2020 / 2010-2019 / 2000-2009 / 1990-1999 / Patents / Book Chapters top
2020
G. M. Beneventi, M. Krug, D. Reger, N. Jux, D. M. Guldi, J. Photochem. Photobiol. C 2023, 100602.
M. Kinzelmann, D. Reger, V. Warmbrunn, D. Lungerich, N. Jux, T. Drewello, Chem. Commun. 2023, 59, 5882–5885.
137 „Photophysical characterization of a ruthenium-based tetrameric pentacene complex„
Y. Hou, I. Papadopoulos, M. J. Ferguson, N. Jux, R. R. Tykwinski, D. M. Guldi, J. Porphyrins Phthalocyanines 2023, 27, 686 – 693.
H. Hölzel, P. Haines, R. Kaur, D. Lungerich, N. Jux, D. M. Guldi, J. Am. Chem. Soc. 2022, 144, 20, 8977–8986.
M. Ammon, M. Devarajulu, Y. Liu, M. Gurrath, D. Lungerich, N. Jux, B. Meyer, S. Amier, Surface Science 2022, 723, 122097.
134 „On the adsorption of different tetranaphthylporphyrins on Cu(111) and Ag(111),
Surface Science„
J. Brox, R. Adhikari, M. Shaker, M. Ruppel, N. Jux, H. Marbach, S. Jaekel, H.-P. Steinrück, Surface Science 2022, 720, 122047.
133 „Acylation of Hexaphenylbenzene for the Synthesis of [5]Cumulenes„
M. A. Johnson, M. M. Martin, K. Cocq, N. Jux, M. J. Ferguson, R. R. Tykwinski, Eur. J. Org. Chem. 2022, e202101467.
J. Köbl, C. C. Fernández, L.-M. Augustin, E. Y. Kataev, S. Franchi, N. Tsud, C. Pistonesi, M. E. Pronsato, N. Jux, O. Lytken, F. J. Williams, H.-P. Steinrück, Surface Science 2022, 716, 121955.
B. Grau, M. Dill, F. Hampel, A. Kahnt, N. Jux, S. B. Tsogoeva, Angew. Chem. Int. Ed. 2021, 60, 22307–22314.
D. Lungerich, H. Hölzel, K. Harano, N. Jux, K. Y. Amsharow, E. Nakamuram, ACS Nano 2021, 15, 8, 12804–12814.
D. Reger, P. Haines, K. Y. Amsharov, J. A. Schmidt, T. Ullrich, S. Bönisch, F. Hampel, A. Görling, J. Nelson, K. E. Jelfs, D. M. Guldi, N. Jux, Angew. Chem. Int. Ed. 2021, 60, 18073–18081.
128 „Wet-Chemically Prepared Porphyrin Layers on Rutile TiO2(110)„
D. Wechsler, C. C. Fernández, J. Köbl, L.-M. Augustin, C. Stumm, N. Jux, H.-P. Steinrück, F. J. Williams, O. Lytken, Molecules 2021, 26, 10, 2871.
127 „Crystal Engineering of Sterically Shielded Hexa-peri-hexabenzocoronenes„
D. Reger, F. Hampel, N. Jux, Australian Journal of Chemistry 2021, 74, 7, 564-567.
R. Adhikari, J. Kuliga, M. Ruppel, N. Jux, H. Marbach, H.-P. Steinrück, J. Phys. Chem. C 2021, 125, 13, 7204–7212.
P. Haines, R. Kaur, M. M. Martin, M. B. Minameyer, S. Frühwald, S. Bönisch, D. Lungerich, F. Hampel, A. Görling, T. Drewello, N. Jux, D. M. Guldi, Adv. Energy Mater. 2021, 11, 2100158–2100171.
124 „Addressing Environmental Challenges of Porphyrin Mixtures Obtained from Statistical Syntheses„
H. Hölzel, M. Muth, D. Lungerich, N. Jux, Chemistry–Methods 2021, 1, 142–147.
P. Haines, D. Reger, J. Träg, V. Strauss, D. Lungerich, D. Zahn, N. Jux, D. M. Guldi, Nanoscale 2021, 13, 801–809.
122 „Metalation of 2HTCNPP on Ag(111) with Zn: Evidence for the Sitting atop Complex at Room Temperature„
J. Kuliga, R. C. de Campos Ferreirra, R. Adhikari, S. Massicot, M. Lepper, H. Hölzel, N. Jux, H. Marbach, A. de Siervo, H.-P. Steinrück, ChemPhysChem 2021, 22, 396–403.
