Publications

2020 / 2010-2019 / 2000-2009 / 1990-1999 / Patents / Book Chapters top

2020

139 „Towards understanding the competition of electron and energy transfer in “molecular” nanographenes on the example of hexa-peri-hexabenzocoronene„

G. M. Beneventi, M. Krug, D. Reger, N. Jux, D. M. Guldi, J. Photochem. Photobiol. C 2023, 100602.

138 „Superhelicenes in the gas phase: experimental and computational evidence of stable radical cation dimers„

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.

136 „Probing Charge Management across the π-Systems of Nanographenes in Regioisomeric Electron Donor–Acceptor Architectures„

H. Hölzel, P. Haines, R. Kaur, D. Lungerich, N. Jux, D. M. Guldi, J. Am. Chem. Soc. 2022, 144, 20, 8977–8986.

135 „Adsorption and self-assembly of a mono-cyano Zn-tetraphenylporphyrin derivative on KBr(001) and MgO(001)„

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.

132 „Benzohydroxamic acid on rutile TiO2(110)-(1×1)– a comparison of ultrahigh-vacuum evaporation with deposition from solution„

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.

131 „Four-Step Domino Reaction Enables Fully Controlled Non-Statistical Synthesis of Hexaarylbenzene with Six Different Aryl Groups„

B. Grau, M. Dill, F. Hampel, A. Kahnt, N. Jux, S. B. Tsogoeva, Angew. Chem. Int. Ed. 2021, 60, 22307–22314.

130 „A Singular Molecule-to-Molecule Transformation on Video: The Bottom-Up Synthesis of Fullerene C₆₀ from Truxene Derivative C₆₀H₃₀„

D. Lungerich, H. Hölzel, K. Harano, N. Jux, K. Y. Amsharow, E. Nakamuram, ACS Nano 2021, 15, 8, 12804–12814.

129 „A Family of Superhelicenes: Easily Tunable, Chiral Nanographenes by Merging Helicity with Planar π Systems„

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.

126 „Self-Assembled 2D-Coordination Kagome, Quadratic, and Close-Packed Hexagonal Lattices Formed from a Cyano-Functionalized Benzoporphyrin on Cu(111)„

R. Adhikari, J. Kuliga, M. Ruppel, N. Jux, H. Marbach, H.-P. Steinrück, J. Phys. Chem. C 2021, 125, 13, 7204–7212.

125 „Screening Nanographene-Mediated Inter(Porphyrin) Communication to Optimize Inter(Porphyrin–Fullerene) Forces„

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.

123 „On the photophysics of nanographenes – investigation of functionalized hexa-peri-hexabenzocoronenes as model systems„

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.

119 „A Functional Hexaphenylbenzene Library Comprising of One, Three and Six Peripheral Rylene-Diimide Substituents„

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„

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.

115 „Panchromatic light funneling through the synergy in hexabenzocoronene–(metallo)porphyrin– fullerene assemblies to realize the separation of charges„

M. Wolf, D. Lungerich, S. Bauroth, M. Popp, B. Platzer, T. Clark, H. L. Anderson, N. Jux, D. M. Guldi, Chem. Sci. 2020, 11, 7123–7132.

114 „Formation of Highly Ordered Molecular Porous 2D Networks from Cyano-Functionalized Porphyrins on Cu(111)„

113 „Investigations of Low-Symmetrical Tetraaryltetrabenzoporphyrins Produced by Mixed Condensation Reactions„

M. 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.

108 „Positive Charge on Porphyrin Ligand and Nature of Metal Center Define Basic Physicochemical Properties of Cationic Manganese and Iron Porphyrins in Aqueous Solution„

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.

102 „Metalation and coordination reactions of 2H-meso-trans-di(p-cyanophenyl)porphyrin on Ag(111) with coadsorbed cobalt atoms„

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.

97 „Adsorption of cyano-​functionalized porphyrin on Cu(111) and Ag(111)​: From molecular wires to ordered supramolecular two-​dimensional aggregates„

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.

