Publikationen

203.       D. Timmer, M. Gittinger, T. Quenzel, S. Stephan, Y. Zhang, M. F. Schumacher, A. Lützen, M. Silies, S. Tretiak, J.-H. Zhong, A. De Sio, C. Lienau, Nat. Commun. 2023, zur Publikation eingereicht.

”Plasmon mediated coherent population oscillations in molecular aggregates”

202.       M. Zuhayra, A. Lützen, M. A. Ruiz, Acta Cryst. C 2023, zur Publikation angenommen.

”The X-ray-Determined Structure of the Technetium Complex [Tc2(µ-CO)2(CO)6(NC5H5)2] Revisited: [Tc2(µ-OMe)2(CO)6(NC5H5)2] as the Right Formulation”

201.       D. Giavazzi, M. F. Schumacher, L. Grisanti, M. Anzola, F. Di Maiolo, J. Zablocki, A. Lützen, M. Schiek, A. Painelli, J. Mater. Chem. C 2023, 11, 8307-8321. DOI: 10.1039/D2TC05555D .

”A Marvel of Chiral Squaraine Aggregates: chiroptical specra beyond the exciton model”

200.       M. Zenka, J. Preinl, E. Pertermann, A. Lützen, K. Tiefenbacher, Eur. J. Inorg. Chem. 2023, 26, e202300110. DOI: 10.1002/ejic.202300110 .

”Synthesis of a water and base-stable iminopyridine-based cage able to bind larger organic anions”

200.       R. Bernhardt, M. Manrho, J. Zablocki, L. Rieland, A. Lützen, M. Schiek, K. Meerholz, J. Zhu, T. L. C. Jansen, J. Knoester, P. H. M. Van Loosdrecht, J. Am. Chem. Soc. 2022, 144, 19372–19381. DOI: 10.1021/jacs.2c07064 .

                ”Structural Disorder as the Origin of Optical Properties and Spectral Dynamics in Squaraine Nano–Aggregates”

199.       D. Timmer, F. Zheng, M. Gittinger, T. Quenzel, D. C. Lünemann, K. Winte, Y. Zhang, M. E. Madjet, J. Zablocki, A. Lützen, J.-H. Zhong, A. De Sio, T. Frauenheim, S. Tretiak, C. Lienau, J. Am. Chem. Soc. 2022, 144, 19150-19162. DOI: 10.1021/jacs.2c08682 .

                ”Charge Delocalization and Vibronic Couplings in Quadrupolar Squaraine Dyes”

198.       X.-L. Li, L. Zhao, J. Wu, H. Zhao, W. Shi, A. Lützen, A. K. Powell, P. Cheng, J. Tang, Chem. Sci. 2022, 13, 10048-10056. DOI: 10.1039/D2SC03156F .

197.       F. Balzer, N. J. Hestand, J. Zablocki, G. Schnakenburg, A. Lützen, M. Schiek, J. Phys. Chem. C 2022, 126, 13802-13813. DOI: 10.1021/acs.jpcc.2c03665 .

“Spotlight on Charge-Transfer Excitons in Crystalline Textured n-Alkyl Anilino Squaraine Thin Films“

196.       F. Balzer, M. F. Schumacher, S. Matiello, M. Schulz, J. Zablocki, M. Schmidtmann, K. Meerholz, S. N. Sariciftci, L. Beverina, A. Lützen, M. Schiek, Isr. J. Chem. 2022, 62, e202100079. DOI: 10.1002/ijch.202100079 .

“The Impact of Chiral Citronellyl-Functionalization on Indolenine and Anilino Squaraine Thin Films“

195.       A. S. Jenniches, J. Bahr, D. Püschner, T. J. Keller, S. Hütgens, K. Gratzfeld, F. Spahlholz, A. Eslam, A. Lützen, Langmuir 2022, 38, 6602-6611. DOI: 10.1021/acs.langmuir.2c00462 .

“Influence of different substitution patterns of dendron units on the 2D crystalline aggregation of small molecules on HOPG surfaces“

1934.       T. Qenzel, D. Timmer, M. Gittinger, J. Zablocki, F. Zheng, M. Schiek, A. Lützen, T. Frauenheim, S. Tretiak, M. Silies, J.-H. Zhong, A. De Sio, C. Lienau, ACS Nano 2022, 16, 4693-4704. DOI: 10.1021/acsnano.1c11398 .

                ”Plasmon-enhanced exciton delocalization in squaraine-type molecular aggregates”

 “Subcomponent Self-Assembly of Circular Helical Dy6L6 and Bipyramidal Dy12L8 Architectures Directed via Second-Order Template Effects“

193. F. Balzer, M. F. Schumacher, S. Matiello, M. Schulz, J. Zablocki, M. Schmidtmann, K. Meerholz, S. N. Sariciftci, L. Beverina, A. Lützen, M. Schiek, Isr. J. Chem. 2021, zur Publikation angenommen. DOI: 10.1002/ijch.202100079   .
“The Impact of Chiral Citronellyl-Functionalization on Indolenine and Anilino Squaraine Thin Films“

192. G. Hoffrichter, A. Lützen, Org. Chem. Front. 2021, 8, 5810-5820. DOI: 10.1039/D1QO01173A   . ”Allosteric Binding of Sodium Deoxycholate by a Bis(β-cyclodextrin)-2,2´-bipyridine Receptor”

191. M. Hardy, J. Tessarolo, J. J. Holstein, N. Struch, N. Wagner, R. Weisbarth, M. Engeser, J. Beck, S. Horiuchi, G. H. Clever, A. Lützen, Angew. Chem. 2021, 133, 22736-22743. DOI: 10.1002/ange.202108792;    Angew. Chem. Int. Ed. 2021, 60, 22562-22569. DOI:10.1002/anie.202108792   .
”Eine Familie von Heterobimetallischen Würfeln zeigt Spin-Crossover-Verhalten nahe Raumtemperatur“
“A family of heterobimetallic cubes shows spin-crossover behaviour near room temperature“

190. T. Grothe, T. Böhm, K. Habashy, O. S. Abdullaeva, J. Zablocki, A. Lützen, K. Dedek, M. Schiek, A. Ehrmann, Phys. Status Solidi B 2021, 258, 2000543. DOI: 10.1002/pssb.202000543   .
“Optical index matching, flexible electrospun substrates for seamless organic photocapacitive sensors“

189. J. Anhäuser, A. Lützen, M. Engeser, ChemPlusChem. 2020, 84, 2528-2533.DOI: 10.1002/cplu.202000697   . “Charge state-dependent fragmentation of [2.2]paracyclophane-based metallosupra-molecular cyclic helicates in the gas phase“

188. M. Hardy, M. Engeser, A. Lützen, Beilstein J. Org. Chem. 2020, 16, 2701-2708. DOI: 10.3762/bjoc.16.220   . “A Heterobimetallic Tetrahedron from a Linear Platinum(II)-Bis(acetylide) Metalloligand“

187. J. Zablocki, M. Schulz, G. Schnakenburg, L. Beverina, P. Warzanowski, A. Revelli, M. Grüninger, F. Balzer, K. Meerholz, A. Lützen, M. Schiek, J. Phys. Chem. C 2020, 124, 22721-22732. DOI: 10.1021/acs.jpcc.0c07498   . “Structure and Anisotropic Dielectric Function of n-Alkyl Anilino Squaraine Thin Films“

186. M. Hardy, A. Lützen, Chem. Eur. J. 2020, 26, 13332-13346. DOI: 10.1002/chem.202001602   .
“Better Together: Functional Heterobimetallic Macrocyclic and Cage-like Assemblies“

185. A. Jarzebski, G. Schnakenburg, A. Lützen, ChemPlusChem 2020, 84, 1455-1464. DOI: 10.1002/cplu.202000387   . “Chiral self-sorting effects in the self-assembly of metallosupramolecular aggregates comprising ligands derived from Tröger’s base“

184. J. Zablocki, D. Hertel, O. Arteaga, J. Anhäuser, R. Puttreddy, J. J. Holstein, G. H. Clever, K. Rissanen, K. Meerholz, A. Lützen, M. Schiek Chirality 2020, 32, 619-632. DOI: 10.1002/chir.23213   . “Polymorphic Chiral Squaraine Crystallites in Textured Thin Films“

