[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/iminoborane-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki41\/iminoborane-wikipedia\/","headline":"Iminoborane – Wikipedia","name":"Iminoborane – Wikipedia","description":"From Wikipedia, the free encyclopedia Class of chemical compounds Chemical compound Structure of tBuN=B-tBu (tBu = tert-butyl). The B-N bond","datePublished":"2015-06-22","dateModified":"2015-06-22","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki41\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/7\/7f\/TBuN%3DB-tBu_%28CETSUP%29.png\/220px-TBuN%3DB-tBu_%28CETSUP%29.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/7\/7f\/TBuN%3DB-tBu_%28CETSUP%29.png\/220px-TBuN%3DB-tBu_%28CETSUP%29.png","height":"136","width":"220"},"url":"https:\/\/wiki.edu.vn\/en\/wiki41\/iminoborane-wikipedia\/","about":["Wiki"],"wordCount":4828,"articleBody":"From Wikipedia, the free encyclopediaClass of chemical compoundsChemical compound  Structure of tBuN=B-tBu (tBu = tert-butyl). The B-N bond distance is 126 pm.[1]Iminoboranes comprise a group of organoboron compounds with the formula RB=NR’. They are electronically related to acetylenes but are usually more reactive due to the polarity.[2][3]Structure and bonding[edit]The parent iminoborane, HB=NH, is produced by the photolysis of H3BNH3.[4][5][6] Bonding in iminoboranes can be described by two resonance structures:[7]"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/iminoborane-wikipedia\/#breadcrumbitem","name":"Iminoborane – Wikipedia"}}]}]