Journal of the Chemical Society Perkin Transactions 2 · 1998 · 33 citations · 23 references
Inorganic CompoundCharge-transfer ComplexEngineeringBiochemistryNatural SciencesPolyiodide SaltsAryl Radical CationOrganometallic ElectrochemistryOrganic ChemistryMolecular ComplexChemistryHalogenationInterfacial ChemistryBiomolecular EngineeringInitial Oxidation
The reaction of iodine and 9-methylacridine in methylene chloride results not in the formation of a charge-transfer complex as with acridine, but in the iodine-rich salt [ICH2C13H8N–H]4(I8)(I5)2, 8, where a proton on the methyl group has been replaced by an iodine. In toluene, the reaction produces both a charge-transfer complex ICH2C13H8N–I2, 9, and a salt [CH3–acridine(H)]2(I7)(I5), 10. Polyiodide salt formation can be explained by the availability of a facile reaction pathway from the aryl radical cation which results from initial oxidation by I2.
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International Tables for X-Ray Crystallography
P. P. Ewald · Nature · 1953 · 5.3K citations · Full text
A Text-Book of Practical Organic Chemistry
J. W. Cook · Nature · 1948 · 3.5K citations
A. Martin de P. Nicholas, Donald R. Arnold · Canadian Journal of Chemistry · 1982 · 191 citations