{"id":2599,"date":"2010-10-16T12:10:21","date_gmt":"2010-10-16T11:10:21","guid":{"rendered":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599"},"modified":"2010-10-18T14:40:19","modified_gmt":"2010-10-18T13:40:19","slug":"hypervalency-is-it-real","status":"publish","type":"post","link":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599","title":{"rendered":"Hypervalency: Is it real?"},"content":{"rendered":"<div class=\"kcite-section\" kcite-section-id=\"2599\">\n<p>The Wikipedia page on <a href=\"http:\/\/en.wikipedia.org\/wiki\/Hypervalent_molecule\" target=\"_blank\">hypervalent compounds<\/a> reveals that the concept is almost as old as that of normally valent compounds. The definition there, \u00a0is &#8220;a molecule that contains one or more\u00a0<a title=\"Main group element\" href=\"http:\/\/en.wikipedia.org\/wiki\/Main_group_element\">main group elements<\/a> formally bearing more than eight\u00a0<a title=\"Electron\" href=\"http:\/\/en.wikipedia.org\/wiki\/Electron\">electrons<\/a> in their\u00a0<a title=\"Valence shell\" href=\"http:\/\/en.wikipedia.org\/wiki\/Valence_shell\">valence shells<\/a>&#8221; (although it could equally apply to e.g. transition elements that would contain e.g. more than 18 electrons in their valence shell). The most extreme example would perhaps be of iodine (or perhaps xenon). The normal valency of iodine is one (to formally complete the octet in the valence shell) but of course compounds such as IF<sub>7<\/sub> imply the valency might reach 7 (and by implication that the octet of electrons expands to 14). So what of IF<sub>7<\/sub>? Well, there is a problem due to the high electronegativity of the fluorine. One could argue that the bonds in this molecule are ionic, and hence that the valence electrons really reside in lone pairs on the F. Thus the apparently hypervalent PF<sub>5<\/sub> could be written PF<sub>4<\/sub><sup>+<\/sup>&#8230;F<sup>&#8211;<\/sup>, in which case the P is not really hypervalent after all. We need a compound with un-arguably covalent bonds. Well, what about IH<sub>7<\/sub>? One might probably still argue about ionicity (for example H<sup>+<\/sup>&#8230;IH<sub>6<\/sub><sup>&#8211;<\/sup>) but that puts electrons on I and not H, and hence does not change any hypervalency on the iodine. Surely, if hypervalency is a real phenomenon, it should manifest in IH<sub>7<\/sub>?<\/p>\n<p><div id=\"attachment_2601\" style=\"width: 227px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2601\" class=\"size-full wp-image-2601\" title=\"IH7\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('yellow');jmolApplet([600,600],'load wp-content\/uploads\/2010\/10\/IH7.log;frame 14;set measurementUnits Angstroms;delay 5;vectors on;vectors 4;vectors scale 5.0; color vectors purple; vibration 15;animation mode loop;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg\" alt=\"\" width=\"217\" height=\"238\" \/><p id=\"caption-attachment-2601\" class=\"wp-caption-text\">IH7. A true hypervalent molecule? Click for 3D<\/p><\/div>A reasonably high level calculation (B3LYP\/Def2-TZVPP with pseudopotential on I to absorb relativistic effects) <a href=\"http:\/\/hdl.handle.net\/10042\/to-5221\" target=\"_blank\">shows<\/a> the molecule to be a minimum, with D<sub>5h<\/sub> symmetry. An NBO analysis shows 46 core (i.e. non-valence) electrons. These arise from a Kr core (=36) plus a filled iodine 5d shell of 10 electrons. So, only the 5s\/5p orbitals can be used for valence bonding. The total minimal basis which one can construct valence molecular orbitals from is thus I 5s, 5p and H 1s, a total of eleven AOs, into which 14 electrons must pair up into 7 doubly-occupied molecular orbitals. Now, the real issue is whether this occupancy corresponds to seven I-H covalent single bonds, each with a two-electron Lewis pair. If so, the molecule is hypervalent! The occupied MOs are shown below.<\/p>\n<table border=\"0\">\n<tbody>\n<tr>\n<td>\n<p><div id=\"attachment_2604\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2604\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo16_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-16.jpg\" alt=\"\" width=\"150\" height=\"147\" \/><p id=\"caption-attachment-2604\" class=\"wp-caption-text\">MO 16 (E2&#39;). Click for 3D<\/p><\/div><\/td>\n<td>\n<p><div id=\"attachment_2605\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2605\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo15_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-15.jpg\" alt=\"\" width=\"150\" height=\"143\" \/><p id=\"caption-attachment-2605\" class=\"wp-caption-text\">MO 15 (E2&#39;)<\/p><\/div><\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<p><div id=\"attachment_2606\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2606\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo14_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-14.jpg\" alt=\"\" width=\"150\" height=\"122\" \/><p id=\"caption-attachment-2606\" class=\"wp-caption-text\">MO 14 (A1&#39;)<\/p><\/div><\/td>\n<\/tr>\n<tr>\n<td>\n<p><div id=\"attachment_2607\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2607\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo13_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-13.jpg\" alt=\"\" width=\"150\" height=\"174\" \/><p