June 26, 2019



45) H. M. Moura, H. Peterlik, and M. M. Unterlass*: “Green Hydrothermal Synthesis Yields Perylenebisimide-SiO2 Hybrid Materials with Solution-Like Fluorescence and Photoredox Activity”, J. Mater. Chem. A, 2022, accepted.
44) A. Moretton, J. Slyskova, M. E. Simaan, M. Meyenberg, E. A. Arasa-Verge, C. Keskinöz, D. A. Cerrón-Infantes, M. M. Unterlass, and J. I. Loizou*: “Clickable Cisplatin Derivates as Versatile Tools to Probe the DNA Damage Response to Chemotherapy”, Frontiers in Oncology, 2022, accepted.
43) F. A. Amaya-García and M. M. Unterlass*: “Synthesis of 2,3-Diarylquinoxaline Carboxylic Acids in High Temperature Water”, Synthesis, 2022, accepted.


42) M. Reiter, A. Khorsand Kheirabad, M. M. Unterlass*, and J. Yuan*: “Siloxane-based main-chain poly(ionic liquid)s via Debus-Radziszewski reaction“, ACS Polym. Au, 2021, accepted.

41) E. Fujiwara, R. Ishige, D. A. Cerrón-Infantes, M. J. Taublaender, M. M.  Unterlass,* and S. Ando*: Compression and Thermal Expansion Behaviors of Highly Crystalline Polyimide Particles Prepared from Poly(amic acid) and Monomer Salts“, Macromolecules, 2021, accepted. doi: 10.1021/acs.macromol.1c00779

40) M. Lahnsteiner, M. Caldera, H. M. Moura, D. A. Cerrón-Infantes, J. Roeser, T. Konegger, A. Thomas, J. Menche, and M. M. Unterlass*: “Hydrothermal Polymerization of Porous Aromatic Polyimide Networks and Machine Learning-Assisted Computational Morphology Evolution Interpretation“, J. Mater. Chem. A, 2021, 9, 19754-19769. doi: 10.1039/d1ta01253c 

39) V. Sulzgruber, M. M. Unterlass, T. Cavalli, H. Walter: “Micro-encapsulated phase-change material for the application in thermal energy storage“, J. Energy Resour. Technol. 2021, 144(5), 052001. doi: 10.1115/1.4051734

38) M. Reiter, A. M. Anton, J. Chang, F. Kremer, M. M. Unterlass*, and J. Yuan*: “Tuning the glass transition of siloxane-based poly(ionic liquid)s towards high ion conductivity“, J. Polym. Sci., 2021, 1. doi: 10.1002/pol.20210200

37) F. A. Amaya-García, M. Caldera, A. Koren, S. Kubicek, J. Menche, and M. M. Unterlass*: “Green hydrothermal synthesis of fluorescent 2,3-diarylquinoxalines and large-scale computational comparison to existing alternatives“, ChemSusChem, 2021, 14, 1-12. doi:  10.1002/cssc.202100433. (Cover page)

36) J. Essmeister,  M. J. Taublaender, T. Koch, D. A. Cerrón-Infantes, M. M. Unterlass and T. Konegger*: “High modulus polyimide particle-reinforcement of epoxy composites“, Mater. Adv., 2021, 2, 2278-2288. doi: 10.1039/D0MA00980F

35b) M. M. Unterlass*: “Recent advances in hydrothermal materials synthesis“, J. Mater. Chem. A, 2021, 9, 661-662. doi: 10.1039/D0TA90284E

35a) M. M. Unterlass*: “Recent advances in hydrothermal materials synthesis“, Mater. Adv., 2021, 2, 538-539 . doi: 10.1039/d0ma90053b


34fC. A. Urbina-Blanco et al. [for full autor list see 34a]: “A diverse view of science to catalyse change“, J. Am. Chem. Soc. 2020. doi: 10.1021/jacs.0c07877

34eC. A. Urbina-Blanco et al. [for full autor list see 34a]: “A diverse view of science to catalyse change“, Croat. Chem. Acta, 2020, 93(1). doi: 10.5562/diversity2020

34dC. A. Urbina-Blanco et al. [for full autor list see 34a]: “A diverse view of science to catalyse change“, Chem. Sci., 2020, Advance Article. doi: 10.1039/D0SC90150D