121 „Pyridinic Nanographenes by Novel Precursor Design„
D. Reger, K. Schöll, F. Hampel, N. Jux, Chem. Eur. J. 2021, 27, 1984–1989.
120 „Oxidative Cyclodehydrogenation Reactions with Tetraarylporphyrins„
M. M. Martin, C. Oleszak, F. Hampel, N. Jux, Eur. J. Org. Chem. 2020, 6758–6762.
C. Dusold, B. Platzer, P. Haines, D. Reger, N. Jux, D. M. Guldi, A. Hirsch, Chem. Eur. J. 2020, (doi.org/10.1002/chem.202004273).
118 „Hexa-peri-hexabenzocoronene decorated with an allenylidene ruthenium complex – almost aflyswatter„
R. Lorenz, D. Reger, R. Weller, N. Jux, N. Burzlaff, Dalton Trans. 2020, 49, 13134–13141.
117 „Synthesis and Photophysical Properties of Hexabenzocoronene-Tetrabenzoporphyrin Architectures„
M. Ruppel, L.-P. Gazetas, D. Lungerich, N. Jux, Eur. J. Org. Chem. 2020, 6352–6360.
116 „Gas-Phase Transformation of Fluorinated Benzoporphyrins to Porphyrin-Embedded Conical Nanocarbons„
D. Lungerich, J. F. Hitzenberger, M. Ruppel, T. Döpper, M. Witt, I. Ivanović‐Burmazović, A. Görling, N. Jux, T. Drewello, Chem. Eur.J. 2020, 26, 12180 –12187.
, 11, 7123–7132.
Chem. Sci. 2020M. Ruppel, L.-P. Gazetas, D. Lungerich, F. Hampel, N. Jux, J. Org. Chem. 2020, 85, 7781–7792.
112 „A Hexabenzocoronene-Based Helical Nanographene„
M. M. Martin, F. Hampel, N. Jux, Chem. Eur. J. 2020, 26, 10210 –10212.
111 „A Comprehensive Study on Tetraaryltetrabenzoporphyrins„
M. Ruppel, D. Lungerich, S. Sturm, R. Lippert, F. Hampel, N. Jux, Chem. Eur. J. 2020, 26, 3287–3296.
2010-2019
110 „Multiple‐Porphyrin Functionalized Hexabenzocoronenes„
M. M. Martin, D. Lungerich, F. Hampel, J. Langer, T. K. Ronson, N. Jux, Chem. Eur.J. 2019, 25, 15083–15090.
109 „Porphyrin-rylene-diimide-hexabenzocoronene triads„
M. M. Martin, C. Dusold, A. Hirsch, N. Jux, J. Porphyrins Phthalocyanines 2019, 23, 2–10.
A. Franke, A. Scheitler, I. Kenkel, R. Lippert, A. Zahl, D. Balbinot, N. Jux, I. Ivanović-Burmazović, Inorganic Chemistry 2019, 58, 9618-9630.
107 „Electronic Communication across Porphyrin Hexabenzocoronene Isomers„
M. M. Martin, D. Lungerich, P. Haines, F. Hampel, N. Jux, Angew. Chem. Int. Ed. 2019, 58, 8932-8937.
106 „Porphyrin-Hexaphenylbenzene Conjugates via Mixed Cyclotrimerization Reactions„
M. M. Martin, M. Dill, J. Langer, N. Jux, J. Org. Chem. 2019, 84, 1489-1499.
105 „Building from Ga-Porphyrins: Synthesis of Ga-Acetylide Complexes Using Acetylenes and Polyynes„
V. Walter, Y. Gao, N. Grzegorzek, M. Krempe, F. Hampel, N. Jux, R. R. Tykwinski, Angew. Chem. Int. Ed. 2019, 59, 494-498.
104 „Superbenzene-Porphyrin Gas-Phase Architectures Derived from Intermolecular Dispersion Interactions„
D. Lungerich, J. F. Hitzenberger, F. Hampel, T. Drewello, N. Jux, Chem. Eur. J. 2018, 24, 15818-15824.

103 „Synthesis and Photophysical Properties of Hexaphenylbenzene-Pyrrolo[3,2-b]pyrroles„
R. Stezycki, D. Reger, H. Hoelzel, N. Jux, D. T. Gryko, Synlett. 2018, 29, 2529-2534.
J. Kuliga, L. Zhang, M. Lepper, D. Lungerich, H. Hoelzel, N. Jux, H.-P. Steinrueck, H. Marbach, Phys. Chem. Chem. Phys. 2018, 20, 25062-25068.
