ABSTRACT
Metal-free oxidative C-C coupling by using polyalkoxybenzene-derived diaryliodonium(III) salts as both the oxidant and aryl source has been developed. These salts can induce single-electron-transfer (SET) oxidation to yield electron-rich arenes and subsequently transfer the polyalkoxyphenyl group into in situ generated aromatic radical cations to produce biaryl products. The reaction is promoted by a Lewis acid that activates the iodonium salts. It has been revealed that the reactivity of the salts under acidic conditions is quite different to their known behavior under basic conditions. The reactivity preference of a series of iodonium salts in the SET oxidation and their ligand transfer abilities have been systematically investigated and the results are summarized in this report.
Subject(s)
Benzene Derivatives/chemistry , Onium Compounds/chemistry , Catalysis , Electron Transport , Electrons , Ligands , Oxidative CouplingABSTRACT
We have successfully established an efficient route to the core structure of donor-acceptor head-to-tail (H-T)-linked regioregular oligothiophenes, which includes the following key synthetic steps, that is, hypervalent iodine induced direct and regioselective coupling of thiophenes and the use of the obtained bithiophenes as excellent coupling substrates for the Suzuki and Stille couplings. The versatility of this new approach is highlighted in the dramatic improvement of the yield (ca. 59 % overall yield) of MK-2, a high-performance organic dye, for photovoltaic applications.
Subject(s)
Coloring Agents/chemistry , Coloring Agents/chemical synthesis , Heterocyclic Compounds/chemistry , Iodine/chemistry , Metals/chemistry , Thiophenes/chemical synthesis , Catalysis , Molecular Structure , Stereoisomerism , Thiophenes/chemistryABSTRACT
The intermolecular C-H cross-coupling between aromatic ethers has been achieved for the first time using perfluorinated hypervalent iodine(III) compounds as extreme single-electron-transfer (SET) oxidants. The demonstrations of this specific coupling could provide a direct route to valuable oxygenated mixed naphthalene-benzene biaryls 3 only, without formation of other biaryl-derived byproducts.
Subject(s)
Benzene Derivatives/chemistry , Benzene Derivatives/chemical synthesis , Hydrocarbons, Fluorinated/chemistry , Hydrocarbons, Iodinated/chemistry , Naphthalenes/chemistry , Naphthalenes/chemical synthesis , Catalysis , Combinatorial Chemistry Techniques , Metals , Oxidation-ReductionABSTRACT
A new synthetic concept for obtaining unsymmetrical biaryl coupling products by an oxidative method is reported. Our synthetic strategy casts light on the reaction intermediate for switching the reactivity of 3-substituted thiophenes. On the basis of this strategy, a novel direct method for the synthesis of head-to-tail bithiophenes using hypervalent iodine(III) reagents has been developed.
Subject(s)
Iodine/chemistry , Thiophenes/chemistry , Thiophenes/chemical synthesis , Molecular Structure , Oxidation-Reduction , StereoisomerismABSTRACT
In this manuscript, we report clear evidence for the generation of aromatic cation radicals produced by using [hydroxy(tosyloxy)iodo]benzene (HTIB) in fluoroalcohol solvents such as 2,2,2-trifluoroethanol (TFE) and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP). The single-electron-transfer (SET) oxidation ability of HTIB to give cation radicals was first established by ESR and UV measurements. The reaction was broadly applied to various thiophenes, and unique thienyliodonium salts were directly synthesized by this method in excellent yields without the production of any harmful byproducts.
