Publikationen
149 S. Höger, J. M. Lupton
From π‑Conjugated Rods to Shape-Persistent Rings, Wheels, and Ladders: The Question of Rigidity
Acc. Chem. Res. 2024, XXXX, XXX, XXX-XXX. doi.org/10.1021/acs.accounts.4c00383.
148 S. Höger, P. Krämer, J. Kohn, D. A. Hofmeister, M. Kersten, C. Sterzenbach, A. Gres, A. Hansen, S.S. Jester, S. Grimme
Size-Increased All-Phenylene Molecular Spoked Wheels – A Combined Theoretical and Experimental Approach
Angew. Chem. Int Ed. 2024, e202411092.
147 S. C. Rickert, S.-X. L. Luo, J. Bahr, J. Kohn, M. Xue, A. Hansen, S. Grimme, S.-S. Jester, T. M. Swager, S. Höger
Flexible Phenanthracene Nanotubes for Explosive Detection
J. Am. Chem. Soc. 2024, 146, 2986-2996.
146 D. Kalle, J. Bahr, T. J. Keller, J. B. Kleine Büning, S. Grimme, M. Bursch, S.-S. Jester, S. Höger
Modular Bicyclophane-Based Molecular Platforms
Chem. Eur. J. 2023, DOI: 10.1002/chem.202302662.
145 N. Schmickler, D. A. Hofmeister, J. Bahr, J. Schedlbauer, S.-S. Jester, J. M. Lupton, S. Höger
An Azobenzene-Clamped Bichromophore
Organic Materials 2022, 4, 153-162.
144 T. Eder, D. Kraus, S. Höger, J. Vogelsang, J. M. Lupton
Vibrations Responsible for Luminescence from HJ-Aggregates of Conjugated Polymers Identified by Cryogenic Spectroscopy of Single Nanoparticles
ACS Nano 2022, 16, 6382–6393. doi.org/10.1021/acsnano.2c00472
143 D. Grabowski, S. Alef, S. Becker, U. Müller, G. Schnakenburg, S. Höger
Condensation of pyrylium salts with mixed anhydrides: aryl ethers, aryl amines and sterically congested aromatics
Org. Chem. Front. 2022, 9, 294 - 298. doi.org/10.1039/D1QO01419F
142 S. A. Meißner, T. Eder, T. J. Keller, D. A. Hofmeister, S. Spicher, S.-S. Jester, J. Vogelsang, S. Grimme, J. M. Lupton, S. Höger
Nanoscale π-conjugated ladders
Nature Communications 2021,12, 6614. https://doi.org/10.1038/s41467-021-26688-9
141 V. M. Freixas, P. Wilhelm, T. Nelson, F. Hinderer, S. Höger, S. Tretiak, J. M. Lupton, S. Fernandez-Alberti
Excitation Energy Transfer between bodipy Dyes in a Symmetric Molecular Excitonic Seesaw
J. Phys Chem. A 2021, 125, 8404-8416.
140 G. Poluektov, T. J. Keller, A. Jochemich, A. Krönert, U. Müller, S. Spicher, S. Grimme, S.-S. Jester, S. Höger
Supramolecular Nanopatterns of Molecular Spoked Wheels with Orthogonal Pillars: The Observation of a Fullerene Haze
Angew. Chem. Int. Ed. 2021, 60, 27264-27270. 10.1002/anie.20211186.
139 C. Sterzenbach, T. J. Keller, D. Kraus, J. M. Lupton, S.-S. Jester, S. Höger
Expanded all-Phenylene Molecular Spoked Wheels: Cutouts of Graphenylene-3
Organic Chemistry Frontiers 2021, 8, 4980-4985. DOI: 10.1039/D1QO00876E
138 T. J. Keller, C. Sterzenbach, J. Bahr, T. L. Schneiders, M. Bursch, J. Kohn, T. Eder, J. M. Lupton, S. Grimme, S. Höger, S.-S. Jester
Nanopatterns of molecular spoked wheels as gianthomologues of benzene tricarboxylic acids
Chem. Sci. 2021, 12, 9352-9358. https://doi.org/10.1039/D1SC01381E
137 G. J. Hedley, T. Schröder, F. Steiner, T. Eder, F. J. Hofmann, S. Bange, D. Laux, S. Höger, P. Tinnefeld, J. M. Lupton, J. Vogelsang
Picosecond time-resolved photon antibunching measures nanoscale exciton motion and the true number of chromophores
Nature Communications 2021, 12, 1, 1327, https://doi.org/10.1038/s41467-021-21474-z.
136 S. Henzel, S. Becker, D. Hennen, T. J. Keller, J. Bahr, S.-S. Jester, S. Höger
Highly Strained Nanoscale Bicyclophane Monolayers Entering the Third Dimension: A Combined Synthetic and Scanning Tunneling Microscopy Investigation
ChemPlusChem 2021, 86, 803-811. https://doi.org/10.1002/cplu.202100099
135 J. Schedlbauer, P. Wilhelm, L. Grabenhorst, M. E. Federl, B. Lalkens, F. Hinderer, U. Scherf, S. Höger, P. Tinnefeld, S. Bange, J. Vogelsang, J. M. Lupton
Ultrafast Single-Molecule Fluorescence Measured by Femtosecond Double-Pulse Excitation Photon Antibunching
Nano-Lett. 2020, 20, 2, 1074-1079. DOI: 10.1021/acs.nanolett.9b04354.
