1b:I[76749,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 1c:I[3486,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 1d:I[41892,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 1e:I[17707,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 1f:I[66528,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 20:I[63176,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 21:I[87099,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 22:I[26200,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"Group"] 23:I[23365,["/_next/static/chunks/f9f65a69b09cd00d.js","/_next/static/chunks/1ba21a8e081e29d1.js","/_next/static/chunks/0383663887945ae7.js","/_next/static/chunks/5bf36002c846d2d8.js","/_next/static/chunks/63561dcd578bd4db.js","/_next/static/chunks/29d2646804fd1cab.js","/_next/static/chunks/2060b26370dc6c0a.js"],"default"] 24:T52b,We disclose the synthesis and structural characterization of the first acid-free anionic oxoborane, [K(2.2.2-crypt)][(HCDippN)₂BO] (1) (Dipp = 2,6- ⁱPr₂C₆H₃), which is isoelectronic with classical carbonyl compounds. 1 can readily be accessed from its borinic acid by a simple deprotonation/sequestration sequence. Crystallographic and density functional theory (DFT) analyses support the presence of a polarized terminal B═O double bond. Subsequent π bond metathesis converts the B═O bond to a heavier B═S containing system, affording the first anionic thioxoborane [K(2.2.2-crypt)][(HCDippN)₂BS] (2), isoelectronic with thiocarbonyls. Facile B═O bond cleavage can also be achieved to access B-H and B-Cl bonds and, via a remarkable oxide (O^2-) ion abstraction, to generate a borenium cation [(HCDippN)₂B(NC₅H₅)][OTf] (4). By extension, 1 can act as an oxide transfer agent to organic substrates, a synthetic role traditionally associated with transition-metal compounds. Hence we show that B-O linkages, which are often considered to be thermody

Kieran Porteous

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