183. L. Volbach, N. Struch, F. Bohle, F. Topić, G. Schnakenburg, A. Schneider, S. Grimme, K. Rissanen, A. Lützen, Chem. Eur. J. 2020, 26, 3335-3347. DOI: 10.1002/chem.201905070   .
“Influencing the self-sorting behavior of [2.2]paracyclophane based ligands by introducing isostructural binding motifs“

182. M. Hardy, N. Struch, J. J. Holstein, G. Schnakenburg, N. Wagner, M. Engeser, J. Beck, G. H. Clever, A. Lützen, Angew. Chem. 2020, 132, 3221-3226. DOI: 10.1002/ange.201914629;    Angew. Chem. Int. Ed. 2020, 59, 3195-3200. DOI: 10.1002/anie.201914629   .
“Dynamische Komplex-zu-Komplex Umwandlungen heterobimetallischer Systeme beeinflussen die Käfigstruktur oder den Spinzustand von Eisen(II)ionen“
“Chemical Stimuli Change the Structure or the Spin State of Iron(II) Ions within Heterobimetallic Cages via Dynamic Complex-to-Complex Transformations“

181. F. Balzer, O. S. Abdullaeva, A. Maderitsch, M. Schulz, A. Lützen, M. Schiek, Phys. Status Solidi B 2020, 257, 1900570. DOI: 10.1002/pssb.201900570   .
“Nanoscale Polarization-Resolved Surface Photovoltage of a Pleochroic Squaraine Thin Film“

180. M. Gaedke, F. Witte, J. Anhäuser, H. Hupatz, H. V. Schröder, A. Valkonen, K. Rissanen, A. Lützen, B. Paulus, C. A. Schalley, Chem. Sci. 2019, 10, 10003-10009. DOI: 10.1039/c9cs03694f   .
“Chiroptical inversion of a planar chiral redox-switchable rotaxane“

179. L. M. Mesquita, J. Anhäuser, D. Bellaire, S. Becker, A. Lützen, S. Kubik, Org. Lett. 2019, 21, 6442-6446. DOI: 10.1021/acs.orglett.9b02338   . “Palladium(II)-Mediated Assembly of a M2L2 Macrocycle and M3L6 Cage from a Cyclopeptide-Derived Ligand“

178. J. Anhäuser, R. Putteddy, L. Glanz, A. Schneider, M. Engeser, K. Rissanen, A. Lützen, Chem. Eur. J. 2019, 25, 12294-12297. DOI: 10.1002/chem.201903164   .
“Subcomponent self-assembly of a cyclic tetranuclear Fe(II) helicate in a highly diastereoselective self-sorting manner “

177. A. Kiesilä, N. K. Beyeh, J. Moilanen, R. Puttreddy, S. Götz, K. Rissanen, P. Barran, A. Lützen, E. Kalenius, Org. Biomol. Chem. 2019, 17, 6980-6984. DOI: 10.1039/C9OB01383K   .
“Thermodynamically driven Self-assembly of Pyridinearene to Hexameric Capsules“

176. Y. Lorenz, J. Anhäuser, A. Lützen, M. Engeser, J. Am. Soc. Mass Spectrom. 2019, 30, 2007-2013. DOI: 10.1007/s13361-019-02218-2   . “[2.2]Paracyclophane bis(pyridine)-based metallosupramolecular rhombs in the gas phase: Competitive cleavage of non-covalent and weak covalent bonds“

168.        A. Ehrmann, T. Grothe, T. Böhm, K. Habashy, O. Abdullaeva, M. Schiek, J. Parisi, M. Schulz, A. Lützen, K. Dedek, Chem. Ing. Tech. 2018, 90, 1214-1215. “Spincoaten organischer Dünnschichten auf elektrogesponnene Nanovliese und -membranen“

167.        M. Käseborn, J. J. Holstein, G. H. Clever, A. Lützen, Angew. Chem. 2018, 130, 12349-12353. DOI: 10.1002/ange.201806814;    Angew. Chem. Int. Ed. 2018, 57, 12171-12175. DOI: 10.1002/anie.201806814   . “Ein rotaxanartiges Käfig-im-Ring-Strukturmotiv für ein metallosupramolekulares Pd6L12-Aggregat“; “A Rotaxane-like Cage-in-Ring Structural Motif for a Metallosupramolecular Pd6L12 Aggregate“

166.        M. Schulz, J. Zablocki, O. S. Abdullaeva, F. Balzer, A. Lützen, O. Arteaga, M. Schiek, Nat. Commun. 2018, 9, 2413. DOI: 10.1038/s41467-018-04811-7   . “Giant Circular Dichroism of Enantiopure Prolinol-Dervived Squaraine Thin Films“

165.        M. Hardy, N. Struch, F. Topić, G. Schnakenburg, K. Rissanen, A. Lützen, Inorg. Chem. 2018, 57, 3507-3515 (Forum Article). DOI: 10.1021/acs.inorgchem.7b02516   . “Stepwise Construction of Heterobimetallic Cages by an Extended Molecular Library Approach“

164.       M. Luft, B. Gross, M. Schulz, A. Lützen, M. Schiek, N. Nilius, J. Chem. Phys. 2018, 148, 074702. DOI: 10.1063/1.5017826   . “Adsorption of Squaraine Molecules on Au(111) and Ag(001) Surfaces: Role of the Substrate Symmetry“

163.        M.-C. Melcher, C. Olagnon, C. Tenten, A. Lützen, D. Strand,  Chem. Eur. J. 2018, 24, 2344-2348. DOI: 10.1002/chem.201704816   . “Control of enantioselectivity in rhodium(I)-catalysis by planar chiral dibenzo[a,e]cyclo-octatetraenes“

162.        B. Ingenfeld, S. Straub, C. Frömbgen, A. Lützen, Synthesis. 2018, 50, 676-684 DOI: 10.1055/s-0036-1589127   . “Synthesis of monofunctionalized calix[5]arenes“

161.        N. Struch, F. Topić, G. Schnakenburg, K. Rissanen, A. Lützen, Inorg. Chem. 2018, 57, 241-250. DOI: 10.1021/acs.inorgchem.7b02412   . “Electron-deficient pyridylimines: New building blocks for metallosupramolecular chemistry“

160.        F. Balzer, H. Kollmann, M. Schulz, M. Schmidtmann, G. Schnakenburg, A. Lützen, C. Lienau, M. Silies, M. Schiek, Cryst. Growth Des. 2017, 17, 6455-6466. DOI: 10.1021/acs.cgd.7b01131   . “Formation of Excitoniuc Molecular Aggregates in Polymorphic, Textured Thin Films of an Anilino Squarine with Branched Alkyl Side Chains“

159.        D. Scheunemann, O. Kolloge, S. Wilken, J. Parisi, M. Schulz, A. Lützen, M. Schiek, Appl. Phys. Lett. 2017, 111, 18502. DOI: 10.1063/1.4996080   . “Revealing the Recombination Dynamics in Squaraine-Based Bulk-Heterojunction Solar Cells“

158.        N. Struch, C. Frömbgen, G. Schnakenburg, A. Lützen, Eur. J. Org. Chem. 2017, 4984-4989. DOI: 10.1002/ejoc.201700921   . “Diastereoselective Formation of Homochiral Helicates via Subcomponent Self-Assembly“

157.        A. Kiesilä, L. Kivijäri, N. K. Beyeh, J. Moilanen, M. Groessi, F. Topic, T. Rothe, S. Götz, K. Rissanen, A. Lützen, E. Kalenius, Angew. Chem. 2017, 129, 11082-11087. DOI: 10.1002/ange.201704054;    Angew. Chem. Int Ed. 2017, 56, 10942-10946. DOI: 10.1002/anie.2017004054   . ”Simultane endo- und exo-Komplexbildung von Pyridin[4]aren-Dimeren mit neutralen und anionischen Gästen”; “Simultaneous Endo and Exo Complex Formation of Pyridin[4]arene with Neutral and Anionic Guests“