134 T. Eder, J. Vogelsang, S. Bange, K. Remmerssen, D. Schmitz, S.-S. Jester, T. J. Keller, S. Höger, J. M. Lupton
Interplay Between J- and H-Type Coupling in Aggregates of π-Conjugated Polymers: A Single-Molecule Perspective
Angew. Chem. Int. Ed. 2019, 58, 18898–18902. DOI: 10.1002/anie.201912374.
133 T. J. Keller, J. Bahr, K. Gratzfeld, N. Schönfelder, M. A. Majeweski, M. Stępień, S. Höger, S.-S. Jester
Nanopatterns of arylene–alkynylene squares on graphite: self-sorting and intercalation
Beilstein J. Org. Chem. 2019, 15, 1848-1855.
132 P. Wilhelm, J. Vogelsang, S. Höger, J. M. Lupton
Homo-FRET in π-Conjugated Polygons: Intermediate-Strength Dipole-Dipole Coupling Makes Energy Transfer Reversible
Nano Lett. 2019, 19, 8, 5483–5488. DOI: 10.1021/acs.nanolett.9b01998.
131 P. Wilhelm, J. Vogelsang, N. Schönfelder, S. Höger, J. M. Lupton
Anomalous Linear Dichroism in Bent Chromophores of π-conjugated Polymers: Departure from the Franck-Condon Principle
Phys. Rev. Lett. 2019, 122, 057402.
130 M. Hündgen, K. A. Maier, S. Höger, S.-S. Jester
Supramolecular nanopatterns of H-shaped molecules
Chem. Commun., 2018, 54, 10558-10561.
129 C. Schweez, S. Höger
A Nanosize Phenylene-Ethynylene-Butadiynylene [2]Catenane
Chem. Eur. J. 2018, 24, 12006-12009. 10.1002/chem.201802567.
128 C. Allolio, T. Stangl, T. Eder, D. Schmitz, J. Vogelsang, S. Höger, D. Horinek, J. M. Lupton
H-Aggregation Effects between π-Conjugated Chromophores in Cofacial Dimers and Trimers: Comparison of Theory and Single-Molecule Experiment
J. Phys. Chem. B 2018, 122, 6431-6441. DOI: 10.1021/acs.jpcb.8b01188
127. M. Kremer, M. Kersten, S. Höger
Efficient catalytic vicinal diamination of arylene diimides
Org. Chem. Front. 2018, 5, 1825-1829. DOI: 10.1039/C8QO00222C.
126. P. Wilhelm, J. Schedlbauer, F. Hinderer, D. Hennen, S. Höger, J. Vogelsang, J. M. Lupton
Molecular excitonic seesaws
PNAS 2018, 115, E3626-E3634. doi.org/10.1073/pnas.1722229115.
125. T. Eder, T. Stangl, M. Gmelch, K. Remmerssen, D. Laux, S. Höger, J. M. Lupton, J. Vogelsang
Switching between H- and J-type electronic coupling in single conjugated polymer aggregates
Nature Communications 2017, 8, 1641. doi:10.1038/s41467-017-01773-0.
124. H. Matsuoka, M. Retegan, L. Schmitt, S. Höger, F. Neese, O. Schiemann
Time-Resolved EPR and Theoretical Investigations of Metal-Free Room-Temperature Triplet Emitters
J. Am. Chem. Soc. 2017, 139, 12968–12975. DOI: 10.1021/jacs.7b04561.
123. A. Idelson, C. Sterzenbach, S.-S. Jester, C. Tschierske, U. Baumeister, S. Höger
A Liquid-Crystalline Phenylene-Based Shape-Persistent Molecular Spoked Wheel
J. Am. Chem. Soc. 2017, 139, 4429–4434. DOI: 10.1021/jacs.6b13020
122. P. Wilhelm, J. Vogelsang, G. Poluektov, N. Schönfelder, T. J. Keller, S.-S. Jester, S. Höger, J. M. Lupton
Molecular polygons probe the role of intramolecular strain in the photophysics of p-conjugated chromophores
Angew. Chem. 2017, 129, 1254–1258; Angew. Chem. Int. Ed. 2017, 56, 1234–1238.
121. D. Würsch, R. May, G. Wiederer, S.-S. Jester, S. Höger, J. Vogelsang, J. M. Lupton
Interactions between π-conjugated chromophores in a giant molecular spoked wheel
Chem. Commun. 2017, 53, 352-355. DOI:10.1039/c6cc08396j
120. W. Ratzke, L. Schmitt, H. Matsuoka, C. Bannwarth, M. Retegan, S. Bange, P. Klemm, F. Neese, S. Grimme, O. Schiemann, J. M. Lupton, S. Höger
Effect of Conjugation Pathway in Metal-Free Room-Temperature Dual Singlet–Triplet Emitters for Organic Light-Emitting Diodes
J. Phys. Chem. Lett. 2016, 7, 4802–4808. DOI: 10.1021/acs.jpclett.6b01907
119. D. Würsch, F. J. Hofmann, T. Eder, A. V. Aggarwal, A. Idelson, S. Höger, J. M. Lupton, J. Vogelsang
Molecular Water Lilies: Orienting Single Molecules in a Polymer Film by Solvent Vapor Annealing
J. Phys. Chem. Lett., 2016, 7, 4451–4457.
118. F. Hinderer, R. May, S.-S. Jester, S. Höger
Monodisperse (p-Phenylene-Butadiynylene)s: GPC Conversion Factors and Self-Assembled Monolayers
Macromolecules 2016, 49, 5, 1816–182110. 1021/acs.macromol.5b02666.
