Issue 0, 1967

Boron hydride derivatives. Part XI. Iodination of decaborane

Abstract

Hillman's work on the iodination of decaborane has been extended to include the reaction between decaborane and iodine chloride in the presence of aluminium chloride. The yields of products are consistent only with an electrophilic substitution mechanism. It has also been shown that deuterium migration occurs in µ,µ′,µ″,µ‴, 5,6,7,8,9,10-decadeuteriodecaborane under the influence of hydrogen iodide. Hillman's “5-iododecaborane” is in consequence 1-iododecaborane.

Article information

Article type
Paper

J. Chem. Soc. A, 1967, 132-133

Boron hydride derivatives. Part XI. Iodination of decaborane

M. H. G. Wallbridge, J. Williams and R. L. Williams, J. Chem. Soc. A, 1967, 132 DOI: 10.1039/J19670000132

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements