Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13 C and 15 N CPMAS NMR investigations

• Published in: Magnetic resonance in chemistry Vol. 51; no. 12; pp. 788 - 794
• Main Authors: Jaźwiński, Jarosław, Kamieński, Bohdan, Sadlej, Agnieszka
• Format: Journal Article
• Language: English
• Published: 01-12-2013
• ISSN: 0749-1581; 1097-458X
• DOI: 10.1002/mrc.4017

Complexation properties of dimeric rhodium(II) tetracarboxylates have been utilised in chemistry, spectroscopy and organic synthesis. Particularly, the combination of these rhodium salts with multifunctional ligands results in the formation of coordination polymers, and these are of interest because of their gas‐occlusion properties. In the present work, the polymeric adducts of rhodium(II) tetraacetate with flexible ligands exhibiting conformational variety, ethane‐1,2‐diamine, propane‐1,3‐diamine and their
N
,
N
′‐dimethyl‐ and
N
,
N
,
N
′,
N
′‐tetramethyl derivatives, have been investigated by means of elemental analysis,
13
C CPMAS NMR,
15
N CPMAS NMR and density functional theory modelling. Elemental analysis and NMR spectra indicated the axial coordination mode and regular structures of (1 : 1)
n
oligomeric chains in the case of adducts of ethane‐1,2‐diamine,
N
,
N
′‐dimethylethane‐1,2‐diamine
N
,
N
,
N
′,
N
′‐tetramethylethane‐1,2‐diamine and
N
,
N
,
N
′,
N
′‐tetramethylpropane‐1,3‐diamine. Propane‐1,3‐diamine and
N
,
N
′‐dimethylpropane‐1,3‐diamine tended to form heterogeneous materials, composed of oligomeric (1 : 1)
n
chains and the additive of dirhodium units containing equatorially bonded ligands. Experimental findings have been supported by density functional theory modelling of some hypothetical structures and gauge‐invariant atomic orbital calculations of NMR chemical shifts. Copyright © 2013 John Wiley & Sons, Ltd.