High-Symmetry Coordination Cages via Self-Assembly

2002 ◽  
Vol 35 (11) ◽  
pp. 972-983 ◽  
Author(s):  
S. Russell Seidel ◽  
Peter J. Stang
ChemInform ◽  
2003 ◽  
Vol 34 (5) ◽  
Author(s):  
S. Russell Seidel ◽  
Peter J. Stang

2020 ◽  
Author(s):  
Daniel B. Straus ◽  
Robert J. Cava

The design of new chiral materials usually requires stereoselective organic synthesis to create molecules with chiral centers. Less commonly, achiral molecules can self-assemble into chiral materials, despite the absence of intrinsic molecular chirality. Here, we demonstrate the assembly of high-symmetry molecules into a chiral van der Waals structure by synthesizing crystals of C<sub>60</sub>(SnI<sub>4</sub>)<sub>2</sub> from icosahedral buckminsterfullerene (C<sub>60</sub>) and tetrahedral SnI4 molecules through spontaneous self-assembly. The SnI<sub>4</sub> tetrahedra template the Sn atoms into a chiral cubic three-connected net of the SrSi<sub>2</sub> type that is held together by van der Waals forces. Our results represent the remarkable emergence of a self-assembled chiral material from two of the most highly symmetric molecules, demonstrating that almost any molecular, nanocrystalline, or engineered precursor can be considered when designing chiral assemblies.


2012 ◽  
Vol 134 (19) ◽  
pp. 8042-8045 ◽  
Author(s):  
Xiao-Ping Zhou ◽  
Jie Liu ◽  
Shun-Ze Zhan ◽  
Ju-Rong Yang ◽  
Dan Li ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Samuel Edward Walker ◽  
Stephanie A Boer ◽  
Thomas Malcomson ◽  
Martin J. Paterson ◽  
Kellie Tuck ◽  
...  

Control of self-sorting regimes is achieved through adjustment of steric interactions in self-assembled coordination cages. The self-assembly regime of dynamic mixtures of heteroleptic cages is followed by HPLC to show...


2002 ◽  
Vol 99 (8) ◽  
pp. 4911-4915 ◽  
Author(s):  
L. Pirondini ◽  
F. Bertolini ◽  
B. Cantadori ◽  
F. Ugozzoli ◽  
C. Massera ◽  
...  

2014 ◽  
Vol 43 (11) ◽  
pp. 4587-4592 ◽  
Author(s):  
Marina Frank ◽  
Lennard Krause ◽  
Regine Herbst-Irmer ◽  
Dietmar Stalke ◽  
Guido H. Clever

The self-assembly of heterogeneous or homogeneous cages from a mixture of ligands is a function of the ligand length and reaction kinetics.


2002 ◽  
Vol 99 (8) ◽  
pp. 4932-4936 ◽  
Author(s):  
C. J. Kuehl ◽  
Y. K. Kryschenko ◽  
U. Radhakrishnan ◽  
S. R. Seidel ◽  
S. D. Huang ◽  
...  

2020 ◽  
Vol 16 ◽  
pp. 2701-2708
Author(s):  
Matthias Hardy ◽  
Marianne Engeser ◽  
Arne Lützen

Employing 4-ethynylaniline as a simple organic ligand we were able to prepare the stable trans-bis(acetylide)platinum(II) complex [Pt(L1)2(PBu3)2] as a linear metalloligand. The reaction of this metalloligand with iron(II) cations and pyridine-2-carbaldehyde according to the subcomponent self-assembly approach yielded decanuclear heterobimetallic tetrahedron [Fe4Pt6(L2)12](OTf)8. Thus, combination of these two design concepts – the subcomponent self-assembly strategy and the complex-as-a-ligand approach – ensured a fast and easy synthesis of large heterobimetallic coordination cages of tetrahedral shape with a diameter of more than 3 nm as a mixture of all three possible T-, S 4- and C 3-symmetric diastereomers. The new complexes were characterized by NMR and UV–vis spectroscopy and ESI mass spectrometry. Using GFN2-xTB we generated energy-minimized models of the diastereomers of this cage that further corroborated the results from analytical findings.


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