Beauftragter für Öffentlichkeitsarbeit

Technische Hochschule Nürnberg Georg Simon Ohm, Nürnberg:

Seit 09/2019 Professor für Anorganische Chemie

Novaled GmbH (SAMSUNG-Gruppe), Dresden:

08/2012 – 08/2019 Gruppenleiter, Laborleiter & Projektleiter. 

Entwicklung von Löcher-Injektionskonzepten für die Anwendung in der organischen Elektronik.

Institut für Angewandte Photophysik, Technische Universität Dresden:

07/2007 – 07/2012 Wissenschaftlicher Mitarbeiter und Leiter der Synthesegruppe.

Synthese, Evaluation und Optimierung organischer und anorganischer Halbleiter-Materialien für die Anwendung in organischen Solarzellen und organischen Leuchtdioden (OLED).

Institut für Chemie, Technische Universität Berlin:

11/2002 – 06.2007 Wissenschaftlicher Mitarbeiter (mit Lehraufgaben).

Synthese und Struktur von Komplexverbindungen der Hauptgruppen- und Übergangsmetalle, sowie Lanthanoide.

01/2002 – 08/2005 Promotion zum Dr. rer. nat. (Herbert Schumann).

Titel: „Synthese und Eigenschaften neuer Organoaluminium-Komplexe“.

10/1998 – 12/2001 Chemie-Studium. Abschluss als Diplom-Chemiker.

G. A. Razuvaev Institut für Organometall-Chemie, Russische Akademie der Wissenschaften, Nizhny Novgorod, Russland:

02/2007 – 05/2007 Gastwissenschaftler als Humboldt-Stipendiat (Feodor Lynen-Forschungsstipendium der Alexander von Humboldt-Stiftung).

Technische Fachhochschule Berlin:

10/1994 – 07/1998 Chemie-Studium (Angewandte Chemie). Abschluss als Diplom-Ingenieur (FH).

Diplomarbeit bei Prof. Dr. Norbert Auner (Humboldt-Universität zu Berlin).

ZERO-Lack GmbH & Co. KG:

08/1992 – 9/1994 Forschung/Entwicklung und Qualitätskontrolle.

Kollegschule des Kreises Minden-Lübbecke:

08/1989 – 07/1992 Ausbildung zum Chemisch-technischen Assistenten.

Feodor Lynen-Forschungsstipendium der Alexander von Humboldt-Stiftung (2006)

Graduierten-Kolleg (2001)

Klaus-Koch-Studienpreis (2002)

Allgemeine Chemie

Anorganische Chemie

Moderne Themen der Anorganischen Chemie

Metallorganik

Nanoskalierte Funktionsmaterialien

Organische Halbleiter

Materialwissenschaften

Anwendung von "Molecular Modelling" in der Molekülchemie

Materialwissenschafte & interdisziplinäre Forschung zu molekularen Funktionsmaterialien

• Metallorganische Substanzen für die CVD oder Katalyse
• Organische Halbleitermaterialien für die Organische Optoelektronik
• Photoaktive Materialien (Photovoltaik, Emission)
• Batterie-Materialien
• Nanostrukturierte Metall- & Halbleiterpartikel
• Metallorganische Gerüstverbindungen (MOF)
• Modellierung chemischer Systeme (Molecular Modelling)

Substanzklassen

• Stark Lewis-saure Metallkomplexe
• Komplexe mit Fluor-haltigen Liganden
• Koordinationspolymere
• Redox-aktive organische Moleküle & Komplexe für den Ladungstransfer
• Elektronenarme organische und anorganische Moleküle mit hohen Oxidationspotentialen
• Funktionalisierte Nanopartikel

Phänomene

• Injektion und Transport von Ladungsträgern
• Ladungsspeicherung
• Stabilität bzw. Instabilität bei Verdampfungsprozessen (z.B. CVD)
• Filmbildung dünner Schichten in nm-Bereich
• Oberflächenchemie selbstorganisierender Monoschichten
• Absorption und Ladungs-Transfer-Phänomen

Techniken

• Synthesen unter Schutzgas im mg bis multi g-Maßstab
• Anwendung quantenchemischen Methoden (DFT) zur Erklärung oder Vorhersage chemischer Phänomene

Allgemeine Chemie (1. Semester B-AC)

Anorganische Stoffchemie Praktikum (2. Semester B-AC)

Grundlagen und Anwendungen der Metallorganik (6. Semester B-AC)

Spezielle Präparative Techniken (6. Semester B-AC)

Nanoskalierte Funktionsmaterialien (in Vorbereitung, M-AC)

Molecular Modelling für Anwender (in Vorbereitung, B-AC)

Artikel (67)
Patente (40)
Review (1)
Dissertation (1)

Zeitschriftenbeiträge

(1) Falkenberg, C.; Hummert, M.; Meerheim, R.; Schuenemann, C.; Olthof, S.; Koerner, C.; Riede, M. K.; Leo, K. Naphthalenetetracarboxylic Diimide Derivatives: Molecular Structure, Thin Film Properties and Solar Cell Applications. Z. Phys. Chem. (Muenchen, Ger. ) 2018, 232 (9-11), 1717–1732. DOI: 10.1515/zpch-2017-1077.

