Radical Photochemical Reactions

Single-electron-mediated alkyl transfer affords a novel mechanism for transmetalation, enabling cross-coupling under mild conditions. Here, general conditions are reported for cross-coupling of secondary alkyltrifluoroborates with an array of aryl bromides mediated by an Ir photoredox catalyst and a Ni cross-coupling…

• İDRİS KARAKAYA

A new photoredox catalyst system for atom transfer radical polymerization is developed on the basis of visible light photocatalysis using dimanganese decacarbonyl (Mn2(CO)10) that initiates and controls the polymerization at ambient temperature. The polymerization was performed by a Mn2(CO)10–alkyl halide system with…

• MUSTAFA ÇİFTÇİ

The efficient generation of aryl radicals from arylboronic acids by manganese(III) acetate is described. In aromatic solvents, in situ generated aryl radicals afford the corresponding biaryls in very good yields. This method works selectively, and yields are better than those from similar, previously described methods…

Single-electron transmetalation has emerged as an enabling paradigm for the cross-coupling of Csp(3) hybridized organotrifluoroborates. Cross-coupling of α-alkoxymethyltrifluoroborates with aryl and heteroaryl bromides has been demonstrated by employing dual catalysis with a combination of an iridium photoredox cataly…

• İDRİS KARAKAYA

Free radical reactions have become increasingly important, as well as a very attractive tool, in organic synthesis within the last two decades, due to their powerful, selective, specific, and mild reaction abilities. Mn(OAc)3 mediated oxidative free radical reactions have been extensively developed in the last twenty…

Diarylmethylamines are of great interest due to their prevalence in pharmaceutical chemistry. As a result, new methods for their synthesis are in demand. Herein, we report a versatile protocol for the synthesis of diarylmethylamine derivatives involving palladium-catalyzed arylation of in situ generated 2-azaallyl ani…

• BARIŞ YÜCEL

Abstract Summary: Thiophene was polymerized by means of UV irradiation using diphenyliodonium hexafluorophosphate as a photoinitiator. An initiation mechanism involving electron transfer from photochemically generated onium radical cations to thiophene was proposed. N‐Ethoxy‐2‐methylpyridinium hexafluorophosphate and…

A visible light sensitive photoinitiator system for the cationic polymerization of typical monomers, e.g. of oxiranes such as cyclohexene oxide, of vinyl ethers such as n -butyl vinyl ether, and of other vinyl monomers such as N -vinylcarbazole, using highly conjugated thiophene derivatives is described. The cationic…

• EMRULLAH GÖRKEM GÜNBAŞ

A visible light sensitive photoinitiator system for the cationic polymerization of typical monomers, e.g. of oxiranes such as cyclohexene oxide, of vinyl ethers such as n -butyl vinyl ether, and of other vinyl monomers such as N -vinylcarbazole, using highly conjugated thiophene derivatives is described. The cationic…

• BİNNUR TEMEL

Photoisomerization processes involving five isomers of cytosine were induced by narrowband tunable UV irradiation of matrix-isolated monomers of the compound. Irradiation of an argon matrix containing cytosine monomers with UV λ = 313 nm laser light resulted in syn↔anti photoisomerizations between the two imino-oxo fo…

• RUI FAUSTO MARTINS RIBEIRO DA SILVA LOURENÇO

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• CANAN VARLIKLI

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• ŞULE ERTEN ELA