6533b839fe1ef96bd12a670e

RESEARCH PRODUCT

Role of the Open-Shell Character on the Pressure-Induced Conductivity of an Organic Donor-Acceptor Radical Dyad

Manuel SoutoManuel SoutoImma RateraRoser ValentíHarald Olaf JeschkeNicola CasatiConcepció RoviraMaria Chiara GulloHengbo CuiJaume VecianaFabio Montisci

subject

010405 organic chemistryChemistryRadicalOrganic ChemistryGeneral ChemistryOrganic radical010402 general chemistry01 natural sciencesCatalysisDonor-acceptor3. Good health0104 chemical sciencesSingle-component conductorDelocalized electronchemistry.chemical_compoundCrystallographyUnpaired electronTetrathiafulvaleneCharge carrierIsostructuralElectronic band structureOpen shellPolychlorotriphenylmethylTetrathiafulvalene

description

Single‐component conductors based on neutral organic radicals have received a lot of attention due to the possibility that the unpaired electron can serve as a charge carrier without the need of a previous doping process. Although most of these systems are based on delocalized planar radicals, we present here a nonplanar and spin localized radical based on a tetrathiafulvalene (TTF) moiety, linked to a perchlorotriphenylmethyl (PTM) radical by a conjugated bridge, which exhibits a semiconducting behavior upon application of high pressure. The synthesis, electronic properties, and crystal structure of this neutral radical TTF‐Ph‐PTM derivative (1) are reported and implications of its crystalline structure on its electrical properties are discussed. On the other hand, the non‐radical derivative (2), which is isostructural with the radical 1, shows an insulating behavior at all measured pressures. The different electronic structures of these two isostructural systems have a direct influence on the conducting properties, as demonstrated by band structure DFT calculations.

https://doi.org/10.1002/chem.201800881