E-mail a Wiley Online Library Link

Niko Fischer, Prof. Dr. Thomas M. Klapötke, Sebastian Rappenglück and Jörg Stierstorfer Cover Picture: The Reactivity of 5-Cyanotetrazole towards Water and Hydroxylamine (ChemPlusChem 10/2012) ChemPlusChem 77

Version of Record online: 10 OCT 2012 | DOI: 10.1002/cplu.201290043

Thumbnail image of graphical abstract

The cover picture outlines the formation of 5-cyanotetrazole from sodium azide and sodium cyanide, which can be further converted into its hydrolysis products tetrazole-5-carboxamide and tetrazole-5-carboxamide oxime. Both products were deprotonated to form the respective hydroxylammonium salts. Among other nitrogen-rich salts of tetrazole-5-carboxamide oxime, they were structurally characterized. The silver salt of 5-cyanoetetrazole is an example of rarely described crystal structures of silver tetrazolate salts. A full account can be found in the Full Paper by T. Klapötke and co-workers on page 877 ff.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field