We create molecular switches,
responsive polymers and BN-PAHs designed as functional
emitters for OLED and circularly polarized luminescence
applications.
Otto Diels Institute54.338° N / 10.122°
EEst. in Kiel · 2010
Group Members 01
The Staubitz Group in Kiel
Group excursion
Together by the Kiel waterfront
Principal Investigator
Full Professor · Chair of Organic
Chemistry
Prof. Dr.
Anne Staubitz
Anne Staubitz studied biochemistry at the University
of Tübingen and worked with Paul Knochel at LMU Munich
on novel Grignard reagents. She completed her PhD with
Varinder Aggarwal at the University of Bristol and
continued there as a postdoctoral researcher with Ian
Manners, investigating main-group inorganic polymers
and catalytic dehydrocoupling reactions of group 13/15
adducts.
She began her independent career as an assistant
professor at Kiel University in 2010, moved to the
University of Bremen as a W2 professor in 2015 and
became a W3 professor in 2020. In 2024, she returned to
Kiel as Chair of Organic Chemistry.
Her research focuses on molecular switches,
switchable polymer systems and their materials-science
applications, as well as organotin heterocycles and
organic frameworks containing group 13 and group 15
elements.
Listed chronologically by the start of their time in the
group.
01
Hinrich Reller
MA · Supervisor: —
06.2024 – 02.2025
02
Lukas Geese
BA · Supervisor: CE
07.2024 – 09.2024
03
Hannes Voß
BA · Supervisor: CE
09.2024 – 01.2025
04
Henrik Paul
BA · Supervisor: CE
09.2024 – 01.2025
05
Beshr Madaraty
MA · Supervisor: CE
11.2024 – 05.2025
06
Thuy Chinh Ta
MA · Supervisor: THK
04.2025 – 10.2025
07
Briga Klopp
BA · Supervisor: CE
05.2025 – 09.2025
08
Tobias Sieve
MA · Supervisor: CE
05.2025 – 11.2025
09
Dennis Kerber
BA · Supervisor: THK
07.2025 – 11.2025
10
Christopher Freytag
BA · Supervisor: HKR
07.2025 – 11.2025
11
Hacer Burak
BA · Supervisor: CE
08.2025 – 12.2025
12
Sandro Paap
BA · Supervisor: CE
08.2025 – 11.2025
13
Leon Bartelt
BA · Supervisor: JL
09.2025 – 12.2025
14
Jannis-Laurin Kuntsch
BA · Supervisor: HKR
10.2025
15
Jenny Gröger
BA · Supervisor: HKR
11.2025
16
Briga Klopp
BA · Supervisor: JL
12.2025 – 03.2026
17
Malin Kaak
MA · Supervisor: CE
12.2025 – 06.2026
18
Dennis Lindstedt
BA · Supervisor: HKR
05.2026 – 08.2026
Research 02
From Molecular Design to Material Impact
From a molecular event to a material-scale function: we
design every level of the system.
01Molecular switches
Azobenzene-based molecular switches
We design and synthesise azobenzene photoswitches with
exceptionally long thermal half-lives by combining
macrocyclic architectures with strategic fluorination,
while precisely controlling geometry and light-driven
switching behaviour.
02Responsive materials
Switchable polymer films and hydrogels
We translate molecular switching into macroscopic
function in photobendable polymer films, responsive
hydrogels and other light-controlled soft materials.
03Circularly polarized
luminescence
BN-PAH materials for CPL
We design chiral boron- and nitrogen-doped polycyclic
aromatic hydrocarbons with intense circularly polarized
luminescence, combining rigid helicene architectures with
high fluorescence efficiency and enhanced CPL
brightness.
04OLED · TADF
BN-PAH OLED emitters
Our current research focuses on boron- and
nitrogen-doped polycyclic aromatic hydrocarbons as TADF
materials for efficient OLED emitters, with precisely
tuned excited states and thermally activated delayed
fluorescence.
05Cross-coupling ·
Catalysis
Selective synthesis
We develop selective cross-coupling strategies and
heterogeneous catalytic methods for the controlled
preparation of complex functional molecules and
materials.
06Main-group chemistry ·
Optoelectronics
Tin heterocycles
We investigate tin-containing heterocycles such as
stannoles and how their incorporation into conjugated
systems changes optical, electronic and electrochemical
properties. Replacing thiophene units with stannoles can
red-shift absorption and emission, lower optical band
gaps and open routes towards functional low-band-gap
materials.
Funding & Cooperations Partners in discovery
Science grows through collaboration.
Our research is enabled by funding partners and
strengthened through collaborations across chemistry,
materials science and neighbouring disciplines.
01
Funding
Funding partners
We gratefully acknowledge the organisations whose
support makes our research possible.
C. Barwig, R. Colaco, A. Koch, S. Geiger, E. R.
Curticean, I. Wacker, Z. Wang, M. Schmidt, A. Sonn, S.
Pashapour, F. Taheri, R. R. Schröder, A. Staubitz and
C. Selhuber-Unkel, Advanced Intelligent Systems 2026,
8, 2500890.
