scholarly journals Transferring axial molecular chirality through a sequence of on-surface reactions

2020 ◽  
Vol 11 (21) ◽  
pp. 5441-5446 ◽  
Author(s):  
Néstor Merino-Díez ◽  
Mohammed S. G. Mohammed ◽  
Jesús Castro-Esteban ◽  
Luciano Colazzo ◽  
Alejandro Berdonces-Layunta ◽  
...  

The axial chirality of reactants is transferred through multistep on-surface reactions to chiral polymers and to prochiral graphene nanoribbons.

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.


2015 ◽  
Vol 19 (18) ◽  
pp. 1850-1871 ◽  
Author(s):  
Eleftherios K. Pefkianakis ◽  
Georgios Sakellariou ◽  
Georgios C. Vougioukalakis

2016 ◽  
Vol 12 (2) ◽  
pp. 184-191 ◽  
Author(s):  
Julia A. Baimova ◽  
Elena A. Korznikova ◽  
Sergey V. Dmitirev ◽  
Bo Liu ◽  
Kun Zhou
Keyword(s):  

2013 ◽  
Vol 3 (3) ◽  
pp. 291-301 ◽  
Author(s):  
Xiaochen Dong ◽  
Xin Zhao ◽  
Lianhui Wang ◽  
Wei Huang
Keyword(s):  

1996 ◽  
Vol 61 (7) ◽  
pp. 1018-1026 ◽  
Author(s):  
Richard Kubík ◽  
Stanislav Böhm ◽  
Josef Kuthan

Borohydride reduction of titled ketones 1a-1g gave diastereoisomeric mixtures of (Z)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)prop-2-en-1-ols 2a-2g and 3a-3g in which the former ones prevailed. Only individual racemic products were obtained after borohydride reduction of (E)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)-prop-2-en-1-one 4 to corresponding 1-hydroxy derivative 5 and by conversion of (Z)-1-oxo derivative 1a to 1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)propan-1-one (6) with sodium hydrogenselenide. Diastereoselectivity of the borohydride reduction is discussed using the PM3 calculations of the molecules 1a, 2a, 2b, 3a, 3b, 4, 5, and 6.


2019 ◽  
Vol 7 (21) ◽  
pp. 6241-6245 ◽  
Author(s):  
Wei-Wei Yan ◽  
Xiao-Fei Li ◽  
Xiang-Hua Zhang ◽  
Xinrui Cao ◽  
Mingsen Deng

Boron adsorption induces a heavily localized state right at the Fermi level only in the family of W = 3p + 1 and thus spin-splitting occurs spontaneously.


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