id=\"caption-attachment-2607\" class=\"wp-caption-text\">MO 13 (E1&#39;)<\/p><\/div><\/td>\n<td>\n<p><div id=\"attachment_2608\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2608\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo12_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-12.jpg\" alt=\"\" width=\"150\" height=\"138\" \/><p id=\"caption-attachment-2608\" class=\"wp-caption-text\">MO 12 (E1&#39;)<\/p><\/div><\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<p><div id=\"attachment_2609\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2609\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo11_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-11.jpg\" alt=\"\" width=\"150\" height=\"109\" \/><p id=\"caption-attachment-2609\" class=\"wp-caption-text\">MO 11 (A2&#39;&#39;)<\/p><\/div><\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<p><div id=\"attachment_2610\" style=\"width: 160px\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-2610\" class=\"size-full wp-image-2604\" title=\"I-16\" onclick=\"jmolInitialize('..\/Jmol\/');jmolSetAppletColor('white');jmolApplet([450,450],'load wp-content\/uploads\/2010\/10\/IH7_mo10_0.02.jvxl;isosurface &quot;&quot; translucent;zoom 100;spin 3;');\" src=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/I-10.jpg\" alt=\"\" width=\"150\" height=\"145\" \/><p id=\"caption-attachment-2610\" class=\"wp-caption-text\">MO 10 (A1&#39;)<\/p><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>One notices that whilst orbitals 10-14 are clearly bonding in the I-H region, orbitals 15-16 seem antibonding in that region (there is a node along the I-H bond). We are seeing much the same phenomenon that occurs when the bond order of 3 in N<sub>2<\/sub> is reduced to 1 in F<sub>2<\/sub> due to occupancy of anti-bonding orbitals. Can this be quantified? NBO (5.9) analysis reveals the following.<\/p>\n<ol>\n<li>The effective (pseudopotential) core has 28 electrons, and the outer core 18. The valence orbitals contain 13.79, and only 0.21 electrons are Rydberg (higher shell). So little occupancy of e.g. 6s\/6p then!<\/li>\n<li> The Wiberg bond index indicates each H has a total bond order of very close to 1 (its natural valence state), whilst I is 3.45.  Remember that the maximum total bond index of a covalently bound atom using a pure octet of valence electrons is 4 (8\/2, think carbon). The iodine is NOT hypervalent!<\/li>\n<li>So why, if its not hypervalent, is it so strongly hypercoordinate? Well, there are 14 valence electrons, but they do NOT all occupy the I-H regions, which have bond orders between 0.46 (equatorial) or 0.57 (axial). The only other place they can be is in the H-H regions! Consider the bond order values between say hydrogen <strong>2<\/strong> to the four other equatorial atoms <strong>4,5,7,8<\/strong>. They are respectively 0.05, 0.15, 0.05, 0.15. So each hydrogen has a total bond order of 1, but only slightly more than half of this comes from the I-H, the rest comes from H-H. To put it another (approximate) way, of the 14 valence electrons, ~8 might be considered to be associated with I-H bonds, and ~6 with H-H bonds.  The hypervalency has been in effect absorbed into the H-H regions. This means no atom in this molecule is at all hypervalent.<\/li>\n<li>Well, if the iodine is not hypervalent, and some of its valence electrons occupy I-H anti-bonding orbitals, why is it stable at all (in the sense that all the vibrations are real, and it&#8217;s clearly a minimum in the potential energy surface). Here, I merely speculate. Iodine has a large core charge, and hence the inner core electrons are starting to exhibit relativistic contractions. This effect stabilizes the outer 5s\/5p electrons, and so occupancy of \u00a0anti-bonding MOs generated from such AOs is not so unfavourable as one might expect. Perhaps, the \u00a0hypercoordination shown by \u00a0IH<sub>7<\/sub> is after all a relativistic effect rather than a hypervalent effect? \u00a0In which case, what will \u00a0AsH<sub>7<\/sub> show?<\/li>\n<\/ol>\n<p>So, what might have been an archetypal covalent hypervalent molecule is no such! IH<sub>7<\/sub> shows entirely normal valencies, one for H and the iodine does not even reach four (if anything, its sub-valent rather than hypervalent). One may be entitled to ask if ANY main group element exhibits hypervalency!<\/p>\n<!-- kcite active, but no citations found -->\n<\/div> <!-- kcite-section 2599 -->","protected":false},"excerpt":{"rendered":"<p>The Wikipedia page on hypervalent compounds reveals that the concept is almost as old as that of normally valent compounds. The definition there, \u00a0is &#8220;a molecule that contains one or more\u00a0main group elements formally bearing more than eight\u00a0electrons in their\u00a0valence shells&#8221; (although it could equally apply to e.g. transition elements that would contain e.g. more [&hellip;]<\/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,"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":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7],"tags":[2649,74,142],"ppma_author":[2661],"class_list":["post-2599","post","type-post","status-publish","format-standard","hentry","category-hypervalency","tag-hypervalency","tag-pence","tag-potential-energy-surface"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Hypervalency: