{"id":166711,"date":"2021-01-29T20:15:34","date_gmt":"2021-01-29T17:15:34","guid":{"rendered":"https:\/\/en.buradabiliyorum.com\/synthesizing-organic-molecules-with-a-long-helical-structure\/"},"modified":"2021-01-29T20:15:34","modified_gmt":"2021-01-29T17:15:34","slug":"synthesizing-organic-molecules-with-a-long-helical-structure","status":"publish","type":"post","link":"https:\/\/buradabiliyorum.com\/en\/synthesizing-organic-molecules-with-a-long-helical-structure\/","title":{"rendered":"#Synthesizing organic molecules with a long helical structure"},"content":{"rendered":"

“#Synthesizing organic molecules with a long helical structure<\/strong>”<\/p>\n

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\"Coiling
\n Helical molecules with a large diameter are symbolized as a spirally rising dragon.https:\/\/doi.org\/10.1002\/chem.202005357 Credit: Eiji Tsurumaki, Chemistry-A European Journal<\/i>
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Scientists at Tokyo Institute of Technology<\/a> (Tokyo Tech) produced and extensively characterized novel organic molecules with a long helical structure. Unlike previous helical molecules, these longer compounds exhibit special interactions between coils that could give rise to interesting optical and chemical properties with app<\/a>lications in light polarization, catalysis, and molecular springs.<\/p>\n


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More often than not, organic molecules with unique 3-D structures bear physicochemical properties that cannot be found in other types of compounds. Helicenes, chains of simple benzene rings that adopt a helical structure, are a good example. These molecules, which resemble a spring, have interesting applications in optics and as chemical sensors or catalysts. However, it is still difficult to synthesize long helicenes; the longest one ever made was sixteen benzene rings long, which amounted to a helical structure with slightly more than two full turns and a half.<\/p>\n

In a recent study published in Chemistry\u2014A European Journal<\/i>, a team of scientists at Tokyo Tech mixed things up by synthesizing a different type of organic molecule with a helical structure. Unlike helicenes, the basic unit of their compounds was anthracene, a linear chain of three aromatic rings. In previous works, the team had managed to synthesize [3]HA, which stands for “helical anthracene with three anthracene units.” However, as Professor Shinji Toyota, the corresponding author of the study, explains, “[3]HA was not long enough to reach a full turn. Therefore, it did not exhibit some of the peculiar characteristics that arise from the interactions between different ‘layers’ of the helical structure in a face-to-face fashion.”<\/p>\n

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\"Coiling
\n By strategically fusing anthracene units, molecules with a helical shape can be obtained. Those longer than three units exhibit peculiar interactions between helical “layers” in a face-to-face fashion. Credit: Chemistry-A European Journal<\/i>
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Using a carefully planned step-by-step process, the scientists managed to synthesize [4]HA and [5]HA, which they proceeded to characterize through a variety of experiments backed by theoretical calculations. They verified the composition and structure of the compounds using proton nuclear magnetic resonance and X-ray analysis. These findings were confirmed through density functional theory calculations, a widely used approach used to make quantum mechanical models of electronic and nuclear structures.<\/p>\n

Then, the researchers quantified the stability of the different helical anthracenes by using them in a virtual chemical reaction that changed them into flat molecules. Interestingly, the stability of 3[HA] was almost the same as that of [4]HA and [5]HA. This indicates that the destabilizing forces that naturally appear in longer molecular chains ([4]HA and [5]HA) actually canceled out with the new face-to-face stabilizing interactions between different helical layers. These interactions between layered anthracene moiety was visualized by Non-Covalent Interaction (NCI) analysis. The effect of these new interactions was also apparent in the photoemission properties of the longer molecules; their emission bands upon excitation were longer-lived, highlighting the fact that excited states were preserved longer.<\/p>\n

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\"Coiling
\n The green region in the NCI plot indicates weak interactions. Credit: Chemistry-A European Journal<\/i>
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Finally, the scientists explored the helical inversion process in the new, longer compounds. This inversion refers to the process of left-handed spirals changing into right-handed ones and vice versa. Some attractive optical properties such as circular polarization are lost if left- and right-handed spirals are present in equal proportion. This motivated the team to analyze the stepwise process by which each helical structure changes directions.<\/p>\n

Overall, this study provides some much-needed insight into a new type of helical molecule. Already looking ahead, Toyota comments on future works involving these exciting compounds: “Extending helical anthracenes further and producing them with a single coiling direction remains a challenge, and so does testing their performance as molecular springs. Our team is currently working on synthesizing even longer molecules and performing structural modifications.” Only time will tell what’s in line for helical structures when longer ones finally spring up!<\/p>\n\n

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Modulating helical nanostructures in liquid crystal phase by molecular design\n <\/p><\/div>\n

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\n More information:<\/strong>
\n Kei Fujise et al, Construction of Helical Structures with Multiple Fused Anthracenes: Structures and Properties of Long Expanded Helicenes, Chemistry \u2013 A European Journal<\/i> (2020). DOI: 10.1002\/chem.202004720<\/a><\/p><\/div>\n
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\n Tokyo Institute of Technology
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Citation<\/strong>:
\n Coiling them up: Synthesizing organic molecules with a long helical structure (2021, January 29)
\n retrieved 30 January 2021
\n from https:\/\/phys.org\/news<\/a>\/2021-01-molecules-helical.html<\/p>\n

This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
\n part may be reproduced without the written permission. The content is provided for information purposes only.<\/p><\/div>\n<\/p><\/div>\n