(2) Lorenz-Rothe, M.; Schellhammer, K. S.; Jaegeler-Hoheisel, T.; Meerheim, R.; Kraner, S.; Hein, M. P.; Schuenemann, C.; Tietze, M. L.; Hummert, M.; Ortmann, F.; Cuniberti, G.; Koerner, C.; Leo, K. From Fluorine to Fluorene-A Route to Thermally Stable aza-BODIPYs for Organic Solar Cell Application. Adv. Electron. Mater. 2016, 2 (10), n/a. DOI: 10.1002/aelm.201600152.

(3) Curiel, D.; Montoya, M. M.; Hummert, M.; Riede, M.; Leo, K. Doped-carbazolocarbazoles as hole transporting materials in small molecule solar cells with different architectures. Org. Electron. 2015, 17, 28–32. DOI: 10.1016/j.orgel.2014.11.013.

(4) Hofmann, S.; Hummert, M.; Scholz, R.; Luschtinetz, R.; Murawski, C.; Will, P.-A.; Hintschich, S. I.; Alex, J.; Jankus, V.; Monkman, A. P.; Luessem, B.; Leo, K.; Gather, M. C. Engineering Blue Fluorescent Bulk Emitters for OLEDs: Triplet Harvesting by Green Phosphors. Chem. Mater. 2014, 26 (7), 2414–2426. DOI: 10.1021/cm500602y.

(5) Leo, K.; Hummert, M. Doping effects on charge transport in organic materials. Woodhead Publ. Ser. Electron. Opt. Mater. 2013, 39, 102–142. DOI: 10.1533/9780857098764.1.102.

(6) Schuenemann, C.; Petrich, A.; Schulze, R.; Wynands, D.; Meiss, J.; Hein, M. P.; Jankowski, J.; Elschner, C.; Alex, J.; Hummert, M.; Eichhorn, K.-J.; Leo, K.; Riede, M. Diindenoperylene derivatives: A model to investigate the path from molecular structure via morphology to solar cell performance. Org. Electron. 2013, 14 (7), 1704–1714. DOI: 10.1016/j.orgel.2013.04.006.

(7) Fedushkin, I. L.; Lukoyanov, A. N.; Tishkina, A. N.; Maslov, M. O.; Ketkov, S. Y.; Hummert, M. Compounds with Direct Gallium-Lanthanum and Gallium-Zinc Bonds. Organometallics 2011, 30 (13), 3628–3636. DOI: 10.1021/om200313u.

(8) Gentschow, S.-A.; Kohl, S. W.; Bauer, W.; Hummert, M.; Grohmann, A. Bond Activation in Iron(II)-Coordinated Polypodal Phosphane Ligands. Eur. J. Inorg. Chem. 2011 (4), 556–566. DOI: 10.1002/ejic.201001014.

(9) Gresser, R.; Hoyer, A.; Hummert, M.; Hartmann, H.; Leo, K.; Riede, M. Homoleptic Co(II), Ni(II), Cu(II), Zn(II) and Hg(II) complexes of bis-(phenyl)-diisoindol-aza-methene. Dalton Trans. 2011, 40 (14), 3476–3483. DOI: 10.1039/c0dt01655a.

(10) Gresser, R.; Hummert, M.; Hartmann, H.; Leo, K.; Riede, M. Synthesis and Characterization of Near-Infrared Absorbing Benzannulated Aza-BODIPY Dyes. Chem. - Eur. J. 2011, 17 (10), 2939. DOI: 10.1002/chem.201002941.

(11) Meiss, J.; Hermenau, M.; Tress, W.; Schuenemann, C.; Selzer, F.; Hummert, M.; Alex, J.; Lackner, G.; Leo, K.; Riede, M. Tetrapropyl-tetraphenyl-diindenoperylene derivative as a green absorber for high-voltage stable organic solar cells. Phys. Rev. B: Condens. Matter Mater. Phys. 2011, 83 (16), 165305/1. DOI: 10.1103/physrevb.83.165305.

(12) Meiss, J.; Hummert, M.; Petrich, A.; Pfuetzner, S.; Leo, K.; Riede, M. Tetrabutyl-tetraphenyl-diindenoperylene derivatives as alternative green donor in bulk heterojunction organic solar cells. Sol. Energy Mater. Sol. Cells 2011, 95 (2), 630–635. DOI: 10.1016/j.solmat.2010.09.030.

(13) Tress, W.; Petrich, A.; Hummert, M.; Hein, M.; Leo, K.; Riede, M. Imbalanced mobilities causing S-shaped IV curves in planar heterojunction organic solar cells. Appl. Phys. Lett. 2011, 98 (6), 063301/1. DOI: 10.1063/1.3553764.