96 „Highly Regioselective Alkylation of Hexabenzocoronenes: Fundamental Insights into the Covalent Chemistry of Graphene„

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.

95 „On the critical role of the substrate: the adsorption behavior of tetrabenzoporphyrins on different metal surfaces„

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.

93 „Unexpected Michael Additions on the Way to 2.3,​8.9-​Dibenzanthanthrenes with Interesting Structural Properties„

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.

85 „2H-​Tetrakis(3,​5-​di-​tert-​butyl)​phenylporphyrin on a Cu(110) Surface: Room-​Temperature Self-​Metalation and Surface-​Reconstruction-​Facilitated Self-​Assembly„

L. Zhang, M. Lepper, M. Stark, R. Schuster, D. Lungerich, N. Jux, H.-P. Steinrück, H. Marbach, Chem. Eur. J. 2016, 22, 3347-3354.

84 „Making the invisible visible: improved electrospray ion formation of metalloporphyrins​/-​phthalocyanines by attachment of the formate anion (HCOO-​)„

J. Hitzenberger, C. Damann, N. Lang, D. Lungerich, M. Garcia-Iglesias, G. Bottari, T. Torres, N. Jux, T. Drewello, Analyst 2016, 141, 1347-1355.

83 „Reversible thermally induced phase transition in ordered domains of Co(II)​-​5,​10,​15,​20-​tetrakis-​(3,​5-​di-​tert-​butylphenyl)​-​porphyrin on Cu(111)„

M. Stark, S. Ditze, M. Thomann, D. Lungerich, N. Jux, H.-P. Steinrück, H. Marbach, Surface Science 2016, 650, 255-262.

82 „Role of Specific Intermolecular Interactions for the Arrangement of Ni(II)​-​5, 10, 15, 20-​Tetraphenyltetrabenzoporphyrin on Cu(111)„

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.

81   „Reactions of Superoxide with Iron Porphyrins in the Bulk and the Near-​Surface Region of Ionic Liquids„

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.

79       „Self-​assembly and coverage dependent thermally induced conformational changes of Ni(II)​-​meso-​tetrakis(4-​tert-​butylphenyl)​benzoporphyrin on Cu(111)„

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.

76. „Insights in Reaction Mechanistics: Isotopic Exchange during the Metalation of Deuterated Tetraphenyl-​21,​23D-​porphyrin on Cu(111)„

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.

74     „Synthesis and first X-​ray structure of a hexa-​peri-​hexabenzocoronene-​fullerene-​dyad: a model for an inter-​carbon-​allotrope hybrid“

A. Kratzer, J. M. Englert, D. Lungerich, F. W. Heinemann, N. Jux, A. Hirsch, Faraday Discussions 2014, 173, 297-310.

73     „Reverse Spin-Crossover and High-Pressure Kinetics of the Heme Iron Center Relevant for the Operation of Heme Proteins under Deep-Sea Conditions“

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.

69     „The dissociation behaviour of a singly and doubly charged (cationised) aza-​crown ether​/metalloporphyrin-​conjugate: Metal-​induced reactivity and Coulomb explosions“

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.

66     „Poly-Ortho-Functionalizable Tetraarylporphycene Platform–Synthesis of Octa-cationic Derivatives Towards the Layer-by-Layer Design of Versatile Graphene Oxide Photoelectrodes“

W. Brenner, J. Malig, R. D. Costa, D. M. Guldi, N. Jux,  Adv. Mater. 2013, 25, 2314-2318.

65     „Toward Multifunctional Wet Chemically Functionalized Graphene-Integration of Oligomeric, Molecular, and Particulate Building Blocks that Reveal Photoactivity and Redox Activity“

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.

62     „Solution behavior of iron(III) and iron(II) porphyrins in DMSO and reaction with superoxide. Effect of neighboring positive charge on thermodynamics, kinetics and nature of iron-(su)peroxo product“

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.

