{"id":21925,"date":"2020-03-11T13:22:51","date_gmt":"2020-03-11T13:22:51","guid":{"rendered":"https:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=21925"},"modified":"2020-03-11T13:44:14","modified_gmt":"2020-03-11T13:44:14","slug":"the-singlet-and-open-shell-higher-spin-states-of-4-6-and-8-annulenes-and-their-kekule-vibrational-modes","status":"publish","type":"post","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925","title":{"rendered":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes"},"content":{"rendered":"
\n

In 2001, Shaik and co-workers published the first of several famous review articles on the topic\u00a0A Different Story of \u03c0-Delocalization. The Distortivity of \u03c0-Electrons and Its Chemical Manifestations<\/i>[1]<\/a><\/span>. The main premise was that the delocalized \u03c0-electronic component of benzene is unstable toward a localizing distortion and is at the same time stabilized by resonance relative to a localized reference structure.\u00a0<\/i> Put more simply, the specific case of benzene has six-fold symmetry because of the twelve C-C \u03c3-electrons and not the six \u03c0-electrons. In 2009,\u00a0I commented here on this concept, via a calculation of the quintet state of benzene<\/a> in which two of the six \u03c0-electrons are excited from bonding into anti-bonding \u03c0-orbitals, thus reducing the total formal \u03c0-bond orders around the ring from three to one. I focused on a particular vibrational normal mode, which is usefully referred to as the Kekul\u00e9<\/em><\/strong> mode, since it lengthens three bonds in benzene whilst shortening the other three. In this case the stretching wavenumber increased by ~207 cm-1 when the total \u03c0-bond order of benzene was reduced from three to one by spin excitation. In other words, each C-C bond gets longer when the \u03c0-electrons are excited, but the C-C bond itself gets stronger (in terms at least of the Kekul\u00e9<\/em> mode).\u2020<\/sup>\u00a0This behaviour is called a violation of Badger’s rule[2]<\/a><\/span> for the relationship between the length of a bond and its stretching force constant.\u00a0<\/p>\n

This blog has come about because\u00a0I wanted to revisit my original calculations and complete them with a calculation for a\u00a0heptet<\/strong> state of benzene in which three \u03c0-electrons are promoted from bonding into anti-bonding \u03c0-orbitals, thus resulting in a total \u03c0-bond order of zero<\/strong>.\u00a0For completness, I here present the results not only for benzene but for some other small-annulene systems, both charged and neutral. These are all done at the coupled-cluster level of theory, both CCSD and CCSD(T), along with two basis set levels (see DOI: 10.14469\/hpc\/6624<\/a>\u00a0for the whole collection of calculations).\u2021<\/sup><\/p>\n

Before discussing the other systems, let your eye drop down the table below to the entries in red. These show the force constants for the singlet, quintet and heptet states of benzene vs<\/em> the optimized C-C bond length for each (at the same level of theory). These confirm the earlier result in revealing that the quintet state (total ring \u03c0-bond order 1) has a longer bond but a stronger force constant for the Kekul\u00e9<\/em> mode than the singlet state (total ring \u03c0-bond order 3). The heptet state now has a normal length C-C single bond (total ring \u03c0-bond order 0) but a Kekul\u00e9\u00a0<\/em>distorsion force constant higher than benzene itself!\u00a0<\/p>\n

Things now start to get more complicated. Firstly, for benzene itself, reducing the remaining \u03c0-bond order from 1 to 0 on exciting from quintet to heptet substantially reduces the force constant. So one might conclude that reducing an annulene total \u03c0-bond order does not always result in an increase in force constant. Badger’s rule is not always violated and the distortivity of \u03c0-electrons\u00a0<\/i>may not be a linear phenomenon.<\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
State<\/th>\nMethod<\/th>\n“Kekule”
\nMode, cm-1<\/sup><\/th>\n		FC,
\nmDyne\/\u00c5<\/th>\n		Reduced
\nmass, AMU<\/th>\n		Bond
\nlength, \u00c5<\/th>\n		\n

