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Dinitrogen complexation with main group radicals
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DOI：10.1039/c0sc00345j.png)
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摘要
En 中文
In this report we present data from hyperfine sublevel correlation spectroscopy (HYSCORE), an electron paramagnetic resonance (EPR) spectroscopic technique, that reveals weak but distinct interactions between several main group element radicals and physically dissolved dinitrogen in solution. These interactions are the basis for a well-defined coordination of N-2 to the paramagnetic centers. The complexes formed are primarily of the van der Waals-type but also feature a non-negligible orbital overlap between dinitrogen and the radicals' SOMO. Our spectroscopic findings are strongly supported by experiments with isotope-labeled N-15(2), spectral simulations and quantum chemical and density functional theory (DFT) calculations. Formation of such complexes is unexpected when considering the small polarizability of dinitrogen but steric effects like formation of a binding pocket may facilitate their formation. The sensitivity, selectivity, and resolution of HYSCORE with respect to the detection of weak hyperfine couplings is needed to identify such complexes that are probably the result of a subtle interplay of induced van der Waals forces between N-2, the solvent and the dissolved radicals.
Keyword:
PERSISTENT RADICALS
AZO-COMPOUNDS
NITROGEN
SPECTROSCOPY
CAGE
DECOMPOSITION
ACTIVATION
RESONANCE
CHEMISTRY
ATOMS
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期刊
IF:
7.4
论文数:
1.7W
被引数:
9.3W
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