(14) Wrackmeyer, M. S.; Hein, M.; Petrich, A.; Meiss, J.; Hummert, M.; Riede, M. K.; Leo, K. Dicyanovinyl substituted oligothiophenes: Thermal stability, mobility measurements, and performance in photovoltaic devices. Sol. Energy Mater. Sol. Cells 2011, 95 (12), 3171–3175. DOI: 10.1016/j.solmat.2011.06.022.

(15) Cui, H.; Hummert, M.; Dechert, S.; Rosenthal, Esther C. E. Structural diversity of chlorido methoxido- and ethoxido-oxidovanadium(V) complexes: Two-dimensional network, dimer, and unusual syn-oriented V=O functionality. Inorg. Chem. Commun. 2010, 13 (6), 769–773. DOI: 10.1016/j.inoche.2010.03.043.

(16) Fedushkin, I. L.; Lukoyanov, A. N.; Tishkina, A. N.; Fukin, G. K.; Lyssenko, K. A.; Hummert, M. Reduction of Digallane [(dpp-bian)Ga[bond]Ga(dpp-bian)] with Group 1 and 2 Metals. Chem. - Eur. J. 2010, 16 (25), 7563–7571. DOI: 10.1002/chem.201000377.

(17) Fedushkin, I. L.; Maslova, O. V.; Hummert, M.; Schumann, H. One- and Two-Electron-Transfer Reactions of (dpp-Bian)Sm(dme)3. Inorg. Chem. 2010, 49 (6), 2901–2910. DOI: 10.1021/ic902439x.

(18) Meiss, J.; Hummert, M.; Ziehlke, H.; Leo, K.; Riede, M. Organic solar cells with very high fill factor and voltage using tetrapropyl-tetraphenyl-diindenoperylene as green donor. Phys. Status Solidi RRL 2010, 4 (11), 329–331. DOI: 10.1002/pssr.201004310.

(19) Wrackmeyer, M. S.; Hummert, M.; Hartmann, H.; Riede, M. K.; Leo, K. Structure-property relationship of acceptor-substituted oligothiophenes. Tetrahedron 2010, 66 (45), 8729–8733. DOI: 10.1016/j.tet.2010.09.004.

(20) Cuevas, A.; Geis, L.; Pintos, V.; Chiozzone, R.; Sanchiz, J.; Hummert, M.; Schumann, H.; Kremer, C. Synthesis, molecular structure and magnetic properties of a rhenium(IV) compound with catechol. J. Mol. Struct. 2009, 921 (1-3), 80–84. DOI: 10.1016/j.molstruc.2008.12.031.

(21) Dominguez, S.; Torres, J.; Gonzalez-Platas, J.; Hummert, M.; Schumann, H.; Kremer, C. Thermodynamic stability and crystal structure of lanthanide complexes with di-2-pyridyl ketone. J. Coord. Chem. 2009, 62 (1), 108–119. DOI: 10.1080/00958970802474797.

(22) Schumann, H.; Kuse, K.; Hummert, M.; Pickardt, J. Transition metal and lanthanide complexes of 1,4,7,10-tetraallyl- and 1,4,7,10-tetra-3-butenyl-1,4,7,10-tetraazacyclododecane. Z. Naturforsch. , B: J. Chem. Sci. 2009, 64 (1), 93–100.

(23) Schumann, H.; Steffens, A.; Hummert, M. Synthesis, x-ray structures and catalytic activity of new alkyne complexes of the alkaline earth metals. Z. Anorg. Allg. Chem. 2009, 635 (6-7), 1041–1047. DOI: 10.1002/zaac.200900159.

(24) Fedushkin, I. L.; Chudakova, V. A.; Hummert, M.; Schumann, H. Electron release and proton acceptance reactions of (dpp-BIAN)Mg(THF)3. Z. Naturforsch. , B: J. Chem. Sci. 2008, 63 (2), 161–168. DOI: 10.1515/znb-2008-0208.

(25) Fedushkin, I. L.; Lukoyanov, A. N.; Fukin, G. K.; Ketkov, S. Y.; Hummert, M.; Schumann, H. Synthesis, molecular structure and DFT study of [(dpp-bian)Ga-M(Et2O)3] (M = Li, Na; dpp-bian = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene). Chem. - Eur. J. 2008, 14 (28), 8465–8468. DOI: 10.1002/chem.200801267.

(26) Fedushkin, I. L.; Lukoyanov, A. N.; Hummert, M.; Schumann, H. C-O bond cleavage of diethyl ether and tetrahydrofuran by [(dpp-BIAN)AlI(Et2O)] [dpp-BIAN = 1,2-bis[(2,6-di-iso-propylphenyl)imino]acenaphthene]. Z. Anorg. Allg. Chem. 2008, 634 (2), 357–361. DOI: 10.1002/zaac.200700411.

(27) Fedushkin, I. L.; Morozov, A. G.; Hummert, M.; Schumann, H. Alkylmagnesium complexes with the rigid dpp-bian ligand {dpp-bian = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene}. Eur. J. Inorg. Chem. 2008 (10), 1584–1588. DOI: 10.1002/ejic.200700816.

