Issue 2, 1998
From the journal:

Journal of Chemical Research, Synopses

Diazepines. Part 30.1 A Comparison between the Extent of Delocalisation of Electrons in a Vinamidine and its Protonated Form. Crystal and Molecular Structure of Two 2,3-Dihydro-1,4-diazepines

Magnus Brisander,   Steven G. Harris,   Douglas Lloyd,   Hamish McNab  and  Simon Parsons  

Abstract

An X-ray study of two 2,3-dihydro-1,4-diazepine bases shows that their vinamidine systems are made up of alternate single and double bonds, in contrast to the derived monocations which contain fully delocalised vinamidinium structures.

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Article information

DOI
https://doi.org/10.1039/A705112C
Article type
Paper

J. Chem. Res. (S), 1998, 72-73

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Diazepines. Part 30.1 A Comparison between the Extent of Delocalisation of Electrons in a Vinamidine and its Protonated Form. Crystal and Molecular Structure of Two 2,3-Dihydro-1,4-diazepines

M. Brisander, S. G. Harris, D. Lloyd, H. McNab and S. Parsons, J. Chem. Res. (S), 1998, 72 DOI: 10.1039/A705112C

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