101 „Controlling the Self-Metalation Rate of Tetraphenylporphyrins on Cu(111) via Cyano Functionalization„
M. Lepper, J. Koebl, L. Zhang, M. Meusel, H. Hoelzel, D. Lungerich, N. Jux, A. de Siervo, B. Meyer, H.-P. Steinrueck, H. Marbach, Angew. Chem. Int. Ed. 2018, 57, 10074-10079.

100 „Synthesis of a porphyrin-hexaarylbenzene-hexabenzocoronene triad„
M. M. Martin, N. Jux, J. Porphyrins Phthalocyanines 2018, 22, 454-460.
99 „Oxa[7]superhelicene: A π-Extended Helical Chromophore Based on Hexa-peri-hexabenzocoronenes„
D. Reger, P. Haines, F. W. Heinemann, D. M. Guldi, N. Jux, Angew. Chem. Int. Ed. 2018, 57, 5938-5942.
98 „Screening Supramolecular Interactions between Carbon Nanodots and Porphyrins„
A. Cadranel, V. Strauss, J. T. Margraf, K. A. Winterfeld, C. Vogl, L. Djordjevic, F. Arcudi, H. Hoelzel, N. Jux, M. Prato, D. M. Guldi, J. Am. Chem. Soc. 2018, 140, 904-907.
M. Lepper, T. Schmitt, M. Gurrath, M. Raschmann, L. Zhang, M. Stark, H. Hoelzel, N. Jux, B. Meyer, M. A. Schneider, H.-P. Steinrueck, H. Marbach, J. Phys. Chem. 2017, 121, 26361-26371.
J. Holzwarth, K. Y. Amsharov, D. I. Sharapa, D. Reger, K. Roshchyna, D. Lungerich, N. Jux, F. Hauke, T. Clark, A. Hirsch, Angew. Chem. Int. Ed. 2017, 56, 12184-12190.
L. Zhang, M. Lepper, M. Stark, T. Menzel, D. Lungerich, N. Jux, W. Hieringer, H.-P. Steinrueck, H. Marbach, Phys. Chem. Chem. Phys. 2017, 19, 20281-20289.
94 „Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties„
F. Ammon, S. T. Sauer, R. Lippert, D. Lungerich, D. Reger, F. Hampel, N. Jux, Org. Chem. Front. 2017, 4, 861-870.
C. Reus, M. P. Lechner, M. Schulze, D. Lungerich, C. Diner, M. Gruber, J. M. Stryker, F. Hampel, N. Jux, R. Tykwinski, Chem. Eur. J. 2016, 22, 9097-9101.
92 „Catching metallic nitride endohedral fullerenes in organic and aqueous media„
V. Strauss, S. G. Radhakrishnan, J. Malig, N. Jux, D. M. Guldi, J. Porphyrins Phthalocyanines 2016, 20, 1025-1033.
91 „Pyridyl-endcapped Polyynes: Stabilized Wire-like Molecules„
M. Krempe, R. Lippert, F. Hampel, I. Ivanović-Burmazović, N. Jux, R. Tykwinski, Angew. Chem. Int. Ed. 2016, 55, 14802-14806.
90 „Three Short Stories about Hexaarylbenzene-Porphyrin Scaffolds„
D. Lungerich, J. F. Hitzenberger, W. Donaubauer, T. Drewello, N. Jux, Chem. Eur. J. 2016, 22, 16755-16759.

89 „Zinc Porphyrin Metal-Center Exchange at the Solid-Liquid Interface„
M. Franke, F. Marchini, N. Jux, H.-P. Steinrueck, O. Lytken, F. J. Williams, Chem. Eur. J. 2016, 22, 8520-8524.

88 „Benzoporphyrins: Selective Co-sensitization in Dye-Sensitized Solar Cells„
F. Lodermeyer, R. D. Costa, J. Malig, N. Jux, D. M. Guldi, Chem. Eur. J. 2016, 22, 7851-7855.
87 „A Strategy towards the Multigram Synthesis of Uncommon Hexaarylbenzenes„
D. Lungerich, D. Reger, H. Hoelzel, R. Riedel, M .M. J. C. Martin, F. Hampel, N. Jux, Angew. Chem. Int. Ed. 2016, 55, 5602-5605.
86 „[18]Annulene put into a new perspective„
D. Lungerich, A. V. Nizovtsev, F. W. Heinemann, F. Hampel, K. Meyer, G. Majetich, P. v. R. Schleyer, N. Jux, Chem. Commun. 2016, 52, 4710-4713.