156.        A. Jarzebski, C. Tenten, C. Bannwarth, G. Schnakenburg, S. Grimme, A. Lützen, Chem. Eur. J. 2017, 23, 12380-12386. DOI: 10.1002/chem.201702125   . “Diastereoselective Self-Assembly of a Neutral Dinuclear Double-Stranded Zinc(II) Helicate via Narcissistic Self-Sorting“

155.        N. Struch, F. Topić, K. Rissanen, A. Lützen, Dalton Trans. 2017, 46, 10809-10813. DOI: 10.1039/c7dt02182h   . “Electron-deficient trifluoromethyl-substituted sub-components affect the properties of M4L4 tetrahedral cages“

154.        J. Linnet, A. R. Walther, O. Albrektsen, L. Tavares, R. L. Eriksen, P. Baunegaard, W. Jensen, A. Osadnik, S. Hassing, A. Lützen, J. Kjelstrup-Hansen, Org. Electr. 2017, 46, 270-275. DOI: 10.1016/j.orgel.2017.04.019   . “Enhanced photoresponsivity in organic field effect transistors by silver nanoparticles“

153.        C. Stobe, I. Pyka, A. Linke, S. Müller, G. Schnakenburg, S. R. Waldvogel, A. Lützen, ChemPlusChem 2017, 82, 758-769. DOI: 10.1002/cplu.201700105   . “Synthesis of 9,9’-Spirobifluorenes and 4,5-Diaza-9,9’-spirobifluorenes and their Application as Affinity Materials for Quartz Crystal Microbalances“

152.        F. Balzer, R. Resel, A. Lützen, M. Schiek, J. Chem. Phys. 2017, 146, 134704. DOI: 10.1063/1.497948   . “Quasi-One-Dimensional Cyano-Phenylene Aggregates: Uniform Molecule Alignment Contrasts Varying Electrostatic Surface Potential“

151.        M. Schulz, M. Mack, O. Kolloge, A. Lützen, M. Schiek, Phys. Chem. Chem. Phys. 2017, 19, 6996-7008. DOI: 10.1039/c7cp00306d   . “Organic Photodiodes from Homochiral Squaraine Compounds with Strong Circular Dichroism“

150.        N. Struch, C. Bannwarth, T. Ronson, Y. Lorenz, B. Mienert, N. Wagner, M. Engeser, E. Bill, R. Puttreddy, K. Rissanen, J. Beck, S. Grimme, J. R. Nitschke, A. Lützen, Angew. Chem. 2017, 129, 5012-5017. DOI: 10.1002/ange.201700832;    Angew. Chem. Int. Ed. 2017, 56, 4930-4935. DOI: 10.1002/anie.201700832   . ”Ein achtkerniger metallosupramolekularer Würfel mit Spin Crossover Eigenschaften”; “An Octanuclear Metallosupramolecular Cage Designed to Exhibit Spin-Crossover Behavior“

145.        F. Balzer, R. Sun, J. Parisi, H.-G. Rubahn, A. Lützen, M. Schiek, Thin Solid Films 2015, 597, 104-111. DOI: 10.1016/j.tsf.2015.11.014    “Epitaxial Growth of a Methoxy-Functionalized Quaterphenylene on Alkali Halide Surfaces“

144.        N. Struch, G. Schnakenburg, A. Lützen, Acta Cryst. C 2015, 71, 1048-1052. DOI: 10.1107/S2053229615020409   . “A novel crystal structure of {tris[4-(1H-pyrazol-3-yl-kN2)-3-aza-but-3-enyl]amine-kN}-iron(II) bis(tetrafluoridoborate) methanol monosolvate featuring low-spin configuration“

143.        N. Struch, J. G. Brandenburg, G. Schnakenburg, N. Wagner, J. Beck, S. Grimme, A. Lützen, Eur. J. Inorg. Chem. 2015, 5503-5510. DOI: 10.1002/ejic.201501057   . “A case study on mechanical strain in supramolecular complexes to manipulate the spin state of iron(II) centres“

142.        S. Kietzmann, C. Strelow, L. Tavares, A. Schramm, J.-P. Penttinen, T. V. Hakkarainen, A. Osadnik, A. Lützen, J. Kjelstrup-Hansen, A. Mews, T. Kipp, ACS Photonics 2015, 2, 1532-1538. DOI: 10.1021/acsphotonics.5b00349   . “Fluorescent NaT2 Molecular Films as Light-Emitting and Light-Confining Material in Rolled-Up AlInP Semiconductor Microtube Resonators“

141.        A. Jarzebski, C. Bannwarth, C. Tenten, C. Benkhäuser, G. Schnakenburg, S. Grimme, A. Lützen, Synthesis 2015, 47, 3118-3132 (Feature Article). DOI: 10.1055/s-0035-1560181   . “Synthesis, Chiral Resolution, and Absolute Configuration of Functionalized Tröger’s Base Derivatives: Part III“

140.        V. Göker, S. R. Kohl, F. Rominger, G. Meyer-Eppler, L. Volbach, G. Schnakenburg, A. Lützen, A. S. K. Hashmi, J. Organomet. Chem. 2015, 795, 45-52. DOI: 10.1016/j.jorganchem.2015.03.010   . “Chiral [2.2]-Paracyclophane-based NAC- and NHC-Gold(I) Complexes“

139.        M. Berg, S. Nozinovic, M. Engeser, A. Lützen, Eur. J. Org. Chem. 2015, 5966-5978. DOI: 10.1002/ejoc.201500657   . “A cholesterol containing pH-sensitive bistable [2]rotaxane“

138.        Ö. V. Rúnarsson, C. Benkhäuser, N. J. Christensen, J. Artachio Ruiz, E. Ascic, M. Harmata, V. Snieckus, K. Rissanen, P. Fristrup, A. Lützen, K. Wärnmark, J. Org. Chem. 2015, 80, 8142-8149. DOI : 10.1021/acs.joc   . 5.b01239. “Resolution and Determination of the Absolute Configuration of a Twisted Bis-Lactam Analogue of Tröger’s Base: a Comparative Spectroscopic and Computational Study“

137.        M. Mirion, L. Andernach, C. Stobe, J. Barjau, D. Schollmeyer, T. Opatz, A. Lützen, S. R. Waldvogel, Eur. J. Org. Chem. 2015, 4876-4882. DOI:10.1002/ejoc.201500600   . “Synthesis and Isolation of Optically Pure Cyclopenta[b]benzofurans based on Products from Anodic Oxidation of 2,4-Dimethylphenol“

136.        K. J. Hintze, A. Lützen, T. Bredow, J. Comput. Chem. 2015, 36, 1467-1472. DOI:10.1002/jcc.23950   . “Structure and stability of supramolecular crown-ether complexes“

135.        C. Benkhäuser, A. Lützen, Beilstein J. Org. Chem. 2015, 11, 693-700. DOI:10.3762/bjoc.11.79   . “Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting“

134.        A. Lützen, “Supramolecular organization of -conjugated oligomers”, in Towards bottom-up self-organization in supramolecular soft matter - prototypical examples of recent advances, Ed. S. C. Müller, J. Parisi, Springer Series Material Sciences Vol. 217, Stuttgart, 2015, S. 195-236. ISBN 978-3-319-19409-7   .

