Catalytic Synthesis of Pyridine

Kline, Charles H.; Turkevich, John

doi:10.1021/ja01238a031

Cited by 12 publications

(3 citation statements)

References 2 publications

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“…Partial infrared data with assignments (8,14,15) are given in Table 3. The anion bands tend to be intense and broad, particularly in the S-0 (or C1-0) stretching regions, and to some extent mask the neutral ligand vibrations.…”

Section: Compound (K) (Mm S-i) (Mm S-i) (Mm S-i) (Mm S-i)mentioning

confidence: 99%

Synthesis, spectroscopic and magnetic properties of some pyrazine-bridged iron(II) sulfonate complexes

Haynes¹,

Sams²,

Thompson³

1988

Can. J. Chem.

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Six new pyrazine-bridged complexes of iron(II) have been prepared and studied using magnetic susceptibility, differential scanning calorimetry, and vibrational, electronic, and Mössbauer spectroscopic methods. Fe(pyz)(CF3SO3)2 exhibits a susceptibility maximum at 4.4 K and analysis of the magnetic data according to a two-dimensional S = 2 system in the (isotropic) Heisenberg limit yields best-fit values of J = −0.26 cm−1 and g = 2.20. Variable temperature Mössbauer spectra between 4.2 and 1.6 K are also reported for this compound and show the onset of magnetic hyperfine splitting below ~3.8 K. Analysis of magnetic data for Fe(pyz)2(CH3SO3)2 and Fe(pyz)2(CF3SO3)2•CH3OH according to the two-dimensional Heisenberg model also indicates the presence of weak antiferromagnetic exchange in these complexes (J = −0.18 and −0.20 cm−1, respectively). No clear evidence for magnetic concentration was obtained from our studies on Fe(pyz)2(CIO4)2, Fe(pyz)(p-CH3C6H4SO3)2, and Fe(pyz)(p-CH3C6H4SO3)2•2CH3OH; any antiferromagnetic coupling in these complexes must be considerably weaker than in the other complexes studied.

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Section: Compound (K) (Mm S-i) (Mm S-i) (Mm S-i) (Mm S-i)mentioning

confidence: 99%

Synthesis, spectroscopic and magnetic properties of some pyrazine-bridged iron(II) sulfonate complexes

Haynes¹,

Sams²,

Thompson³

1988

Can. J. Chem.

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show abstract

“…In addition, seven commercial catalysts (The Harshaw Chemical Co.) were obtained for evaluation. Ferric oxide (Fe-0101) 13.…”

Section: Experimental Workmentioning

confidence: 99%

Catalyst Evaluation for Synthesis of Phenylpyridine from Butadiene and Benzonitrile

Janz¹,

McCulloch²,

Timpane³

1953

Ind. Eng. Chem.

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“…Pyrolysis of diethylamine gave rise to small yields of pyrrole (11,12,13) and N-ethyl aniline gave traces of indole (14) while N.N. dimethyl-o-toluidine gave relatively good yields of 1. methyl indole (15).…”

Section: Synthesismentioning

confidence: 99%

Nitrogen in oil shale and shale oil. IV. Pyrolytic reactions involving the formation and decomposition of tar bases

Mapstone¹

1949

Journal and Proceedings of the Royal Society of New South Wales

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Catalytic Synthesis of Pyridine

Cited by 12 publications

References 2 publications

Synthesis, spectroscopic and magnetic properties of some pyrazine-bridged iron(II) sulfonate complexes

Synthesis, spectroscopic and magnetic properties of some pyrazine-bridged iron(II) sulfonate complexes

Catalyst Evaluation for Synthesis of Phenylpyridine from Butadiene and Benzonitrile

Nitrogen in oil shale and shale oil. IV. Pyrolytic reactions involving the formation and decomposition of tar bases

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