Publications

29.

G. L. Schulz*, M. Mastalerz, C.-Q. Ma, M. Wienk, R. Janssen, P. Bäuerle*, Synthesis and Photovoltaic Performance of Pyrazinoquinoxaline Containing Conjugated Thiophene-Based Dendrimers and Polymers, Macromolecules 2013, 46, 2141-2151.

28.

M. Mastalerz*, Modular Synthesis of Shape-Persistent Organic Cage Compounds: Precursors for a New Class of Permanent Porous Materials, Synlett 2013, DOI: 10.1055/s-0032-1318328.

27b.

M. W. Schneider, I. M. Oppel, A. Griffin, M. Mastalerz*, Postmodifizierung der Hohlräume poröser formstabiler organischer Käfigverbindungen, Angew. Chem. 2013, 125, 3699-3704.

27a.

M. W. Schneider, I. M. Oppel, A. Griffin, M. Mastalerz*, Post-Modification of the Interior of Porous Shape-Persistent Organic Cage Compounds, Angew. Chem. Int. Ed. 2013, 52, 3611-3615.

26.

M. Brutschy, M. W. Schneider, M. Mastalerz*, S. R. Waldvogel*, Porous Organic Cage Compounds as Highly Potent Affinity Materials for Sensing by Quartz Crystal Microbalances, Adv. Mater. 2012, 24, 6049-6052.

25.

M. W. Schneider, H.-J. S. Hauswald, R. Stoll, M. Mastalerz*, A Shape-Persistent Exo-functionalized [4+6] Cage Compound with a Very High Specific Surface Area, Chem. Commun. 2012, 48, 9861-9863.

24.

M. Mastalerz*, Permanent Porous Materials from Discrete Organic Molecules – Towards Ultrahigh Surface Areas, Chem. Eur. J. 2012, 18, 10082-10091.

23b.

M. Mastalerz*, I. M. Oppel, Rationale Herstellung eines extrinsisch porösen Molekülkristalls mit einer außergewöhnlich großen spezifischen Oberfläche, Angew. Chem. 2012, 124, 5345-5348.

23a.

M. Mastalerz*, I. M. Oppel, Rational Construction of an Extrinsic Porous Organic Crystal with an Exceptional High Surface Area, Angew. Chem. Int. Ed. 2012, 51, 5252-5255; (judged as „Very Important Paper“ by all referees).

Highlighted in Angewandte Chemie: A. I. Cooper, Angew. Chem. Int. Ed. 2012, 51, 7892-7894.

Highlighted in Nachrichten der Chemie: F. Beuerle, Nachr. Chem. 2013, 3, 265-266.

22.

M. W. Schneider, L. G. Lechner, M. Mastalerz*, Uniform Porous Nanospheres from Discrete Shape-persistent Organic Cage Compounds, J. Mater. Chem. 2012, 22, 7113-7116.

21.

M. W. Schneider, I. M. Oppel, M. Mastalerz*, Exo-Functionalized Shape Persistent [2+3]-Cage Compounds – Influence of Molecular Rigidity on Formation and Permanent Porosity, Chem. Eur. J. 2012, 18, 4156-4160.

20b.

M. Mastalerz*, Rationales Design multifunktionaler Nanoporen durch Mischen passender Moleküle, Angew. Chem. 2012, 124, 604-606.

20a.

M. Mastalerz*, Rational Design of Multifunctional Nanopores by Mixing Matching Molecules, Angew. Chem.Int. Ed. 2012, 51, 584-586.

19.

J. Hamacek*, D. Poggiali, S. Zebret, B. El Aroussi, C. Besnard, M. W. Schneider, M. Mastalerz, Building large supramolecular nanocapsules with europium cations, Chem. Commun. 2012, 48, 1281-1283.

18.

M. W. Schneider, I. M. Oppel, H. Ott, L. G. Lechner, H.-J. S. Hauswald, R. Stoll, M. Mastalerz*, Periphery-Substituted [4+6] Salicylbisimine Cage Compounds with Exceptional High Surface Areas: Influence of the Molecular Structure on Nitrogen Sorption Properties, Chem. Eur. J. 2012, 18, 836-847.

17.

M. Mastalerz*, H.-J. S. Hauswald, R. Stoll, Metal-assisted Salphen Organic Frameworks (MaSOFs) with High Surface Areas and Narrow Pore-Size Distributions, Chem. Commun.2012, 48, 130-132.

Among the top ten most accessed articles in November 2011.

16.

M. Mastalerz*, Iris M. Oppel, Synthesis of Tetrahedral Shape-Persistent Tetranuclear Metal-salphens, Eur. J. Org. Chem. 2011, 5971-5980.

15.

M. Mastalerz*, S. Sieste, M. Cenić, I. M. Oppel, Two-Step Synthesis of Hexaammonium Triptycene: An Air-Stable Building Block for Condensation Reactions to Extended Triptycene Derivatives, J. Org. Chem. 2011,76, 6389-6393.