L. Zhang, M. Lepper, M. Stark, R. Schuster, D. Lungerich, N. Jux, H.-P. Steinrück, H. Marbach, Chem. Eur. J. 2016, 22, 3347-3354.
J. Hitzenberger, C. Damann, N. Lang, D. Lungerich, M. Garcia-Iglesias, G. Bottari, T. Torres, N. Jux, T. Drewello, Analyst 2016, 141, 1347-1355.
M. Stark, S. Ditze, M. Thomann, D. Lungerich, N. Jux, H.-P. Steinrück, H. Marbach, Surface Science 2016, 650, 255-262.

M. Lepper, L. Zhang, M. Stark, S. Ditze, D. Lungerich, N. Jux, W. Hieringer, H.-P. Steinrück, H. Marbach, J. Chem. Phys. C 2015, 119, 19897-19905.
A. Dees, N. Jux, O. Tröppner, K. Dürr, R. Lippert, M. Schmid, B. Küstner, S. Schlücker, H.-P. Steinrück, J. M. Gottfried, I. Ivanović-Burmazović, Inorg. Chem. 2015, 54, 6862-6872.
80 „Axial coordination of pyridyl-containing pentacenes to porphyrins„
A. Waterloo, R. Lippert, N. Jux, R. Tykwinski, J. Coord. Chem. 2015, 68, 3088-3098.
L. Zhang, M. lepper, M. Stark, D. Lungerich, N. Jux, W. Hieringer, H.-P. Steinrück, H. Marbach, Phys. Chem. Chem. Phys. 2015, 17, 13066-13073.
78. „Supramolecular order and structural dynamics: An STM study of 2H-tetraphenylporphycene on Cu(111)„
M. Stark, J. Träg, S. Ditze, W. Brenner, N. Jux, H.-P. Steinrück, H. Marbach, J. Chem. Phys. 2015, 142, 101925/1-101925-6.
77. „Dibenzoporphycene – Platform for the Generation of Fused Porphycenes„
W. Brenner, N. Jux, Eur. J. Org. Chem. 2015, 242-246.
M. Roeckert, M. Franke, Q. Tariq, D. Lungerich, N. Jux, M. Stark, A. Kaftan, S. Ditze, H. Marbach, M. Laurin, J. Libuda, H.-P. Steinrueck, O. Lytken, J. Phys. Chem. C, 2014, 118, 26729-26736.
75 „Superbenzene-porphyrin conjugates“
D. Lungerich, J. F. Hitzenberger, M. Marcia, F. Hampel, T. Drewello, N. Jux, Angew. Chem. Int. Ed. 2014, 53, 12231-12235.
A. Kratzer, J. M. Englert, D. Lungerich, F. W. Heinemann, N. Jux, A. Hirsch, Faraday Discussions 2014, 173, 297-310.
O. Troeppner, R. Lippert, T. E. Shubina, A. Zahl, N.Jux, I. Ivanović-Burmazović, Angew. Chem. Int. Ed. 2014, 53, 11452-11457.
72 „Integrating metalloporphycenes into p-type NiO-based dye-sensitized solar cells“
S. Feihl, R. D. Costa, W. Brenner, J. T. Margraf, R. Casillas, O. Langmar, A. Browa, T. E. Shubina, T. Clark, N. Jux, D. M. Guldi, Chem. Commun. 2014, 50, 11339-11342.
71 „Effect of ferrocene-substituted porphyrin RL-91 on Candida albicans biofilm formation“
R. Lippert, S. Vojnovic, A. Mitrovic, N. Jux, I. Ivanovic-Burmazovic, B. Vasiljevic, N. Stankovic, Bioorg. Med. Chem. Letters 2014, 24, 3506-3511.
70 „On the Energetics of Conformational Switching of Molecules at and Close to Room Temperature“
S. Ditze, M. Stark, F. Buchner, A. Aichert, N. Jux, N. Luckas, A. Goerling, W. Hieringer, J. Hornegger, H.-P. Steinrueck, H. Marbach, J. Am. Chem. Soc. 2014, 136, 1609-1616.
J. Li, K. Duerr, M. von Gernler, N. Jux, I. Ivanovic-Burmazovic, T. Drewello, Int. J. Mass Spectrom. 2013, 354-355, 406-413.