133.        A. Osadnik, A. Lützen, Arkivoc 2015 (II), 40-51 (commemorative issue in honor of Prof. Jürgen Martens. DOI:10.3998/ark.5550190.p008.833   . “Synthesis of functionalized thiophene/phenylen co-oligomers by direct arylation of thiophenes“

132.        A. Osadnik, A. Lützen, Synthesis 2014, 46, 2976-2982. DOI: 10.1055/s-0034-1378894   . “Synthesis of Symmetrically Functionalized Oligo(het)arylenes Containing Phenylene, Thiophene, Benzothiophene, Furane, Benzofurane, Pyridine, and/or Pyridimine Groups“

131.        C. Stobe, R. Seto, A. Schneider, A. Lützen, Eur. J. Org. Chem. 2014, 6513-6518. DOI: 10.1002/ejoc.201402738   . “Synthesis, Chiral Resolution, and Absolute Configuration of C2-symmetric, chiral 9,9’-spirobifluorenes“

130.        R. Hovorka, T. Piehler, G. Meyer-Eppler, S. Hytteballe, M. Engeser, F. Topić, K. Rissanen, A. Lützen, Chem. Eur. J. 2014, 20, 13253-13258. DOI: 10.1002/chem.201403414   . “Unexpected Self-Assembly of a Homochiral Metallosupramolecular M4L4-Catenane“

129.        C. Gütz, R. Hovorka, N. Struch, J. Bunzen, G. Meyer-Eppler, Z.-W. Qu, S. Grimme, F. Topić, K. Rissanen, M. Cetina, M. Engeser, A. Lützen, J. Am. Chem. Soc. 2014, 136, 11830-11838. DOI: 10.1021/ja506327c   . “Enantiomerically Pure Trinuclear Helicates via Diastereoselective Self-Assembly and Characterization of their Redox Chemistry“

128.        G. Meyer-Eppler, R. Sure, A. Schneider, G. Schnakenburg, S. Grimme, A. Lützen, J. Org. Chem. 2014, 79, 6679-6687. DOI: 10.1021/jo501212t   . “Synthesis, Chiral Resolution, and Absolute Configuration of Dissymmetric 4,15-Difunctionalized [2.2]Paracyclophanes“

127.        C. Kremer, A. Lützen, Chem. Eur. J. 2014, 20, 8852-8855. DOI: 10.1002/chem.201403503   . “Allosteric Binding of Capsaicin by a Bis(β-Cyclodextrin)-2,2’-Bipyridine Receptor“

126.        G. Meyer-Eppler, F. Topić, G. Schnakenburg, K. Rissanen, A. Lützen, Eur. J. Inorg. Chem. 2014, 2495-2501. DOI: 10.1002/ejic.201402057   . “Chiral Self-Sorting of trans-Chelating Chiral Ligands upon Formation of Pd(II) Complexes“

125.        X. Liu, L. Tavares, A. Osadnik, J. Larsen Lausen, J. Kongsted, A. Lützen, H.-G. Rubahn, J. Kjelstrup-Hansen, Org. Electr. 2014, 15, 1273-1281. DOI: 10.1016/j.orgel.2014.02.023   . “Low-voltage organic phototransistors based on naphthyl end-capped oligothiophene nanofibers“

124.        A. Liesenfeld, A. Lützen, Beilstein J. Org. Chem. 2014, 10, 826-831. DOI:10.3762/bjoc.10.78   . “Molecular Recognition of isomeric protonated Amino Acid Esters monitored by ESI-Mass Spectrometry “

123.        C. Kremer, G. Schnakenburg, A. Lützen, Beilstein J. Org. Chem. 2014, 10, 814-824. DOI:10.3762/bjoc.10.77   . “Towards Allosteric Receptors – Synthesis of β-Cyclodextrin-Functionalized 2,2’-Bipyridines and Their Metal Complexes“

122.        G. Meyer-Eppler, L. Küchler, C. Tenten, C. Benkhäuser, S. Brück, A. Lützen, Synthesis 2014, 46, 1085-1090. DOI: 10.1055/s-0033-1338598   . “Cheap and Easy Synthesis of highly Functionalised (Het-)Aryl Iodides via Aromatic Finkelstein Reaction“

121.        C. Klein, C. Gütz, M. Bogner, F. Topić, K. Rissanen, A. Lützen, Angew. Chem. 2014, 126, 3814-3817, DOI: 10.1002/ange.201400626   ; Angew. Chem. Int. Ed. 2014, 53, 3739-3742. DOI: 10.1002/anie.201400626   . “Ein enantiomerenreines metallosupramolekulares Pd4L8-Aggregat mit neuartigem Strukturmotiv: Bildung durch einen Anionen-Templateffekt“; “A NewStructural Motif for an Enantiomerically Pure Metallosupramolecular Pd4L8 Aggregate via Anion Templating“

120.        F. Balzer, R. Sun, A. Lützen, H.-G. Rubahn, M. Schiek Proc. SPIE 2014, 8983, 89830M. DOI 10.1117/12.2040434   . “Epitaxial growth of a methoxy-functionalized organic semiconductor on dielectric surfaces“

119.        R. Hovorka, S. Hytteballe, T. Piehler, G. Meyer-Eppler, F. Topić, K. Rissanen, M. Engeser, A. Lützen, Beilstein J. Org. Chem. 2014, 10, 432-441. DOI: 10.3762/bjoc.10.40   . “Self-assembly of metallosupramolecular rhombi from chiral concave 9,9’-spirobifluorene-derived bis(pyridine) ligands“

118.        F. Balzer, M. Schiek, A. Osadnik, I. Wallmann, J. Parisi, H.-G. Rubahn, A. Lützen, Phys. Chem. Chem. Phys. 2014, 16, 5747-5754. DOI:10.1039/C3CP53881H   . “Substrate Steered Crystallization of Naphthyl End-Capped Oligothiophenes into Nanowires: The Influence of Methoxy-Functionalization“

117.        C. Gütz, R. Hovorka, C. Klein, Q.-Q. Jiang, C. Bannwarth, M. Engeser, C. Schmuck, W. Assenmacher, W. Mader, F. Topić, K. Rissanen, S. Grimme, A. Lützen, Angew. Chem. 2014, 126, 1719-1724, DOI: 10.1002/ange.201308651;    Angew. Chem. Int. Ed. 2014, 53, 1693-1698. DOI: 10.1002/anie.201308651   . “Enantiomerenreine [M6L12]- oder [M12L24]-Polyeder aus flexiblen Bis(pyridine)-Liganden”; “Enantiomerically Pure M6L12 or M12L24-Polyhedra from Flexible Chiral Bis(Pyridine) Ligands“

116.        S. Brück, C. Krause, L. Beverina, R. Turrisi, W. Saak, A. Lützen, H. Borchert, M. Schiek, J. Parisi, Phys. Chem. Chem. Phys. 2014, 16, 1067-1077. DOI:10.1039/C3CP54163K   . “Impact of the N,N-Alkylation of Anilino-Squaraines on Photovoltaic Performance in Bulk Heterojunction Solar Cells“

115.        C. Gütz, R. Hovorka, C. Stobe, N. Struch, F. Topić, G. Schnakenburg, K. Rissanen, A. Lützen, Eur. J. Org. Chem. 2014, 206-216. DOI: 10.1002/ejoc.20130134   . “Self-sorting effects in the self-assembly of metallosupramolecular rhombi from chiral BINOL-derived bis(pyridine) ligands“

114.        T. Reimers, G. Haberhauer, C. Benkhäuser, F. P. Schmidtchen, A. Lützen, U. Lüning, Eur. J. Org. Chem. 2013, 7556-7566. DOI: 10.1002/ejoc.201300830   . “Enantiopure chiral concave N-heterocyclic carbene precursors“

113.        R. Hovorka, M. Engeser, A. Lützen, Int. J. Mass Spectrom. 2013, 354/355, 152-158; DOI: 10.1016/j.ijms.2013.07.002   . “Electron capture dissociation of a self-assembled tetranuclear metallosupramolecular complex in the gas phase“

112.        C. Gütz, R. Hovorka, G. Schnakenburg, A. Lützen, Chem. Eur. J. 2013, 19, 10890-10894; DOI: 10.1002/chem.201301499   . “Homochiral Supramolecular M2L4-Cages via High-Fidelity Self-Sorting of Chiral Ligands“

111.        G. Meyer-Eppler, E. Vogelsang, C. Benkhäuser, G. Schnakenburg, A. Schneider, A. Lützen, Eur. J. Org. Chem. 2013, 4523-4532. DOI: 10.1002/ejoc.201300412   . “Synthesis, resolution, and absolute configuration of dissymmetric 4,12-difunctionalized [2.2]paracyclophanes“

110.        C. Kremer, A. Lützen, Chem. Eur. J. 2013, 19, 6162-6196; DOI:10.1002/chem.201203814   . “Artificial Allosteric Receptors“

109.        M. Berg, A. Lützen, “Structural Aspects of Helicates“ in Metallofoldamers: Supramolecular Architectures from Helicates to Biomimetics, Ed. G. Maayan, M. Albrecht, Wiley-VCH, Weinheim, 2013, S.125-158.