(28) Fedushkin, I. L.; Tishkina, A. N.; Fukin, G. K.; Hummert, M.; Schumann, H. Zinc complexes with the chelating amido-imino ligand [1-n-butyl-2-(2,6-diisopropylphenyl)iminoacenaphthen-1-yl]-2,6-diisopropylphenylamide (L): synthesis, molecular structure and reactivity of [(L)ZnCl]2, (L)Zn-nBu and (L)ZnN(SiMe3)2. Eur. J. Inorg. Chem. 2008 (3), 483–489. DOI: 10.1002/ejic.200700796.

(29) Kremer, C.; Morales, P.; Torres, J.; Castiglioni, J.; Gonzalez-Platas, J.; Hummert, M.; Schumann, H.; Dominguez, S. Novel lanthanide-iminodiacetate frameworks with hexagonal pores. Inorg. Chem. Commun. 2008, 11 (8), 862–864. DOI: 10.1016/j.inoche.2008.04.020.

(30) Piskunov, A. V.; Mescheryakova, I. N.; Fukin, G. K.; Baranov, E. V.; Hummert, M.; Shavyrin, A. S.; Cherkasov, V. K.; Abakumov, G. A. Oxidation by oxygen and sulfur of tin(IV) derivatives containing a redox-active o-amidophenolate ligand. Chem. - Eur. J. 2008, 14 (32), 10085–10093. DOI: 10.1002/chem.200801203.

(31) Rosenthal, Esther C. E.; Cui, H.; Hummert, M. A novel oxovanadium(V) complex of 2-(2-butoxyethoxy)ethanolate with high catalytic activities for polymerization and epoxidation. Inorg. Chem. Commun. 2008, 11 (8), 918–920. DOI: 10.1016/j.inoche.2008.04.037.

(32) Cuevas, A.; Kremer, C.; Hummert, M.; Schumann, H.; Lloret, F.; Julve, M.; Faus, J. Magnetic properties and molecular structures of binuclear (2-pyrazinecarboxylate)-bridged complexes containing Re(IV) and M(II) (M = Co, Ni). Dalton Trans. 2007 (3), 342–350. DOI: 10.1039/b611888g.

(33) Fedushkin, I. L.; Lukoyanov, A. N.; Hummert, M.; Schumann, H. Coordination of benzene to a sodium cation. Russ. Chem. Bull. 2007, 56 (9), 1765–1770. DOI: 10.1007/s11172-007-0274-y.

(34) Fedushkin, I. L.; Lukoyanov, A. N.; Ketkov, S. Y.; Hummert, M.; Schumann, H. [(dpp-bian)Ga-Ga(dpp-bian)] and [(dpp-bian)Zn-Ga(dpp-bian)]: synthesis, molecular structures, and DFT studies of these novel bimetallic molecular compounds. Chem. - Eur. J. 2007, 13 (25), 7050–7056. DOI: 10.1002/chem.200700736.

(35) Fedushkin, I. L.; Skatova, A. A.; Eremenko, O. V.; Hummert, M.; Schumann, H. Synthesis and molecular structure of two zinc complexes of 1,2-bis[(trimethylsilyl)imino]acenaphthene. Z. Anorg. Allg. Chem. 2007, 633 (10), 1739–1742. DOI: 10.1002/zaac.200700231.

(36) Kohl, S. W.; Kuse, K.; Hummert, M.; Schumann, H.; Muegge, C.; Janek, K.; Weisshoff, H. New synthetic routes for 1-benzyl-1,4,7,10-tetraazacyclododecane and 1,4,7,10-tetraazacyclododecane-1-acetic acid ethyl ester, important starting materials for metal-coded DOTA-based affinity tags. Z. Naturforsch. , B: J. Chem. Sci. 2007, 62 (3), 397–406. DOI: 10.1515/znb-2007-0313.

(37) Schumann, H.; Freckmann, Dominique M. M.; Schutte, S.; Dechert, S.; Hummert, M. Organometallic compounds of the lanthanides. Part 181. Alkyllanthanide carbene complexes. Z. Anorg. Allg. Chem. 2007, 633 (5-6), 888–892. DOI: 10.1002/zaac.200700028.

(38) Schumann, H.; Hummert, M.; Lukoyanov, A. N.; Chudakova, V. A.; Fedushkin, I. L. Organometallic compounds of the lanthanides. 182. Calcium and neodymium complexes containing the dpp-BIAN ligand system: synthesis and molecular structure of [(dpp-BIAN)CaI(THF)2]2 and [(dpp-BIAN)NdCl(THF)2]2. Z. Naturforsch. , B: J. Chem. Sci. 2007, 62 (9), 1107–1111. DOI: 10.1515/znb-2007-0901.

(39) Schumann, H.; Hummert, M.; Lukoyanov, A. N.; Fedushkin, I. L. Sodium cation migration above the diimine ¤Ç-system of solvent coordinated dpp-BIAN sodium aluminum complexes (dpp-BIAN = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene). Chem. - Eur. J. 2007, 13 (15), 4216–4222. DOI: 10.1002/chem.200601649.

