Organic cage compounds–from shape-persistency to function G Zhang, M Mastalerz Chemical Society Reviews 43 (6), 1934-1947, 2014 | 610 | 2014 |
Rational construction of an extrinsic porous molecular crystal with an extraordinary high specific surface area M Mastalerz, IM Oppel Angewandte Chemie International Edition 51 (21), 5252-5255, 2012 | 485 | 2012 |
Shape‐persistent organic cage compounds by dynamic covalent bond formation M Mastalerz Angewandte Chemie International Edition 49 (30), 5042-5053, 2010 | 428 | 2010 |
A salicylbisimine cage compound with high surface area and selective CO2/CH4 adsorption M Mastalerz, MW Schneider, IM Oppel, O Presly Angewandte Chemie International Edition 50 (5), 1046-1051, 2011 | 425 | 2011 |
A permanent mesoporous organic cage with an exceptionally high surface area G Zhang, O Presly, F White, IM Oppel, M Mastalerz Angewandte Chemie International Edition 53 (6), 1516-1520, 2014 | 413 | 2014 |
Porous shape-persistent organic cage compounds of different size, geometry, and function M Mastalerz Accounts of Chemical Research 51 (10), 2411-2422, 2018 | 302 | 2018 |
Porous organic cage compounds as highly potent affinity materials for sensing by quartz crystal microbalances. M Brutschy, MW Schneider, M Mastalerz, SR Waldvogel Advanced Materials (Deerfield Beach, Fla.) 24 (45), 6049-6052, 2012 | 231 | 2012 |
A shape‐persistent quadruply interlocked giant cage catenane with two distinct pores in the solid state G Zhang, O Presly, F White, IM Oppel, M Mastalerz Angewandte Chemie International Edition 53 (20), 5126-5130, 2014 | 222 | 2014 |
The Next generation of shape‐persistant zeolite analogues: covalent organic frameworks M Mastalerz Angewandte Chemie International Edition 47 (3), 445-447, 2008 | 214 | 2008 |
Permanent Porous Materials from Discrete Organic Molecules—Towards Ultra‐High Surface Areas M Mastalerz Chemistry–A European Journal 18 (33), 10082-10091, 2012 | 207 | 2012 |
Chiral Self‐Sorting of [2+ 3] Salicylimine Cage Compounds D Beaudoin, F Rominger, M Mastalerz Angewandte Chemie International Edition 56 (5), 1244-1248, 2017 | 174 | 2017 |
Periphery‐Substituted [4+ 6] Salicylbisimine Cage Compounds with Exceptionally High Surface Areas: Influence of the Molecular Structure on Nitrogen Sorption Properties MW Schneider, IM Oppel, H Ott, LG Lechner, HJS Hauswald, R Stoll, ... Chemistry–A European Journal 18 (3), 836-847, 2012 | 172 | 2012 |
Post-modification of the interior of porous shape-persistent organic cage compounds. MW Schneider, IM Oppel, A Griffin, M Mastalerz Angewandte Chemie International Edition 52 (13), 2013 | 150 | 2013 |
Exo‐Functionalized Shape‐Persistent [2+ 3] Cage Compounds: Influence of Molecular Rigidity on Formation and Permanent Porosity MW Schneider, IM Oppel, M Mastalerz Chemistry–A European Journal 18 (14), 4156-4160, 2012 | 129 | 2012 |
A Pyrene‐Fused N‐Heteroacene with Eleven Rectilinearly Annulated Aromatic Rings B Kohl, F Rominger, M Mastalerz Angewandte Chemie International Edition 54 (20), 6051-6056, 2015 | 115 | 2015 |
Formtreue organische Käfigverbindungen durch dynamische Bildung kovalenter Bindungen M Mastalerz Angewandte Chemie 122 (30), 5164-5175, 2010 | 107 | 2010 |
Synthesis of a Rigid C3v‐Symmetric Tris‐salicylaldehyde as a Precursor for a Highly Porous Molecular Cube SM Elbert, F Rominger, M Mastalerz Chemistry–A European Journal 20 (50), 16707-16720, 2014 | 104 | 2014 |
A shape-persistent exo-functionalized [4+ 6] imine cage compound with a very high specific surface area MW Schneider, HJS Hauswald, R Stoll, M Mastalerz Chemical Communications 48 (79), 9861-9863, 2012 | 104 | 2012 |
Direct gravimetric sensing of GBL by a molecular recognition process in organic cage compounds M Brutschy, MW Schneider, M Mastalerz, SR Waldvogel Chemical Communications 49 (75), 8398-8400, 2013 | 99 | 2013 |
One-pot synthesis of a shape-persistent endo-functionalised nano-sized adamantoid compound M Mastalerz Chemical communications, 4756-4758, 2008 | 97 | 2008 |