Data<\/p>\n

DOI<\/p>\n<\/th>\n<\/tr>\n

Cyclobutadiene, dication<\/th>\n<\/tr>\n
1<\/sup>A1g<\/sub><\/td>\nCCSD(T)\/Def2-TZVPP<\/td>\n1383a<\/sup><\/td>\n5.4102<\/td>\n6.5340<\/td>\n1.449<\/td>\n6920<\/a><\/th>\n<\/tr>\n
1329b<\/sup><\/td>\n8.0442<\/td>\n7.7338<\/td>\n<\/tr>\n
3<\/sup>B1g<\/sub><\/td>\nCCSD\/Def2-TZVPP<\/td>\n-2195a<\/sup><\/td>\n-33.0943<\/td>\n11.6515<\/td>\n1.589<\/td>\n6944<\/a><\/th>\n<\/tr>\n
-2211b<\/sup><\/td>\n-17.6740<\/td>\n6.1313<\/td>\n<\/tr>\n
3<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-TZVPP<\/td>\n-2171a<\/sup><\/td>\n-32.2296<\/td>\n11.6023<\/td>\n1.593<\/td>\n6933<\/a><\/th>\n<\/tr>\n
-2189b<\/sup><\/td>\n-16.0614<\/td>\n5.6844<\/td>\n<\/tr>\n
Cyclobutadiene<\/th>\n<\/tr>\n
3<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1422a<\/sup><\/td>\n7.7848<\/td>\n6.5340<\/td>\n1.444<\/td>\n6634<\/a><\/th>\n<\/tr>\n
1373b<\/sup><\/td>\n7.9700<\/td>\n7.1807<\/td>\n<\/tr>\n
CCSD(T)\/Def-SVP<\/td>\n1395<\/td>\n7.2647<\/td>\n6.3381<\/td>\n1.449<\/td>\n6643<\/a><\/th>\n<\/tr>\n
1345<\/td>\n7.6931<\/td>\n7.2202<\/td>\n<\/tr>\n
CCSD\/Def2-TZVPP<\/td>\n1392<\/td>\n6.9173<\/td>\n6.0600<\/td>\n1.438<\/td>\n6671<\/a><\/th>\n<\/tr>\n
1342<\/td>\n8.0252<\/td>\n7.5582<\/td>\n<\/tr>\n
CCSD(T)\/Def2-TZVPP<\/td>\n1360<\/td>\n7.2647<\/td>\n6.3381<\/td>\n1.449<\/td>\n6672<\/a><\/th>\n<\/tr>\n
1310<\/td>\n7.7044<\/td>\n7.6151<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
5<\/sup>B1g<\/td>\nCCSD\/Def2-SVP<\/td>\n1192<\/td>\n2.2102<\/td>\n2.6391<\/td>\n1.566<\/td>\n6635<\/a><\/th>\n<\/tr>\n
1088<\/td>\n4.9656<\/td>\n7.1153<\/td>\n<\/tr>\n
CCSD(T)\/Def-SVP<\/td>\n1176<\/td>\n2.0739<\/td>\n2.5452<\/td>\n1.569<\/td>\n6644<\/a><\/th>\n<\/tr>\n
1069<\/td>\n4.7829<\/td>\n7.0983<\/td>\n<\/tr>\n
CCSD\/Def-TZVPP<\/td>\n1177<\/td>\n1.8783<\/td>\n2.3023<\/td>\n1.563<\/td>\n6636<\/a><\/th>\n<\/tr>\n
1067<\/td>\n5.0294<\/td>\n7.5000<\/td>\n<\/tr>\n
CCSD(T)\/Def-TZVPP<\/td>\n1157<\/td>\n1.7555<\/td>\n2.2253<\/td>\n1.568<\/td>\n6678<\/a><\/th>\n<\/tr>\n
1045<\/td>\n4.8322<\/td>\n7.5073<\/td>\n<\/tr>\n
Cyclobutadiene Di-anion (isoelectronic with benzene)<\/th>\n<\/tr>\n
1<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1283<\/td>\n5.9023<\/td>\n6.0872<\/td>\n1.470<\/td>\n6652<\/a><\/th>\n<\/tr>\n
1233<\/td>\n6.3831<\/td>\n7.1172<\/td>\n<\/tr>\n
CCSD(T)\/Def2-SVP<\/td>\n1258<\/td>\n5.5888<\/td>\n5.9952<\/td>\n1.475<\/td>\n6653<\/a><\/th>\n<\/tr>\n
1209<\/td>\n6.1657<\/td>\n7.1565<\/td>\n<\/tr>\n
CCSD\/Def2-TZVPP<\/td>\n1216<\/td>\n4.3487<\/td>\n4.9883<\/td>\n1.467<\/td>\n6676<\/a><\/th>\n<\/tr>\n
1165<\/td>\n6.2282<\/td>\n7.7827<\/td>\n<\/tr>\n
CCSD(T)\/Def2-TZVPP<\/td>\n1187<\/td>\n4.1223<\/td>\n4.9621<\/td>\n1.473<\/td>\n6679<\/a><\/th>\n<\/tr>\n
1138<\/td>\n6.0103<\/td>\n7.8734<\/td>\n<\/tr>\n
Benzene<\/th>\n<\/tr>\n
1<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1337<\/td>\n4.9922<\/td>\n4.7425<\/td>\n1.401<\/span><\/strong><\/td>\n6623<\/a><\/th>\n<\/tr>\n
1308<\/td>\n10.7126<\/span><\/strong><\/td>\n10.6244<\/td>\n<\/tr>\n
CCSD(T)\/Def2-SVP<\/td>\n1359<\/td>\n6.9812<\/td>\n6.4190<\/td>\n1.405<\/td>\n6647<\/a><\/th>\n<\/tr>\n
1339<\/td>\n11.3860<\/td>\n10.7785<\/td>\n<\/tr>\n
CCSD\/Def2-TZVPP<\/td>\n1309<\/td>\n3.5714<\/td>\n3.5358<\/td>\n1.392<\/td>\n6646<\/a><\/th>\n<\/tr>\n
1273<\/td>\n10.1936<\/td>\n10.6709<\/td>\n<\/tr>\n