(40) Skatova, A. A.; Fedushkin, I. L.; Maslova, O. V.; Hummert, M.; Schumann, H. Synthesis and structures of new conformationally rigid 1-aza-1,3-dienes of the acenaphthene series. Russ. Chem. Bull. 2007, 56 (11), 2284–2289. DOI: 10.1007/s11172-007-0360-1.

(41) Sun, J.; Cheng, Z.; Nie, Y.; Schumann, H.; Hummert, M. Novel titanium complexes bearing two chelating phenoxy-imine ligands and their catalytic performance for ethylene polymerization. Appl. Organomet. Chem. 2007, 21 (4), 268–274. DOI: 10.1002/aoc.1185.

(42) Fedushkin, I. L.; Khvoinova, N. M.; Piskunov, A. V.; Fukin, G. K.; Hummert, M.; Schumann, H. New acenaphthene-1,2-diimine and its reduction to the tetraanion. Molecular structures of 1,2-bis[(trimethylsilyl)imino]acenaphthene and its lithium derivatives. Russ. Chem. Bull. 2006, 55 (4), 722–730. DOI: 10.1007/s11172-006-0320-1.

(43) Fedushkin, I. L.; Lukoyanov, A. N.; Fukin, G. K.; Hummert, M.; Schumann, H. Reduction of aromatic ketones with the (dpp-BIAN)AlI(Et2O) complex. Russ. Chem. Bull. 2006, 55 (7), 1177–1183. DOI: 10.1007/s11172-006-0396-7.

(44) Fedushkin, I. L.; Hummert, M.; Schumann, H. Molecular structures and NMR studies of lithium and germanium(II) complexes of a new chelating amido-imino ligand obtained by addition of nBuLi to 1,2-bis(arylimino)acenaphthene. Eur. J. Inorg. Chem. 2006 (16), 3266–3273. DOI: 10.1002/ejic.200600265.

(45) Kohl, S. W.; Heinemann, F. W.; Hummert, M.; Bauer, W.; Grohmann, A. Ligand cleavage put into reverse: P-C bond breaking and remaking in an alkylphosphane iron complex. Chem. - Eur. J. 2006, 12 (16), 4313–4320. DOI: 10.1002/chem.200501577.

(46) Kohl, S. W.; Heinemann, F. W.; Hummert, M.; Bauer, W.; Grohmann, A. Solvent dependent reactivity: solvent activation vs. solvent coordination in alkylphosphane iron complexes. Dalton Trans. 2006 (47), 5583–5592. DOI: 10.1039/b610792c.

(47) Kohl, S. W.; Heinemann, F. W.; Hummert, M.; Weisshoff, H.; Grohmann, A. Tetra- and triphosphane pyridine podands and their cobalt(II) and nickel(II) complexes. Eur. J. Inorg. Chem. 2006 (19), 3901–3910. DOI: 10.1002/ejic.200600530.

(48) Lukoyanov, A. N.; Fedushkin, I. L.; Hummert, M.; Schumann, H. Aluminum complexes with mono-and dianionic diimine ligands. Russ. Chem. Bull. 2006, 55 (3), 422–428. DOI: 10.1007/s11172-006-0273-4.

(49) Lukoyanov, A. N.; Fedushkin, I. L.; Schumann, H.; Hummert, M. Monoalkylaluminium complexes stabilized by a rigid dianionic diimine ligand: synthesis, solid state structure, and dynamic solution behaviour of (dpp-BIAN)air (R = Me, Et, iBu). Z. Anorg. Allg. Chem. 2006, 632 (8-9), 1471–1476. DOI: 10.1002/zaac.200600033.

(50) Schumann, H.; Decher, S.; Girgsdies, F.; Heymer, B.; Hummert, M.; Hyeon, J.-Y.; Kaufmann, J.; Schutte, S.; Wernik, S.; Wassermann, B. C. Synthesis and characterization of new intramolecularly nitrogen-stabilized organoaluminum- and organogallium alkoxides. Z. Anorg. Allg. Chem. 2006, 632 (2), 251–263. DOI: 10.1002/zaac.200500382.

(51) Trifonov, A. A.; Lyubov, D. M.; Fedorova, E. A.; Fukin, G. K.; Schumann, H.; Muhle, S.; Hummert, M.; Bochkarev, M. N. Chloro, alkyl and aryl complexes of rare earth metals supported by bulky tetrasubstituted guanidinate ligands. Eur. J. Inorg. Chem. 2006 (4), 747–756. DOI: 10.1002/ejic.200500641.

(52) Fedushkin, I. L.; Chudakova, V. A.; Fukin, G. K.; Dechert, S.; Hummert, M.; Schumann, H. Protonation of magnesium and sodium complexes containing dianionic diimine ligands. Molecular structures of 1,2-bis{(2,6-diisopropylphenyl)imino}acenaphthene (dpp-BIAN), [(dph-BIAN)H2(Et2O)], and [(dpp-BIAN)HNa(Et2O)]. Russ. Chem. Bull. 2005, 53 (12), 2744–2750. DOI: 10.1007/s11172-005-0185-8.