108.        T. Weilandt, N. L. Löw, G. Schnakenburg, J. Daniels, M. Nieger, C. A. Schalley, A. Lützen, Chem. Eur. J. 2012, 18, 16665-16676. DOI:10.1002/chem.201202771   . “Exploring the palladium and platinum bis(pyridyl) complex motif - do substituents affect NMR spectroscopic, X-ray crystallographic, (tandem) mass spectrometric, and isothermal titration calorimetry data following chemical intuition?“

107.        E. Skovsen, P. Siemesen, J. Fiutowski, A. Osadnik, A. Lützen, S. I. Bozhevolnyi, H.-G. Rubahn, K. Pedersen, Opt. Express 2012, 20, 16715-16725. DOI: 10.1364/OE.20.016715   . “Local excitation of surface plasmon polaritons by second-harmonic generation in crystalline organic nanofibers“

106.        C. J. Shaffer, D. Schröder, C. Gütz, A. Lützen, Angew. Chem. 2012, 124, 8221-8224, DOI: 10.1002/ange.201203163;    Angew. Chem. Int. Ed. 2012, 51, 8097-8100. DOI: 10.1002/anie.201203163   . “Intramolekulare C-H Aktivierung mit flexibler Ester-Verknüpfung“; “Intramolecular C-H Bond Activation through a Flexible Ester Linkage“

105.        C. Keil, F. Müntze, M. Schiek, A. Lützen, D. Schlettwein, Proc. MRS 2012, 1402: mrsf11-1402-u08-42. DOI: 10.1557/opl.2012.366   . “Influence of an Applied Electric Field on the Conduction Characteristics of a Bithienyl-Capped Biphenylene and Biphenyl-Capped Oligothiophenes in Organic Field-Effect Transistor Structures “

104.        R. W. Troff, R. Hovorka, T. Weilandt, A. Lützen, M. Cetina, M. Nieger, D. Lentz, K. Rissanen, C. A. Schalley, J. Chem. Soc., Dalton Trans. 2012, 41, 8410-8420. DOI: 10.1039/C2DT30190C   . “Equipping metallo-supramolecular macrocycles with functional groups: Assemblies of pyridine-substituted urea ligands“

103.        J. Fiutowski, C. Maibohm, O. Kostiucenko, A. Osadnik, A. Lützen, H.-G. Rubahn, Proc. SPIE 2012, 84242H. DOI: 10.1117/12.922109   . “Surface structure enhanced second harmonic generation in organic nanofibers“

102.        F. Balzer, M. Schiek, A. Osadnik, A. Lützen, H.-G. Rubahn, Proc. SPIE 2012, 8258, 825809. DOI:10.1117/12.908449    “Organic Nanofibers from Squarylium Dyes: Local Morphology, Optical, and Electronical Properties“

101.        C. Benkhäuser-Schunk, B. Wezisla, K. Urbahn, U. Kiehne, J. Daniels, G. Schnakenburg, F. Neese, A. Lützen, ChemPlusChem 2012, 77, 396-403. DOI: 10.1002/cplu.201200029   . “Synthesis, Resolution, and Absolute Configuration of Difunctionalized Tröger’s Base Derivatives. Part II“

100.        K. Bordo, M. Schiek, A. Ghazal, I. Wallmann, A. Lützen, F. Balzer, H.-G. Rubahn, J. Phys. Chem. C 2011, 115, 20882-20887   . DOI: 10.1021/jp204980n    “Parallelly and Normally Surface-Aligned Organic Nanofiber Arrays“

99.          F. Balzer, M. Schiek, I. Wallmann, A. Schäfer, A. Lützen, H.-G. Rubahn, Proc. SPIE 2011, 8094, 809409; DOI:10.1117/12.893374    “Stability of Organic Nanowires“

98.          C. Kremer, A. Lützen, Synthesis 2011, 210-212. DOI: 10.1055/s-0030-1258342   . “Synthesis of diisothiocyanato-functionalized 2,2’-bipyridines“

97.          X. Liu, H. Budinov, J. Kjelstrup-Hansen, I. Wallmann, M. Schiek, A. Lützen, H.-G. Rubahn, Org. Electr. 2010, 11, 1096-1102. DOI: 10.1016/j.orgel   . 2010.03.015. “AC-biased organic light-emitting field-effect transistors from naphthyl end-capped oligothiophenes“

96.          T. Piehler, A. Lützen, Z. Naturforsch. B. 2010, 65b, 329-336 (issue dedicated to Prof. Dr. R. Saalfrank). “Diastereoselective self-assembly of enantiomerically pure C2-symmetric dinuclear silver(I) and copper(I) complexes from a bis(2,2’-bipyridine) substituted 9,9’-spirobifluorene ligand“

95.          T. Weilandt, U. Kiehne, J. Bunzen, G. Schnakenburg, A. Lützen, Chem. Eur. J. 2010, 16, 2418-2426. DOI: 10.1002/chem.200902993   . “Self-Discriminating Self-Assembly of Dinuclear Heterochiral Rhombs from Tröger’s Base Derived Bis(pyridyl) Ligands“

94.          H. Staats, A. Lützen, Beilstein J. Org. Chem. 2010, 6, No. 10 (special issue on supramolecular chemistry). “Size selective recognition of small esters by a negative allosteric hemicarcerand“

93.          A. Lützen, ChemCatChem 2010, 2, 1212-1214. DOI: 10.1002/cctc.201000198   . “Self-assembled molecular reaction vessels reloaded “

92.          N. Dalla Favera, U. Kiehne, J. Bunzen, S. Hytteballe, A. Lützen, C. Piguet, Angew. Chem. 2010, 122, 129-132, DOI: 10.1002/ange.200904614;    Angew. Chem. Int. Ed. 2010, 49, 125-128. DOI: 10.1002/anie.200904614   . “Intermetallic Interactions Within Solvated Polynuclear Complexes: A Misunderstood Concept“

91.          C. Gütz, A. Lützen, Synthesis 2010, 85-90. DOI: 10.1055/s-0029-1217082    “Synthesis of 2,2’-Bipyridines via Suzuki-Miyaura Cross-Coupling“

90.          F. Balzer, M. Schiek, A. Lützen, H.-G. Rubahn, Chem. Mater. 2009, 21, 4759-4767. DOI: 10.1021/cm802850s   . “Self organized growth of organic thiophene-phenylene nanowires on silicate surfaces“

89.          J. Bunzen, U. Kiehne, C. Benkhäuser-Schunk, A. Lützen, Org. Lett. 2009, 11, 4786-4789. DOI: 10.1021/ol901958v   . “Immobilization of Bis(bipyridine) BINOL Ligands and their Use in Chiral Resolution“

88.          J. Iwicki, C. Näther, M. Schiek, A. Lützen, H.-G. Rubahn, K. Rossnagel, L. Kipp, Mater. Lett. 2009, 63, 2399-2401 DOI: 10.1016/j.matlet.2009.07.054   . “Crystal structure of 1,4’’’-Dimethoxy-4,1’:4’,1’’:4’’,1’’’-quaterphenylene“

87.          H. Staats, F. Eggers, O. Haß, F. Fahrenkrug, J. Matthey, U. Lüning, A. Lützen, Eur. J. Org. Chem. 2009, 4777-4792. DOI: 10.1002/ejoc200900642   . “Towards allosteric receptors – Synthesis of Resorcinarene-Functionalized 2,2’-Bipyridines and their Metal complexes“

86.          F. Balzer, M. Schiek, A. Lützen, H.-G. Rubahn Proc. SPIE 2009, 7393. DOI: 10.1117/12.825891   . “Self-Assembly of thiophene/phenylene co-oligomers“

85.          J. Bunzen, M. Hapke, A. Lützen, Eur. J. Org. Chem. 2009, 3885-3894. DOI: 10.1002/ejoc200900232   . “The Influence of Different Spacer Lengths on the Selectivity of Self-Assembly Processes of Bis(bipyridine) BINOL-Helicates“

84.          J. Bunzen, R. Hovorka, A. Lützen, J. Org. Chem. 2009, 74, 5228-5236. DOI: 10.1021/jo900254r   . “Surprising Substituent Effects on the Self-Assembly of Helicates from Bis(bipyridine)-BINOL Ligands“

83.          M. Schiek, F. Balzer, K. Al-Shamery, A. Lützen, H.-G. Rubahn, J. Phys. Chem. C 2009, 113, 9601-9608. DOI: 10.1021/jp9008465   . “Nanoaggregates from Thiophene/Phenylene Co-oligomers“

82.          T. Weilandt, U. Kiehne, G. Schnakenburg, A. Lützen, Chem. Commun. 2009, 2320-2322. DOI: 10.1039/b819335e   . “Diastereoselective Self-Assembly of Dinuclear Heterochiral Metallosupramolecular Rhombs in a Self-Discriminating Process“

81.          F. Balzer, M. Schiek, A. Lützen, H.-G. Rubahn, “Organic Nanofibers from PPTPP“ in Interface controlled organic thin films, Ed. H.-G. Rubahn, H. Sitter, G. Horowitz, K. Al-Shamery, Springer Proceedings in Physics Vol. 129, Berlin, 2009, S. 11-18.