34cC. A. Urbina-Blanco et al. [for full autor list see 34a]: “A diverse view of science to catalyse change“, Can. J. Chem., 2020, 00, 1-4. doi: 10.1139/cjc-2020-0323

34b) C. A. Urbina-Blanco et al. [for full autor list see 34a]: “A diverse view of science to catalyse change“, Angew. Chem. Int. Ed., 2020, 59, 2-7. doi10.1002/anie.202009834

34aC. A. Urbina-Blanco, S. Z. Jilani, I. R. Speight, M. J. Bojdys, T. Friščić, J. F. Stoddart, T. L. Nelson, J. Mack, R. A. S. Robinson, E. A. Waddell, J. L. Lutkenhaus, M. Godfrey, M. I. Abboud, S. O. Aderinto, D. Aderohunmu, L. Bibič, J. Borges, V. M. Dong, L. Ferrins, F. M. Fung, T. John, F. P. L. Lim, S. L. Masters, D. Mambwe, P. Thordarson, M.-M. Titirici, G. D. Tormet-González, M. M. Unterlass, A. Wadle, V. W.-W. Yam, and Y.-W. Yang : “A diverse view of science to catalyse change“, Nat. Chem., 2020. doi: 10.1038/s41557-020-0529-x

33) A. S. Abd-El-Aziz, M. Antonietti, C. Barner-Kowollik, W. H. Binder, A. Böker, C. Boyer, M. R. Buchmeiser, S. Z. D. Cheng, F. D’Agosto, G. Floudas, H. Frey, G. Galli, J. Genzer, L. Hartmann, R. Hoogenboom, T. Ishizone, D. L. Kaplan, M. Leclerc, A. Lendlein, B. Liu, T. E. Long, S. Ludwigs, J.-F. Lutz, K. Matyjaszewski, M. A. R. Meier, K. Müllen, M. Müllner, B. Rieger, T. P. Russell, D. A. Savin, A. D. Schlüter, U. S. Schubert, S. Seiffert, K. Severing, J. B. P. Soares, M. Staffilani, B. S. Sumerlin, Y. Sun, B. Z. Tang, C. Tang, P. Théato, N. Tirelli, O. K. C. Tsui, M. M. Unterlass, P. Vana, B. Voit, S. Vyazovkin, C. Weder, U. Wiesner, W.‐Y. Wong, C. Wu, Y. Yagci, J. Yuan, and G. Zhang: “The Next 100 Years of Polymer Science“, Macromol. Chem. Phys., 2020, 2000216. doi: 10.1002/macp.202000216

32) H. M. Moura and M. M. Unterlass*: “Biogenic Metal Oxides“, Biomimetics, 20205, 29. doi: 10.3390/biomimetics5020029

31b) [OPEN ACCESS] M. J. Taublaender, S. Mezzavilla, S. Thiele, F. Glöcklhofer, and M. M. Unterlass*: “Hydrothermale Synthese von konjugierten Polymeren am Beispiel von Pyrronpolymeren und Polybenzimidazolen“, Angew. Chem., 2020, 132, 15050-15060. doi: 10.1002/ange.202000367

31a) [OPEN ACCESS] M. J. Taublaender, S. Mezzavilla, S. Thiele, F. Glöcklhofer, and M. M. Unterlass*: “Hydrothermal Generation of Conjugated Polymers on the Example of Pyrrone Polymers and Polybenzimidazoles”, Angew. Chem. Int. Ed., 2020, 59, 15050-15060. doi: 10.1002/anie.202000367 (Back cover page)

30) L. Hartmann*, M. Staffilani*, and M. M. Unterlass*: “Polymers for the Future”, Macromol. Chem. Phys., 2020, 221, 2000077. doi: 10.1002/macp.202000077


29) M. J. Taublaender, M. Reiter, and M. M. Unterlass*: ”Highly Crystalline, Nanostructured Polyimide Microparticles via Green and Tunable Solvothermal Polymerization”, Macromolecules, 201952(16), 6318-6329. doi: 10.1021/acs.macromol.9b00985

28) G. Sinn, G. Singer, L. Jocher, M. M. Unterlass, H. Rennhofer, U. Windberger, J. Wendrinsky, W. Stöger, K. H. Semlitsch, and H. C. Lichtenegger*: “Mechanical and Fracture Mechanical Properties of Matrix-Reinforced Carbon Fiber Composites with Carbon Nanotubes“, Key. Eng. Mater., 2019, 809, 615-619. doi: 10.4028/www.scientific.net/KEM.809.615