68 „HBC-porphyrin – close contact chromophores“
J. M. Englert, J. Malig, V. Zamolo, A. Hirsch, N. Jux, Chem. Commun. 2013, 49, 4827-4829.
67 „Electron Accepting Porphycenes on Graphene“
R. D. Costa, J. Malig, W. Brenner, N. Jux, D. M. Guldi, Adv. Mater. 2013, 25, 2600-2605.
W. Brenner, J. Malig, R. D. Costa, D. M. Guldi, N. Jux, Adv. Mater. 2013, 25, 2314-2318.
J. Malig, N. Jux, D. M. Guldi, Acc. Chem. Res. 2013, 46, 53-64.
64 „Synthesis and physico-chemical properties of porphycenes“
W. Brenner, J. Malig, C. Oelsner, D. M. Guldi, N. Jux, J. Porphyrins Phthalocyanines 2012, 16, 651-662.
63 „Integrating Water-Soluble Graphene into Porphyrin Nanohybrids“
J. Malig, C. Romero-Nieto, N. Jux, D. M. Guldi, Adv Mater. 2012, 24, 800-805.
K. Duerr, O. Troeppner, J. Olah, J. Li, A. Zahl, T. Drewello, N. Jux, J. N. Harvey, I. Ivanović-Burmazović, Dalton Trans. 2012, 41, 546-557.
G. Katsukis, J. Malig, C. Schulz-Drost, S. Leubner, N. Jux, D. M. Guldi, ACS Nano 2012, 6, 1915-1924.
60 „A Facile Route to Water-Soluble Coronenes and Benzo[ghi]perylenes“
C. D. Schmidt, N. Lang, N. Jux, A. Hirsch, Chem. Eur. J. 2011, 17, 5289-5299.
59 „Towards Tunable Graphene/Phthalocyanine-PPV Hybrid Systems“
J. Malig, N. Jux, D. Kiessling, J.-J. Cid, P. Vazquez, T. Torres, D. M. Guldi, Angew. Chem. Int. Ed. 2011, 50, 3561-3565.
J. Malig, V. Strauss, P. Groenningen, D. M. Guldi, N. Jux, J. Porphyrins Phthalocyanines 2011, 15, 1317-1325.
H. Maid, P. Böhm, S. Huber, W. Bauer, W. Hummel, N. Jux, H. Gröger, Angew. Chem. Int. Ed. 2011, 50, 2397-2400.
J.-F. Gnichwitz, R. Marczak, F. Werner, N. Lang, N. Jux, D. M. Guldi, W. Peukert, A. Hirsch, J. Am. Chem. Soc. 2010, 132, 17910-17920.
55 „Studies on an iron(iii)-peroxo porphyrin. Iron(iii)-peroxo or iron(ii)-superoxo?“
K. Dürr, J. Olah, R. Davydov, M. Kleiman, J. Li, N. Lang, R. Puchta, E. Hübner, T. Drewello, J. N. Harvey, N. Jux, I. Ivanović-Burmazović, Dalton Trans. 2010, 39, 2049-2056.
K. Dürr, N. Jux, A. Zahl, R. van Eldik, I. Ivanović-Burmazović, Inorg. Chem. 2010, 49, 11254-11260.
53 „Annulation and Arylation Stabilize New Porphyrinoids“
N. Jux, Angew. Chem. 2009, 121, 4348-4350; Angew. Chem. Int. Ed.2009, 48, 4284-4286.
A. Brausam, S. Eigler, N. Jux, R. van Eldik, Inorg. Chem. 2009, 48, 7667-7678.
51 „Spectroscopic study of NH-tautomerism in novel cycloketo-tetraphenylporphyrins„
E. A. Ermilov, B. Büge, S. Jasinski, N. Jux, B. Röder, J. Chem. Phys. 2009, 130, 134509/1-134509/8
G. M. A. Rahman, V. Sgobba, A. Troeger, D. M. Guldi, N. Jux, M. N. Tchoul, W. T. Ford, A. Mateo-Alonso, M. Prato, Chem. Eur. J. 2008, 14, 8837-8836.
K. Rosenlehner, T. Schunk, N.Jux, M. Brettreich, A. Hirsch, Org. Biomol. Chem. 2008, 6, 2697-2705.
48 „Novel cycloketo tetraphenylporphyrins: spectroscopic study of structure-properties relationships„
E. A. Ermilov, S. Jasinski, N. Jux, B. Röder, Proceedings of SPIE-The International Society for Optical Engineering 2008, 7049, 704905/1-704905/11.