Highlighted in SYNFACTS: T. M. Swager, J. B. Goods, Synfacts 2011, 10, 1076.

14.

M. Mastalerz*, H. J. E. Rivera, I. M. Oppel, G. Dyker*, Supramolecular Single-Stranded Calix[4]arene Helices – A Crystal Engineering Approach Towards Homochiral Assemblies. CrystEngComm 2011, 13, 3979-3982.

13b.

M. Mastalerz*, M. W. Schneider, I. M. Oppel, O. Presly, Eine Salicylbisimin Käfigverbindung mit großer spezifischer Oberfläche und selektiver CO₂/CH₄-Adsorption, Angew. Chem. 2011, 123, 1078-1083 (judged as “Very Important Paper” by all referees).

13a.

M. Mastalerz*, M. W. Schneider, I. M. Oppel, O. Presly, A Salicylbisimine Cage Compound with High Surface Area and Selective CO₂/CH₄ Adsorption, Angew. Chem. Int. Ed. 2011, 50, 1046-1051.

Highlighted in Angewandte Chemie: A. I. Cooper, Angew. Chem. Int. Ed. 2011, 50, 996-998.
Highlighted in Nachrichten der Chemie: A. Krüger, Nachr. Chem. 2012, 3, 266-267.

12b.

M. Mastalerz*, Formtreue organische Käfigverbindungen durch dynamische Bildung kovalenter Bindungen, Angew. Chem. 2010, 122, 5164-5175.

12a.

M. Mastalerz*, Shape Persistent Organic Cage Compounds by Dynamic Covalent Bond Formation, Angew. Chem. Int. Ed. 2010, 49, 5042-5053.

11.

M. Mastalerz*, V. Fischer, C.-Q. Ma, R. A. J. Janssen, P. Bäuerle*, Conjugated Oligothienyl-Dendrimers Based on a Pyrazino[2,3-g]quinoxaline Core, Org. Lett. 2009, 11, 4500-4503.

10.

M. Mastalerz*, I. M. Oppel, K. Merz, G. Dyker*, Tetrapyridoxycalix[4]arene and its Copper(II)-Complex: Activation of a Tecton for Self-Inclusion Polymers, J. Incl. Phenom. Macrocycl. Chem. 2009, 64 (1-2), 157-161.

9.

M. Mastalerz*, One-pot synthesis of an endo-functionalized shape-persistent nano-sized adamantoid cage compound, Chem. Commun. 2008, 4756-4758.

8.

M. Mastalerz*, H. J. E. Rivera, W. Hüggenberg, K. Merz, I. M. Oppel, G. Dyker*, Pyridoxycalix[4]arene Palladium(II) Complexes as Tectons for Self-Inclusion Polymers, CrystEngComm 2008, 10, 1120-1122.

7b.

M. Mastalerz*, Die nächste Generation formstabiler Zeolith-Analoga: Kovalent­gebundene Organische Netzwerkverbindungen, Angew. Chem. 2008, 120, 453-455.

7a.

M. Mastalerz*, The Next Generation of Shape-Persistent Zeolite-Analoga: Covalent Organic Frameworks, Angew. Chem. Int. Ed. 2008, 47, 445-447.

6.

M. Mastalerz, G. Dyker*, U. Flörke, G. Henkel, I. M. Oppel, K. Merz, Oligophenylcalix[4]arenes as Potential Precursors for Funnelenes and Calix[4]triphenylenes: Syntheses and Preliminary Cyclodehydration Studies, Eur. J. Org. Chem. 2006, 4951-4962.

5.

M. Mastalerz, W. Hüggenberg, G. Dyker*, Photochemistry of Styrylcalix[4]arenes, Eur. J. Org. Chem. 2006, 3977-3987.

4.

M. Mastalerz, G. Dyker*, Synthesis and Spectroscopic Properties of a Novel Bisspirocalixarene, Synlett 2006, 1419-1421.

3.

G. Dyker*, M. Mastalerz, I. M. Müller, K. Merz, K. Koppe, Solvent Dependent Pseudopolymorphism of Trispyridoxycalix[4]arene: cone- vs partial-cone Conformation, Eur. J. Org. Chem. 2005, 4963-4966.

2.

G. Dyker*, M. Mastalerz, I. M. Müller, Electron-rich Cavitands via Fourfold Sonogashira Cross-Coupling Reaction of Calix[4]arenes and Bromopyridines – Effect of the Nitrogen Position on Complexation Abilities, Eur. J. Org. Chem. 2005, 3801-3812.

1.

G. Dyker*, M. Mastalerz, K. Merz, From a Calix[4]arene to a Hexameric Supracycle, Eur. J. Org. Chem. 2003, 4355-4362.

2.

M. Mastalerz*, Konjugierte Oligomere und Polymere, Nachr. Chem. 2009, 57, 1240. (Conference Report)

1.

M. Mastalerz*, Konjugierte Polymere und Oligomere, Nachr. Chem. 2007, 55, 1248. (Conference Report)