scholarly journals Charge Redistribution and Spin Polarization Driven by Correlation Induced Electron Exchange in Chiral Molecules

Nano Letters ◽  
2021 ◽  
Vol 21 (7) ◽  
pp. 3026-3032
Author(s):  
Jonas Fransson
2017 ◽  
Vol 114 (10) ◽  
pp. 2474-2478 ◽  
Author(s):  
Anup Kumar ◽  
Eyal Capua ◽  
Manoj K. Kesharwani ◽  
Jan M. L. Martin ◽  
Einat Sitbon ◽  
...  

Noncovalent interactions between molecules are key for many biological processes. Necessarily, when molecules interact, the electronic charge in each of them is redistributed. Here, we show experimentally that, in chiral molecules, charge redistribution is accompanied by spin polarization. We describe how this spin polarization adds an enantioselective term to the forces, so that homochiral interaction energies differ from heterochiral ones. The spin polarization was measured by using a modified Hall effect device. An electric field that is applied along the molecules causes charge redistribution, and for chiral molecules, a Hall voltage is measured that indicates the spin polarization. Based on this observation, we conjecture that the spin polarization enforces symmetry constraints on the biorecognition process between two chiral molecules, and we describe how these constraints can lead to selectivity in the interaction between enantiomers based on their handedness. Model quantum chemistry calculations that rigorously enforce these constraints show that the interaction energy for methyl groups on homochiral molecules differs significantly from that found for heterochiral molecules at van der Waals contact and shorter (i.e., ∼0.5 kcal/mol at 0.26 nm).


1996 ◽  
Vol 74 (11-12) ◽  
pp. 863-874 ◽  
Author(s):  
Joachim Kessler

Exactly 30 years ago the ICPEAC was held for the first time in Canada. At this conference in Québec first results on spin-polarization phenomena in low-energy electron scattering were presented. In the following years spin-polarization effects played an increasing role at the ICPEAC and its satellite conferences. This contribution gives a perspective of this development in the past 30 years. It outlines fundamental directions of development, shows how they interact, and gives an account of their usefulness for a better understanding of collision physics. In the first part, processes are discussed where the polarization effects are caused by either the spin–orbit interaction or the exchange interaction alone. Experimental results on such processes can be used to study the role of these spin-dependent interactions in electron-atom collisions. In recent years more complicated processes have been studied where the two spin-dependent effects can no longer be disentangled. Examples of such processes are elastic scattering from atoms with unsaturated spins, inelastic scattering, and spin-selected coincidence experiments. Major progress in spin-dependent scattering from chiral molecules will also be reported. The enormous progress of this field in the past 30 years could only be made by a number of novel developments in the production and detection of electron polarization.


Science ◽  
2018 ◽  
Vol 360 (6395) ◽  
pp. 1331-1334 ◽  
Author(s):  
Koyel Banerjee-Ghosh ◽  
Oren Ben Dor ◽  
Francesco Tassinari ◽  
Eyal Capua ◽  
Shira Yochelis ◽  
...  

It is commonly assumed that recognition and discrimination of chirality, both in nature and in artificial systems, depend solely on spatial effects. However, recent studies have suggested that charge redistribution in chiral molecules manifests an enantiospecific preference in electron spin orientation. We therefore reasoned that the induced spin polarization may affect enantiorecognition through exchange interactions. Here we show experimentally that the interaction of chiral molecules with a perpendicularly magnetized substrate is enantiospecific. Thus, one enantiomer adsorbs preferentially when the magnetic dipole is pointing up, whereas the other adsorbs faster for the opposite alignment of the magnetization. The interaction is not controlled by the magnetic field per se, but rather by the electron spin orientations, and opens prospects for a distinct approach to enantiomeric separations.


Author(s):  
О. Мирославович Карбованець ◽  
Мирослав Іванович Карбованець ◽  
Володимир Юрійович Лазур ◽  
М. В. Хома

2020 ◽  
Author(s):  
Dung Do

<p>Chiral molecules with their defined 3-D structures are of paramount importance for the study of chemical biology and drug discovery. Having rich structural diversity and unique stereoisomerism, chiral molecules offer a large chemical space that can be explored for the design of new therapeutic agents.<sup>1</sup> Practically, chiral architectures are usually prepared from organometallic and organocatalytic processes where a transition metal or an organocatalyst is tailor-made for desired reactions. As a result, developing a method that enables rapid assembly of chiral complex molecules under metal- and organocatalyst-free condition represents a daunting challenge. Here we developed a straightforward route to create a chiral 3-D structure from 2-D structures and an amino acid without any chiral catalyst. The center of this research is the design of a <a>special chiral spiroimidazolidinone cyclohexadienone intermediate</a>, a merger of a chiral reactive substrate with multiple nucleophillic/electrophillic sites and a transient organocatalyst. <a>This unique substrate-catalyst (“subcatalyst”) dual role of the intermediate enhances </a><a>the coordinational proximity of the chiral substrate and catalyst</a> in the key Aza-Michael/Michael cascade resulting in a substantial steric discrimination and an excellent overall diastereoselectivity. Whereas the “subcatalyst” (hidden catalyst) is not present in the reaction’s initial components, which renders a chiral catalyst-free process, it is strategically produced to promote sequential self-catalyzed reactions. The success of this methodology will pave the way for many efficient preparations of chiral complex molecules and aid for the quest to create next generation of therapeutic agents.</p>


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