117. C. Schweez, P. Shushkov, S. Grimme, S. Höger
Synthesis and Dynamics of Nanosize Phenylene-Ethynylene-Butadiynylene Rotaxanes and the Role of Shape Persistence
Angew. Chem. 2016, 128, 3389-3394; Angew. Chem. Int. Ed. 2016, 55, 3328-3333. DOI: 10.1002/anie.201509702R2 and 10.1002/ange.201509702R2
116. S. K. Maier, G. Poluektov, S.-S. Jester, H. M. Möller, S. Höger
Fast Oxidative Cyclooligomerization towards Low- and High-Symmetry Thiophene Macrocycles
Chem. Eur. J. 2016, 22, 1379 –1384. DOI: 10.1002/chem.
115. T. Stangl, P. Wilhelm, K. Remmerssen, S. Höger, J. Vogelsang, J. M. Lupton
Mesoscopic quantum emitters from deterministic aggregates of conjugated polymers
PNAS 2015, 112, E5560-E5566.
114. A. Thiessen, D. Würsch, S.-S. Jester, A. V. Aggarwal, S. Bange, J. Vogelsang, S. Höger, J. Lupton
Exciton Localization in Extended π-electron Systems: Comparison of Linear and Cyclic Structures
J. Phys. Chem. Part B 2015, 119, 9949-9958.
113. T. Stangl, P. Wilhelm, D. Schmitz, K. Remmerssen, S. Henzel, S.-S. Jester, S. Höger, J. Vogelsang, J. Lupton
Temporal Fluctuations in Excimer-like Interactions between π-conjugated Chromophores
J. Phys. Chem. Lett. 2015, 6, 1321-1326.
112. H. G. Börner, S. Höger, S. Rosselli, S. S. Sheiko
Synthesis of Conjugates Combining Macromolecular Brushes and Rigid Macrocycles
Polymer 2015, 72, 422-427. http://dx.doi.org/10.1016/j.polymer.2015.02.059
111. R. May, S.-S. Jester, S. Höger
A Giant Molecular Spoked Wheel
J. Am. Chem. Soc. 2014, 136, 16732–16735.
110. S.-S. Jester, A. V. Aggarwal, D. Kalle, S. Höger
Molecular spoked carbazole wheels: Self-assembly at the solid/liquid interface
Beilstein J. Org. Chem. 2014, 10, 2783–2788.
109. S.-S. Jester, J. Vollmeyer, F. Eberhagen, S. Höger
Self-assembled monolayers of shape-persistent macrocycles on graphite: interior design and conformational polymorphism
Beilstein J. Org. Chem. 2014, 10, 2774–2782.
108. J. Burdyńska, Y. Li, A. V. Aggarwal, S. Höger, S. S. Sheiko, K. Matyjaszewski
Synthesis and Arm Dissociation in Molecular Stars with a Spoked Wheel Core and Bottlebrush Arms
J. Am. Chem. Soc. 2014, 136, 12762-12770.
107. S. Höger
Chemical Templates
Beilstein J. Org. Chem. 2014, 10, 1670-1671.
106. G. Rauch, S. Höger
N-Alkylated and N,N-Dialkylated 1,6-Diaminoperylene Diimides via Copper Catalyzed Direct Aromatic Amination
Chem. Commun., 2014, 50, 5659 – 5661. DOI:10.1039/C4CC02124J.
105. J. Vollmeyer, U. Baumeister, S. Höger
The Influence of Intraannular Templates on the Liquid Crystallinity of Shape-Persistent Macrocycles
Beilstein J. Org. Chem. 2014, 10, 910-920.
104. D. Schmitz, S. Höger
Preferential oxidative addition in mixed iodo/bromo quinquephenylenes
Tetrahedron, 2014, 70, 3726-3729.
103. D. Chaudhuri, E. Sigmund, A. Mayer, L. Röck, P. Klemm, S. Lautenschlager, A. Schmid, S. R. Yost, T. Van Voorhis, S. Bange, S. Höger, J. M. Lupton
Metal-free OLED triplet emitters by side-stepping Kasha’s rule
Angew. Chem. 2013, 125, 13691–13694; Angew. Chem. Int. Ed. 2013, 52, 13449–13452. DOI: 10.1002/anie.201307601.
102. G. Ohlendorf, C. W. Mahler, S.-S. Jester, G. Schnakenburg, S. Grimme, S. Höger
Highly strained phenylene bicyclophanes
Angew. Chem. 2013, 125, 12308–12312. DOI: 10.1002/ange.201306299; Angew. Chem. Int. Ed. 2013, 46, 12086-12090 .
101. V. Aggarwal, A. Thiessen, A. Idelson, D. Kalle, D. Würsch, T. Stangl, F. Steiner, S.-S. Jester, J. Vogelsang, S. Höger, J. M. Lupton
Fluctuating exciton localization in giant p-conjugated spoked-wheel macrocycles
Nature Chemistry 2013, 5, 964–970. doi:10.1038/nchem.1758.
