Molecular Chirality in Chemistry and Biology: Historical Milestones

2013 ◽  
Vol 96 (9) ◽  
pp. 1617-1657 ◽  
Author(s):  
Joseph Gal
Keyword(s):  
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.


Author(s):  
Alberta Ferrarini ◽  
Pier Luigi Nordio
Keyword(s):  

Science ◽  
1998 ◽  
Vol 282 (5397) ◽  
pp. 2247-2250 ◽  
Author(s):  
R. K. Kondru ◽  
P. Wipf ◽  
D. N. Beratan

Science ◽  
1996 ◽  
Vol 273 (5282) ◽  
pp. 1686-1688 ◽  
Author(s):  
N. P. M. Huck ◽  
W. F. Jager ◽  
B. de Lange ◽  
B. L. Feringa

Soft Matter ◽  
2012 ◽  
Vol 8 (30) ◽  
pp. 7773 ◽  
Author(s):  
Hale Ocak ◽  
Belkız Bilgin-Eran ◽  
Marko Prehm ◽  
Carsten Tschierske

2012 ◽  
Vol 48 (40) ◽  
pp. 4809-4811 ◽  
Author(s):  
Noriko Fujimoto ◽  
Mio Matsumura ◽  
Isao Azumaya ◽  
Shizuka Nishiyama ◽  
Hyuma Masu ◽  
...  

2015 ◽  
Vol 51 (52) ◽  
pp. 10506-10509 ◽  
Author(s):  
Alberto Insuasty ◽  
Carmen Atienza ◽  
Juan Luis López ◽  
Nazario Martín

The supramolecular organization of new fullerene derivatives endowed with peptides as biomolecular templates affords ordered nanofibers of several micrometres length based on hydrogen bonds and π–π interactions.


2006 ◽  
Vol 118 (7) ◽  
pp. 1019-1019 ◽  
Author(s):  
Ayyappanpillai Ajayaghosh ◽  
Reji Varghese ◽  
Subi Jacob George ◽  
Chakkooth Vijayakumar
Keyword(s):  

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