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7-(Fur-2-yl)benzotriazinyl 1 is the first example of a hydrazyl radical dimer with a thermally accessible triplet state. The triplet exciton (|D| = 0.018 cm(-1), |E| = 0.001 cm(-1)) was observed by solid-state VT-EPR spectroscopy between 5 and 140 K. VT crystallography, DFT calculations and magnetic susceptibility studies reveal a strong temperature dependence of the intra-dimer exchange interaction with J/k ~ -254 + 0.0007T(2).

A comparative study of two structural isomers highlights the advantages of bifuran vs. bithiophene units in conjugated systems, such as higher fluorescence, solubility, and increased stability of the oxidized species. Importantly, we have found that the small bifuran unit bestows the advantages found in longer oligofurans, and should be considered in the rational design of π-conjugated systems.

We show that interactions between the electrode surface and the transition metal during the initial step of metal nanoparticle formation can be utilized to control the formation and size of metal nanoparticles deposited on a conducting surface. Pt nanoparticles formed on the PEDOS surface are of smaller size compared to the PEDOT surface.

A Raman spectroscopic analysis revealed that π-conjugation does not reach saturation at least up to the octamer in long α-oligofurans and spreads over 14-15 furan units in the polyfuran. Comparing DFT calculations with experimental results suggests that a considerable amount of HF exchange is required to reproduce computationally the observed conjugation.

We report that linear oligomers of furan, which is a biodegradable molecule directly obtainable from biomass, could be used as organic semiconductors and show field effect mobilities similar to those of the corresponding thiophene analogues. Efficient fluorescence and increased solubility of oligofurans and their derivatives are two other important advantages for their application in organic electronics.

An interesting change in mechanism (from concerted to biradical) is described for the reaction of acenes (benzene through pentacene) with molecular oxygen (either singlet oxygen, 1Deltag-O2, or triplet oxygen, 3Sigmag-O2).

Clean endocyclic C-O bond cleavage has been achieved in the reactions of 5-membered phosphate triesters with various nucleophiles.