27) G. Singer, G. Sinn, H. Rennhofer, R. Schuller, T. A. Grünewald, M. M.  Unterlass, U. Windberger, and H.C. Lichtenegger*: “High performance functional composites by in-situ orientation of carbon nanofillers“, Compos. Struct., 2019, 215, 178-184. doi: 10.1016/j.compstruct.2019.02.020

26) M. Rimmele, K. Ableidinger, A. V. Marsh, N. J. Cheetham, M. J. Taublaender, A. Buchner, J. Prinz, J. Fröhlich, M. M. Unterlass, M. Heeney, and F. Glöcklhofer*: “Thioalkyl- and Sulfone-Substituted Poly(p-Phenylene Vinylene)s“, Polym. Chem., 2019, 10, 738-750. doi: 10.1039/C8PY01717D


25) [OPEN ACCESS] G. Singer, P. Siedlaczek, G. Sinn, H. Rennhofer, M. Mičušík, M. Omastová , M. M. Unterlass, J. Wendrinsky, V. Milotti, F. Fedi, T. Pichler, and Helga C. Lichtenegger*: “Acid Free Oxidation and Simple Dispersion Method of MWCNT for High-Performance CFRP“, Nanomaterials, 2018, 8(11), 912-930. doi10.3390/nano8110912

24) [OPEN ACCESS] D. A. Cerrón-Infantes and M. M. Unterlass*: “Síntesis Ecoamigables de Colorantes“, Rev. Quim., 2018, 32(1), 18-31.

23b) [OPEN ACCESS] M. J. Taublaender, F. Glöcklhofer, M. Marchetti-Deschmann, and M. M. Unterlass*: “Grüne und rasche hydrothermale Kristallisation und Synthese vollständig konjugierter aromatischer Verbindungen“, Angew. Chem., 2018130, 12450-12454. doi: 10.1002/ange.201801277

23a) [OPEN ACCESS] M. J. Taublaender, F. Glöcklhofer, M. Marchetti-Deschmann, and M. M. Unterlass*: “Green and Rapid Hydrothermal Crystallization and Synthesis of Fully Conjugated Aromatic Compounds“, Angew. Chem.Int. Ed., 201857, 12270-12274. doi: 10.1002/anie.201801277

22) M. M. Unterlass*, S. Ando*, and O. K. C. Tsui*: “Polymer Morphology and Characterization“, Macromol. Chem. Phys., 2018219, 1800001-1800002. doi: 10.1002/macp.201800001. (Editorial to the special issue “Polymer Morphology and Characterization” guest edited by M. M. Unterlass, S. Ando and O. K. C. Tsui)

21a) M. M. Unterlass*: “Hot Water Generates Crystalline Organic Materials” Angew. Chem. Int. Ed. 201857, 2292-2294. doi: 10.1002/anie.201713359

21b) M. M. Unterlass*: “Heißes Wasser ermöglicht Kristallinität in organischen Materialien“, Angew. Chem., 2018130, 2314-2316. doi: 10.1002/ange.201713359

20) [OPEN ACCESS] M. J. Taublaender, M. Reiter, and M. M. Unterlass*:  “Exerting Additive-Assisted Morphological Control During Hydrothermal Polymerization“, Macromol. Chem. Phys., 2018, 219, 1700397-170407. doi: 10.1002/macp.201700397


19) G. Singer, H. Rennhofer, G. Sinn, M. M. Unterlass, J. Wendrinsky, U. Windberger, and H. C. Lichtenegger*: “Processing of Carbon Nanotubes and Carbon Nanofibers towards High Performance Carbon Fiber Reinforced Polymers“, Key Eng. Mater, 2017, 742, 31-37. doi: 10.4028/www.scientific.net/KEM.742.31

18) [OPEN ACCESS] M. M. Unterlass*: “Geomimetics and Extreme Biomimetics Inspired by Hydrothermal Systems – What Can We Learn from Nature for Materials Synthesis“, Biomimetics, 2017, 2(2), 8-27. doi: 10.3390/biomimetics2020008