Y. Appiarius, S. Míguez-Lago, P. Puylaert, N. Wolf,
S. Kumar, M. Molkenthin, D. Miguel, T. Neudecker, M.
Juríček, A. G. Campaña and A. Staubitz, Chemical
Science 2024, 15, 466-476.
P.J. Gliese, Y. Appiarius, T. Scheele, E. Lork, T.
Neudecker and A. Staubitz, Acta Crystallographica
Section E Crystallographic Communications 2023 , 79,
1012-1016.
G. Wittstock, M. Bäumer, W. Dononelli, T. Klüner, L.
Lührs, C. Mahr, L.V. Moskaleva, M. Oezaslan, T. Risse,
A. Rosenauer, A. Staubitz, J. Weissmüller and A.
Wittstock, Chemical Reviews 2023 , 123, 6716-6792.
Y. Appiarius, P.J. Gliese, S.A.W. Segler, P. Rusch,
J. Zhang, P.J. Gates, R. Pal, L.A. Malaspina, K.
Sugimoto, T. Neudecker, N.C. Bigall, S. Grabowsky, A.A.
Bakulin and A. Staubitz, The Journal of Physical
Chemistry C 2022 , 126, 4563-4576.
F. Kleemiss, A. Justies, D. Duvinage, P. Watermann,
E. Ehrke, K. Sugimoto, M. Fugel, L.A. Malaspina, A.
Dittmer, T. Kleemiss, P. Puylaert, N.R. King, A.
Staubitz, T.M. Tzschentke, R. Dringen, S. Grabowsky and
J. Beckmann, Journal of Medicinal Chemistry 2020 , 63,
12614-12622.
S. Urrego-Riveros, M. Bremer, J. Hoffmann, A.
Heitmann, T. Reynaldo, J. Buhl, P. J. Gates, F. D.
Sönnichsen, M. Hissler, M. Gerken and A. Staubitz,
Organic Chemistry Frontiers 2019, 6, 3636-3643.
I.-M. Ramirez y Medina, M. Rohdenburg, F.
Mostaghimi, S. Grabowsky, P. Swiderek, J. Beckmann, J.
Hoffmann, V. Dorcet, M. Hissler and A. Staubitz,
Inorganic Chemistry 2018 , 57, 12562-12575.
J. Strüben, J. Hoffmann, D. Presa-Soto, C. Näther
and A. Staubitz, Acta Crystallographica Section E
Crystallographic Communications 2016 , 72,
1590-1594.
V. Blackstone, S. Pfirrmann, H. Helten, A. Staubitz,
A. Presa Soto, G.R. Whittell and I. Manners, Journal of
the American Chemical Society 2012 , 134,
15293-15296.
A. Staubitz, M.E. Sloan, A.P.M. Robertson, A.
Friedrich, S. Schneider, P.J. Gates, J. Schmedt auf der
Günne and I. Manners, Journal of the American Chemical
Society 2010 , 132, 13332-13345.
Cyclic voltammetry reveals oxidation and reduction
potentials, electrochemical reversibility and redox
stability, helping us understand the electronic
properties of molecular switches and emitter
materials.
Responsible: Christoph
Eschen
Compact PGSTAT204 potentiostat/galvanostat
Maximum current: ±400 mA; compliance voltage:
±20 V
Operation in 2-, 3- and 4-electrode
configurations
Gas-tight TSC 1600 closed cell with
glassy-carbon electrode
Ag pseudo-micro reference electrode for the
gas-tight cell
Classical cell with Ag/AgCl reference,
platinum-sheet counter electrode and
interchangeable 2 mm glassy-carbon working
electrode
Control and data evaluation with NOVA
software
External-device triggering for in-situ
spectroelectrochemistry
Polarized optical microscopy (POM) uses crossed
polarizers to reveal birefringence, textures, phase
transitions and molecular ordering that are not
visible in ordinary bright-field microscopy.
Responsible: Thore Klüwer · Thuy
Chinh Ta
Olympus BH-2 POM with trinocular head for
simultaneous observation and image capture
Panasonic camera with MTV-3 C-mount adapter and
Philips live monitor
Instec J035 heating stage with adjustable
target temperature and heating rate
10× eyepieces with 4×, 10×, 20× and 40×
objectives
Thorlabs upLED sources for wavelength-selective
irradiation of samples in quartz cuvettes or NMR
tubes, enabling photostationary-state and
photoswitching studies.
Responsible: Hinrich Reller
M365L3: 365 nm
M415L4: 415 nm · 170 mW cm⁻²
M455L4: 455 nm · 177 mW cm⁻²
M530L4: 530 nm · 164 mW cm⁻²
M590L4: 590 nm · 144 mW cm⁻²
MWWHL4 white LED: 400–800 nm · 166 mW cm⁻²
upLEDs operated at 1000 mA
Thorlabs LCL1582-M plano-concave lens (f = −75
mm) for focusing and collimation
Typical LED-to-sample distance: 3 cm; cuvette
experiments performed with stirring