Is it real? - Henry Rzepa&#039;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=2599\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Hypervalency: Is it real? - Henry Rzepa&#039;s Blog\" \/>\n<meta property=\"og:description\" content=\"The Wikipedia page on hypervalent compounds reveals that the concept is almost as old as that of normally valent compounds. The definition there, \u00a0is &#8220;a molecule that contains one or more\u00a0main group elements formally bearing more than eight\u00a0electrons in their\u00a0valence shells&#8221; (although it could equally apply to e.g. transition elements that would contain e.g. more [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599\" \/>\n<meta property=\"og:site_name\" content=\"Henry Rzepa&#039;s Blog\" \/>\n<meta property=\"article:published_time\" content=\"2010-10-16T11:10:21+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2010-10-18T13:40:19+00:00\" \/>\n<meta property=\"og:image\" content=\"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg\" \/>\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=\"4 minutes\" \/>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Hypervalency: Is it real? - Henry Rzepa&#039;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=2599","og_locale":"en_GB","og_type":"article","og_title":"Hypervalency: Is it real? - Henry Rzepa&#039;s Blog","og_description":"The Wikipedia page on hypervalent compounds reveals that the concept is almost as old as that of normally valent compounds. The definition there, \u00a0is &#8220;a molecule that contains one or more\u00a0main group elements formally bearing more than eight\u00a0electrons in their\u00a0valence shells&#8221; (although it could equally apply to e.g. transition elements that would contain e.g. more [&hellip;]","og_url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599","og_site_name":"Henry Rzepa&#039;s Blog","article_published_time":"2010-10-16T11:10:21+00:00","article_modified_time":"2010-10-18T13:40:19+00:00","og_image":[{"url":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg","type":"","width":"","height":""}],"author":"Henry Rzepa","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Henry Rzepa","Estimated reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#article","isPartOf":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599"},"author":{"name":"Henry Rzepa","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#\/schema\/person\/2b40f7b9c872a4dc1547e040a11b6281"},"headline":"Hypervalency: Is it real?","datePublished":"2010-10-16T11:10:21+00:00","dateModified":"2010-10-18T13:40:19+00:00","mainEntityOfPage":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599"},"wordCount":899,"commentCount":5,"image":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#primaryimage"},"thumbnailUrl":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg","keywords":["Hypervalency","pence","potential energy surface"],"articleSection":["Hypervalency"],"inLanguage":"en-GB","potentialAction":[{"@type":"CommentAction","name":"Comment","target":["https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#respond"]}]},{"@type":"WebPage","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599","url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599","name":"Hypervalency: Is it real? - Henry Rzepa&#039;s Blog","isPartOf":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#primaryimage"},"image":{"@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#primaryimage"},"thumbnailUrl":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg","datePublished":"2010-10-16T11:10:21+00:00","dateModified":"2010-10-18T13:40:19+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=2599#breadcrumb"},"inLanguage":"en-GB","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599"]}]},{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#primaryimage","url":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg","contentUrl":"http:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/wp-content\/uploads\/2010\/10\/IH7.jpg"},{"@type":"BreadcrumbList","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/?p=2599#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog"},{"@type":"ListItem","position":2,"name":"Hypervalency: Is it real?"}]},{"@type":"WebSite","@id":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/#website","url":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/","name":"Henry Rzepa&#039;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-FV","jetpack-related-posts":[],"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","0":null,"1":"","2":"","3":"","4":"","5":"","6":"","7":"","8":""}],"_links":{"self":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts\/2599","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=2599"}],"version-history":[{"count":0,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=\/wp\/v2\/posts\/2599\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=2599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=2599"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=2599"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/www.ch.ic.ac.uk\/rzepa\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fppma_author&post=2599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}