Bismole Explained

Bismole is a theoretical heterocyclic organic compound, a five-membered ring with the formula C4H4BiH. It is classified as a metallole. It can be viewed as a structural analog of pyrrole, with bismuth replacing the nitrogen atom of pyrrole. The unsubstituted compound has not been isolated due to the high energy of the Bi-H bond. Substituted derivatives, which have been synthesized, are called bismoles.

Reactions

2,5-Bis(trimethylsilyl)-3,4-dimethyl-1-phenyl-1H-bismole, for example, can be formed by the reaction of (1Z,3Z)-1,4-bis(trimethylsilyl)-1,4-diiodobuta-2,3-dimethyl-1,3-diene and diiodophenylbismuthine. Bismoles can be used to form ferrocene-like sandwich compounds.[1]

See also

Notes and References

  1. Book: Berge , John M. . 4.22.7  - Functions Containing Arsenic, Antimony or Bismuth with a Metalloid, R12C=C(AsR22)SiR33 etc . Katritzky . Alan R. . Alan R. Katritzky . Meth-Cohn . Otto . Rees . Charles W. . Charles Rees . Gordon W. . Kirby . 1995 . Synthesis: Carbon with Two Heteroatoms, Each Attached by a Single Bond . Comprehensive Organic Functional Group Transformations . 4 . . 1038–1040 . 978-0-08-042325-8 . https://books.google.com/books?id=0RQEsfYCuBcC&pg=PA1038.