CCSD(T)\/Def2-TZVPP<\/td>\n1328<\/td>\n5.6130<\/td>\n5.4004<\/td>\n1.398<\/td>\n6710<\/a><\/th>\n<\/tr>\n
1306<\/td>\n10.9097<\/td>\n10.8588<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
5<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1600<\/td>\n17.4689<\/td>\n11.5855<\/td>\n1.463<\/strong><\/span><\/td>\n6626<\/a><\/th>\n<\/tr>\n
1597<\/td>\n17.4799<\/strong><\/span><\/td>\n11.6274<\/td>\n<\/tr>\n
CCSD\/Def2-TZVPP<\/td>\n1572<\/td>\n17.1041<\/td>\n11.7511<\/td>\n1.455<\/td>\n6669<\/a><\/th>\n<\/tr>\n
1571<\/td>\n17.1770<\/td>\n11.8198<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
7<\/sup>B1u<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1361<\/td>\n11.0797<\/td>\n10.1574<\/td>\n1.550<\/span><\/strong><\/td>\n6632<\/a><\/th>\n<\/tr>\n
1355<\/td>\n12.4274<\/strong><\/span><\/td>\n11.4839<\/td>\n<\/tr>\n
Cyclo-octatetraene Dication (isoelectronic with benzene)<\/th>\n<\/tr>\n
1<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1750<\/td>\n21.4531<\/td>\n11.8876<\/td>\n1.414<\/td>\n6648<\/a><\/th>\n<\/tr>\n
1750<\/td>\n21.5770<\/td>\n11.9620<\/td>\n<\/tr>\n
CCSD(T)\/Def2-SVP<\/td>\n1707<\/td>\n20.4695<\/td>\n11.9226<\/td>\n1.420<\/td>\n6673<\/a><\/th>\n<\/tr>\n
1707<\/td>\n20.5570<\/td>\n11.9773<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
5<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1702<\/td>\n20.4349<\/td>\n11.9684<\/td>\n1.444<\/td>\n6663<\/a><\/th>\n<\/tr>\n
1702<\/td>\n20.4690<\/td>\n11.9899<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
7<\/sup>B1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1460<\/td>\n14.8761<\/td>\n11.8407<\/td>\n1.511<\/td>\n6675<\/a><\/th>\n<\/tr>\n
1460<\/td>\n15.0578<\/td>\n11.9890<\/td>\n<\/tr>\n
Cyclo-octatetraene<\/th>\n<\/tr>\n
3<\/sup>B2g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1777<\/td>\n22.3143<\/td>\n11.9956<\/td>\n1.409<\/td>\n6637<\/a><\/th>\n<\/tr>\n
1777<\/td>\n22.3176<\/td>\n11.9976<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
7<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1637<\/td>\n18.9335<\/td>\n11.9851<\/td>\n1.484<\/td>\n6639<\/a><\/th>\n<\/tr>\n
1637<\/td>\n18.9464<\/td>\n11.9941<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
9<\/sup>B1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1441<\/td>\n14.6711<\/td>\n11.9988<\/td>\n1.553<\/td>\n6640<\/a><\/th>\n<\/tr>\n
1441<\/td>\n14.6723<\/td>\n11.9998<\/td>\n<\/tr>\n
CCSD(T)\/Def2-SVP<\/td>\n1421<\/td>\n13.4795<\/td>\n11.3256<\/td>\n1.555<\/td>\n6677<\/a><\/th>\n<\/tr>\n
\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Cyclo-octatetraene dianion<\/th>\n<\/tr>\n
1<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1731<\/td>\n21.1621<\/td>\n11.9903<\/td>\n1.419<\/td>\n6695<\/a><\/th>\n<\/tr>\n
1731<\/td>\n21.1668<\/td>\n11.9937<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
5<\/sup>A1g<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1642<\/td>\n19.0214<\/td>\n11.9711<\/td>\n1.461<\/td>\n6698<\/a><\/th>\n<\/tr>\n
1642<\/td>\n19.0408<\/td>\n11.9852<\/td>\n<\/tr>\n
\n
\n<\/td>\n<\/tr>\n
9<\/sup>B2u<\/sub><\/td>\nCCSD\/Def2-SVP<\/td>\n1517<\/td>\n16.0290<\/td>\n11.8174<\/td>\n1.528<\/td>\n6700<\/a><\/th>\n<\/tr>\n
1517<\/td>\n16.1516<\/td>\n11.9186<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