47 „The Porphyrin Twist: Hückel and Möbius Aromaticity“
N. Jux, Angew. Chem. Int. Ed. 2008, 47, 2543-2546.
46 „Testing Electron Transfer within Molecular Associates Built around Anionic C60 and C70 Dendrofullerenes and a Cationic Zinc Porphyrin„
G. H. Sarova, U. Hartnagel, D. Balbinot, S. Sali, N. Jux, A. Hirsch, D. M. Guldi, Chem. Eur. J. 2008, 14, 3137-3145.
45 „Synthesis and photophysical studies of porphyrin-ferrocene conjugates„
H. Mansour, M. E. El-Khouly, S. Y. Shaban, O. Ito, N. Jux, J. Porphyrins Phthalocyanines 2008, 10, 719-728.
44 „Polymorphism of Porphyrin Molecules on Ag(111) and how to weave a rigid monolayer„
F. Buchner, K. Comanici, N. Jux, H.-P. Steinrück, H. Marbach. J. Phys. Chem. 2007, 111, 13531-13538.
T. E. Shubina, H. Marbach, K. Flechtner, A. Kretschmann, N. Jux, F. Buchner, H.-P. Steinrück, T. Clark, J. M. Gottfried, J. Am. Chem. Soc. 2007, 129, 9476-9483.
42 „Intracellular uptake and phototoxicity of 31,32-didehydrophytochlorin-fullerene hexaadducts“
F. Rancan, M. Helmreich, A. Mölich, N. Jux, A. Hirsch, B. Röder, F. Böhm, Photochemistry and Photobiology 2007, 83, 1330-1338.
F. Rancan, M. Helmreich, A. Mölich, E. A. Ermilov, N. Jux, B. Röder, A. Hirsch, F. Böhm, Bioconjugate Chem. 2007, 18, 1078-1086.
T. Lukasczyk, K. Flechtner, L. R. Merte, N. Jux, F. Maier, J. M. Gottfried, H.-P. Steinrück, J. Phys. Chem. C. 2007, 111, 3090-3098.
39 „Photoinduced Energy and Electron Transfer Processes in Hexa-pyropheo-phorbide a- fullerene [C60] molecular systems„
M. Regehly, E. A. Ermilov, M. Helmreich, A. Hirsch, N. Jux, B. Röder, J. Phys. Chem. B. 2007, 111, 998-1006.
J.-E. Jee, S. Eigler, N. Jux, A. Zahl, R. van Eldik, Inorg. Chem. 2007, 46, 3336-3352.
37 „Iron(III) Complex of a Crown Ether-Porphyrin Conjugate and the Reversible Binding of Superoxide„
K. Dürr, B. P. Macpherson, R. Warratz, F. Hampel, F. Tuczek, M. Helmreich, N. Jux, I. Ivanović-Burmazovića, J. Am. Chem. Soc. 2007, 129, 4217-4228.
36 „Novel Synthetic Cyclo-Keto-Tetraphenylporphyrins„
S. Jasinski, E. A. Ermilov, N. Jux, B. Röder, Eur. J. Org. Chem. 2007, 1075-1084.
35 „Supramolecular Assemblies of Different Carbon Nanotubes for Photoconversion Processes„
V. Sgobba, G. M. A. Rahman, D. M. Guldi, N. Jux, S. Campidelli, M. Prato, Adv. Mater. 2006, 18, 2264-2269.
34 „Interactions in SWNT/pyrene/porphyrin nanohybrids„
C. Ehli, G. M. A. Rahman, N. Jux, D. Balbinot, D. M. Guldi, F. Paolucci, M. Maraccio, D. Paolucci, M. Melle-Franco, F. Zerbetto, S. Campielli, M. Prato, J. Am. Chem. Soc. 2006, 128, 11222-11231.
33 „The formation and energy transfer in pheophorbide a-DAB-dendrimers and pyropheophorbide a – fullerene C60 hexaadduct molecular systems„
B. Röder, E. A. Ermilov, S. Hackbarth, M. Helmreich, N. Jux, Proceedings of SPIE-The International Society for Optical Engineering 2006, 6192, 465-507.
32 „Electrophoresis of electrostatically assembled fullerene–porphyrin conjugates„
U. Hartnagel, D. Balbinot, N. Jux, A.Hirsch, Org. Biomol. Chem. 2006, 4, 1785-1795.
J.-E. Jee, M. Wolak, D. Balbinot, N. Jux, A. Zahl, R. van Eldik, Inorg. Chem. 2006, 453, 1326-1337.
30 „Carbon nanotube nanocomposites: quasi 1-dimensional structures for electron transfer„
D. M. Guldi, G. M. A. Rahman, N. Jux, D. Balbinot, U. Hartnagel, N. Tagmatarchis, M. Prato, Proceedings of SPIE-The International Society for Optical Engineering 2005, 5929, 1-11.
