Pawel Pieranski – crystallographer of liquids and Alfred-Saupe-prize laureate 2019
H.-S. Kitzerow, Liquid Crystals Today 28 (2019) 23–30.

Phase Transformation Behavior of Polylactide Probed by Small Angle Light Scattering and Calorimetry
N. Schmidt, S. KeukerBaumann, J. Meyer, K. Huber, Journal of Polymer Science Part B: Polymer Physics 57 (2019) 1483–1495.

Controlling Self-Assembly with Light and Temperature
N. Carl, W. Müller, R. Schweins, K. Huber, Langmuir 36 (2019) 223–231.

Ion-selective binding as a new trigger for micellization of block copolyelectrolytes with two anionic blocks
N. Carl, S. Prévost, R. Schweins, K. Huber, Soft Matter 15 (2019) 8266–8271.

Self-Assembly of Fibrinogen in Aqueous, Thrombin-Free Solutions of Variable Ionic Strengths
B. Hämisch, A. Büngeler, C. Kielar, A. Keller, O. Strube, K. Huber, Langmuir 35 (2019) 12113–12122.

Joining of blanks by cold pressure welding: Incremental rolling and strategies for surface activation and heat treatment
H.C. Schmidt, W. Homberg, A.G. Orive, G. Grundmeier, B. Duderija, I. Hordych, S. Herbst, F. Nürnberger, H.J. Maier, Materialwissenschaft Und Werkstofftechnik 50 (2019) 924–939.

Joining of blanks by cold pressure welding: Incremental rolling and strategies for surface activation and heat treatment
H.C. Schmidt, W. Homberg, A.G. Orive, G. Grundmeier, B. Duderija, I. Hordych, S. Herbst, F. Nürnberger, H.J. Maier, Materialwissenschaft Und Werkstofftechnik 50 (2019) 924–939.

Kinetics of thermal decomposition of PMMA at different heating rates and in a wide temperature range
O.P. Korobeinichev, .. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu, Thermochimica Acta 671 (2018) 17–25.

Effect of ionic strength on the structure and elongational kinetics of vimentin filaments
C. G. Lopez, O. Saldanha, A. Aufderhorst-Roberts, C. Martinez-Torres, M. Kuijs, G.H. Koenderink, S. Köster, K. Huber, Soft Matter 14 (2018) 8445–8454.

Insight into Fast Nucleation and Growth of Zeolitic Imidazolate Framework-71 by In Situ Static Light Scattering at Variable Temperature and Kinetic Modeling
S. Saha, M. Wiebcke, K. Huber, Crystal Growth &;amp; Design 18 (2018) 4653–4661.

Secondary Particle Formation during the Nonaqueous Synthesis of Metal Oxide Nanocrystals
P. Stolzenburg, B. Hämisch, S. Richter, K. Huber, G. Garnweitner, Langmuir 34 (2018) 12834–12844.

Liquid crystalline dithienothiophene derivatives for organic electronics
J. Vollbrecht, P. Oechsle, A. Stepen, F. Hoffmann, J. Paradies, T. Meyers, U. Hilleringmann, J. Schmidtke, H. Kitzerow, Organic Electronics 61 (2018) 266–275.

Influence of s/s-carbon ratio of vertically standing carbon nanostructures produced by pulsed laser-treatment on PAN-based carbon fibers
K. Engelkemeier, K.-P. Hoyer, M. Schaper, Materials Letters 236 (2018) 752–756.

Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization
X. Yu, M.-T. Picker, M. Schneider, A. Herberg, S. Pascual, L. Fontaine, D. Kuckling, Macromolecular Chemistry and Physics 219 (2017).

Liquid crystals and precious metal: from nanoparticle dispersions to functional plasmonic nanostructures
B. Atorf, T. Funck, T. Hegmann, S. Kempter, T. Liedl, K. Martens, H. Mühlenbernd, T. Zentgraf, B. Zhang, H.-S. Kitzerow, M. Urbanski, Liquid Crystals (2017) 1–19.

Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts
M. Kley, A. Kempter, V. Boyko, K. Huber, Langmuir 33 (2017) 6071–6083.

Insight into the Final Step of the Supramolecular Buildup of Eumelanin
A. Büngeler, B. Hämisch, K. Huber, W. Bremser, O.I. Strube, Langmuir 33 (2017) 6895–6901.

Inverter circuits on freestanding flexible substrate using ZnO nanoparticles for cost-efficient electronics
F.F. Vidor, T. Meyers, K. Müller, G.I. Wirth, U. Hilleringmann, Solid-State Electronics 137 (2017) 16–21.

The International Liquid Crystal Society 1990–2015
D. Dunmur, H.-S. Kitzerow, Liquid Crystals Today 25 (2016) 24–29.

Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione
M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508.