a<\/sup>Unprojected, with possible Dushinsky coupling b<\/sup>Projected from Dushinksky coupling. In all cases, the excited states show -ve force constants for out of plane deformations, but the in-plane Kekule modes are all +ve except for the first entry.<\/small><\/p>\n

I will now make some short comments about the other ring systems reported above.<\/p>\n

\n
    \n
  1. Cyclobutadiene, dication<\/strong>. The Kekul\u00e9 mode is very similar to benzene, but based clearly on just two \u03c0-electrons rather than six. There are two ways of forming a triplet state by exciting one of the two \u03c0-electrons to give a total \u03c0-bond order of zero. Both give a C-C distance a little longer than that typical of cyclobutanes (1.56\u00c5). These triplet states however are not equilibrium species but transition states for the dissociation into two molecules of acetylene radical cation, a reaction driven no doubt by the large coulomb repulsions found for a di-cation.<\/li>\n
  2. Cyclobutadiene<\/strong>. The singlet ground state has Jahn-Teller effects (which by the way are absent from all the other excited states reported here), but the triplet state again has a Kekul\u00e9 mode is very similar to benzene. Removing all the \u03c0-bond orders in the quintet reduces the Kekul\u00e9 force constant. This is in contrast to benzene itself.<\/li>\n
  3. Cyclobutadiene, di-anion<\/strong>. Only the singlet state was calculable (the excited states did not converge), and now the Kekul\u00e9 force constant is distinctly lower than benzene, probably again due to coulombic repulsions of the di-anion coupled with greater Pauli repulsions of the additional electrons. One other vibrational mode is worth showing here, the Eu<\/sub> mode (\u03bd 1267 cm-1<\/sup>) which shows interesting charge localisation into a carbon-centred anion and a delocalised allylic anion.\"\"<\/a><\/li>\n
  4. Cyclo-octatetraene Dication<\/strong>. Although isoelectronic with benzene, it shows very different behaviour. As the spin-multiplicity increases, so the Kekul\u00e9 force constant decreases and the bond length increases, in accordance with Badger's rule. Again, another vibration (E3u<\/sub>, \u03bd 1544 cm-1<\/sup>) shows charge localisation to give a 1,4-separated di-cation.\"\"<\/a><\/li>\n
  5. Cyclo-octatetraene<\/strong>. The triplet has a total ring \u03c0-bond order 3 (with two electrons in non-bonded orbitals) and a C-C bond length similar to benzene itself. The nonet state total ring \u03c0-bond order is reduced to 0, with a C-C length again identical to a single bond. As with the di-cation, the force constant is reduced as the bond length increases, in accordance with Badger's rule.<\/li>\n
  6. Cyclo-octatetraene di-anion<\/strong> is similar to the neutral system in following Badger's rule.<\/li>\n<\/ol>\n

