{"id":22311,"date":"2022-03-16T11:42:03","date_gmt":"2022-03-16T05:57:03","guid":{"rendered":"https:\/\/www.revoscience.com\/en\/?p=22311"},"modified":"2022-03-16T11:42:15","modified_gmt":"2022-03-16T05:57:15","slug":"changing-the-handedness-of-molecules","status":"publish","type":"post","link":"https:\/\/www.revoscience.com\/en\/changing-the-handedness-of-molecules\/","title":{"rendered":"Changing the handedness of molecules"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Researchers at Kanazawa University report in Proceedings of the National Academy of Sciences a responsive molecular system that, through chemical reactions, inverses its chirality before becoming racemic.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Molecules that have the ability to change their structure in response to a chemical or physical stimulus are called \u2018responsive molecules\u2019.\u00a0 <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">This type of molecule plays an important role in signal transduction at the nanoscale.\u00a0 The typical time profile of a structural change of a responsive molecule follows an exponential relaxation.\u00a0 However, molecular systems with non-typical time responses, such as e.g. chemical oscillators (whose structure switches periodically between two states), offer advanced functionalities and are also intensively investigated.\u00a0 <\/p>\n\n\n\n<figure class=\"wp-block-image size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-675x403.png\" alt=\"\" class=\"wp-image-22312\" width=\"839\" height=\"501\" title=\"\" srcset=\"https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-675x403.png 675w, https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-670x400.png 670w, https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-194x116.png 194w, https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png 677w\" sizes=\"auto, (max-width: 839px) 100vw, 839px\" \/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Shigehisa Akine and colleagues from Kanazawa University have now designed a particular responsive molecule in which the chirality (\u2018handedness\u2019) changes in a non-exponential fashion.\u00a0 The achievement is a breakthrough in the field of responsive systems as the chirality change happens in a unimolecular system \u2014 not, as has often been the case before, in supramolecular assemblies.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The researchers\u2019 responsive molecule has six exchangeable sites; it can be written as [LCo<sub>3<\/sub>X<sub>6<\/sub>]<sup>3+<\/sup>, where X stands for a ligand at each of the six sites.\u00a0 The molecule has two forms, a \u2018left-handed\u2019 (abbreviated \u2018<em>M<\/em>\u2019) and a \u2018right-handed\u2019 (abbreviated \u2018<em>P<\/em>\u2019) version.\u00a0<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">In solution, the two forms will occur, in a given ratio.\u00a0 Akine and colleagues started from the molecule where X is a particular chiral amine labeled\u00a0<strong>A<\/strong>\u00a0(chiral means that the ligand and its mirror image cannot be superimposed, and amine refers to a type of molecular group containing nitrogen).\u00a0 <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">In a methanol solution, the\u00a0<em>P<\/em>\/<em>M<\/em>\u00a0ratio of [LCo<sub>3<\/sub><strong>A<\/strong><sub>6<\/sub>]<sup>3+<\/sup>\u00a0was 88:12, meaning that the right-handed version was dominant.\u00a0 The scientists then looked at what happened when exchanging the chiral\u00a0<strong>A<\/strong>\u00a0groups with piperidine (another, but achiral, amine).<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Because of the achirality of the piperidine groups, the resulting [LCo<sub>3<\/sub>(piperidine)<sub>6<\/sub>]<sup>3+<\/sup>&nbsp;solution should become \u2018racemic\u2019, which means that any effects of chirality are compensated.&nbsp; This is indeed what happened, but the researchers discovered that before reaching the racemic state after two days, the solution first switched from originally&nbsp;<em>P<\/em>-dominant to&nbsp;<em>M<\/em>-dominant after 7 minutes, with maximum&nbsp;<em>M<\/em>-dominance after 60 \u2013 120 minutes.&nbsp; Remarkably, a similar transient chirality inversion was not observed for the reverse reaction, [LCo<sub>3<\/sub>(piperidine)<sub>6<\/sub>]<sup>3+<\/sup>&nbsp;to [LCo<sub>3<\/sub><strong>A<\/strong><sub>6<\/sub>]<sup>3+<\/sup>, for which the solution changed monotonically from racemic to&nbsp;<em>P<\/em>-dominant.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Akine and colleagues note that their [LCo<sub>3<\/sub>X<sub>6<\/sub>]<sup>3+<\/sup>\u00a0responsive molecule is the first unimolecular platform displaying a transient chirality inversion and that the unique chirality change happens on the timescale of minutes to hours, which could be potentially useful for time-dependent functional materials related to human activity.\u00a0 Quoting the scientists: \u201cthis result will provide an important insight into the science of autonomously driven materials.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Molecules that have the ability to change their structure in response to a chemical or physical stimulus are called \u2018responsive molecules\u2019.\u00a0 <\/p>\n","protected":false},"author":2,"featured_media":22312,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[17],"tags":[],"class_list":["post-22311","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-research"],"featured_image_urls":{"full":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"thumbnail":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-200x200.png",200,200,true],"medium":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-670x400.png",670,400,true],"medium_large":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"large":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-675x403.png",675,403,true],"1536x1536":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"2048x2048":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"ultp_layout_landscape_large":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"ultp_layout_landscape":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"ultp_layout_portrait":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",600,358,false],"ultp_layout_square":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",600,358,false],"newspaper-x-single-post":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",677,404,false],"newspaper-x-recent-post-big":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-550x360.png",550,360,true],"newspaper-x-recent-post-list-image":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system-95x65.png",95,65,true],"web-stories-poster-portrait":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",640,382,false],"web-stories-publisher-logo":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",96,57,false],"web-stories-thumbnail":["https:\/\/www.revoscience.com\/en\/wp-content\/uploads\/2022\/03\/molecular-system.png",150,90,false]},"author_info":{"info":["RevoScience"]},"category_info":"<a 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