J.-E. Jee, S. Eigler, F. Hampel, N. Jux, M. Wolak, A. Zahl, G. Stochel, R. van Eldik, Inorg. Chem. 2005, 44, 7717-7731.
28 „Functional SWNT Nanohybrids – Associating SWNTs with Water Soluble Enzyme Model Systems„
D. M. Guldi, G. M. A. Rahman, N. Jux, D. Balbinot, U. Hartnagel, N. Tagmatarchis, M. Prato, J. Am. Chem. Soc. 2005, 127, 9830-9838.
27 „Dissipation of Electronic Excitation Energy within a C60 [6:0]-Hexaadduct Carry-ing 12 Pyropheophorbide a Moieties„
M. Helmreich, E. A. Ermilov, M. Meyer, N. Jux, A. Hirsch, B. Röder, J. Am. Chem. Soc. 2005, 127, 8376-8385.
F. Rancan, M. Helmreich, A. Mölich, N. Jux, A. Hirsch, B. Röder, C. Witt, F. Böhm, J. Photochem. Photobiol. B: Biology 2005, 80, 1-8.
25 „Trap formation and energy transfer in the hexapyropheophorbide a – fullerene C60 hexaadduct molecular system„
E.A. Ermilov, St. Hackbarth, S. Al-Omari, M. Helmreich, N. Jux, A. Hirsch, B. Röder, Opt. Commun. 2005, 250, 95-104.
D. M. Guldi, G. M. A. Rahman, N. Jux, D. Balbinot, N. Tagmatarchis, M. Prato, Chem. Commun. 2005, 2038-2040.
23 „Single-Wall Carbon Nanotubes as Integrative Building Blocks for Solar-Energy Conversion„
D. M. Guldi, G. M. A. Rahman, M. Prato, N. Jux, S. Qin, W. Ford, Angew. Chem. Int. Ed. 2005, 44, 2015-2018.
22 „Synthesis of novel pyropheophorbide a-fullerene conjugates„
M. Helmreich, A. Hirsch, N. Jux, J. Porphyrins Phthalocyanines 2005, 9, 130-137.
21 „Integrating Single-Wall Carbon Nanotubes into Donor–Acceptor Nanohybrids„
D. M. Guldi, G. M. A. Rahman, N. Jux, N. Tagmatarchis, M. Prato, Angew. Chem. Int. Ed. 2004, 43, 5526-5530.
20 „Donor-acceptor nanoensembles of soluble carbon nanotubes„
D. M. Guldi, G. N. A Rahman, J. Ramey, M. Marcaccio, D. Paolucci, F. Paolucci, S. Qin, W. T. Ford, D. Balbinot, N. Jux, N. Tagmatarchis, M. Prato, Chem. Commun. 2004, 2034-2035.
19 „Transient absorption spectroscopy of a monofullerene C60-bis-(pyropheophorbide a) molecular system in polar and nonpolar environments„
S. Al-Omari, E. A. Ermilov, M. Helmreich, N. Jux, A. Hirsch, B. Röder, Appl. Phys. B 2004, 79, 617-622.
E. A. Ermilov, S. Al-Omari, M. Helmreich, N. Jux, A. Hirsch, B. Röder, Opt. Commun. 2004, 234, 245-252.
17 „Photophysical properties of fullerene-dendron-pyropheophorbide supra-molecules„
E. A. Ermilov, S. Al-Omari, M. Helmreich, N. Jux, A. Hirsch, B. Röder, Chem. Phys. 2004, 301, 27-31.
16 „Introducing the Staudinger phosphazene reaction to porphyrin chemistry„
N. H. Huyen, U. Jannsen, H. Mansour, N. Jux, J. Porphyrins Phthalocyanines 2004, 8, 1356-1365.
15 „Multi-component redox gradients on photoactive electrode surfaces„
D. M. Guldi, I. Zilbermann, G. Anderson, A. Li, D. Balbinot, N. Jux, M. Hatzimarinaki, A. Hirsch, M. Prato, Chem. Commun. 2004, 726-727.
