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Inside Back Cover: Designed Enclosure Enables Guest Binding Within the 4200 Å3 Cavity of a Self‐Assembled Cube (Angew. Chem. Int. Ed. 19/2015) 下载免费PDF全文
William J. Ramsay Filip T. Szczypiński Dr. Haim Weissman Dr. Tanya K. Ronson Dr. Maarten M. J. Smulders Prof. Boris Rybtchinski Prof. Jonathan R. Nitschke 《Angewandte Chemie (International ed. in English)》2015,54(19):5793-5793
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Dr. Tanya K. Ronson Chandan Giri Dr. N. Kodiah Beyeh Antti Minkkinen Filip Topić Dr. Julian J. Holstein Prof. Kari Rissanen Dr. Jonathan R. Nitschke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(10):3374-3382
Subtle differences in metal–ligand bond lengths between a series of [M4L6]4? tetrahedral cages, where M=FeII, CoII, or NiII, were observed to result in substantial differences in affinity for hydrophobic guests in water. Changing the metal ion from iron(II) to cobalt(II) or nickel(II) increases the size of the interior cavity of the cage and allows encapsulation of larger guest molecules. NMR spectroscopy was used to study the recognition properties of the iron(II) and cobalt(II) cages towards small hydrophobic guests in water, and single‐crystal X‐ray diffraction was used to study the solid‐state complexes of the iron(II) and nickel(II) cages. 相似文献
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Dr. Matthias Otte Petrus F. Kuijpers Dipl.‐Chem. Oliver Troeppner Prof. Dr. Ivana Ivanović‐Burmazović Prof. Dr. Joost N. H. Reek Prof. Dr. Bas de Bruin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(31):10170-10178
The synthesis of a new, cubic M8L6 cage is described. This new assembly was characterised by using NMR spectroscopy, DOSY, TGA, MS, and molecular modelling techniques. Interestingly, the enlarged cavity size of this new supramolecular assembly allows the selective encapsulation of tetra(4‐pyridyl)metalloporphyrins (MII(TPyP), M=Zn, Co). The obtained encapsulated cobalt–porphyrin embedded in the cubic zinc–porphyrin assembly is the first example of a catalytically active encapsulated transition‐metal complex in a cubic M8L6 cage. The substrate accessibility of this system was demonstrated through radical‐trapping experiments, and its catalytic activity was demonstrated in two different radical‐type transformations. The reactivity of the encapsulated CoII(TPyP) complex is significantly increased compared to free CoII(TPyP) and other cobalt–porphyrin complexes. The reactions catalysed by this system are the first examples of cobalt–porphyrin‐catalysed radical‐type transformations involving diazo compounds which occur inside a supramolecular cage. 相似文献