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Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule

Angewandte Chemie International Edition, 2019-03, Vol.58 (13), p.4200-4204

International ed. in English, 2019

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A Comprehensive Study of Extended Tetrathiafulvalene Cruciform Molecules for Molecular Electronics: Synthesis and Electrical Transport Measurements

Journal of the American Chemical Society, 2014-11, Vol.136 (47), p.16497-16507

2014

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Subphthalocyanine-radiaannulene scaffold - a multi-electron acceptor and strong chromophore

Chemical communications (Cambridge, England), 2018, Vol.54 (22), p.2763-2766

2018

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Azadioxatriangulenium: Synthesis and Photophysical Properties of Reactive Dyes for Bioconjugation

European journal of organic chemistry, 2015-10, Vol.2015 (28), p.6351-6358

2015

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Synthesis and properties of sulfur-functionalized triarylmethylium, acridinium and triangulenium dyes

Beilstein journal of organic chemistry, 2019-09, Vol.15 (1), p.2133-2141

2019

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Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule

Angewandte Chemie, 2019-03, Vol.131 (13), p.4244-4248

2019

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Rational Design of Bright Long Fluorescence Lifetime Dyad Fluorophores for Single Molecule Imaging and Detection

Journal of the American Chemical Society, 2021-01, Vol.143 (3), p.1377-1385

2021

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Inside Cover: Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule (Angew. Chem. Int. Ed. 13/2019)

Angewandte Chemie International Edition, 2019-03, Vol.58 (13), p.4068-4068

2019

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Thieno‐Fused Subporphyrazines: A New Class of Light Harvesters

Chemistry : a European journal, 2017-11, Vol.23 (64), p.16194-16198

2017

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Assessing The Key Photophysical Properties of Triangulenium Dyes for DNA Binding by Alteration of the Fluorescent Core

Chemistry : a European journal, 2021-02, Vol.27 (7), p.2523-2536

2021

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Subphthalocyanine-radiaannulene scaffold - a multi-electron acceptor and strong chromophoreElectronic supplementary information (ESI) available: Synthesis protocols, NMR spectra, UV-vis absorption, fluorescence, electrochemical and computational data. See DOI: 10.1039/c8cc00028j

2018-03

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Evaluation of Ebselen-azadioxatriangulenium as redox-sensitive fluorescent intracellular probe and as indicator within a planar redox optode

Dyes and pigments, 2020-02, Vol.173, p.107866, Article 107866

2020

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Diazaoxatriangulenium: synthesis of reactive derivatives and conjugation to bovine serum albumin

Organic & biomolecular chemistry, 2016-01, Vol.14 (3), p.1091-1101

2016

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Extended Triangulenium Ions: Syntheses and Characterization of Benzo-Bridged Dioxa- and Diazatriangulenium Dyes

Journal of organic chemistry, 2019-03, Vol.84 (5), p.2556-2567

2019

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Diazaoxatriangulenium: synthesis of reactive derivatives and conjugation to bovine serum albuminElectronic supplementary information (ESI) available: Nomenclature of triangulenium ions, data for quantum yield determinations, labelling procedure, parameters describing the time-dependent photophysical properties, tryptophan quenching experiments, and NMR spectra. See DOI: 10.1039/c5ob02293b

2016-01

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Triazatriangulene as Binding Group for Molecular Electronics

Langmuir, 2014-12, Vol.30 (49), p.14868-14876

2014

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Acetylenic scaffolding with subphthalocyanines - synthetic scope and elucidation of electronic interactions in dimeric structuresElectronic supplementary information (ESI) available: NMR spectra, X-ray crystal data, and computational data. CCDC 1550013. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob01907f

2017-11

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Molecular Heterojunctions of Oligo(phenylene ethynylene)s with Linear to Cruciform Framework

Advanced functional materials, 2015-03, Vol.25 (11), p.1700-1708

2015

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Emissive Photoconversion Products of an Amino-triangulenium Dye

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2016-05, Vol.120 (20), p.3554-3561

2016

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Dihydroazulene–Buckminsterfullerene Conjugates

Journal of organic chemistry, 2012-10, Vol.77 (20), p.8922-8932

2012

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Acetylenic scaffolding with subphthalocyanines - synthetic scope and elucidation of electronic interactions in dimeric structures

Organic & biomolecular chemistry, 2017, Vol.15 (46), p.9809-9823

2017

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Fluorescence switching with subphthalocyanine-dihydroazulene dyads

Molecular systems design & engineering, 2019-02, Vol.4 (1), p.199-205

2019

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Diamine anchored molecular junctions of oligo(phenylene ethynylene) cruciform

Chinese chemical letters, 2018-02, Vol.29 (2), p.271-275

2018

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Tuning the p Ka of a pH Responsive Fluorophore and the Consequences for Calibration of Optical Sensors Based on a Single Fluorophore but Multiple Receptors

ACS sensors, 2019-03, Vol.4 (3), p.764-773

2019

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Molecular Junctions Based on SAMs of Cruciform Oligo(phenylene ethynylene)s

Langmuir, 2012-02, Vol.28 (8), p.4016-4023

2012

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Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule

A Comprehensive Study of Extended Tetrathiafulvalene Cruciform Molecules for Molecular Electronics: Synthesis and Electrical Transport Measurements

Subphthalocyanine-radiaannulene scaffold - a multi-electron acceptor and strong chromophore

Azadioxatriangulenium: Synthesis and Photophysical Properties of Reactive Dyes for Bioconjugation

Synthesis and properties of sulfur-functionalized triarylmethylium, acridinium and triangulenium dyes

Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule

Rational Design of Bright Long Fluorescence Lifetime Dyad Fluorophores for Single Molecule Imaging and Detection

Inside Cover: Fluorometric Recognition of Nucleotides within a Water‐Soluble Tetrahedral Capsule (Angew. Chem. Int. Ed. 13/2019)

Thieno‐Fused Subporphyrazines: A New Class of Light Harvesters

Assessing The Key Photophysical Properties of Triangulenium Dyes for DNA Binding by Alteration of the Fluorescent Core

Subphthalocyanine-radiaannulene scaffold - a multi-electron acceptor and strong chromophoreElectronic supplementary information (ESI) available: Synthesis protocols, NMR spectra, UV-vis absorption, fluorescence, electrochemical and computational data. See DOI: 10.1039/c8cc00028j

Evaluation of Ebselen-azadioxatriangulenium as redox-sensitive fluorescent intracellular probe and as indicator within a planar redox optode

Diazaoxatriangulenium: synthesis of reactive derivatives and conjugation to bovine serum albumin

Extended Triangulenium Ions: Syntheses and Characterization of Benzo-Bridged Dioxa- and Diazatriangulenium Dyes

Triazatriangulene as Binding Group for Molecular Electronics

Molecular Heterojunctions of Oligo(phenylene ethynylene)s with Linear to Cruciform Framework

Emissive Photoconversion Products of an Amino-triangulenium Dye

Dihydroazulene–Buckminsterfullerene Conjugates

Acetylenic scaffolding with subphthalocyanines - synthetic scope and elucidation of electronic interactions in dimeric structures

Fluorescence switching with subphthalocyanine-dihydroazulene dyads

Diamine anchored molecular junctions of oligo(phenylene ethynylene) cruciform

Tuning the p Ka of a pH Responsive Fluorophore and the Consequences for Calibration of Optical Sensors Based on a Single Fluorophore but Multiple Receptors

Molecular Junctions Based on SAMs of Cruciform Oligo(phenylene ethynylene)s

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