Publications

2017

61.    Xin-Yue Hu, Wen-Shan Zhang, Frank Rominger, Irene Wacker, Rasmus R. Schröder,
         Michael Mastalerz*, Transforming a chemically labile [2+3] imine cage into a robust
         carbamate cage, Chem. Commun. 2017, 53, 8616 - 8619.


61

 

60.    Elisabeth H. Menke, David Leibold, Vincent Lami, Y. J. Hofstetter, Michael Mastalerz*, Yana Vaynzof*, Triptycene-trisaroyleneimidazoles as non-fullerene acceptors – Influence of side-chains on solubility, device morphology and performance, Org. Electronics 2017, 47, 211-219.

60

59.    Elisabeth H. Menke, David Leibold, Alexander P. Ullrich, Yana Vaynzof, Michael Mastalerz*, Planar versus triptycenylene end-capped aroyleneimidazoles as electron acceptors in organic photovoltaics, Org. Chem. Front. 2017, 4, 834-838.

59

58.  Daniel Beaudoin, Frank Rominger, Michael Mastalerz*, Chiral Self-Sorting of [2+3]-Salicylimine Cage Compounds, Angew. Chem. Int. Ed. 2017, 56, 1244-1248.

58

57.    Sven M. Elbert, Philippe Wagner, Thines Kanagasundaram, Frank Rominger, Michael Mastalerz*, Boroquinol Complexes with fused Extended Aromatic Backbones – Synthesis and Optical Properties, Chem. Eur. J. 2017, 23, 935-945. HOT Paper!

57

 

2016

56.   Daniel Beaudoin, Frank Rominger, Michael Mastalerz*, Chirality-assisted synthesis of a very large octameric hydrogen-bonded capsule, Angew. Chem. Int. Ed. 2016, 55, 15599-15603.

56

Highlighted in Nachrichten der Chemie 03/2017 (Trendberichte)
 

55.   Kevin Baumgärtner, Ana Lucia Meza Chincha, Andreas Dreuw, Frank Rominger, Michael Mastalerz*, A Conformationally Stable Contorted Hexabenzoovalene, Angew. Chem. Int. Ed. 2016, 55, 15594-15598.

55

54.    Gang Zhang*, Frank Rominger, Michael Mastalerz*, Hydrogen-bonded chains and networks of triptycene based triboronic acid and tripyridinone, Cryst. Growth & Design 2016, 16, 5542-5548.

54

53.   Daniel Beaudoin, Frank Rominger, Michael Mastalerz*, Synthesis and Chiral Resolution of C3-symmetric Tribenzotriquinacenes, Eur. J. Org. Chem. 2016, 4470-4472.

​​53

52.   Gang Zhang, Frank Rominger, Ute Zschieschang, Hagen Klauk, Michael Mastalerz*, Facile Synthetic Approach to a large Variety of soluble Diarenoperylenes, Chem. Eur. J. 2016, 22, 14840-14845.

52a

51.  Gang Zhang, Vincent Lami, Frank Rominger, Yana Vaynzof, Michael Mastalerz*, Rigid Conjugated Twisted Truxene-Dimers and Trimers as Electron Acceptors, Angew. Chem. 2016. 128, 4045-4049; Angew. Chem. Int. Ed. 2016, 55, 3977-3981.

51

Highlighted in: T. M. Swager, Q. Zhang, Synfacts 2016, 12, 478.

Highlighted in Nachrichten der Chemie 03/2017 (Trendberichte)

50.   F. Maass, A. Stein, B. Kohl, L. Hahn, L. H. Gade, M. Mastalerz, P. Tegeder*, Substrate-directed growth of N-heteropolycyclic molecules on a metal surface, J. Phys., Chem. C 2016, 120, 2866−2873.

50

49.    Gang Zhang, Frank Rominger, Michael Mastalerz*, Fused π-extended Truxenes via a
         Threefold Borylation as Key Step, Chem. Eur. J. 2016, 22, 3084-3093. (Hot Paper!).

49

48.    Michael Mastalerz*, Single-handed Towards Nano-sized Organic Molecules, Angew. Chem.
         Int. Ed.
2016, 55, 45-47.

 

45a


47.    Elisabeth H. Menke, Vincent Lami, Yana Vaynzof, Michael Mastalerz*, π-Extended Rigid Triptycene-Trisaroylenimidazoles as Electron Acceptors, Chem. Commun. 2016, 52, 1048-1051.

               47

Highlighted in Nachrichten der Chemie 03/2017 (Trendberichte)

46.   Bernd Kohl, Mercedes V. Bohnwagner, Frank Rominger, Hubert Wadepohl, Andreas Dreuw, Michael Mastalerz*, Attractive Dispersion Interactions versus Steric Repulsion of Tert-Butyl groups in the Crystal Packing of D3h-symmetric Tris(quinoxalinophenanthrophenazine), Chem.Eur. J. 2016, 22, 646-655.

