{"id":14037,"date":"2015-05-22T16:16:20","date_gmt":"2015-05-22T15:16:20","guid":{"rendered":"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=14037"},"modified":"2015-05-22T16:16:20","modified_gmt":"2015-05-22T15:16:20","slug":"r-x%e2%89%a1x-r-g-n-lewis-100-year-old-idea","status":"publish","type":"post","link":"https:\/\/rzepa.net\/blog\/2015\/05\/22\/r-x%e2%89%a1x-r-g-n-lewis-100-year-old-idea\/","title":{"rendered":"R-X\u2261X-R: G. N. Lewis&#8217; 100 year old idea."},"content":{"rendered":"<p>As I have noted <a href=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=9973\" target=\"_blank\" rel=\"noopener\">elsewhere<\/a>, Gilbert N. Lewis wrote a famous paper entitled &#8220;<em>the atom and the molecule<\/em>&#8220;, the centenary of which is coming up.[cite]10.1021\/ja02261a002[\/cite] In a short and rarely commented\u00a0upon remark, he speculates about the shared electron pair structure of acetylene,\u00a0\u00a0R-X\u2261X-R (R=H, X=C). It could, he suggests, take up three forms. H-C:::C-H and two more which I show as he drew them. The first of these would now be called a<em> bis-carbene<\/em> and the second a <em>biradical<\/em>.<\/p>\n<p><img decoding=\"async\" src=\"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2013\/03\/Lewis.svg\" alt=\"\" \/><\/p>\n<p>In 1916, it was too early for Lewis to speculate what the geometries of such species might be, and in particular the C&#8230;C (or generalising, X&#8230;X) distance, and the two angles, one for each X. Well, we do not need to speculate, we can perform a search of the crystal structure database. Here it is\u00a0(R &lt; 0.05, no errors, no disorder):<\/p>\n<p><a href=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2015\/05\/Lewis-CC4.jpg\"><img decoding=\"async\" class=\"aligncenter size-full wp-image-14040\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2015\/05\/Lewis-CC4.jpg\" alt=\"Lewis-CC4\" width=\"440\" \/><\/a><\/p>\n<p>A little more explanation of this 4-dimensional plot is needed:<\/p>\n<ol>\n<li>The two angles are plotted as X and Y.<\/li>\n<li>The X&#8230;X distance is plotted as colour, with red representing the longest distances and blue the shortest<\/li>\n<li>The size of each &#8220;bin&#8221; is represented by the radius of the circle; small circles represent few examples, larger circles represent more examples in each &#8220;bin&#8221; defined by a regular range of angles.<\/li>\n<\/ol>\n<p>There are one or two off-diagonal\u00a0 &#8220;outliers&#8221;, each of which probably deserves individual inspection. But dealing just with the obvious clusters, the overwhelmingly largest is for both angles of ~180\u00b0, and these are the triple bonds we know and love. As far as I know, Lewis was the first to propose a triple bond between two atoms, but if anyone reading this blog knows of an antecedent, do let me know.\u00a0The next cluster is for angles of ~109\u00b0 and these are clearly<em> bis-carbenes.<\/em> These all occur when X \u2260 C.\u00a0There are two small clusters worthy of note; one ~130\u00b0 and one ~90\u00b0. The latter are mostly Pb-Pb and Sn-Sn, where the bonding is unhybridised pure p.<\/p>\n<p>One of the limitations of searching for crystal structures is that the spin state of each molecule is never given. The biradical structure given by Lewis could well have a triplet ground state, and perhaps that might have very characteristic angles (~130\u00b0 ?). It would be great to identify a genuine example of this biradical form!<\/p>\n<p>As usual, the search itself took around 10 minutes, and it provides much interesting food for thought; not bad for a 100-year-old idea!<\/p>\n<hr \/>\n<h4>Acknowledgments<\/h4>\n<p>This post has been cross-posted in PDF format at <a href=\"https:\/\/doi.org\/10.15200\/winn.143326.61507\" rel=\"noopener\" target=\"_blank\">Authorea<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>As I have noted elsewhere, Gilbert N. Lewis wrote a famous paper entitled &#8220;the atom and the molecule&#8220;, the centenary of which is coming up.[cite]10.1021\/ja02261a002[\/cite] In a short and rarely commented\u00a0upon remark, he speculates about the shared electron pair structure of acetylene,\u00a0\u00a0R-X\u2261X-R (R=H, X=C). It could, he suggests, take up three forms. H-C:::C-H and two [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4,9,11],"tags":[361,362,542,589,1023,1058,1098,1755,1826,1828],"class_list":["post-14037","post","type-post","status-publish","format-standard","hentry","category-chemical-it","category-historical","category-interesting-chemistry","tag-carbene","tag-carbenes","tag-chemistry","tag-cluster-chemistry","tag-food","tag-functional-groups","tag-gilbert-n-lewis","tag-non-kekule-molecule","tag-organic-chemistry","tag-organic-compounds"],"_links":{"self":[{"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/posts\/14037","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/comments?post=14037"}],"version-history":[{"count":0,"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/posts\/14037\/revisions"}],"wp:attachment":[{"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/media?parent=14037"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/categories?post=14037"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rzepa.net\/blog\/wp-json\/wp\/v2\/tags?post=14037"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}