14 „Electrostatic assemblies of fullerene porphyrin hybrids towards long-lived charge separation„
D. Balbinot, S. Atalick, D. M. Guldi, M. Hatzimarinaki, A. Hirsch, N. Jux, J. Phys. Chem. B 2003, 107, 13273-13279.
R. Weiss, F. Pühlhofer, N. Jux, K. Merz, Angew. Chem. Int. Ed. 2002, 41, 3815-3817.
12 „Polymalonates derived from ortho-bromomethylated tetraarylporphyrins„
N. Jux, Proceedings of ECSOC-3, [and] Proceedings of ECSOC-4, Sept. 1-30, 1999 and 2000, 2000, 578-583.
11 „o-(Bromomethyl) Substituted Tetraarylporphyrin Building Blocks„
N. Jux, Org. Lett. 2000, 2, 2129-2132.
10 „26π-Porphyrinoide: Moleküle mit exzeptionellen spektroskopischen Eigen-schaften„
M. Bröring, H.-J. Dietrich, J. Dörr, G. Hohlneicher, J. Lex, N. Jux, C. Pütz, M. Roeb, H. Schmickler, E. Vogel, Angew. Chem. Int. Ed. 2000, 39, 1105-1108.
E. Vogel, N. Jux, J. Dörr, T. Pelster, T. Berg, H.-S. Böhm, F. Behrens, J. Lex, D. Bremm, G. Hohlneicher, Angew. Chem. Int. Ed. 2000, 39, 1101-1105.
8 „Synthesis and X-ray Characterization of an Oktaalkynyldibenzooctade-hydro[12]annulene“
J. D. Tovar, N. Jux, T. Jarosson, S. I. Khan, Y. Rubin, J. Org. Chem. 1997, 62, 3432-3433.
7 „Ein ungewöhnlich stabiles Pentaethinylcyclopentadienyl-Radikal“
N. Jux, K. Holczer, Y. Rubin, Angew. Chem. 1996, 108, 2116-2120; Angew. Chem. Int. Ed. 1996, 35, 1986-1990.
6 „Redox properties of novel tetrapyrroles: expanded porphycenes„
C. Bernard, J. P. Gisselbrecht, M. Gross, N. Jux, E. Vogel, J. Electroanal. Chem. 1995, 381, 159-166.
5 „Triplet spin alignment of ‘stretched porphycenes’ „
A. Berman, H. Levanon, E. Vogel, N. Jux, Chem. Phys. Lett. 1993, 211, 549-554.
4 „Photophysics and Photochemistry of 22π and 26π Acetylene-Cumulene Porphyrinoids„
D. O. Mártire, N. Jux, P. F. Aramendía, R. M. Negri, J. Lex, S. E. Braslavsky, K. Schaffner, E. Vogel, J. Am. Chem. Soc. 1992, 114, 9969-9978.
3 „Porphyrin – Strukturvarianten„
N. Jux, GIT Fachz. Lab. 1991, 35, 567-572.
2 „Die Porphyrin-Homologen: [22]Porphyrin(2.2.2.2), ein ‘gestrecktes’ Porphycen„
E. Vogel, N. Jux, E. Rodriguez-Val, J. Lex, H. Schmickler, Angew. Chem. Int. Ed. 1990, 29, 1387-1390.
1 „Acetylen-Cumulen-Porphyrinoide„
N. Jux, P. Koch, H. Schmickler, J. Lex, E. Vogel, Angew. Chem. Int. Ed. 1990, 29, 1385-1387.
Patents
P1 „Cyclo-Keto-Tetraphenylporphyrins as Sensitizers for the Photodynamic Therapy of Tumors“ S. Jasinski, N. Jux, E. Ermilov, B. Röder, eingereicht beim Europäischen Patentamt am 10. März 2006; Aktenzeichen 06 075 595.6.
Book Chapters
B1 „Novel Pyropheophorbide Fullerene conjugates as part of Modular Carrier Systems in PDT and as promising units in Artificial Photosynthesis„
E.A. Ermilov, M. Helmreich, N. Jux, B. Röder, Chemical Physics Research Trends -Horizons in World Physics, B.V. Arnold (Ed.), Nova Science Publishers, Vol. 252, 2007, ISBN: 1-60021-554-8.
B2 „Targeting Strategies for Tetrapyrrole-Based Photodynamic Therapy„
N. Jux, B. Röder, Handbook of Porphyrin Science, K. M. Kadish, K. M. Smith, R. Guilard (Ed.), World Scientific, Vol. 4, 2010, 325-402; ISBN: 13 978-981-4280-16-7.
B3 „Coordination Chemistry of Crown Ether-Porphyrin Conjugates„
N. Jux, Handbook of Porphyrin Science, K. M. Kadish, K. M. Smith, R. Guilard (Ed.), World Scientific, Vol. 24, 2010, 181-269; ISBN: 978-981-4397-65-0 (Vol. 24).