100. M. F. G. Klein, F. M. Pasker, S. Kowarik, D. Landerer, M. Pfaff, M. Isen, D. Gerthsen, U. Lemmer, S. Höger, A. Colsmann
Carbazole-Phenylbenzotriazole Copolymers as Absorber Material in Organic Solar Cells
Macromolecules 2013, 46, 3870-3878.
99. V. Manninen, M. Niskanen, T. I. Hukka, F. Pasker, S. Claus, S. Höger, J. Baek, T. Umeyama, H. Imahori, H. Lemmetyinen
Conjugated donor–acceptor (D–A) copolymers in inverted organic solar cells – a combined experimental and modelling study
J. Mater. Chem. A 2013, 1, 7451-7462.
98. A. V. Aggarwal, S.-S. Jester, S. Mehdizadeh Taheri, S. Förster, S. Höger
Molecular Spoked Wheels: Synthesis and Self-Assembly Studies on Rigid Nanoscale 2D Objects
Chem. Eur. J. 2013, 19, 4480–4495.
97. D. Baran, F. M. Pasker, S. Le Blanc, G. Schnakenburg, T. Ameri, S. Höger, C. J. Brabec
Introducing a New Triazoloquinoxaline-Based Fluorene Copolymer for Organic Photovoltaics: Synthesis, Characterization, and Photovoltaic Properties
J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 987-992.
96. T. Stangl, S. Bange, D. Schmitz, D. Würsch, S. Höger, J. Vogelsang, J. M. Lupton
Temporal Switching of Homo-FRET Pathways in Single-Chromophore Dimer Models of π-Conjugated Polymers
J. Am. Chem. Soc. 2013, 135, 78-81.
95. M. F. G. Klein, F. Pasker, H. Wettach, I. Gadaczek, T. Bredow, P. Zilkens, P. Vöhringer, U. Lemmer, S. Höger, A. Colsmann
Oligomers Comprising 2-Phenyl-2H-benzotriazole Building Blocks for Solution-Processable Organic Photovoltaic Devices
J. Phys. Chem. C 2012, 116, 16358-16364.
94. M. Saracino, S. Breuer, G. Barati, E. Sak, K. Hingerl, U. Müller, M. Müller, S. Höger, K. Wandelt
The impact of intramolecular π-coupling and steric flexibility on the ordering of organic films at solid/liquid-interfaces
Surf. Sci. 2013, 607, 74-81.
93. S.-S. Jester, E. Sigmund, L. M. Röck, S. Höger
Hierarchical Self-Assembly of Polycyclic Heteroaromatic Stars into Snowflake Patterns
Angew. Chem. 2012, 124, 8683–8687; Angew. Chem. Int. Ed. 2012, 51, 8555-8559.
92. J. Vollmeyer, S.-S. Jester, F. Eberhagen, T. Prangenberg, W. Mader, S. Höger
Gels of shape-persistent macrocycles: the role of the interior
Chem. Commun. 2012, 48, 6547-6549.
91. D. Chaudhuri, D. Li, E. Sigmund, H. Wettach, S. Höger, J. M. Lupton
Plasmonic surface enhancement of dual fluorescence and phosphorescence emission from organic semiconductors: effect of exchange gap and spin-orbit coupling
Chem. Commun. 2012, 48, 6675-6677.
90. S. Liu, D. Schmitz, S.-S. Jester, N. J. Borys, S. Höger, J. M. Lupton
Coherent and Incoherent Interactions between Cofacial π-Conjugated Oligomer Dimers in Macrocycle Templates
J. Phys. Chem. B 2013, 117, 4197-4203.
89. A. Marchanka, S. K. Maier, S. Höger, M. van Gastel
Photoinduced charge separation in an organic donor-acceptor hybrid molecule
J. Phys. Chem. B 2011, 115, 13526–13533.
88. A. Thiessen, H. Wettach, K. Meerholz, F. Neese, S. Höger, D. Hertel
Control of electronic properties of triphenylene by substitution
Org. Electron. 2012, 13, 71-83.
87. F. M. Pasker, M. F. G. Klein, M. Sanyal, E. Barrena, U. Lemmer A. Colsmann, S. Höger
Photovoltaic response to structural modifications on a series of conjugated polymers based on 2-aryl-2H-benzotriazoles
J. Polym. Sci., Part A: Polym. Chem. 2011, 49, 5001-5011.
86. T. Kudernac, N. Shabelina, W. Mamdouh, S. Höger, S. De Feyter
STM visualisation of counterions and effect of charges on self-assembled monolayers of macrocycles
Beilstein J. Nanotechnol. 2011, 2, 674-680.
85. S. K. Maier, S.-S. Jester, U. Müller, W.M. Müller, S. Höger
An oxidative coupling route to macrocyclic thiophenes and its application in the synthesis of a donor/acceptor hybrid molecule
Chem. Commun. 2011, 47, 11023-11025.
84. E. Sigmund, S. Höger
Definierte Cyclooligomere mittels Recycling-Gelpermeationschromatographie (recGPC): Einblicke in die zweidimensionale supramolekulare Organisation molekularer Polygone
Analytik News 2011, 1-6, Publ.-Datum 3.8.2011.
83. S.-S. Jester, A. Idelson, D. Schmitz, F. Eberhagen, S. Höger
Shape-Persistent Linear, Kinked, and Cyclic Oligo(phenylene-ethynylene-butadiynylenes)s: Self-Assembled Monolayers
Langmuir 2011, 27, 8205-8215.
