All Outputs (25)

A bifurcated molecular pentad capable of sequential electronic energy transfer and intramolecular charge transfer (2015)
Journal Article
Harriman, A., Stachelek, P., Sutter, A., & Ziessel, R. (2015). A bifurcated molecular pentad capable of sequential electronic energy transfer and intramolecular charge transfer. Physical Chemistry Chemical Physics, 17(39), 26175-26182. https://doi.org/10.1039/c5cp03932k

An extended molecular array, comprising three distinct types of chromophores and two additional redox-active subunits, that harvests photons over most of the visible spectral range has been synthesized and characterised. The array exhibits a rich var... Read More about A bifurcated molecular pentad capable of sequential electronic energy transfer and intramolecular charge transfer.

Stepwise photoconversion of an artificial light-harvesting array built from extended BODIPY units (2015)
Journal Article
Harriman, A., Stachelek, P., Sutter, A., & Ziessel, R. (2015). Stepwise photoconversion of an artificial light-harvesting array built from extended BODIPY units. Photochemical & Photobiological Sciences, 14(6), 1100-1109. https://doi.org/10.1039/c5pp00021a

A molecular dyad, comprising two disparate extended boron dipyrromethene (BODIPY) units, has been identified as a potential component of artificial light-harvesting arrays. Highly efficient, intramolecular electronic energy transfer takes place under... Read More about Stepwise photoconversion of an artificial light-harvesting array built from extended BODIPY units.

Fluorescent molecular rotors based on the BODIPY motif: effect of remote substituents (2014)
Journal Article
Bahaidarah, E., Harriman, A., Stachelek, P., Rihn, S., Heyer, E., & Ziessel, R. (2014). Fluorescent molecular rotors based on the BODIPY motif: effect of remote substituents. Photochemical & Photobiological Sciences, 13(10), 1397-1401. https://doi.org/10.1039/c4pp00204k

The ability of an unconstrained boron dipyrromethene dye to report on changes in local viscosity is improved by appending a single aryl ring at the lower rim of the dipyrrin core. Recovering the symmetry by attaching an identical aryl ring on the opp... Read More about Fluorescent molecular rotors based on the BODIPY motif: effect of remote substituents.

Exciplex Emission from a Boron Dipyrromethene (Bodipy) Dye Equipped with a Dicyanovinyl Appendage (2013)
Journal Article
Nano, A., Ziessel, R., Stachelek, P., Alamiry, M. A., & Harriman, A. (2014). Exciplex Emission from a Boron Dipyrromethene (Bodipy) Dye Equipped with a Dicyanovinyl Appendage. ChemPhysChem, 15(1), 177-186. https://doi.org/10.1002/cphc.201300805

The photophysical properties of a prototypic donor–acceptor dyad, featuring a conventional boron dipyrromethene (Bodipy) dye linked to a dicyanovinyl unit through a meso-phenylene ring, have been recorded in weakly polar solvents. The absorption spec... Read More about Exciplex Emission from a Boron Dipyrromethene (Bodipy) Dye Equipped with a Dicyanovinyl Appendage.

Charge-Recombination Fluorescence from Push-Pull Electronic Systems Constructed around Amino-Substituted Styryl-BODIPY Dyes (2013)
Journal Article
Nano, A., Ziessel, R., Stachelek, P., & Harriman, A. (2013). Charge-Recombination Fluorescence from Push-Pull Electronic Systems Constructed around Amino-Substituted Styryl-BODIPY Dyes. Chemistry - A European Journal, 19(40), 13528-13537. https://doi.org/10.1002/chem.201301045

A small series of donor–acceptor molecular dyads has been synthesized and fully characterized. In each case, the acceptor is a dicyanovinyl unit and the donor is a boron dipyrromethene (BODIPY) dye equipped with a single styryl arm bearing a terminal... Read More about Charge-Recombination Fluorescence from Push-Pull Electronic Systems Constructed around Amino-Substituted Styryl-BODIPY Dyes.