Aggregates Promote Efficient Charge Transfer Doping of Poly(3-hexylthiophene).

The doping efficiencies of regioregular (r-Re) and regiorandom (r-Ra) poly(3-hexylthiophene) (P3HT) with 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4-TCNQ) were studied in solution using electron paramagnetic resonance (EPR), (19)F NMR, optical absorption, and Raman spectroscopy. EPR spectra of doped r-Re P3HT possess significantly larger amounts of paramagnetic species than r-Ra P3HT with similar F4-TCNQ loadings (∼0.1% up to 50%), which is confirmed by corresponding optical absorption spectra. (19)F NMR also show a rapid disappearance of the pristine F4-TCNQ signal when small amounts of r-Re P3HT are added due to minority paramagnetic species acting as efficient spin relaxation channels. Raman spectra of both P3HT variants indicate strong interactions with F4-TCNQ, however, the presence of free charges is only detected in r-Re samples owing to its ability to aggregate and adopt ordered conformations allowing for delocalization of hole charges after initial contact with the dopant.

Diamidodipyrrins: versatile bipyrrolic ligands with multiple metal binding modes.

A straightforward, facile synthesis of diamidodipyrromethenes (diamidodipyrrins, DADP (R,R')) is presented. These tetradentate ligands readily form complexes with metal ions such as Ni (2+) and Cu (2+) and can adopt different binding modes with these metals. One version of the ligand (DADP (Ph, iPr )) has been structurally characterized in its "free base" form, as a HBr salt, and as the Ni (2+) and Cu (2+) complexes. A symmetric NNOO donor set is found for the Cu (2+) complex in the solid state, involving two carbonyl oxygen atoms and two dipyrrin nitrogen atoms, and this coordination mode has been confirmed in solution by electron paramagnetic resonance. An asymmetric NNNO binding mode found for the Ni (2+) complex in the solid state persists in solution as revealed by (1)H NMR. The HBr salt form of the ligand shows an intriguing hydrogen-bonded head-to-head dimer arrangement. Experiments show that Cu (2+), but not Ni (2+), can mediate the rapid oxidation of the diamidodipyrromethane precursors to the diamidodipyrromethene ligands in the presence of dioxygen. The work here shows that diamidodipyrrins are a versatile new class of ligands in the area of nonporphyrinic pyrrole-based compounds that merit further investigation.