Skip to main content

Research Repository

Advanced Search

Outputs (5)

Extended ligand conjugation and dinuclearity as a route to efficient platinum-based near-infrared (NIR) triplet emitters and solution-processed NIR-OLEDs (2020)
Journal Article
Shafikov, M. Z., Pander, P., Zaytsev, A. V., Daniels, R., Martinscroft, R., Dias, F. B., Williams, J. G., & Kozhevnikov, V. N. (2021). Extended ligand conjugation and dinuclearity as a route to efficient platinum-based near-infrared (NIR) triplet emitters and solution-processed NIR-OLEDs. Journal of Materials Chemistry C Materials for optical and electronic devices, 9(1), 127-135. https://doi.org/10.1039/d0tc04881j

Near infrared (NIR) emission from molecular materials is typically targeted by using more extended conjugated systems compared to visible-emitting materials. But efficiencies usually fall off due to the combined effects of increasing non-radiative an... Read More about Extended ligand conjugation and dinuclearity as a route to efficient platinum-based near-infrared (NIR) triplet emitters and solution-processed NIR-OLEDs.

Benzannulation via the use of 1,2,4-triazines extends aromatic system of cyclometallated Pt(II) complexes to achieve candle light electroluminescence (2020)
Journal Article
Pander, P., Turnbull, G., Zaytsev, A. V., Dias, F. B., & Kozhevnikov, V. N. (2021). Benzannulation via the use of 1,2,4-triazines extends aromatic system of cyclometallated Pt(II) complexes to achieve candle light electroluminescence. Dyes and Pigments, 184, Article 108857. https://doi.org/10.1016/j.dyepig.2020.108857

This work describes an application of 1,2,4-triazine methodology for the synthesis of novel cyclometallated Pt (II) complexes of C^N type. It is shown that addition of a cyclopenteno unit into the complex structure not only facilitates the fabricatio... Read More about Benzannulation via the use of 1,2,4-triazines extends aromatic system of cyclometallated Pt(II) complexes to achieve candle light electroluminescence.

Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect (2020)
Journal Article
Rodrigues, A. I., Krishnamoorthy, P., Gomes, C. S., Carmona, N., Di Paolo, R. E., Pander, P., Pina, J., Sérgio Seixas de Melo, J., Dias, F. B., Calhorda, M. J., Maçanita, A. L., Morgado, J., & Gomes, P. T. (2020). Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect. Dalton Transactions, 49(29), 10185-10202. https://doi.org/10.1039/d0dt01845g

A group of new boron complexes [BPh2{2N,N’-NC4H3-2-C(H)=N-C6H4X}] (X= 4-Cl 4c, 4-Br 4d, 4-I 4e, 3-Br 4f, 2-Br 4g, 2-I 4h) containing different halogens as substituents in the N-aryl ring have been synthesized and characterized in terms of their mole... Read More about Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect.

Toward Efficient Toxic-Gas Detectors: Exploring Molecular Interactions of Sarin and Dimethyl Methylphosphonate with Metal-Centered Phthalocyanine Structures (2020)
Journal Article
Aldahhak, H., Powroźnik, P., Pander, P., Jakubik, W., Dias, F. B., Schmidt, W. G., Gerstmann, U., & Krzywiecki, M. (2020). Toward Efficient Toxic-Gas Detectors: Exploring Molecular Interactions of Sarin and Dimethyl Methylphosphonate with Metal-Centered Phthalocyanine Structures. Journal of Physical Chemistry C, 124(11), 6090-6102. https://doi.org/10.1021/acs.jpcc.9b11116

The rapid and reliable detection of lethal agents such as sarin is of increasing importance. Here, density-functional theory (DFT) is used to compare the interaction of sarin with single-metal-centered phthalocyanine (MPc) and MPc layer structures to... Read More about Toward Efficient Toxic-Gas Detectors: Exploring Molecular Interactions of Sarin and Dimethyl Methylphosphonate with Metal-Centered Phthalocyanine Structures.

Donor-acceptor 1,2,4,5-Tetrazines Prepared by Buchwald-Hartwig Cross-Coupling Reaction and Their Photoluminescence Turn-on Property by Inverse Electron Demand Diels-Alder Reaction (2020)
Journal Article
Qu, Y., Pander, P. H., Vybornyi, O., Vasylieva, M., Guillot, R., Miomandre, F., Dias, F. B., Skabara, P. J., Data, P., Clavier, G., & Audebert, P. (2020). Donor-acceptor 1,2,4,5-Tetrazines Prepared by Buchwald-Hartwig Cross-Coupling Reaction and Their Photoluminescence Turn-on Property by Inverse Electron Demand Diels-Alder Reaction. Journal of Organic Chemistry, 85(5), 3407-3416. https://doi.org/10.1021/acs.joc.9b02817

A facile efficient synthetic tool, Buchwald-Hartwig cross-coupling reaction, for the functionalization of 1,2,4,5-tetrazines is presented. Important factors affecting the Buchwald-Hartwig cross-coupling reaction have been optimized. Seven new donor-a... Read More about Donor-acceptor 1,2,4,5-Tetrazines Prepared by Buchwald-Hartwig Cross-Coupling Reaction and Their Photoluminescence Turn-on Property by Inverse Electron Demand Diels-Alder Reaction.