Electron transfer from tetracarbonylrhodate(1–) to nitro aromatics: novel interaction of nitro radical anions with a rhodium(I) centre-Reference-Cited by-同舟云学术

Electron transfer from tetracarbonylrhodate(1–) to nitro aromatics: novel interaction of nitro radical anions with a rhodium(I) centre

Published:1995 Issue:23 Volume: Page:2441-2442
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Liu Pey-Horng,Liao Hong-Yueh,Cheng Chien-Hong

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950002441

Reference34 articles.

1. A. J. Fry , in The Chemistry of Amino, Nitroso and Nitro Compounds and their Derivatives: The Chemistry of Functional Groups, Supplement F. ed. S. Patai, Wiley, New York, 1982, part 1, pp. 319–337;

2. STERIC EFFECTS ON NITROGEN HYPERFINE COUPLING IN METHYL SUBSTITUTED MONO- AND DINITROBENZENE ANION RADICALS

3. Homogeneous catalytic carbonylation of nitroaromatics. 5. Kinetics and mechanism of aniline and carbamate formation using ruthenium complex Ru(Ph2PCH2CH2PPh2)(CO)3

4. Kinetic electron spin resonance studies on the photolysis of some carbonyl, nitroso, and nitro compounds

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