80.          J. Bunzen, T. Bruhn, G. Bringmann, A. Lützen, J. Am. Chem. Soc. 2009, 131, 3621-3630. DOI: 10.1021/ja807780j    “Synthesis and Helicate Formation of a New Family of BINOL-based Bis(bipyrdine) Ligands“

79.          I. Wallmann, G. Schnakenburg, A. Lützen, Synthesis 2009, 79-84; DOI: 10.1055/s-0028-1083260   . “Synthesis of Functionalized Oligophenylenes and Oligoarylenes Bearing Heteroaryl Groups“

78.          U. Kiehne, J. Bunzen, A. Lützen, “Self-Assembly Of Dinuclear Helical Metallosupra-molecular Coordination Compounds “ in Activating Unreactive Substrates: The Role of Secondary Interactions, Ed. C. Bolm, E. F. Hahn, Wiley-VCH, Weinheim, 2009, S. 427-446.

77.          S. Zahn, W. Reckien, H. Staats, J. Matthey, A. Lützen, B. Kirchner, Chem. Eur. J. 2009, 15, 2572-2580. DOI: 10.1002/chem.200801374   . “Towards allosteric receptors – Adjustment of the rotation barrier of 2,2’-bipyridine derivatives“

76.          M. Hapke, L. Brandt, A. Lützen, Chem. Soc. Rev. 2008, 37, 2782-2797; DOI: 10.1039/B810973G   . “Versatile Tools in the Construction of Substituted 2,2’-Bipyridines – Cross-coupling Reactions with Tin, Zinc, and Boron Compounds“

75.          M. Zuhayra, A. Alfteimi, L. Papp, U. Lützen, A. Lützen, C. Von Forstner, B. Meller, E. Henze, Bioorg. Med. Chem. 2008, 16, 9121-9126; DOI: 10.1016/j.bmc.2008.09.031   . “Simplified fast and High yielding automated synthesis of [18F]-fluoroethylcholine for prostate cancer imaging“

74.          M. Zuhayra, U. Lützen, A. Lützen, L. Papp, E. Henze, G. Friedrichs, F. Oberdorfer, Inorg. Chem. 2008, 47, 10177-10182; DOI: 10.1021/ic8015063   . “C-H activation of coordinated pyridine: Ortho-pyridyl-di-technetiumhydridocarbonyl metal cyclcus. Crystal structure and dynamic behaviour in solution“

73.          A. Rang, M. Nieger, M. Engeser, A. Lützen, C. A. Schalley, Chem. Commun. 2008, 4789-4791; DOI: 10.1039/b806916f   . “Metallo-supramolecular squares with amino acid decorated bipyridines: Heterochiral self-sorting through self-assembly“

71.          K. Schröder, D. Haase, W. Saak, R. Beckhaus, W. P. Kretschmer, A. Lützen, Organometallics 2008, 27, 1859-1868; DOI: 10.1021/om7012293    “Tetrabenzo[a,c,g,i]fluorenyltitanium-(III) and –(IV) Complexes – Synthesis, Reactions and Catalytic Applications“

72.          I. Wallmann, M. Schiek, R. Koch, A. Lützen, Synthesis 2008, 2446-2450; DOI: 10.1055/s-2008-1067163   . “Synthesis of Monofunctionalized p-Quaterphenylenes“

70.          F. Balzer, M. Schiek, H.-G. Rubahn, K. Al-Shamery, A. Lützen, J. Vac. Sci. & Technol. B 2008, 26, 1619-1623. “Towards a better understanding of the growth of organic nanowires on dielectric surfaces“

69.          U. Kiehne, T. Weilandt, A. Lützen, Eur. J. Org. Chem. 2008, 2056-2064; DOI: 10.1002/ejoc.200701215   . “Self-Assembly of Dinuclear Double- and Triple-Stranded Helicates from Bis(bipyridine) Ligands Derived from Tröger’s Base Analogues“

68.          U. Kiehne, T. Bruhn, G. Schnakenburg, R. Fröhlich, G. Bringmann, A. Lützen, Chem. Eur. J. 2008, 14, 4246-4255; DOI: 10.1002/chem.200701960   . “Synthesis, Resolution, and Absolute Configuration of Difunctionalized Tröger’s Base Derivatives“

67.          S. S. Zhu, H. Staats, K. Brandhorst, J. Grunenberg, F. Gruppi, E. Dalcanale, A. Lützen, K. Rissanen, C. A. Schalley, Angew. Chem. 2008, 120, 800-804; DOI: 10.1002/ange.200703451;    Angew. Chem. Int. Ed. 2008, 47, 788-792; DOI: 10.1002/anie.200703451   . “Anionen bindende Resorcinaren-Cavitanden: die Bedeutung von C-H···Anion-Wechselwirkungen“; “Anion-Binding to Simple Resorcinarene-Based Cavitands: The Importance of C-H···Anion Interactions“

66.          M. Schiek, F. Balzer, K. Al-Shamery, J. Brewer, A. Lützen, H.-G. Rubahn, Small 2008, 4, 176-181; DOI: 10.1002/smll.200700483   . “Organic molecular nanotechnology“

65.          K. Al-Shamery, M. Schiek, R. Koch, A. Lützen, “Tailored organic nanoaggregates generated by self-assembly of designed functionalised p-quaterphenylenes on muscovite mica substrates“ in New organic nanofibers for next generation devices, Ed. K. Al-Shamery, H.-G. Rubahn, H. Sitter, Springer Series in Material Science 101, Berlin, 2008, S. 67-88.

64.          M. Schiek, F. Balzer, K. Al-Shamery, A. Lützen, H.-G. Rubahn, Soft Matter 2008, 4, 277-285; DOI: 10.1039/b713295f   . “Light Emitting Organic Nanoaggregates from Functionalized p-Quaterphenylenes“

63.          U. Kiehne, A. Lützen, Org. Lett. 2007, 9, 5333-5336. “Diastereoselective self-assembly of dinuclear double- and triple-stranded helicates from a D‑isomannide derivative“

62.          U. Kiehne, A. Lützen, Eur. J. Org. Chem. 2007, 5703-5711. “Synthesis of Bis(catechol)-Ligands of Tröger’s Base Derivatives and their Dinuclear Triple-Stranded Complexes with Titanium(IV)-Ions“

61.          M. Madsen, M. Schiek, P. Thomsen, N. L. Andersen, A. Lützen, H.-G. Rubahn, Proc. SPIE 2007, 6769. “Organic nanofiber nanosensors“

60.          F. Balzer, J. Brewer, J. Kjelstrup-Hansen, M. Madsen, M. Schiek, K. Al-Shamery, A. Lützen, H.-G. Rubahn, Proc. SPIE 2007, 6779. “Printed second harmonic active organic nanofiber arrays“

59.          M. Hapke, H. Staats, I. Wallmann, A. Lützen, Synthesis 2007, 2711-2719. “Synthesis of Amino-Functionalized 2,2’-Bipyridines“

58.          U. Kiehne, T. Weilandt, A. Lützen, Org. Lett. 2007, 9, 1283-1286. “Diastereoselective self-assembly of double-stranded helicates from Tröger’s base derivatives“