    I do need to insert some caveats here. The original hypothesis[1]<\/a><\/span> of distortive\u00a0\u03c0-electrons was based on the singlet states (both ground and excited) and the results reported here are based on higher spin states, the assumption being that these are well-described by single reference states or configurations. It may well be that these higher spin states need more complex multi-reference determinants to describe them properly, in which case the coupled-cluster calculations reported here would be inappropriate. Thus for the larger rings, some of the CC calculations either failed to converge for large basis sets or gave some unphysical force constants (i.e. huge). This does tend to suggest that the internal MP expansion performed for coupled-cluster calculations is failing to converge, a well known propensity for systems where a multi-reference determinant is needed.<\/p>\n

    So one should not conclude too firmly that only benzene itself (in this series; there are many other examples to be found in [1]<\/a><\/span>) exhibits Badger’s rule violations. Nonetheless, it would be valuable in the future to know whether the concept of distortivity of \u03c0-electrons can be applied to the small ring annulenes where the \u03c0-bond orders have been progressively reduced down to zero by specifying higher-spin \u03c0-states.<\/p>\n

    \n

    \u2020<\/sup>In 2014, I looked at some of the historical origins<\/a> of this attribution to Kekul\u00e9, and you might also want to read the fascinating discussion by others on this topic.\u2021<\/sup>I thank Sason Shaik for his comments on the above results!<\/p>\n

    References<\/h2>\n
    1. S. Shaik, A. Shurki, D. Danovich, and P.C. Hiberty, \"A Different Story of \u03c0-DelocalizationThe Distortivity of \u03c0-Electrons and Its Chemical Manifestations\", Chemical Reviews<\/i>, vol. 101, pp. 1501-1540, 2001. https:\/\/doi.org\/10.1021\/cr990363l<\/a>\n\n<\/li>\n
    2. R.M. Badger, \"A Relation Between Internuclear Distances and Bond Force Constants\", The Journal of Chemical Physics<\/i>, vol. 2, pp. 128-131, 1934. https:\/\/doi.org\/10.1063\/1.1749433<\/a>\n\n<\/li>\n<\/ol>\n\n<\/div> ","protected":false},"excerpt":{"rendered":"