82. S.-S. Jester, E. Sigmund, S. Höger
Nanopatterning by Molecular Polygons
J. Am. Chem. Soc. 2011, 133, 11062-11065.
81. S.-S. Jester, D. Schmitz, F. Eberhagen, S. Höger
Self-assembled monolayers of clamped oligo(phenylene-ethynylene-butadiynylene)s
Chem. Commun. 2011, 47, 8838-8840. DOI: 10.1039/C1CC12435H
80. F. M. Pasker, S. M. Le Blanc, G. Schnakenburg, S. Höger
Thiophene-2-aryl-2H-benzotriazole-thiophene Oligomers with Adjustable Electronic Properties
Org. Lett. 2011, 13, 2338-2341.
79. S. Höger
Oligomere trennen mit Recycling-GPC
Nachrichten aus der Chemie 2011, 59, 453-455.
78. M. Fritzsche, A. Bohle, D. Dudenko, U. Baumeister, D. Sebastiani, G. Richardt, H. W. Spiess, M. R. Hansen, S. Höger
Empty Helical Nano-Channels with Adjustable Order from Low-Symmetry Macrocycles
Angew. Chem. 2011, 123, 3086–3089; Angew. Chem. Int. Ed. 2011, 50, 3030-3033.
77. A. Meyer, E. Sigmund, F. Luppertz, G. Schnakenburg, I. Gadaczek, T. Bredow, S.-S. Jester, S. Höger
Syntheses and Properties of Thienyl-Substituted Dithienophenazines
Beilstein J. Org. Chem. 2010, 6, 1180-1187.
76. S. Höger, D. Mössinger
Defined linear and cyclic oligomers using recycling-GPC
Shimadzu News 2010, 2, 20-22.
Definierte lineare und zyklische Oligomere mittels Recycling-GPC
Shimadzu News 2010, 2, 20-22.
75. H. Wettach, S. Höger, D. Chaudhuri, J. M. Lupton, F. Liu, E. M. Lupton, S. Tretiak, G. Wang, M. Li, S. De Feyter, S. Fischer, S. Förster
Synthesis and properties of a triphenylene-butadiynylene macrocycle
J. Mater. Chem. 2011, 21 (5), 1404-1415.
74. M. Fritzsche, S.-S. Jester, S. Höger, C. Klaus, N. Dingenouts, P. Linder, M. Drechsler, S. Rosenfeldt
Self-organization of Coil-Ring-Coil Structures into Tubular Supramolecular Polymer Brushes: Synthesis, Morphology, and Growth
Macromolecules 2010, 43, 8379-8388.
73. D. Chaudhuri, H. Wettach, K. van Schooten, S. Liu, E. Sigmund, S. Höger, J. M. Lupton
Tuning the singlet-triplet gap in metal-free phosphorescent p-conjugated polymers
Angew. Chem. 2010, 122, 7880-7883; Angew. Chem. Int. Ed. 2010, 49, 7714-7717. DOI: 10.1002/ange.201003291.
72. S.-S. Jester, N. Shabelina, S. M. Le Blanc, S. Höger
Oligomers and Cyclooligomers of Rigid Phenylene-Ethynylene-Butadiynylenes: Synthesis and Self-Assembled Monolayers
Angew. Chem. Int. Ed. 2010, 49, 6101-6105; Angew. Chem. 2010, 122, 6237-6241.
71. K. Becker, G. Gaefke, J. Rolffs, S. Höger, J. M. Lupton
Quantitative mass determination of conjugated polymers for single molecule conformation analysis: enhancing rigidity with macrocycles
Chem. Commun. 2010, 46, 4686-4688. DOI:10.1039/C0CC00670J
70. D. Mössinger, D. Chaudhuri, T. Kudernac, S. Lei, S. De Feyter, J. M. Lupton, S. Höger
Large All-Hydrocarbon Spoked Wheels of High Symmetry: Modular Synthesis, Photophysical Properties and Surface Assembly
J. Am. Chem. Soc. 2010, 132, 1410-1423.
69. S. Höger
Shape-persistent rings and wheels
Pure and Appl. Chem. 2010, 82, 821-830.
68. T. Chen, G.-B. Pan, H. Wettach, M. Fritzsche, S. Höger, L.-J. Wan, H.-B. Yang, B. H. Northrop, P. J. Stang
2D Assembly of Metallacycles on HOPG by Shape-Persistent Macrocycle Templates
J. Am. Chem. Soc. 2010, 132, 1328-1333.
67. H. Wettach, A. Colsmann, U. Lemmer, N. Rehmann, K. Meerholz, S. Höger
Deep blue organic light-emitting diodes based on triphenylenes
Synthetic Met. 2010, 160, 691-700.
66. J.C. Gielen, A. Ver Heyen, S. Klyatskaya, W. Vanderlinden, S. Höger, J.C. Maan, S. de Feyter, P.C.M. Christianen
Aggregation kinetics of macrocycles detected by magnetic birefringence
J. Am. Chem. Soc. 2009, 131, 14134-14135.
65. D. Mössinger, S.-S. Jester, E. Sigmund, U. Müller, S. Höger
Defined Oligo(p-Phenylene-Butadiynylene)Rods
Macromolecules 2009, 42, 7974-7978.
64. S. Lei, A. Ver Heyen, S. De Feyter, M. Surin, R. Lazzaroni, S. Rosenfeldt, M. Ballauff, P. Lindner, D. Mössinger, S. Höger
Two-Dimensional Oligo(phenylene-ethynylene-butadiynylene)s: All-Covalent Nanoscale Spoked Wheels
Chem. Eur. J. 2009, 15, 2518-2535.
