Staff profile

Journal Article

• Ligand Chirality Transfer from Solution State to the Crystalline Self‐Assemblies in Circularly Polarized Luminescence (CPL) Active Lanthanide Systems
  
  Caffrey, D. F., Gorai, T., Rawson, B., Martínez‐Calvo, M., Kitchen, J. A., Murray, N. S., Kotova, O., Comby, S., Peacock, R. D., Stachelek, P., Pal, R., & Gunnlaugsson, T. (2024). Ligand Chirality Transfer from Solution State to the Crystalline Self‐Assemblies in Circularly Polarized Luminescence (CPL) Active Lanthanide Systems. Advanced Science, 11(18), Article 2307448. https://doi.org/10.1002/advs.202307448
• Circularly Polarized Luminescence Bioimaging Using Chiral BODIPYs: A Model Scaffold for Advancing Unprecedented CPL Microscopy Using Small Full-Organic Probes.
  
  Stachelek, P., Serrano-Buitrago, S., Maroto, B. L., Pal, R., & de la Moya, S. (2024). Circularly Polarized Luminescence Bioimaging Using Chiral BODIPYs: A Model Scaffold for Advancing Unprecedented CPL Microscopy Using Small Full-Organic Probes. ACS Applied Materials and Interfaces, 16(49). https://doi.org/10.1021/acsami.4c14127
• Recent advances in highly-efficient near infrared OLED emitters
  
  dos Santos, P. L., Stachelek, P., Takeda, Y., & Pander, P. (2024). Recent advances in highly-efficient near infrared OLED emitters. Materials Chemistry Frontiers, 8(7), 1731-1766. https://doi.org/10.1039/d3qm01067h
• Rapid handheld time-resolved circularly polarised luminescence photography camera for life and material sciences
  
  De Rosa, D. F., Brook, P., Black, D. J., & Pal, R. (2023). Rapid handheld time-resolved circularly polarised luminescence photography camera for life and material sciences. Nature Communications, 14, Article 1537. https://doi.org/10.1038/s41467-023-37329-8
• Near-Infrared Circularly Polarised Luminescence from Helically Extended Chiral N,N,O,O -Boron Chelated Dipyrromethenes
  
  Algoazy, N., Clarke, R. G., Penfold, T. J., Waddell, P. G., Probert, M. R., Aerts, R., Herrebout, W., Stachelek, P., Pal, R., Hall, M. J., & Knight, J. G. (2022). Near-Infrared Circularly Polarised Luminescence from Helically Extended Chiral N,N,O,O -Boron Chelated Dipyrromethenes. ChemPhotoChem, 6(9), Article e202200090. https://doi.org/10.1002/cptc.202200090
• The Pink Box: Exclusive Homochiral Aromatic Stacking in a Bis-perylene Diimide Macrocycle
  
  Penty, S. E., Zwijnenburg, M. A., Orton, G. R., Stachelek, P., Pal, R., Xie, Y., Griffin, S. L., & Barendt, T. A. (2022). The Pink Box: Exclusive Homochiral Aromatic Stacking in a Bis-perylene Diimide Macrocycle. Journal of the American Chemical Society, 144(27), 12290-12298. https://doi.org/10.1021/jacs.2c03531
• Circularly polarised luminescence laser scanning confocal microscopy to study live cell chiral molecular interactions
  
  Stachelek, P., MacKenzie, L., Parker, D., & Pal, R. (2022). Circularly polarised luminescence laser scanning confocal microscopy to study live cell chiral molecular interactions. Nature Communications, 13(1), Article 533. https://doi.org/10.1038/s41467-022-28220-z
• The Impact of C2 Insertion into a Carbazole Donor on the Physicochemical Properties of Dibenzo[a,j]phenazine-Cored Donor–Acceptor–Donor Triads
  
  Zimmermann Crocomo, P., Kaihara, T., Kawaguchi, S., Stachelek, P., Minakata, S., Silva, P., Data, P., & Takeda, Y. (2021). The Impact of C2 Insertion into a Carbazole Donor on the Physicochemical Properties of Dibenzo[a,j]phenazine-Cored Donor–Acceptor–Donor Triads. Chemistry – A European Journal, 27(53), 13390-13398. https://doi.org/10.1002/chem.202101654
• Are the Rates of Dexter Transfer in TADF Hyperfluorescence Systems Optically Accessible?
  