(53) Fedushkin, I. L.; Skatova, A. A.; Lukoyanov, A. N.; Chudakova, V. A.; Dechert, S.; Hummert, M.; Schumann, H. Reactions of (dpp-BIAN)Mg(thf)3 complex (dpp-BIAN is 1,2-bis{(2,6-diisopropylphenyl)imino}acenaphthene) with halogen-containing reagents. Russ. Chem. Bull. 2005, 53 (12), 2751–2762. DOI: 10.1007/s11172-005-0186-7.

(54) Fedushkin, I. L.; Skatova, A. A.; Fukin, G. K.; Hummert, M.; Schumann, H. Addition of enolisable ketones to (dpp-bian)Mg(THF)3 [dpp-bian = 1,2-bis{(2,6-diisopropylphenyl)imino}acenaphthene]. Eur. J. Inorg. Chem. 2005 (12), 2332–2338. DOI: 10.1002/ejic.200400948.

(55) Fedushkin, I. L.; Skatova, A. A.; Hummert, M.; Schumann, H. Reductive isopropyl radical elimination from (dpp-bian)Mg-iPr(Et2O). Eur. J. Inorg. Chem. 2005 (8), 1601–1608. DOI: 10.1002/ejic.200400973.

(56) Rosenthal, Esther C. E.; Cui, H.; Koch, J.; Escarpa Gaede, P.; Hummert, M.; Dechert, S. Chloride-bridged oxovanadium(V) complexes with alkoxyalkoxide ligands. Synthesis, structure, electrochemistry and reactivities. Dalton Trans. 2005 (18), 3108–3117. DOI: 10.1039/b505750g.

(57) Schumann, H.; Hummert, M.; Lukoyanov, A. N.; Fedushkin, I. L. Monomeric Alkylaluminum Complexes (dpp-BIAN)AlR2 (R = Me, Et, iBu) Supported by the Rigid Chelating Radical-Anionic 1,2-Bis[(2,6-diisopropylphenyl)imino]acenaphthene Ligand (dpp-BIAN). Organometallics 2005, 24 (16), 3891–3896. DOI: 10.1021/om0491037.

(58) Schumann, H.; Suehring, K.; Weimann, R.; Hummert, M. Deca(4-methylbenzyl)ferrocene and -stannocene. Z. Naturforsch. , B: J. Chem. Sci. 2005, 60 (5), 527–532. DOI: 10.1515/znb-2005-0508.

(59) Fedushkin, I. L.; Chudakova, V. A.; Skatova, A. A.; Khvoinova, N. M.; Kurskii, Y. A.; Glukhova, T. A.; Fukin, G. K.; Dechert, S.; Hummert, M.; Schumann, H. Monomeric magnesium and calcium complexes containing the rigid, dianionic 1,2-bis[(2,5-di-tert-butylphenyl)imino]acenaphthene (dtb-BIAN) and 1,2-bis[(2-biphenyl)imino]acenaphthene (bph-BIAN) ligands. Z. Anorg. Allg. Chem. 2004, 630 (4), 501–507. DOI: 10.1002/zaac.200300361.

(60) Fedushkin, I. L.; Skatova, A. A.; Chudakova, V. A.; Khvoinova, N. M.; Baurin, A. Y.; Dechert, S.; Hummert, M.; Schumann, H. Stable germylenes derived from 1,2-bis(arylimino)acenaphthenes. Organometallics 2004, 23 (15), 3714–3718. DOI: 10.1021/om0497846.

(61) Rufanov, K. A.; Ziemer, B.; Hummert, M.; Schutte, S. Synthesis of (indenylidene)phosphoranes - A novel class of ligand precursors for main-group and transition metal organometallics. Eur. J. Inorg. Chem. 2004 (24), 4759–4763. DOI: 10.1002/ejic.200400664.

(62) Schumann, H.; Dechert, S.; Hummert, M.; Lange, Katharina C. H.; Schutte, S.; Wassermann, B. C.; Koehler, K.; Eichhorn, J. Intramolecularly nitrogen-stabilized organoaluminum compounds containing naphthyl, benzyl, and phenyl ligands. Z. Anorg. Allg. Chem. 2004, 630 (8-9), 1196–1204. DOI: 10.1002/zaac.200400033.

(63) Schumann, H.; Fedushkin, I. L.; Hummert, M.; Scarel, G.; Bonera, E.; Fanciulli, M. Crystal and molecular structure of [(╬À5-C5H4SiMe3)2LuCl]2: A precursor for the production of Lu2O3 films. Z. Naturforsch. , B: J. Chem. Sci. 2004, 59 (9), 1035–1038.

(64) Sun, J.; Shan, Y.; Xu, Y.; Cui, Y.; Schumann, H.; Hummert, M. Novel cyclohexyl-substituted salicylaldiminato-nickel(II) complex as a catalyst for ethylene homopolymerization and copolymerization. J. Polym. Sci. , Part A: Polym. Chem. 2004, 42 (23), 6071–6080. DOI: 10.1002/pola.20458.

