{"id":15894,"date":"2016-02-21T19:23:29","date_gmt":"2016-02-21T19:23:29","guid":{"rendered":"http:\/\/www.ch.imperial.ac.uk\/rzepa\/blog\/?p=15823"},"modified":"2016-02-21T19:23:29","modified_gmt":"2016-02-21T19:23:29","slug":"real-hypervalency-in-a-small-molecule","status":"publish","type":"post","link":"https:\/\/www.rzepa.net\/blog\/?p=15894","title":{"rendered":"Real hypervalency in a small molecule."},"content":{"rendered":"
\n

\n\tHypervalency<\/a> is defined as a molecule that contains one or more main group elements formally bearing more than eight  electrons in their  valence shell. One example of a molecule so characterised was CLi6<\/sub>[1]<\/a><\/span> where the description "“carbon can expand its octet of electrons to form this relatively stable molecule<\/em>“ was used. Yet, in this latter case, the octet expansion is in fact an illusion,<\/a> as indeed are many examples that are cited. The octet shell remains resolutely un-expanded. Here I will explore the tiny molecule CH3<\/sub>F2-<\/sup> where two extra electrons have been added to fluoromethane.\n<\/p>\n

\n\tTwo such electrons added to e.g.<\/em> such a methane derivative can be in principle accommodated in two ways:\n<\/p>\n

    \n
  1. \n\t\tThe electrons on carbon could expand the octet shell by populating molecular orbitals constructed using 3s or 3p atomic orbitals (AOs) as well as the normal 2s and 2p shells. This is also the normal "explanation" for expanded octets, the assumption being that as one moves down the rows of the periodic table (e.g. P, S, Cl, etc) these shells become energetically more accessible (e.g. <\/em>the 3d or 4s shell for P, S, Cl etc). In fact, for e.g.<\/em> PF5<\/sub>, the occupancy of such  "Rydberg<\/a>" shells is only ~0.2 electrons, not a significant octet expansion.\n\t<\/li>\n
  2. \n\t\tThe electrons can instead or as well as populate the antibonding molecular orbitals (MOs) formed from just the 2s\/2p AOs. For a methane derivative, there are four bonding MOs (into which the octet of electrons are placed) and four anti-bonding MOs all constructed from the total of eight AOs. Well known examples of populating antibonding MOs are the series N≡N, O=O (singlet), F-F, Ne…Ne where the additional electrons are added to anti-bonding MOs and have the effect of reducing the bond orders from 3 to 2 to 1 to 0. And of course all core shells contain populated bonding and antibonding pairs.\n\t<\/li>\n<\/ol>\n

    \n\tHere are some ωB97XD\/Def2-TZVPPD\/scrf=water calculations. All these species are molecules with all-real vibrations, being stable toward dissociation to e.g. <\/em>CH3<\/sub>–<\/sup> + H–<\/sup> or CH3<\/sub>–<\/sup> + F–<\/sup>.  A transition state for this latter dissocation with IRC[2]<\/a><\/span> can be characterised. In all cases the energy of the highest occupied MO or NBO is -ve, meaning that the electrons are bound, at least in part due to the solvent field applied.\n<\/p>\n\n\n\n\n\n\n\n
    \n\t\t\t\tMolecule\n\t\t\t<\/th>\n\n\t\t\t\tWiberg CH order\n\t\t\t<\/th>\n\n\t\t\t\tWiberg CF order\n\t\t\t<\/th>\n\n\t\t\t\tNatural Populations\n\t\t\t<\/th>\n\n\t\t\t\tE HONBO, au\n\t\t\t<\/th>\n\n\t\t\t\tdataDOI\n\t\t\t<\/th>\n<\/tr>\n
    \n\t\t\t\tCH4<\/sub>2-<\/sup>\n\t\t\t<\/td>\n\n\t\t\t\t0.773\n\t\t\t<\/td>\n\n\t\t\t\t–\n\t\t\t<\/td>\n\n

    \n\t\t\t\t\tC:[core]2S(1.98)2p(3.82)3S( 0.15)4d( 0.01)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tH:1S( 1.00)\n\t\t\t\t<\/p>\n<\/td>\n

    		\n\t\t\t\t-0.144\"CH4\"\n\t\t\t<\/td>\n\n\t\t\t\t[3]<\/a><\/span>\n\t\t\t<\/td>\n<\/tr>\n
    \n\t\t\t\tCH3<\/sub>F2-<\/sup>\n\t\t\t<\/td>\n\n\t\t\t\t0.980\n\t\t\t<\/td>\n\n\t\t\t\t1.213\n\t\t\t<\/td>\n\n

    \n\t\t\t\t\tC:[core]2S(1.05)2p( 3.20)3S(1.26)4p( 0.01)4d( 0.01)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tH:1S( 0.84)2S( 0.01)2p( 0.02)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tF:[core]2S(1.88)2p( 5.61)3S( 0.30)3p( 0.04)3d( 0.01)4p( 0.01)\n\t\t\t\t<\/p>\n<\/td>\n

    		\n\t\t\t\t-0.068
    \"Click

    Click for 3D<\/p><\/div>\n\t\t\t<\/td>\n

    		\n\t\t\t\t[4]<\/a><\/span>\n\t\t\t<\/td>\n<\/tr>\n
    \n\t\t\t\tCH2<\/sub>F<\/font>2<\/sub>2-<\/sup>\n\t\t\t<\/td>\n\n\t\t\t\t0.871\n\t\t\t<\/td>\n\n\t\t\t\t0.897\n\t\t\t<\/td>\n\n