      In 2001, Shaik and co-workers published the first of several famous review articles on the topic\u00a0A Different Story of \u03c0-Delocalization. The Distortivity of \u03c0-Electrons and Its Chemical Manifestations. The main premise was that the delocalized \u03c0-electronic component of benzene is unstable toward a localizing distortion and is at the same time stabilized by resonance relative […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"activitypub_content_warning":"","activitypub_content_visibility":"","activitypub_max_image_attachments":5,"activitypub_interaction_policy_quote":"anyone","activitypub_status":"","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},"jetpack_post_was_ever_published":false},"categories":[4],"tags":[],"ppma_author":[2661],"class_list":["post-21925","post","type-post","status-publish","format-standard","hentry","category-interesting-chemistry"],"yoast_head":"\nThe singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes - Henry Rzepa's Blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes - Henry Rzepa's Blog\" \/>\n<meta property=\"og:description\" content=\"In 2001, Shaik and co-workers published the first of several famous review articles on the topic\u00a0A Different Story of \u03c0-Delocalization. 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The main premise was that the delocalized \u03c0-electronic component of benzene is unstable toward a localizing distortion and is at the same time stabilized by resonance relative […]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925\" \/>\n<meta property=\"og:site_name\" content=\"Henry Rzepa's Blog\" \/>\n<meta property=\"article:published_time\" content=\"2020-03-11T13:22:51+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2020-03-11T13:44:14+00:00\" \/>\n<meta name=\"author\" content=\"Henry Rzepa\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Henry Rzepa\" \/>\n\t<meta name=\"twitter:label2\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"7 minutes\" \/>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes - Henry Rzepa's Blog","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925","og_locale":"en_GB","og_type":"article","og_title":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes - Henry Rzepa's Blog","og_description":"In 2001, Shaik and co-workers published the first of several famous review articles on the topic\u00a0A Different Story of \u03c0-Delocalization. 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The main premise was that the delocalized \u03c0-electronic component of benzene is unstable toward a localizing distortion and is at the same time stabilized by resonance relative […]","og_url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925","og_site_name":"Henry Rzepa's Blog","article_published_time":"2020-03-11T13:22:51+00:00","article_modified_time":"2020-03-11T13:44:14+00:00","author":"Henry Rzepa","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Henry Rzepa","Estimated reading time":"7 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925#article","isPartOf":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925"},"author":{"name":"Henry Rzepa","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#\/schema\/person\/2b40f7b9c872a4dc1547e040a11b6281"},"headline":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes","datePublished":"2020-03-11T13:22:51+00:00","dateModified":"2020-03-11T13:44:14+00:00","mainEntityOfPage":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925"},"wordCount":1354,"commentCount":0,"articleSection":["Interesting chemistry"],"inLanguage":"en-GB","potentialAction":[{"@type":"CommentAction","name":"Comment","target":["https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925#respond"]}]},{"@type":"WebPage","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925","url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925","name":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes - Henry Rzepa's Blog","isPartOf":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#website"},"datePublished":"2020-03-11T13:22:51+00:00","dateModified":"2020-03-11T13:44:14+00:00","author":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#\/schema\/person\/2b40f7b9c872a4dc1547e040a11b6281"},"breadcrumb":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925#breadcrumb"},"inLanguage":"en-GB","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=21925#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog"},{"@type":"ListItem","position":2,"name":"The singlet and open shell higher-spin states of [4], [6] and [8]-annulenes and their Kekul\u00e9 vibrational modes"}]},{"@type":"WebSite","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#website","url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/","name":"Henry Rzepa's Blog","description":"Chemistry with a twist","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-GB"},{"@type":"Person","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#\/schema\/person\/2b40f7b9c872a4dc1547e040a11b6281","name":"Henry Rzepa","image":{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/secure.gravatar.com\/avatar\/897b6740f7f599bca7942cdf7d7914af5988937ae0e3869ab09aebb87f26a731?s=96&d=blank&r=g370be3a7397865e4fd161aefeb0a5a85","url":"https:\/\/secure.gravatar.com\/avatar\/897b6740f7f599bca7942cdf7d7914af5988937ae0e3869ab09aebb87f26a731?s=96&d=blank&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/897b6740f7f599bca7942cdf7d7914af5988937ae0e3869ab09aebb87f26a731?s=96&d=blank&r=g","caption":"Henry Rzepa"},"description":"Henry Rzepa is Emeritus Professor of Computational Chemistry at Imperial College London.","sameAs":["https:\/\/orcid.org\/0000-0002-8635-8390"],"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?author=1"}]}},"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/pDef7-5HD","jetpack-related-posts":[{"id":485,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=485","url_meta":{"origin":21925,"position":0},"title":"Longer is