In situ 1 H nuclear magnetic resonance spectroscopy was used to investigate the processes that occur during the synthesis of 1,3,6,8tetraazatricyclo[4.3.1.1 3,8 ]undecane (TATU). NMR analysis showed a reaction mixture containing more than one compound. The production of these intermediates and colla
Synthesis and characterization of novel triazenes from the reaction of the cyclic aminal 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane (TATU) with diazonium ions
✍ Scribed by Augusto Rivera; Diego González-Salas
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 426 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The reaction of the cyclic aminal 1,3,6,8-tetraazatricyclo[4.3.1.1 3,8 ]undecane (TATU, 4) with diazonium salts resulted in the formation of a new series of bis-triazenes, namely 3,8-bis [(4-methoxyphenyl) 3,6,8-tetraazabicyclo[4.3.1]decane 6c. When aniline derived diazonium salt 5d was coupled with TATU, 3,8-bis(phenyldiazenyl)-1,3,6,8-tetraazabicyclo[4.3.1]decane 6d and bis[1,5-bis-((E)-phenyldiazenyl)-1,3,5-triazepan-3-yl]methane 7 were obtained. These compounds were characterized by HR-MS, 1 H and 13 C NMR and 2D-NMR. Additionally, the structure of compound 7 was confirmed by X-ray crystallography.
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