57.          U. Kiehne, J. Bunzen, H. Staats, A. Lützen, Synthesis 2007, 1061-1069. “Synthesis of substituted 2,2’-bipyridines from 2-bromo- or 2-chloropyridines using [Pd(PPh3)4] as catalyst in a modified Negishi cross-coupling reaction“

56.          A. Lützen, Chemkon 2007, 14, 123-130. “Supramolekulare Chemie – Chemie jenseits des Moleküls“

55.          F. Balzer, M. Schiek, A. Lützen, K. Al-Shamery, H.-G. Rubahn, Proc. SPIE 2007, 6470. “Growth of nanofibers from thiophenes , thiophene-phenylenes, and phenylenes: a systematic study“

54.          M. Schiek, J. Brewer, F. Balzer, A. Lützen, K. Al-Shamery, H.-G. Rubahn, Proc. SPIE 2007, 6475. “Tailored nanoaggregates from functionalised organic molecules“

53.          M. Schiek, K. Al-Shamery, A. Lützen, Synthesis 2007, 613-621. “Synthesis of symmetrically and non-symmetrically para-functionalised para-quaterphenylenes“

52.          M. Schiek, A. Lützen, K. Al-Shamery, F. Balzer, H.-G. Rubahn, Crystal Growth & Design 2007, 7, 229-233. “Organic nanofibers from chloride functionalized para-quaterphenylenes“

51.          J. Brewer, M. Schiek, A. Lützen, K. Al-Shamery, H.-G. Rubahn, Nano Lett. 2006, 6, 2656-2659. “Nanofiber frequency doublers“

50.          K. Schröder, W. Saak, D. Haase, A. Lützen, R. Beckhaus, Organometallics 2006, 25, 3824-3836. “Tetrabenzo[a,c,g,i]fluorenyllithium and η5-Tetrabenzo[a,c,g,i]fluorenyltitanium Complexes“

49.          M. Schiek, A. Lützen, K. Al-Shamery, F. Balzer, H.-G. Rubahn, Surf. Sci. 2006, 600, 4030-4033. “Nanofibers from methoxy functionalized para-phenylene molecules“

48.          U. Biermann, A. Lützen, J.-O. Metzger, Eur. J. Org. Chem, 2006, 2631-2637. “Synthesis of Enantiomerically Pure 2,3,4,6-Tetrasubstituted Tetrahydropyrans by Prins-Type Cyclization of Methyl Ricinoleate and Aldehydes“

47.          M. Diekmann, G. Bockstiegel, A. Lützen, M. Friedmann, W. Saak, D. Haase, R. Beckhaus, Organometallics 2006, 25, 339-348. “Chiral bis(h5,h1-Pentafulvene)Titanium Complexes“

46.          O. Hass, A. Schierholt, M. Jordan, A. Lützen, Synthesis 2006, 519-526. “Improved Synthesis of Monohalogenated Cavitands and their Use in the Synthesis of further Functionalized Cavitands“

45.          P. Ghosh, G. Federwisch, M. Kogej, C. A. Schalley, D. Haase, W. Saak, A. Lützen, and R. M. Gschwind, Org. Biomol. Chem. 2005, 3, 2691-2700. “Controlling the Rate of Shuttling Motions in [2]Rotaxanes by Electrostatic Interactions: A Cation as Tunable Brake“

44.          M. Albrecht,I. Janser, A. Lützen, M. Hapke, R. Fröhlich, P. Weis, Chem. Eur. J. 2005, 11, 5742-5748. “5,5’-Diamino-2,2’-bipyridine: A versatile building block for the synthesis of bipyridine/catechol ligands which form homo- and heteronuclear helicates“

43.          F. Thiemann, T. Piehler, D. Haase, W. Saak, A. Lützen, Eur. J. Org. Chem. 2005, 1991-2001. “Synthesis of Enantiomerically PureDissymmetric 2,2’-Disubstituted 9,9’-Spirobifluorenes“

42.          M. Schiek, A. Lützen, R. Koch, K. Al-Shamery, F. Balzer, R. Frese, H.-G. Rubahn, Appl. Phys. Lett. 2005, 86, 153107. “Nanofibers from functionalized para-phenylene molecules“

41.          A. Scherer, K. Kollak, A. Lützen, M. Friedemann, D. Haase, W. Saak, R. Beckhaus, Eur. J. Inorg. Chem. 2005, 1003-1010. “Low Valent Titanium Pentafulvene Complexes - Formation of Binuclear Titanium Nitrogen Complexes“

40.          A. Lützen, Angew. Chem. 2005, 117, 1022-1025; Angew. Chem. Int. Ed. 2005, 44, 1000-1002. “Durch Selbstorganisationsprozesse gebildete molekulare Kapseln – sogar mehr als nur nanoskalierte Reaktionsgefäße“; “Self-assembled molecular capsules – even more than nano-sized reaction vessels“

39.          U. Kiehne, A. Lützen, Synthesis 2004, 1687-1695. “Synthesis of 2,8-Disubstituted Analogues of Troeger’s Base“

38.          M. Wilhelm, S. Deeken, E. Berssen, W. Saak, A. Lützen, R. Koch, H. Strasdeit, Eur. J. Inorg. Chem. 2004, 2301-2312. “The First Structurally Authenticated Organomercury Thioether Complexes––Mercury–Carbon Bond Activation Related to the Mechanism of the Bacterial Enzyme Organomercurial Lyase“

37.          M. Fu, A. Koulman, M. van Rijssel, A. Lützen, M. K. de Boer, M. R. Tyl, G. Liebezeit, Toxicon 2004, 43, 355-363. “Chemical Characterisation of three Haemolytic Compounds from Fibrocapsa japonica (Raphidophyceae)“

36.          C. A. Schalley, A. Lützen, M. Albrecht, Chem. Eur. J. 2004, 10, 1072-1080. “Approaching supramolecular functionality“

35.          A. Lützen, “Recognition of Carbohydrates“ in The Encyclopedia of Supramolecular Chemistry, Ed. J. W. Steed, J. L. Atwood, Marcel Dekker, New York, 2004, 169-177.

34.          A. Lützen, “Carbohydrate recognition by artificial receptors“ in Highlights in Bioorganic Chemistry, Ed. C. Schmuck, H. Wennemers, WILEY-VCH, Weinheim, 2004, S. 109-119.

33.          A. Lützen, V. Wittmann, “Recognition of carbohydrates in biological systems“ in Highlights  in Bioorganic Chemistr, Ed. C. Schmuck, H. Wennemers, WILEY-VCH, Weinheim, 2004, S. 119-123.

32.          S. Fürmeier, M. S. F. Lie Ken Jie, A. Lützen, J. O. Metzger, Eur. J. Org. Chem. 2003, 4874-4878. “Expanding the Field of Phosphorus-containing Fatty Acid Derivatives: Synthesis of 1,2-Oxaphospholene Derivatives and Alkenyl Phosphonates from α-Keto allenes“

31.          A. Lützen, M. Hapke, H. Staats, J. Bunzen, Eur. J. Org. Chem. 2003, 3948-3957. “Synthesis of differently disubstituted 2,2'-bipyridines by a modified Negishi cross coupling reaction“

30.          A. Lützen, F. Thiemann, S. Meyer, Synthesis 2002, 2771-2778. “Synthesis of a Tetra(BINOL)-Substituted Spirobifluorene“

29.          A. Lützen, M. Hapke, S. Meyer, Synthesis 2002, 2289-2295. “Synthesis of Bis(BINOL) substituted 2,2'-Bipyridines and their Late Transition Metal Ion Complexes“

28.          C. A. Schalley, T. Müller, P. Linnartz, M. Witt, M. Schäfer, A. Lützen, Chem. Eur. J. 2002, 8, 3538-3551. “Mass Spectrometric Characterization and Gas Phase Chemistry of Self-Assembling Supramolecular Squares and Triangles“

27.          A. Lützen, M. Hapke, Eur J. Org. Chem. 2002, 2292-2297. “Synthesis of 5-monosubstituted 2,2'-bipyridines from substituted 2-chloropyridines through modified Negishi cross-coupling reaction“

