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J. Chem. Soc., Perkin Trans. 2, 11, p. 2280-2286

DOI: 10.1039/b004270f

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The solid- and solution-state structures of 2-nitrosopyridine and its 3-and 4-methyl derivatives

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

2-Nitrosopyridine, 1, 3-methyl-2-nitrosopyridine, 2, and 4-methyl-2-nitrosopyridine, 3, exist in organic solvents as monomer-azodioxy dimer equilibria with the dimers predominating at ambient temperatures. In the case of compounds 1 and 3 only the Z-dimers co-exist with the monomers, whereas for compound 2 both Z- (major) and E- (minor) dimers are present with the monomer. Variable temperature H-1 NMR bandshape analysis and 2D-EXSY spectra of 1-3 provided thermodynamic and kinetic data for the dissociation equilibria Z- (or E-) dimer reversible arrow 2 monomer, DeltaH(empty set) values being in the range 53-58 kJ mol(-1) and DeltaG double dagger (298.15 K) values in the range 70-82 kJ mol(-1). An X-ray crystal structure of 1 identified the compound as a Z-dimeric species with the two pyridine rings twisted by 62.7 degrees and their heterocyclic N atoms pointing towards each other.