stronger.","author":"Henry Rzepa","date":"June 6, 2009","format":false,"excerpt":"The iconic diagram below represents a cornerstone of organic chemistry. Generations of chemists have learnt early on in their studies of the subject that these two representations of where the electron pairs in benzene might be located (formally called electronic resonance or valence bond forms) each contribute ~50% to the\u2026","rel":"","context":"In "Interesting chemistry"","block_context":{"text":"Interesting chemistry","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=4"},"img":{"alt_text":"The Kekule structures of benzene.","src":"https:\/\/i0.wp.com\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2009\/06\/benzene.jpg?resize=350%2C200","width":350,"height":200},"classes":[]},{"id":12329,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=12329","url_meta":{"origin":21925,"position":1},"title":"More (blog) connections spotted. Something new about diphenyl magnesium?","author":"Henry Rzepa","date":"April 17, 2014","format":false,"excerpt":"I have just noticed unexpected links between two old posts, one about benzene, one about diphenyl magnesium\u00a0and\u00a0a link to August Kekul\u00e9.\u2020 The post about benzene dealt with the apparently simple issue of why all the C-C bonds are of equal length. The answer, in brief is purely because of the\u2026","rel":"","context":"In "Interesting chemistry"","block_context":{"text":"Interesting chemistry","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=4"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":1903,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=1903","url_meta":{"origin":21925,"position":2},"title":"Carbobenzene: benzene with a difference","author":"Henry Rzepa","date":"April 16, 2010","format":false,"excerpt":"Some molecules, when you first see them, just intrigue. So it was with carbobenzene, the synthesis of a derivative of which was recently achieved by Remi Chauvin and co-workers. Two additional carbon atoms have been inserted into each of the six C-C bonds in benzene. The structure shows two resonance\u2026","rel":"","context":"In "General"","block_context":{"text":"General","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=1"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/04\/carbobenzene.jpg?resize=350%2C200","width":350,"height":200},"classes":[]},{"id":12583,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=12583","url_meta":{"origin":21925,"position":3},"title":"Kekul\u00e9’s vibration: A modern example of its use.","author":"Henry Rzepa","date":"June 6, 2014","format":false,"excerpt":"Following the discussion here of Kekul\u00e9's suggestion of what we now call a vibrational mode (and which in fact now bears his name), I thought I might apply the concept to a recent molecule known as [2.2]paracyclophane. The idea was sparked by Steve Bachrach's latest post, where the \"zero-point\" structure\u2026","rel":"","context":"In "Historical"","block_context":{"text":"Historical","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=565"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":22996,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=22996","url_meta":{"origin":21925,"position":4},"title":"An interesting aromatic molecule found in Titan’s atmosphere: Cyclopropenylidene","author":"Henry Rzepa","date":"November 7, 2020","format":false,"excerpt":"Cyclopropenylidene must be the smallest molecule to be aromatic due to \u03c0-electrons, with just three carbon atoms and two hydrogen atoms. It has now been detected in the atmosphere of Titan, one of Saturn's moons and joins benzene, another aromatic molecule together with the protonated version of cyclopropenylidene, C3H3+ also\u2026","rel":"","context":"In "Interesting chemistry"","block_context":{"text":"Interesting chemistry","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=4"},"img":{"alt_text":"","src":"","width":0,"height":0},"classes":[]},{"id":2046,"url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2046","url_meta":{"origin":21925,"position":5},"title":"Chemistry with a super-twist: A molecular trefoil knot, part 1.","author":"Henry Rzepa","date":"May 31, 2010","format":false,"excerpt":"Something important happened in chemistry for the first time about 100 years ago. A molecule was built (nowadays we would say synthesized) specifically for the purpose of investigating a theory. It was cyclo-octatetraene or (CH)8, and it was made by Willst\u00e4tter and Waser to try to find out if benzene,\u2026","rel":"","context":"In "Interesting chemistry"","block_context":{"text":"Interesting chemistry","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?cat=4"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/05\/metallatrefoil.jpg?resize=350%2C200","width":350,"height":200},"classes":[]}],"jetpack_likes_enabled":false,"authors":[{"term_id":2661,"user_id":1,"is_guest":0,"slug":"admin","display_name":"Henry Rzepa","avatar_url":"https:\/\/secure.gravatar.com\/avatar\/897b6740f7f599bca7942cdf7d7914af5988937ae0e3869ab09aebb87f26a731?s=96&d=blank&r=g","author_category":"1","first_name":"Henry","last_name":"Rzepa","user_url":"https:\/\/orcid.org\/0000-0002-8635-8390","job_title":"","description":"Henry Rzepa is Emeritus Professor of Computational Chemistry at Imperial College London."}],"_links":{"self":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts\/21925","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=21925"}],"version-history":[{"count":24,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts\/21925\/revisions"}],"predecessor-version":[{"id":21959,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts\/21925\/revisions\/21959"}],"wp:attachment":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=21925"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=21925"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=21925"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fppma_author&post=21925"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}