26.          A. Lützen, M. Hapke, J. Griep-Raming, D. Haase, W. Saak, Angew. Chem. 2002, 114, 2190-2194; Angew. Chem. Int. Ed. 2002, 41, 2086-2089. “Synthese und stereoselektive Selbstorganisation von zwei- und dreisträngigen Helicaten“; “Synthesis and stereoselective self-assembly of double and triple-stranded helicates“

25.          J. Stroot, A. Lützen, M. Friedemann, W. Saak und R. Beckhaus, Z. Anorg. Allg. Chem. 2002, 628, 797-802. “Pentafulvenkomplexe des Titans – Synthese, Struktur und Fluktuierendes Verhalten von Cp’Ti{η6-C5H4=C(p-Tol)2}Cl (Cp’ = Cp*, Cp)”

24.          J. Stroot, R. Beckhaus, D. Haase, W. Saak, A. Lützen, Eur. J. Inorg. Chem. 2002, 1729-1737. “Reactions of Pentafulvene Complexes of Titanium with Carbonyl Compounds – Diastereoselective Synthesis of σ, π-Chelat Complexes with Cp~O Ligands”

23.          A. Lützen, O. Haß, T. Bruhn, Tetrahedron Lett. 2002, 43, 1807-1811. “Synthesis and recognition behavior of an allosteric hemicarcerand“

22.          B. M. O'Leary, T. Szabo, N. Svenstrup,C. A. Schalley, A. Lützen,M. Schäfer, J. Rebek, Jr., J. Am. Chem. Soc. 2001, 123, 11519-11533. “The “Flexiball” Toolkit: A Modular Approach to Self-Assembling Capsules“

21.          W. Uhl, F. Breher, B. Neumüller, A. Lützen, W. Saak, J.Grunenberg, Organometallics 2001, 20, 5478-5484. “Reactions of Carbaalanes with HBF4 and HCl: µ3-Bridging Fluorine Atom in (AlEt)7(C=CHPh)2(CCH2Ph)3(µ3-F) versus Terminal Chlorine Atom in (AlMe)7(AlCl)(CCH2Ph)5H“

20.          W. Uhl, F. Breher, A. Mbonimana, J. Gauss, D. Haase, A. Lützen, W. Saak, Eur. J. Inorg. Chem. 2001, 3059-3066. “New Carbaalanes: (AlMe)8(CCH2Me)5(C≡C-Me) and the THF Adduct (AlMe)8(CCH2Me)5H∙2 THF“

19.          I. Schlemminger, A. Willecke, W. Maison, R. Koch, A. Lützen, J. Martens, J. Chem. Soc., Perkin Trans. 1, 2001, 2804-2816. “Diastereoselective Lewis acid mediated hydrophosphonylation of heterocyclic imines: a stereoselective approach towards α-aminophosphonates“

18.          R. Beckhaus, A. Lützen, D. Haase, W. Saak, J. Stroot, S. Becke, J. Heinrichs, Angew. Chem. 2001, 2112-2115; Angew. Chem. Int. Ed. 2001, 40, 2056-2058. “Ein neuartiger Zugang zu Fulvenkomplexen des Titans – Diastereoselektive Komplexierung von Pentafulvenen an Cyclopentadienyltitan-Fragmente”; “A Novel Route to Fulvene Complexes of Titanium - Diastereoselective Complexation of Pentafulvenes to Cyclopentadienyltitanium Fragments”

17.          O. Westerhoff, A. Lützen, W. Maison, M. Kosten, J. Martens, J. Chem. Soc., Perkin Trans. 1, 2001, 508-513. “Synthesis of novel pipecolic acid derivatives. Part 2. Addition of trimethylsilylcyanide to 3,4,5,6-tetrahydropyridines”

16.          P. Köll, A. Wernicke, J. Kovács, A. Lützen, J. Carbohydr. Chem. 2000, 19, 1019-1047. “Comprehensive Reinvestigation of the reaction of aldoses with Meldrum’s Acid Yielding mainly Chain Extended 3,4-Anhydro-2-deoxy-aldono-1,4-lactones”

15.          W. Uhl, F. Breher, J. Grunenberg, A. Lützen, W. Saak, Organometallics 2000, 19, 4536-4543. “New Carbaalanes Containing Clusters of Aluminum and Carbon Atoms: (AlEt)8(CCH2C6H5)5H, (AlMe)8(CCH2C6H5)5(CºC-C6H5), and (AlMe)7(CCH2CH3)4H2; Quantum Chemical Characterization“

14.          I. Schlemminger, A. Lützen, A. Willecke, W. Maison, R. Koch, W. Saak, J. Martens, Tetrahedron Lett. 2000, 7285-7288. “Highly Diastereoselective Hydrophosphonylation of cyclic imines using BINOL as Chiral Source“

13.          U. Biermann, A. Lützen, M. L. K. Jie, J. O. Metzger, Eur. J. Org. Chem. 2000, 3069-3073. “Regioselective Cationic 1.2- and 1.4-C,C-Bond Forming Additions to Methyl Santalbate, a Conjugated Enyne”

12.          W. Maison, A. Lützen, M. Kosten, I. Schlemminger, O. Westerhoff, J. Martens, J. Chem. Soc., Perkin Trans. 1 2000, 1867-1871. “Multicomponent synthesis of tripeptides containing pipecolic acid derivatives: selective induction of cis- and trans-imide bonds into peptide backbones“

11.          A. Lützen, S. D. Starnes, D. M. Rudkevich, J. Rebek, Jr., Tetrahedron Lett. 2000, 41, 3777-3780. “A self-assembled phthalocyanine dimer”

10.          M. Stöver, A. Lützen, P. Köll, Tetrahedron: Asymmetry 2000, 11, 371-374. “New glyco-oxazolidin-2-ones as chiral auxiliaries in boron-mediated asymmetric aldol reactions”

9.            W. Uhl, A. Lützen, F. Breher, W. Saak, Angew. Chem. 2000, 112, 414-416; Angew. Chem. Int. Ed., 2000, 39, 406-409. “Zwei neue Carbaalane: Verbindungen mit Al7C5- und zu [B11H11]2- isovalenz-elektronischem Al7C4-Cluster”; “Two New Carbaalanes: Compounds with an Al7C5 and a[B11H11]2- Analogous Al7C4 Cluster”

8.            W. Maison, A. Lützen, M. Kosten, I. Schlemminger, O. Westerhoff, J. Martens, J. Chem. Soc., Perkin Trans. I 1999, 3515-3525. “Synthesis of novel pipecolic acid derivatives: a multicomponent approach from 3,4,5,6-tetrahydropyridines”

7.            A. Lützen, A. Renslo, C. A. Schalley, B. M. O’Leary, J. Rebek, Jr., J. Am. Chem. Soc. 1999, 121, 7455-7456. “Encapsulation of Ion-Molecule Complexes: Second-Sphere Supramolecular Chemistry”

6.            J. Kopf, A. Lützen, P. Köll, Acta Cryst. 1999, C55, 1541-1542. “1-N,2-O-Carbonyl-3,5-isopropylidene-1-N(2’[R]-2’-methyl-3’-oxo-pentanoyl)--D-xylofuranosylamine”

5.            W. Maison, M. Kosten, A. Charpy, J. Kintscher-Langenhagen, I. Schlemminger, A. Lützen, O. Westerhoff und J. Martens, Eur. J. Org. Chem. 1999, 2433-2441. “The Synthesis of Novel β-Amino Acids as Intermediates for the Preparation of Bicyclic -Lactams”

4.            A. Lützen, P. Köll, Tetrahedron: Asymmetry 1997, 8, 1193-1206. “D-Xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective aldol reactions”

3.            A. Lützen, P. Köll, Tetrahedron: Asymmetry 1997, 8, 29-32. “D-Xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective acylations and halogenations”

2.            P. Köll, A. Lützen, Tetrahedron: Asymmetry 1996, 7, 637-640. “D-Xylose Derived Oxazolidin-2-ones as Chiral Auxiliaries in Stereoselective Alkylations” 

1.            P. Köll, A. Lützen, Tetrahedron: Asymmetry 1995, 6, 43-46. “Resolution of Racemic Carboxylic and Sulfonic Acids via D-Xylose Derived New Cyclic Carbamate Reagents (Oxazolidin-2-ones)”