63. N. Shabelina, S. Klyatskaya, V. Enkelmann, S. Höger
A simple approach towards shape-persistent nanoscale pyridine macrocycles
Comptes rendus 2009, 12, 430-436.
62. N. Dingenouts, S. Klyatskaya, S. Rosenfeldt, M. Ballauff, S. Höger
Temperature-induced switching between aggregated and non-aggregated states in coil-ring-coil block copolymers
Macromolecules 2009, 42, 5900-5902.
61. H. Wettach, F. Pasker, S. Höger
2-Aryl-2H-benzotriazoles as building blocks for new low-bandgap poly(arylene-ethynylene)s
Macromolecules 2008, 41, 9513-9515.
60. M. J. Walter, N. J. Boys, G. Gaefke, S. Höger, J. M. Lupton
Spacial Anticorrelation between Nonlinear White-Light Generation and Single Molecule Surface-Enhanced Raman Scattering
J. Am.Chem. Soc. 2008, 130 , 16830-16831.
59. C. Mahler, U. Müller, W.M. Müller, V. Enkelmann, C. Moon, G. Brunklaus, H. Zimmermann, S. Höger
Synthesis of highly phenylene substituted p-phenylene oligomers from pyrylium salts
Chem. Commun. 2008, 33, 4816-4818.
58. K. Tahara, S. Lei, D. Mössinger, H. Kozuma, K. Inukai, M. van der Auweraer, F. C. De Schryver, S. Höger, Y. Tobe, S. De Feyter
Giant Molecular Spoked Wheels in Giant Voids: Two-Dimensional Molecular Self-Assembly Goes Big
Chem. Commun. 2008, 3897-3899.
57. G. Gaefke, S. Höger
[3-(Cyanopropyl)diisopropylsilyl] acetylene, a more stable analogue of [3-(Cyanopropyl)dimethylsilyl] acetylene
Synthesis 2008, 14, 2155.
56. K. Becker, M. Fritzsche, S. Höger, J. M. Lupton
Phenylene-Ethynylene Macrocycles as Model Systems of Interchromophoric Interactions in π-Conjugated Macromolecules
J. Phys. Chem. B 2008, 112, 4848-4853.
55. S. Höger, J. Weber, A. Leppert, V. Enkelmann
Shape-Persistent Macrocycles with Intraannular Alkyl Groups:
Some Structural Limits of Discotic Liquid Crystals with an Inverted Structure
Beilstein J. Org. Chem. 2008, 4:1.
54. D. Mössinger, J. Hornung, S. Lei, S. De Feyter, S. Höger
Molecularly Defined Shape-Persistent Two-Dimensional Oligomers: The Covalent Template Approach to Molecular Spoked Wheels
Angew. Chem. 2007, 119, 6926-6930; Angew. Chem. Int. Ed. 2007, 46, 6802-6806.
53. K. Becker, P. G. Lagoudatis, G. Gaefke, S. Höger, J. Lupton
Exciton Accumulation in Pi-Conjugated Wires Encapsulated by Light-Harvesting Macrocycles
Angew. Chem. 2007, 119, 3520-3525; Angew. Chem. Int. Ed. 2007, 46, 3450-3455.
52. M. J. Walter, J. M. Lupton, K. Becker, J. Feldmann, G. Gaefke, S. Höger
Simultaneous Raman and Fluorescence Spectroscopy of Single Conjugated Polymers
Phys. Rev. Lett. 2007, 98, 137401.
51. X. Cheng, A. Ver Heyen, W. Mamdouh, H. Uji-i, F. De Schryver, S. Höger, S. De Feyter
Synthesis and Adsorption of Shape-Persistent Macrocycles Containing Polycyclic Aromatic Hydrocarbons in the Rigid Framework
Langmuir 2007, 23, 1281-1286.
50. S. Höger
High-Yield Synthesis of Shape-Persistent Phenylene-Ethynylene Macrocycles
In: Functional Organic Materials- Synthesis, Strategies and Applications
(Eds. Bunz/Müller), WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2007, 225-260.
49. G. Gaefke, V. Enkelmann, S. Höger
A Practical Synthesis of 1,4-Diiodo-2,5-bis(chloromethyl)benzene and 1,4-Diiodo-
2,5-bis(bromomethyl)benzene
Synthesis 2006, 2971-2973.
48. G.-B. Pan, X.-H. Cheng, S. Höger, W. Freyland
2D-Supramolecular Structures of a Shape-Persistent Macrocycle and Codeposition with Fullerene on HOPG
J. Am. Chem. Soc. 2006, 128, 4218-4219.
47. S. Klyatskaya, N. Dingenouts, C. Rosenauer, B. Müller, S. Höger
Cationic Shape-Persistent Macrocycles: The Unexpected Formation of a Nano-Size Supramolecular Dimer
J. Am. Chem. Soc. 2006, 128, 3150-3151.
46. A. Ziegler, W. Mamdouh, A. V. Heyen, M. Surin, H. Uji-i, M. M. S. Abdel-Mottaleb, F. C. De Schryver, S. De Feyter, R. Lazzaroni, S. Höger
Covalent Template Approach towards Functionalyzed Oligo-Alkyl Substituted Shape-Persistent Macrocycles: Synthesis and Properties of Rings with a Loop
Chem. Mat. 2005, 17, 5670-5683.
