Abstract
Silver(I) complexes of selenones, [LAgNO3] and [AgL2]NO3 (where L is imidazolidine-2-selenone or diazinane-2-selenone and their derivatives) have been prepared and characterized by elemental analysis, IR and NMR (1H, 13C and 107Ag) spectroscopy. An upfield shift in the C=Se resonance of selenones in 13C NMR and a downfield shift in N-H resonance in 1H NMR are consistent with selenium coordination to silver(I). 107Ag NMR, the AgNO3 signal is deshielded by 450-650ppm on coordination to selenones. Greater upfield shifts in 13C NMR were observed for [LAgNO3] compared to [AgL2]NO3 complexes, whereas the opposite trend was observed for 1H and 107Ag NMR chemical shifts.
| Original language | English |
|---|---|
| Pages (from-to) | 539-544 |
| Number of pages | 6 |
| Journal | Journal of Coordination Chemistry |
| Volume | 56 |
| Issue number | 6 |
| DOIs | |
| State | Published - 15 Apr 2003 |
Bibliographical note
Funding Information:This research was supported by the KFUPM Research Committee under project no. CY/NMR-STUDIES/214.
Keywords
- NMR
- Selenones
- Silver(I) complexes
- Spectroscopy
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Materials Chemistry