17) [OPEN ACCESS] L. Leimhofer, B. Baumgartner, M. Puchberger, T. Prochaska, T. Konegger, and M. M. Unterlass*: “Green one-pot synthesis and processing of polyimide-silica hybrid materials“, J. Mater. Chem. A., 2017, 5, 16326-16335. doi: 10.1039/C7TA02498C

16) [OPEN ACCESS] F. Glöcklhofer, A. J. Morawietz, B. Stöger, M. M. Unterlass, and J. Fröhlich*: “Extending the Scope of a New Cyanation: Design and Synthesis of an Anthracene Derivative with an Exceptionally Low LUMO Level and Improved Solubility“, ACS Omega, 20172(4), 1594 – 1600. doi: 10.1021/acsomega.7b00245

15) [OPEN ACCESS] F. Glöcklhofer, A. Peritz, E. Karner, M. J. Bojdys, B. Stadlober, J. Fröhlich, and M. M. Unterlass*: “Dicyano- and Tetracyanopentacene: Foundation of an Intriguing New Class of Easy-to-Synthesize Organic Semiconductors“,  J. Mater. Chem. C, 2017, 5, 2603 – 2610doi: 10.1039/C7TC00143F

14) [OPEN ACCESS] B. Baumgartner, A. Svirkova, J. Bintinger, C. Hametner, M. Marchetti-Deschmann, and M. M. Unterlass*: “Green and highly efficient synthesis of perylene and naphthalene bisimides is nothing but water”, Chem. Commun., 2017, 53, 1229-1232. doi10.1039/C6CC06567H (inside front cover)

Highlights in English:

“Fluorescence Dyes from the Pressure Cooker” on www.tuwien.ac.at “Fluorescence Dyes from the Pressure Cooker” on www.chemeurope.com
“Fluorescence Dyes from the Pressure Cooker” on www.phys.org
“Fluorescence Dyes from the Pressure Cooker” on www.sciencedaily.com
“Fluorescence Dyes from the Pressure Cooker” on www.eurekalert.org

Highlights in German:

“Fluoreszierende Farbstoffe aus dem Druckkochtopf” on www.tuwien.ac.at “Fluoreszierende Farbstoffe aus dem Druckkochtopf” on www.chemie.de
“TU Wien: Organische Pigmente” on www.chz.at and in print (Österreichische Chemiezeitschrift, Jg. 118, Ausgabe 01/2017)
“Einfach zu fluoreszierenden Farbstoffen” at www.chemiextra.com and in print (ChemieXtra, Ausgabe 4/2017)


13b) D. A. Cerrón-Infantes and M. M. Unterlass*: “High-performance polyimide particles with angular shape”, Revisita de Química PUCP, 2016, vol. 30(1-2), 3-6. (invited feature article – front cover – back cover) 

13a) D. A. Cerrón-Infantes and M. M. Unterlass*: “Poliimidas de alto rendimiento con forma angular”, Revisita de Química PUCP, 2016, vol. 30(1-2), 3-6. 

12) M. M. Unterlass*: “Green Synthesis of Inorganic-Organic Hybrid Materials: State of the Art and Future Perspectives”, Eur. J. Inorg. Chem., 20168, 1135-1156. doi: 10.1002/ejic.201501130. (Cover page) – read the author profile here.

11) B. Baumgartner, M. J. Bojdys, P. Skrinjar, and M. M. Unterlass*: “Design Strategies in Hydrothermal Polymerization of Polyimides”, Macromol. Chem. Phys., 2016217, 485-500. doi: 10.1002/macp.201500287 (invited for the Macromolecular Chemistry and Physics “Young Talents in Polymer Science” Issue 2016 – Editorial to the issue can be read here)

Highlighted by: “Hydrothermal Polymerization of Polyimides” on www.materialsviews.com


10) K. Kriechbaum#, D. A. Cerrón-Infantes#, B. Stöger, and M. M. Unterlass*: “Shape-Anisotropic Polyimide Particles by Solid-State Polycondensation of Monomer Salt Single Crystals”, Macromolecules, 201548, 8773-8780. doi10.1021/acs.macromol.5b01545 (# both authors contributed equally)

Highlights in English:

“High-performance material polyimid for the first time with angular shape” on www.tuwien.ac.at
“Polyimide for the first time with angular shape” on www.chemeurope.com
“TU Wien researchers develop new procedure to produce angular polyimide particles” onwww.azom.com
“High-performance material polyimide – for the first time with angular shape” on www.phys.org

Highlights in German:

“Hochleistungsmaterial Polyimid – erstmals eckig” on www.tuwien.ac.at
“Polyimid: Das Runde wird zum Eckigen” on www.derstandard.at
“Polyimid erstmals in Form kantiger Partikel” on www.laborpraxis.vogel.de
“Neues Syntheseverfahren zur Herstellung eckiger Polyimide entwickelt” on www.analytik-news.de
“Hochleistungsmaterial Polyimid – erstmals eckig” on www.materialsgate.de
“Hochleistungsmaterial Polyimid – erstmals eckig“ on www.chemie.de
“Erstmals eckig – Kantige Polyimid-Partikel für höhere Widerstandskraft” in productronic 01|2016

Highlights in other languages:

in Danish: “Polyimid med kanter” in Plast Panorama Scandinavia 04|2016

9) B. Baumgartner, M. Puchberger, and M. M. Unterlass*: “Towards a General Understanding of Hydrothermal Polymerization of Polyimides”, Polym. Chem., 20156, 5773-5781. doi: 10.1039/C5PY00231A  (invited for the Polymer Chemistry Emerging Investigator Issue 2015)

8) [OPEN ACCESS] M. M. Unterlass*: “Creating geomimetic polymers“, Mater. Today, 201518, 242-243. doi: 10.1016/j.mattod.2015.02.013


7) B. Baumgartner, M. J. Bojdys, and M. M. Unterlass*: “Geomimetics for Green Polymer Synthesis: Highly Ordered Polyimides via Hydrothermal Techniques”, Polym. Chem., 20145, 3771-3776. doi: 10.1039/C4PY00263F (Cover page)

Highlighted by:

“Producing stable polymers through hydrothermal synthesis” on www.materialsviews.com
“Wiener Ingenieure kochen Kunststoffe mit Wasserdampf, Hitze und ganz viel Druck” onwww.ingenieur.de (in German only)
“Der Kunststofftrick mit dem Druckkochtopf” on www.derstandard.at (in German only)
“Hochfeste Materialien aus dem Druckkochtopf” on www.tuwien.ac.at (in German only)
“High-Strength Organic Materials Can Be Made Quickly & In Eco-Friendly Way Using Hot Water Vapor” on www.cleantechnica.com
“High-strength materials created under pressure” on www.phys.org
“Wasserdampf statt Giftstoffen“ on www.hitech.at (in German only)
“High-Strength Polymers Made in an Eco-friendly Pressure Cooker” on www.plasticsconnect.com

6M. M. Unterlass*, F. Emmerling, M. Antonietti, and J. Weber: “From dense monomer salt crystals to CO2 selective microporous polyimides via solid-state polymerization” Chem. Commun. 201450, 430-432. doi: 10.1039/C3CC47674J


5) M. Capelot, M. M. Unterlass, F. Tournilhac, and L. Leibler*: “Catalytic Control of the Vitrimer Glass Transition”, ACS MacroLett., 20121, 789-792. doi: 10.1021/mz300239f


4) N. Weber, B. Tiersch, M. M. Unterlass, A. Heilig, and K. Tauer*: “‘Schizomorphic’ Emulsion Copolymerization Particles“, Macromol. Rapid. Commun., 201132, 1925-1929. doi: 10.1002/marc.201100491

3) N. Weber, M. M. Unterlass, and K. Tauer*: “High-Ionic Strength Promotes the Formation of Spherical Copolymer Particles“, Macromol. Chem. Phys., 2011212, 2071-2086. doi: 10.1002/macp.201100206

2M. M. Unterlass, E. Espinosa, F. Boisson, F. D’Agosto*, C. Boisson*, K. Agira, I. Khalakhan, R. Charvet, and J. P. Hill*: “Polyethylenes bearing a terminal porphyrin group“, Chem. Commun., 201147, 7057-7059. doi: 10.1039/C1CC12620B

1M. M. Unterlass, D. Kopetzki, M. Antonietti, and J. Weber*: “Mechanistic study of hydrothermal synthesis of aromatic polyimides“, Polym. Chem., 20112, 1744-1753. doi: 10.1039/C1PY00109D