45. S. Höger
Formtreue Phenylacetylen-Macrocyclen: große Ringe-kleine Ausbeute?
Angew. Chem. 2005, 117, 3872.
44. S. Höger, X. H. Cheng, A.-D. Ramminger, V. Enkelmann, A. Rapp, M. Mondeshki, I. Schnell
Diskotische Flüssigkristalle mit invertierter Struktur
Angew. Chem. 2005, 117, 2862.
43. S. Höger
Shape-Persistent Acetylenic Macrocycles for Ordered Systems
In: Acetylene Chemistry (Eds. Stang/Diederich/Tykwinsky), WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2005, p. 427.
42. X. H. Cheng, S.-S. Jester, S. Höger
Synthesis and Aggregates of Phenylene-Ethynylene Substituted Polycyclic Aromatic Compounds
Macromolecules 2004, 37, 7065.
41. J. Jo, C. Chi, S. Höger, G. Wegner, D. Y. Yoon
Synthesis and Characterization of Monodisperse Oligofluorenes
Chem. Eur. J. 2004, 10, 2681.
40. D. Borissov, A. Ziegler, S. Höger, W. Freyland
SAMs of Shape-Persistent Macrocycles: Structure and Binding on HOPG and Au(111)
Langmuir 2004, 20, 2781.
39. S. Höger
Shape-Persistent Macrocycles: From Molecules to Materials
Chem. Eur. J. 2004, 10, 1320.
38. M. Fischer, G. Lieser, A. Rapp, I. Schnell, W. Mamdouh, S. De Feyter, F. C. De Schryver, S. Höger
Shape-Persistent Macrocycles with Intraannular Polar Groups: Synthesis, Liquid Crystallinity and 2D Organization
J. Am. Chem. Soc. 2004, 126, 214.
37. M. Fischer, S. Höger
Synthesis of a Shape-Persistent Macrocycle with Intraannular Carboxylic Acid Groups,
Tetrahedron 2003, 59, 9441.
36. X. H. Cheng, S. Höger, D. Fenske
Facile Synthesis of alkoxy-functionalized dibenzo[fg,op]naphthacenes
Org. Lett. 2003, 5, 2587.
35. S. Rosselli, A.-D. Ramminger, T. Wagner, G. Lieser, S. Höger
Synthesis and Solid State Organization of Coil-Ring-Coil Block Copolymers
Chem. Eur. J. 2003, 9, 3481.
34. M. Fischer, S. Höger
Synthesis of a Shape-Persistent Macrocycle with Intraannular Sulfonate Groups
Eur. J. Org. Chem. 2003, 441.
33. S. Höger, S. Rosselli, A.-D. Ramminger, V. Enkelmann
A Facile Synthesis of Large Extraannular Functionalized Phenyl-Ethynyl Macrocycles Containing m-Terphenyl Units
Org. Lett. 2002, 4, 4269.
32. S. Höger, D.L. Morrison, K. Bonrad, V. Enkelmann, C. Tschierske
Shape-Persistent Macrocycles with Adaptable Units: New Insights from the Solid State
Mol. Cryst. Liq. Cryst. 2002, 389, 73.
31. J. Jo, S. Höger, G. Wegner, D. Y. Yoon
Synthesis and Characterization of Well-defined Monodisperse Fluorene Oligomers
Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 2002, 43(2), 1118.
30. S. Höger, D.L. Morrison, V. Enkelmann
Solvent Triggering between Conformational States in Amphiphilic Shape-Persistent Macrocycles
J. Am. Chem. Soc. 2002, 124, 6734.
29. S. Höger, K. Bonrad, S. Rosselli, A.-D. Meckenstock, T. Wagner, B. Silier, S. Wiegand, W. Häußler, G. Lieser, V. Scheumann
Shape-Persistent Macrocycles: Building Blocks for Complex Organic and Polymeric Structures
Macromol. Symp. 2002, 177, 185.
28. S. Rosselli, A.-D. Ramminger, T. Wagner, B. Silier, S. Wiegand, W. Häußler, G. Lieser, V. Scheumann, S. Höger
Knäuel-Ring-Knäuel-Blockcopolymere als Bausteine supramolekularer Polymerbürsten
Angew. Chem. 2001, 113, 3233-3237;
Coil–Ring–Coil Block Copolymers as Building Blocks for Supramolecular Hollow Cylindrical Brushes
Angew. Chem. Int. Ed. 2001, 40, 3137-3141.
27. S. Höger, K. Bonrad, A. Mourran, U. Beginn, M. Möller
Synthesis, Aggregation and Adsorption Phenomena of Shape-Persistent Macrocycles with Extraannular Polyalkyl Substituents
J. Am. Chem. Soc. 2001, 123, 5651.
26. S. Höger
Die Palladium-katalysierte Bildung von Arylaminen und -ethern
Chem. unserer Zeit 2001, 35,102.
25. S. Höger
Schablonen machen es möglich (eingeladene Buchrezension)
Nachrichten Chem. 2000, 48, 1138.
24. S. Höger, V. Enkelmann, K. Bonrad, C. Tschierske
Alkylsubstituierte formtreue Makrocyclen: der erste dikotische Flüssigkristall mit starrer Peripherie und flexiblem Kern
Angew. Chem. 2000, 112, 2355-2358.