    \n\t\t\t\t\tC:[core]2S(1.60)2p( 2.64)3S(0.39)3p( 0.01)4d( 0.01)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tH:1S(1.19)2S( 0.06)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tF:[core]2S(1.86)2p( 5.52)3S( 0.01)3p( 0.01)4p( 0.01)\n\t\t\t\t<\/p>\n<\/td>\n

    		\n\t\t\t\t-0.281
    \"Click

    Click for 3D<\/p><\/div>\n\t\t\t<\/td>\n

    		\n\t\t\t\t[5]<\/a><\/span>\n\t\t\t<\/td>\n<\/tr>\n
    \n\t\t\t\tCF4<\/sub>2-<\/sup>\n\t\t\t<\/td>\n\n\t\t\t\t–\n\t\t\t<\/td>\n\n\t\t\t\t0.801\n\t\t\t<\/td>\n\n

    \n\t\t\t\t\tC:[core]2S(1.94)2p( 1.96)3S( 0.19)3p( 0.04)5d( 0.01)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\tF:[core]2S(1.89)2p( 5.54)3p( 0.01)3d( 0.02)\n\t\t\t\t<\/p>\n

    \n\t\t\t\t\t \n\t\t\t\t<\/p>\n<\/td>\n

    		\n\t\t\t\t-0.148\"CF4\"\n\t\t\t<\/td>\n\n\t\t\t\t[6]<\/a><\/span>\n\t\t\t<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
      \n
    1. \n\t\tCH4<\/sub>2- <\/sup>shows only small Rydberg occupancy (< 0.2e), but a significantly reduced bond order for the four C-H bonds (each C-H bonding NBO also has some antibonding character for the other three CHs) and hence the molecule is not truly hypervalent.\n\t<\/li>\n
    2. \n\t\tCH3<\/sub>F2-<\/sup> in contrast shows quite different behavour. The C-H bond order is almost 1 and the C-F bond order is actually >1. Of the two extra electrons, ~1.28 now occupy carbon Rydberg AOs and the fluorine also has significant Rydberg population (~0.36e). So this is a real hypervalent system, in which the total valencies exceed that expected from an octet.\n\t<\/li>\n
    3. \n\t\tCH2<\/sub>F<\/font>2<\/sub>2-<\/sup> is somewhere inbetween the previous two systems. The carbon has modest Rydberg occupancy (~0.4e) but there is also significant occupation of the antibonding MOs. Both the C-H and C-F bond orders are <1.\n\t<\/li>\n
    4. \n\t\tCF4<\/sub>2-<\/sup> shows a further reduction in the C Rydberg occpancy (<0.2) and the C-F bond order is also reduced. This reduction in bond order is also seen in other so-called hypervalent systems such as PF5<\/sub>.\n\t<\/li>\n<\/ol>\n

      \n\tSo of these systems, CH3<\/sub>F2-<\/sup> can be reasonably called hypervalent, whilst the others have much less such character. It does appear that there is a fine balance between placing extra electrons into Rydberg orbitals to expand the "octet" and hence valencies, and placing them in anti-bonding orbitals where the individual valencies are actually reduced. It seems that substituting methane with just one fluorine encourages population of the Rydberg orbitals, but that more fluorines encourage instead population of the antibonding orbitals. What is remarkable is that CH3<\/sub>F2-<\/sup> actually has a (small) barrier to dissociation. The challenge now is to try to design a system which has a significant Rydberg population, a low antibonding population AND is stable to dissociation; this will require some inspiration. So do not hold your breaths!\n<\/p>\n

      \n\t \n<\/div>\n

      References<\/h2>\n
      1. H. Kudo, \"Observation of hypervalent CLi6 by Knudsen-effusion mass spectrometry\", Nature<\/i>, vol. 355, pp. 432-434, 1992. https:\/\/doi.org\/10.1038\/355432a0<\/a>\n\n<\/li>\n
      2. https:\/\/doi.org\/<\/a>\n\n<\/li>\n
      3. H.S. Rzepa, \"C 1 H 4 -2\", 2016. https:\/\/doi.org\/10.14469\/ch\/191837<\/a>\n\n<\/li>\n
      4. H.S. Rzepa, \"C 1 H 3 F 1 -2\", 2016. https:\/\/doi.org\/10.14469\/ch\/191919<\/a>\n\n<\/li>\n
      5. H.S. Rzepa, \"C 1 H 2 F 2 -2\", 2016. https:\/\/doi.org\/10.14469\/ch\/191918<\/a>\n\n<\/li>\n
      6. H.S. Rzepa, \"C 1 F 4 -2\", 2016. https:\/\/doi.org\/10.14469\/ch\/191916<\/a>\n\n<\/li>\n<\/ol>\n\n<\/div> ","protected":false},"excerpt":{"rendered":"

        Hypervalency is defined as a molecule that contains one or more main group elements formally bearing more than eight  electrons in their  valence shell. One example of a molecule so characterised was CLi6 where the description "“carbon can expand its octet of electrons to form this relatively stable molecule“ was used. Yet, in this latter case, […]<\/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":[2246,5],"tags":[1687,1689,1691,510,1425,147,1719,1720,1483,1729,1641,1736,1646],"class_list":["post-15894","post","type-post","status-publish","format-standard","hentry","category-bond-slam","category-hypervalency","tag-antibonding-molecular-orbital","tag-atomic-orbital","tag-block","tag-chemical-bonding","tag-covalent-bond","tag-energy","tag-hypervalent-molecule","tag-hypervalent-systems","tag-molecular-orbital","tag-molecular-orbital-diagram","tag-octet-rule","tag-periodic-table","tag-valence"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/p1gPyz-48m","jetpack_likes_enabled":true,"_links":{"self":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/15894","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=15894"}],"version-history":[{"count":0,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=\/wp\/v2\/posts\/15894\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=15894"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=15894"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.rzepa.net\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=15894"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}