                  46a

45.      Michael Mastalerz*, Gang Zhang, Permanent Porous Organic Cage Compounds, book
           chapter in: Self-Assembled Rings and Cages, Ed. Guido H. Clever, Wiley-VCH, 2016,
           in press

46

           

 

 2015

44.   Michael Mastalerz*, Liquefied Molecular Holes, Nature 2015, 527, 174-176.

44

 

43.     Daniel Beaudoin, Frank Rominger, Michael Mastalerz*, Efficient, scalable syntheses of
          important intermediates in tribenzotriquinacene chemistry, Synthesis 2015, 47, 3846-3848.

43

42.     Bernd Kohl, Frank Rominger, Michael Mastalerz*, Crystal Structures of a Molecule
  Designed Not to Pack Tightly, Chem. Eur. J. 2015,
21, 17308-17313. (selected as
  "Hot Paper")



42b
Highlighted in Chemistry Views (08th November 2015)

41.  Dennis Reinhard, Frank Rominger, Michael Mastalerz*, Synthesis of Triphenylene based Triptycenes via Suzuki-Miyaura Cross-Coupling and Subsequent Scholl Reaction. J. Org. Chem. 2015, 80, 9342-9348.

41b


Highlighted in SYNFACTS: T. M. Swager, J. U. Engelhart, Synfacts 2015, 11, 1263.

40.   Kevin Baumgärtner, Frank Rominger, Michael Mastalerz*, An Oxidative Macrobicyclic ring-opening of a triptycene to a highly functionalized fluorene derivative. J. Org. Chem. 2015, 80, 8881-8886.



                           40a

39.    Bernd Kohl, Frank Rominger, Michael Mastalerz*, A pyrene–fused N-heteroacene with eleven rectilinearly annulated aromatic rings characterized by single-crystal X-ray diffraction, Angew. Chem. Int. Ed. 2015, 54, 6051-6056; Angew. Chem. 2015, 127, 6149-6154.

​​

39b

38.    Dennis Reinhard, Ludger Schöttner, Victor Brosius, Frank Rominger, Michael Mastalerz*, Synthesis of para aryl-substituted salicyldialdehydes, Eur. J Org. Chem. 2015, 15, 3274-3285.

38

 

 

                                                                                   

2014

37.    Bernd Kohl, Lena Charlotte Over, Thorsten Lohr, Mariya Vasylyeva, Frank Rominger, M. Mastalerz*, Selective Even-Numbered Bromination of Triptycene (tristhiadizole), Org. Lett. 2014, 16, 5596-5599.

37a

      

36.    Sven M. Elbert, Frank Rominger, M. Mastalerz*, Synthesis of a Rigid C3v-Symmetric Trissalicylaldehyde as Precursor for a Highly Porous Molecular Cube, Chem. Eur. J. 2014, 20, 16707-16720.

                 36

35.    G.Zhang, O. Presly, F. White, I. M. Oppel, M. Mastalerz*, A Shape-Persistent Quadruply Interlocked Giant Cage Catenane with Two Distinct Pores in the Solid State, Angew. Chem. Int. Ed. 2014, 53, 5126-5130. (Hot Paper!)

35
 

34.    B. Kohl, F. Rominger, M. Mastalerz*, Rigid π-extended triptycenes via a hexaketone precursor, Org. Lett. 2014, 16, 704-707.34

33.    G. Zhang, O. Presly, F. White, I. M. Oppel, M. Mastalerz*, A Permanent Mesoporous Organic Cage with an Exceptionally High Surface Area, Angew. Chem. Int. Ed. 2014, 53, 1516-1520. 33

32.    G. Zhang, M. Mastalerz*, Organic Cage Compounds - From Shape-Persistency to Function, Chem. Soc. Rev. 2014, 43, 1934-1947.

      32
 

                                                  

                                                       2013

31.    M. Mastalerz*, Covalent Crystal Growth (News and Views), Nat. Chem. 2013, 5, 810-811.

31
 

30.    M. Brutschy, M. W. Schneider, M. Mastalerz*, S. R. Waldvogel*, Direct Gravimetric Sensing of GBL by Molecular Recognition Process in Organic Cage Compounds, Chem. Commun. 2013, 49, 8398-8400.

30

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.
 

                            29

28.   M. Mastalerz*, Modular Synthesis of Shape-Persistent Organic Cage Compounds: Precursors  for a New Class of Permanent Porous Materials, Synlett 2013, 24, 781-786.

                      28

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.

27

 

                                                        2012

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.

                                                26

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.

                                                   25

 

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


24

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.

23

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.

               22

 

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.

                                                      21

 

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.

             20

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.

19
 

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.

18
 

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.

17
 

 

                                                                                     2011

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

16
 

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.

15
 

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.

14
 

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 asVery Important Paperby 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.

13

 

 

                                                          2010

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.

 
12
 

 

                                                       2009

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.

11
 

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.

 

 

                                                         2008

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

9
 

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.

8
 

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.

7
 

 

                                                       2006

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.

6
 

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

5

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

 

 

                                                        2005

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.

3
 

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.

2
 

 

                                                         2003

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

 

 

Non peer-reviewed articles

 

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)

 

 

Seitenbearbeiter: E-Mail
Letzte Änderung: 28.07.2017
zum Seitenanfang/up