


Cycloocteno-l,2,3-.seIenadiazole (1) and cyclopentadienyldicurbonylcobalt (2) react in the presence of an excess of elemental sulfur to yield the dithiolene cyclopentudicwyl( 1,2-cyclooctenedith io1ato)cobalt (3). Available evidence indicates that this reaction involves the intermediacy of a cobalt-alkyne complex. Compound 3 is the first example o f a cyclopentadienylcohalt dithiolene bearing aliphatic substituents. Analogous reactions performed using only catalytic quantities of 2 provide high-yield syntheses of bis(cyc1oocteno)-I ,4-dithiin (6) and bis(cyc1oocteno)-I ,4-diselenin (7), whose structures have been determined bv X-ray difraction.


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