23. S. Höger, K. Bonrad
3-Cyanopropy-dimethysilyl acetylene (CPDMS acetylene), a Polar Analogue of Trimethylsilyl acetylene: Synthesis and Applications in the Preparation of Monoprotected Bisacetylenes
J. Org. Chem. 2000, 65, 2243-2045.
22. S. Höger, K. Bonrad, L. Karcher, A.-D. Meckenstock
Structure and Temperature Effects on the Cyclization of Rigid Bisacetylenes
J. Org. Chem. 2000, 65, 1588.
21. S. Höger
Highly Efficient Template-based Preparation of Shape-persistent Macrocyclics
Macromol. Symp. 1999, 142, 185.
20. S. Höger
Highly Efficient Methods for the Preparation of Shape-Persistent Macrocyclics
J. Polym. Sci, Part A 1999, 37, 2685.
19. S. Höger, A.-D. Meckenstock
Template-Directed Synthesis of Shape-Persistent Macrocyclic Amphiphiles with Convergently Arranged Functionalities
Chem. Eur. J. 1999, 5, 1686.
18. S. Höger, A.-D. Meckenstock
High-Yield Synthesis of Macrocycles by the Coupling of Templated Bisacetylenes
Polym. Mater. Sci. Eng. 1999, 80, 106.
17. S. Höger, K. Bonrad, G. Schäfer, V. Enkelmann
2-Bromo-5-iodo-hydroquinone and its symmetrical and unsymmetrical dialkylethers
Z. Naturforsch. 1998, 53b, 960.
16. S. Höger, A.-D. Meckenstock, S. Müller
Synthesis and properties of shape-persistent macrocyclic amphiphiles with switchable amphiphilic portions
Chem. Eur. J. 1998, 4, 2423.
15. S. Höger, A.-D. Meckenstock
Structure Dependent Yield of the Cyclisation of Outside-Templated Bisacetylenes: Catenation or Oligomerization?
Tetrahedron Lett. 1998, 39, 1735.
14. S. Höger, A.-D. Meckenstock, H. Pellen
High-Yield Macrocyclisation via Glaser Coupling of Temporary Covalent Templated Bisacetylenes
J. Org. Chem. 1997, 62, 4556.
13. S. Höger, J. Spickermann, D.L. Morrison, P. Dziezok, H.J. Räder
Aggregates of Shape Persistent Macrocyclic Amphiphiles Detected by MALDI-TOF Spectroscopy
Macromolecules 1997, 30, 3110.
12. S. Höger, S. Müller, L. Karcher
Shape Persistent Macrocycles: Various Isomers and Sizes by the Repetitive Hagihara-Coupling/Desilylating Strategy
Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 1997, 38(1), 72.
11. S. Höger
Synthesis of Bromo-iodo-hydroquinone Monoalkyl Ethers
Liebigs Ann./Recueil 1997, 273.
10. S. Höger
Methoxycarbonyl-Terminated Dendrons via the Mitsunobu Reaction: An Easy Way to Functionalized Hyperbranched Building Blocks
Synthesis 1997, 20.
9. D.L. Morrison, S. Höger
Shape-persistent macrocyclic amphiphiles: molecular reversible coats
J. Chem. Soc. Chem. Commun. 1996, 2313.
8. S. Höger, V. Enkelmann
Synthese und Struktur eines formtreuen makrocyclischen Amphiphils
Angew. Chem. 1995, 107, 2917.
7. M.T. Reetz, S. Höger, K. Harms
Reversibler Protonentransfer-bedingter Phasenübergang im 4,4´-Bipyridiniumsalz der Quadratsäure
Angew. Chem. 1994, 106, 193.
6. C. Zhang, S. Höger, K. Pakbaz, F. Wudl, A. J. Heeger
Improved Efficiency in Green Polymer Light-Emitting Diodes with Air-Stable Elektrodes
Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 1994, 35(1), 329.
5. C. Zhang, S. Höger, K. Pakbaz, F. Wudl, A. J. Heeger
Improved Efficiency in Green Polymer Light-Emitting Diodes with Air-Stable Elektrodes
J. Electron. Mater. 1994, 23, 453.
4. S. Höger, J. J. McNamara, S. Schricker, F. Wudl
Novel Silicon-Substituted, Soluble Poly(phenylenevinylene)s:
Enlargement of the Semiconductor Bandgap
Chem. Mater. 1994, 6, 171.
3. S. Aratani, C. Zhang, K. Pakbaz, S. Höger, F. Wudl, A. J. Heeger
Improved Efficiency in Polymer Light-Emitting Diodes Using Air-Stable Elektrodes
J. Electron. Mater. 1993, 22, 745.
2. C. Zhang, S. Höger, K. Pakbaz, F. Wudl, A. J. Heeger
Yellow Elektroluminescent Diodes Utilising
Poly-(2,5-bis-(5,6-dihydro-cholestanoxy)-1,4-phenylene vinylene)
J. Electron. Mater. 1993, 22, 413.
1. F. Wudl, S. Höger, C. Zhang, K. Pakbaz, A. J. Heeger
Conjugated Polymers for Organic LED´s: Poly(2,5-bis-(3 -5 -cholestanoxy)-
phenylenevinylene) (BCHA-PPV); a Processable, Yellow Light Emitter
Polym. Prepr. (Am. Chem. Soc. Div. Polym. Chem.) 1993, 34(1), 197.