61     „Toward Combining Graphene and QDs: Assembling CdTe QDs to Exfoliated Graphite and Nanographene in Water“

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.

58     „Synthesis and characterization of novel „Clicked“ dimers of unsymmetrically substituted tetraphenylporphyrins“

J. Malig, V. Strauss, P. Groenningen, D. M. Guldi, N. Jux, J. Porphyrins Phthalocyanines 2011, 15, 1317-1325.

57     „Iron catalysis for in situ regeneration of oxidized cofactors by activation and reduction of molecular oxygen: a synthetic metalloporphyrin as a biomimetic NAD(P)H oxidase“

H. Maid, P. Böhm, S. Huber, W. Bauer, W. Hummel, N. Jux, H. Gröger, Angew. Chem. Int. Ed. 2011, 50, 2397-2400.

56     „Efficient synthetic access to cationic dendrons and their application for ZnO nanoparticles surface functionalization: new building blocks for dye-sensitized solar cells“

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.

54     „Volume Profile Analysis for the Reversible Binding of Superoxide to Form Iron(II)-Superoxo/Iron(III)-Peroxo Porphyrin Complexes“

K. Dürr, N. Jux, A. Zahl, R. van Eldik, I. Ivanović-Burmazović, Inorg. Chem. 2010, 49, 11254-11260.

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2000-2009

53     „Annulation and Arylation Stabilize New Porphyrinoids“

N. Jux, Angew. Chem. 2009, 121, 4348-4350; Angew. Chem. Int. Ed.2009, 48, 4284-4286.

52       „Mechanistic Investigations of the Reaction of an Iron(III) Octa-Anionic Porphyrin Complex with Hydrogen Peroxide and the Catalyzed Oxidation of Diammonium-2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonate)„

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

50       „Improving photocurrent generation: supramolecularly and covalently functionalized single-wall carbon nanotubes-polymer/porphyrin donor-acceptor nanohybrids„

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.

49       „Layer-by-Layer Deposition of Molecular Oligoelectrolytes – Investigation of Assembling and Degradation Behaviour„

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.

43     „Principle and Mechanism of Direct Porphyrin Metalation: A Joint Experimental and Theoretical Investigation„

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.

41     „Synthesis and in vitro testing of a pyropheophorbide-a-fullerene-hexakisadduct immunoconjugate for photodynamic therapy„

F. Rancan, M. Helmreich, A. Mölich, E. A. Ermilov, N. Jux, B. Röder, A. Hirsch, F. Böhm, Bioconjugate Chem. 2007, 18, 1078-1086.

40     „Interaction of Co(II)-tetraarylporphyrins with a Ag(111) surface studied with photoelectron spectroscopy„

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.

38     „Influence of an extremely negatively charged porphyrin on the reversible binding kinetics of NO to Fe(III) and the subsequent reductive nitrosylation„

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.

31     „A comparative mechanistic study of the reversible binding of NO to a water-soluble octa-cationic FeIII porphyrin complex„

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.

29     „Kinetic and mechanistic studies on the reaction of nitric oxide with a water-soluble octa-anionic FeIII-porphyrin complex„

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.

26     „Fullerene-pyropheophorbide a complexes as sensitizer for photodynamic therapy: Uptake and photo-induced cytotoxicity on Jurkat cells„

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.

24     „Multiwalled carbon nanotubes in donor-acceptor nanohybrids-towards long-lived electron transfer products„

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.

18     „Steady-state and time-resolved studies on the photophysical properties of fullerene-pyropheophorbide a complexes in polar and nonpolar solvents„

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.

13     „SASAPOS statt Sisyphos: Hocheffiziente 20-stufige Eintopfsynthese eines diskreten organisch-anorganischen Ionenclusters mit Porphyrinkern„

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.

9       „Porphyrine auf Furan-Basis: Tetraoxa[4n+2]porphyrin-Dikationen mit 18π-, 22π- und 26π-Elektronensystem„

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.

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1990-1999

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).

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