{"id":1423,"date":"2010-01-01T12:44:52","date_gmt":"2010-01-01T11:44:52","guid":{"rendered":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=1423"},"modified":"2010-01-01T12:44:52","modified_gmt":"2010-01-01T11:44:52","slug":"contriving-aromaticity-from-s%e2%89%a1c-triple-bonds","status":"publish","type":"post","link":"https:\/\/www.rzepa.net\/blog\/?p=1423","title":{"rendered":"Contriving aromaticity from S\u2261C Triple bonds"},"content":{"rendered":"
\n

In the previous post<\/a>, the molecule F3<\/sub>S-C\u2261SF3<\/sub> was found to exhibit a valence bond isomerism, one of the S-C bonds being single, the other triple, and with a large barrier (~31 kcal\/mol, \u03bd 284i<\/em> cm-1<\/sup>) to interconversion of the two valence-bond forms. So an interesting extension of this phenomenon is shown below:<\/p>\n

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A cyclic form of the SCS Motif. Click for 3D<\/p><\/div>If the same type of valence bond isomerism were to occur, we would now have three C\u2261S triple bonds swapping places with three CS single bonds, a sort of super version of the notation normally shown for benzene itself. If the barrier to this swapping is finite, then the interconversion shown above would be a proper equilibrium (the top arrows), but if there is no barrier, then the interconversion would be a proper resonance (the bottom double-headed arrow). Another way of posing the question is whether the so-called Kekul\u00e9 vibrational mode<\/a> (which in effect represents the motions implied above) has a negative force constant or a positive one respectively for the two sets of arrows shown.<\/p>\n

A B3LYP\/cc-pVTZ calculation (DOI: 10042\/to-3646<\/a>) reveals that the optimized geometry exhibits six equal SC bonds, all 1.616\u00c5 long. Typically, a single SC bond is around 1.82\u00c5, a double 1.65\u00c5 and a triple is about 1.5\u00c5 at the same level of theory, so this C=S bond is clearly at least a double one. A NICS(0) calculation at the centroid has the value of -14.6 ppm, which indicates aromaticity. We conclude the appropriate arrow above is the bottom resonance one, rather than the top equilibrium one. This is confirmed by finding that the Kekul\u00e9 vibrational mode has a strongly positive force constant (\u03bd 1083 cm-1<\/sup>, animated in 3D model above), which contrasts with the negative value (\u03bd 284i<\/em> cm-1<\/sup>) found for bond shifting in F3<\/sub>S-C\u2261SF3<\/sub> itself. Again, comparison indicates that a C\u2261S triple bond has a frequency of around 1400 cm-1<\/sup> and a double around 1200 cm-1<\/sup> (the degenerate C=S non–<\/strong>Kekul\u00e9 vibrational mode for this system is indeed calculated at around 1225 cm-1<\/sup>). So to summarise; a single F3<\/sub>S-C\u2261SF3<\/sub> unit reveals very strong bond alternation, and negative force constant (transition state) for interconversion of the two bond forms, but a cyclic form reveals the opposite behaviour, with no alternation and instead strong aromaticity.<\/p>\n

In part this difference in behaviour must be due to the constraints on the geometry of the cyclic form. F3<\/sub>S-C\u2261SF3<\/sub> interconverts via a highly twisted geometry with C2<\/sub> symmetry, and this twisting is not exactly possible if you create a cyclic equivalent. In part it is also due to the aromatic stabilisation energies. In the resonance above, you should be able to count a total of 12 electrons involved! Nominally, if you try to apply the 4n+2 aromaticity rule, it does not fit, until you realise that in fact you must be dealing with two sets of 6 electrons. The system in fact is a classic double-aromatic, in which six electrons circulate in the plane of the molecule (the \u03c3-set) and six above and below (the \u03c0-set; the MOs for the molecule confirm exactly this interpretation). Notice how this itself contrasts with a similarly aromatic system, the atom swapping in three nitrosonium cations<\/a>, where the Kekul\u00e9 mode force constant was strongly negative.<\/p>\n

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ELF Analysis for F6S3C3. Click for 3D<\/p><\/div>To complete the analysis, the ELF basins (above) reveal the six SC regions to each contain 2.7 electrons, together with three carbon carbene monosynaptic basins. For comparison, a system with a high degree of SC triple character (HCS+<\/sup>) has around 3.8 in the SC region. Perhaps a better model is TfOSCH<\/a> (for which the carbon also has a carbene lone pair), which has 2.6e in the CS region. The carbene lone “pair” for the present molecule integrates to 2.6e each, which totals to a nice octet of electrons around each carbon and to around 7 for each S, confirming that whilst the S is hypervalent<\/strong>, its valence octet is not expanded!). This ELF picture does rather tend to confirm the original resonance structure representation shown at the top.<\/p>\n

All that is needed is is for someone to make this molecule to confirm its properties. Perhaps by trimerising F2<\/sub>SC, itself formed by cheletropic elimination? It is worth noting that the iso-electronic P\/N (e.g.<\/em> of S\/C) analogues are very well known.<\/p>\n

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Phosphonitrilic compounds<\/p><\/div>\n\n<\/div> ","protected":false},"excerpt":{"rendered":"

In the previous post, the molecule F3S-C\u2261SF3 was found to exhibit a valence bond isomerism, one of the S-C bonds being single, the other triple, and with a large barrier (~31 kcal\/mol, \u03bd 284i cm-1) to interconversion of the two valence-bond forms. So an interesting extension of this phenomenon is shown below: If the same […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[5,6],"tags":[41,1525,1526,1529,340],"class_list":["post-1423","post","type-post","status-publish","format-standard","hentry","category-hypervalency","category-interesting-chemistry","tag-aromaticity","tag-hypervalency","tag-interesting-chemistry","tag-pericyclic","tag-south-carolina"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/p1gPyz-mX","jetpack_likes_enabled":true,"_links":{"self":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/1423","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1423"}],"version-history":[{"count":0,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/1423\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1423"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1423"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1423"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}