(65) Fedushkin, I. L.; Skatova, A. A.; Cherkasov, V. K.; Chudakova, V. A.; Dechert, S.; Hummert, M.; Schumann, H. Reduction of benzophenone and 9(10H)-anthracenone with the magnesium complex [(2,6-iPr2C6H3-bian)Mg(THF)3]. Chem. - Eur. J. 2003, 9 (23), 5778–5783. DOI: 10.1002/chem.200305235.

(66) Schumann, H.; Dechert, S.; Schutte, S.; Hyeon, J.-Y.; Hummert, M.; Wassermann, B. C.; Kaminsky, W.; Eisenhardt, A.; Koehler, K.; Eichhorn, J. Oxygen-Stabilized Organoaluminum Compounds as Highly Active Cocatalysts for Ziegler-Natta Olefin Polymerization. Organometallics 2003, 22 (7), 1391–1401. DOI: 10.1021/om020797y.

(67) Schumann, H.; Girgsdies, F.; Dechert, S.; Gottfriedsen, J.; Hummert, M.; Shutte, S.; Pickardt, J. Thermally induced lengthening of weak dative bonds in donor functionalized organoaluminum alkoxides observed by X-ray single crystal diffraction. Z. Anorg. Allg. Chem. 2002, 628 (12), 2625–2630. DOI: 10.1002/1521-3749(200212)628:123.0.co;2-e.

Monographien

(1) Leo, K.; Hummert, M. 3 - Doping effects on charge transport in organic materials. In Handbook of organic materials for optical and (opto)electronic devices:Properties and applications; Ostroverkhova, O., Ed.; Woodhead publishing series in electronic and optical materials, Vol. 39; Woodhead Publ, 2013; pp 102–142. DOI: 10.1533/9780857098764.1.102.

Patentschriften

(1) Gresser, R.; Mueller, T.; Hummert, M.; Riede, M.; Hartmann, H.; Leo, K. Organic semiconductor devices using nitrogen-bridged pyrrole ring-containing heterocyclic compounds and complexes of the compounds (DE102009021881 A1).

(2) Heggemann, U.; Hummert, M. Active organic luminescent display, method for preparing an active OLED display and compound consisting of an organic anion and metal cation (WO2018150050 A1).

(3) Heggemann, U.; Hummert, M. Electronic organic luminescent device with organic borate salt-containing layer, method for preparing the electronic semiconducting device and compound (WO2018150006 A1).

(4) Heggemann, U.; Hummert, M. Electronic semiconducting device, method for preparing the electronic semiconducting device and compound (EP3364475 A1).

(5) Heggemann, U.; Hummert, M.; Rosenow, T.; Furno, M. Electronic device with organic borate salt-containing layer, method for preparing the same and organic luminescent display device comprising the same (WO2018150049 A1).

(6) Heggemann, U.; Hummert, M.; Rosenow, T.; Furno, M. Electronic semiconducting device with an organic semiconductor layer and method for preparing the electronic semiconducting device (WO2018150048 A1).

(7) Heggemann, U.; Hummert, M.; Rosenow, T.; Furno, M. Electronic semiconducting device, such as an OLED device, and method for preparing the electronic semiconducting device (WO2018150051 A1).

(8) Hummert, M.; Bruch, A.; Koehn, C.; Nuellen, M. P. Preparation of substituted 1,2,3-triylidenetris(cyanomethanylylidene)cyclopropanes for vacuum thermal evaporation (VTE), electronic devices and semiconducting materials using them (WO2016097017 A1).

(9) Hummert, M.; Heggemann, U.; Rosenow, T.; Schliebe, U. Coordination complex and electronic device comprising the same (WO2019122071 A1).

(10) Hummert, M.; Heggemann, U.; Rosenow, T.; Schliebe, U. Coordination complex for electronic device (EP3503233 A1).

(11) Hummert, M.; Rosenow, T. Electronic device and method for preparing same (EP3462516 A1).

(12) Hummert, M.; Rosenow, T. Metal amides for use as HIL for an organic light-emitting diode (WO2017029370 A1).

(13) Hummert, M.; Rosenow, T. Triarylamine thick layer doped with metal amides for use as hole injection layer for an organic light-emitting diode (OLED) (WO2017029366 A1).

(14) Hummert, M.; Rosenow, T.; Kalisz, T. Fabricating organic electronic device comprising inverse coordination complex (EP3503234 A1).

(15) Hummert, M.; Rosenow, T.; Kalisz, T. Organic electronic device comprising an inverse coordination complex fabrication (WO2019122081 A1).

(16) Hummert, M.; Senkowskyy, V. Electronic devices, method for preparing devices thereof, and display devices comprising the same (WO2020007741 A1).

(17) Hummert, M.; Willmann, S.; Rosenow, T. Construction of electronic devices with improved voltage, efficiency or lifetime (DE102018118278 A1).