  Haase, N., Danos, A., Pflumm, C., Stachelek, P., Brütting, W., & Monkman, A. P. (2021). Are the Rates of Dexter Transfer in TADF Hyperfluorescence Systems Optically Accessible?. Materials Horizons., 8(6), 1805-1815. https://doi.org/10.1039/d0mh01666g
• The twists and turns of chiral chemistry
  
  MacKenzie, L. E., & Brook, P. (2021). The twists and turns of chiral chemistry. Nature Chemistry, 13(6), 521-522. https://doi.org/10.1038/s41557-021-00729-8
• Electrochemical and Spectroelectrochemical Comparative Study of Macrocyclic Thermally Activated Delayed Fluorescent Compounds: Molecular Charge Stability vs OLED EQE Roll‐Off
  
  Nyga, A., Izumi, S., Higginbotham, H. F., Stachelek, P., Pluczyk, S., de Silva, P., Minakata, S., Takeda, Y., & Data, P. (2020). Electrochemical and Spectroelectrochemical Comparative Study of Macrocyclic Thermally Activated Delayed Fluorescent Compounds: Molecular Charge Stability vs OLED EQE Roll‐Off. Asian Journal of Organic Chemistry, 9(12), 2153-2161. https://doi.org/10.1002/ajoc.202000475
• Thermally Activated Delayed Fluorescent Donor–Acceptor–Donor–Acceptor π-Conjugated Macrocycle for Organic Light-Emitting Diodes
  
  Izumi, S., Higginbotham, H. F., Nyga, A., Stachelek, P., Tohnai, N., Silva, P. de, Data, P., Takeda, Y., & Minakata, S. (2020). Thermally Activated Delayed Fluorescent Donor–Acceptor–Donor–Acceptor π-Conjugated Macrocycle for Organic Light-Emitting Diodes. Journal of the American Chemical Society, 142(3), 1482-1491. https://doi.org/10.1021/jacs.9b11578
• Exploiting trifluoromethyl substituents for tuning orbital character of singlet and triplet states to increase the rate of thermally activated delayed fluorescence
  
  Ward, J. S., Danos, A., Stachelek, P., Fox, M. A., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2020). Exploiting trifluoromethyl substituents for tuning orbital character of singlet and triplet states to increase the rate of thermally activated delayed fluorescence. Materials Chemistry Frontiers, 4(12). https://doi.org/10.1039/d0qm00429d
• Molecular Design Strategies for Color Tuning of Blue TADF Emitters
  
  Stachelek, P., Ward, J. S., dos Santos, P. L., Danos, A., Colella, M., Haase, N., Raynes, S. J., Batsanov, A. S., Bryce, M. R., Monkman, A. P., & Brook, P. (2019). Molecular Design Strategies for Color Tuning of Blue TADF Emitters. ACS Applied Materials and Interfaces, 11(30), 27125-27133. https://doi.org/10.1021/acsami.9b06364
• Ultrafast Through-Space Electronic Energy Transfer in Molecular Dyads Built around Dynamic Spacer Units
  
  Ziessel, R., Stachelek, P., Harriman, A., Hedley, G. J., Roland, T., Ruseckas, A., & Samuel, I. D. (2018). Ultrafast Through-Space Electronic Energy Transfer in Molecular Dyads Built around Dynamic Spacer Units. The Journal of Physical Chemistry A, 122(18), 4437-4447. https://doi.org/10.1021/acs.jpca.8b02415
• End-to-end communication in a linear supermolecule with a BOPHY centre and N,N-dimethylanilino-based terminals
  
  Woodford, O. J., Stachelek, P., Ziessel, R., Algoazy, N., Knight, J. G., & Harriman, A. (2018). End-to-end communication in a linear supermolecule with a BOPHY centre and N,N-dimethylanilino-based terminals. New Journal of Chemistry, 42(7). https://doi.org/10.1039/c7nj04654e
• Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives
  
  Stachelek, P., Alsimaree, A. A., Alnoman, R. B., Harriman, A., & Knight, J. G. (2017). Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A, 121(10), 2096-2107. https://doi.org/10.1021/acs.jpca.6b11131
• Electronic Communication in Closely Connected BODIPY-Based Bichromophores
  
  Stachelek, P., & Harriman, A. (2016). Electronic Communication in Closely Connected BODIPY-Based Bichromophores. The Journal of Physical Chemistry A, 120(41), 8104-8113. https://doi.org/10.1021/acs.jpca.6b08284
• Solvent-Driven Conformational Exchange for Amide-Linked Bichromophoric BODIPY Derivatives
  
  Thakare, S., Stachelek, P., Mula, S., More, A. B., Chattopadhyay, S., Ray, A. K., Sekar, N., Ziessel, R., & Harriman, A. (2016). Solvent-Driven Conformational Exchange for Amide-Linked Bichromophoric BODIPY Derivatives. Chemistry - A European Journal, 22(40), 14356-14366. https://doi.org/10.1002/chem.201602354
• A bifurcated molecular pentad capable of sequential electronic energy transfer and intramolecular charge transfer
  
  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
• Stepwise photoconversion of an artificial light-harvesting array built from extended BODIPY units
  
  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
• Fluorescent molecular rotors based on the BODIPY motif: effect of remote substituents
  
  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. Photochem. Photobiol. Sci., 13(10), 1397-1401. https://doi.org/10.1039/c4pp00204k
• Exciplex Emission from a Boron Dipyrromethene (Bodipy) Dye Equipped with a Dicyanovinyl Appendage
  
  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
• Charge-Recombination Fluorescence from Push-Pull Electronic Systems Constructed around Amino-Substituted Styryl-BODIPY Dyes
  
  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