(18) Koehler, K.; Poetsch, E.; Eichhorn, J.; Schumann, H.; Wassermann, B. C.; Dechert, S.; Hummert, M.; Schutte, S.; Kaminsky, W.; Eisenhardt, A.; Arnold, M. Oxygen-containing organoaluminum complexes for use as cocatalysts in polymerization (WO2004033466 A1).

(19) Leo, K.; Hummert, M.; Falkenberg, C.; Hermenau, M.; Riede, M.; Olthof, S. Organic solar cells (EP2498315 A2).

(20) Meiss, J.; Hummert, M.; Schueppel, R.; Riede, M.; Petrich, A.; Leo, K. Organic solar cell or photodetector with diindenoperylenes for improved light absorption (WO2010133205 A1).

(21) Meiss, J.; Hummert, M.; Schueppel, R.; Riede, M.; Petrich, A.; Leo, K. Organic solar cell or photodetector with diindenoperylenes for improved light absorption (DE102009022408 A1).

(22) Meiss, J.; Riede, M.; Hummert, M.; Leo, K. Inverted or transparent organic solar cell or photodetector having improved absorption (DE102009024956 A1).

(23) Nuellen, M. P.; Hummert, M.; Hartmann, H.; Kaufmann, D.; Savych, I. Organic electronic device, organic semiconducting material and a borane compound (DE102018122708 A1).

(24) Nuellen, M. P.; Hummert, M.; Hartmann, H.; Kaufmann, D. E.; Toguem, S.-M. T. Organic electronic device, organic semiconducting material, a trioxatriborinane compound and the use thereof (DE102020108402 A1).

(25) Rosenow, T.; Hummert, M. Organic light emitting device (WO2020074379 A1).

(26) Rosenow, T.; Hummert, M.; Canzler, T. Organic electronic device having an improved performance, in particular operating voltage and method for producing the organic electronic device (WO2018220218 A1).

(27) Rosenow, T.; Jankus, V.; Hummert, M.; Park, M. J.; Uvarov, V.; Steudel, A. An organic electronic device comprising an anode layer, a cathode layer, at least one emission layer (EML) and at least one hole injection layer (HIL) (WO2021151958 A1).

(28) Rosenow, T.; Jankus, V.; Hummert, M.; Park, M. J.; Uvarov, V.; Steudel, A. An organic electronic device comprising an anode layer, a cathode layer, at least one emission layer (EML) and at least one hole injection layer (HIL) (WO2021151959 A1).

(29) Scholz, S.; Olthof, S.; Hummert, M.; Hermenau, M.; Meerheim, R.; Petrich, A.; Friebe, B. Procedure for the production of fullerene derivatives (DE102010046040 A1).

(30) Uvarov, V.; Hummert, M.; Heggemann, U. Organic electronic device, display device having the same (WO2021123064 A1).

(31) Uvarov, V.; Hummert, M.; Heggemann, U.; Willmann, S. Organic electronic device comprising a compound of formula (1), display device comprising the organic electronic device as well as compounds of formula (1) for use in organic electronic devices (EP3840081 A1).

(32) Uvarov, V.; Hummert, M.; Heggemann, U.; Willmann, S. Organic electronic device comprising a compound of formula (1), display device comprising the organic electronic device as well as compounds of formula (1) for use in organic electronic devices (EP3840075 A1).

(33) Uvarov, V.; Hummert, M.; Heggemann, U.; Willmann, S. Organic electronic device containing copper metal compound, display devices used in organic electronic devices (EP3840074 A1).

(34) Uvarov, V.; Hummert, M.; Heggemann, U.; Willmann, S. Organic electronic device, and display device (WO2021123068 A1).

(35) Uvarov, V.; Hummert, M.; Heggemann, U.; Willmann, S. Organic electronic device, and display device having the same (WO2021123067 A1).

(36) Uvarov, V.; Hummert, M.; Rosenow, T.; Runge, S.; Luschtinetz, R.; Langguth, O. Organic electronic device comprising a compound of formula [B1SO2N-SO2B2]M+ (EP4002508 A1).

(37) Uvarov, V.; Hummert, M.; Rosenow, T.; Runge, S.; Luschtinetz, R.; Langguth, O.; Angermann, J. Organic semiconductor device (WO2022101439 A1).

(38) Uvarov, V.; Nuellen, M. P.; Heggemann, U.; Hummert, M. Semiconductor material comprising pentanedionato metal complex, semiconductor device and electronic device (EP3945125 A1).

(39) Uvarov, V.; Nuellen, M. P.; Heggemann, U.; Hummert, M.; Willmann, S.; Luschtinetz, R. Metal complexes of 3-(2,3,5-trifluoro-6-(trifluoromethyl)pyridin-4-yl)pentane-2,4-dione and similar ligands as semiconductor materials for use in electronic devices (WO2022023260 A1).

(40) Uvarov, V.; Nuellen, M. P.; Heggemann, U.; Hummert, M.; Willmann, S.; Luschtinetz, R. Semiconductor material comprising pentanedionato metal complex, semiconductor device and electronic device (WO2022023278 A1).