Diboron-carbene complexes derived from a geminal dianion

The reaction of the bis(thiophosphinoyl) geminal dianion [C(PPh2S)2]2- with B2Br4(SMe2)2 in toluene afforded the diboron-carbene complex [(SPh2P)2CB]2 (2). The lability of the boron-carbene bond was found in the reaction of the sterically hindered thiophosphinoyl iminophosphoranyl geminal dianion [C...

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Bibliographic Details
Main Authors: Fan, Jun, Yang, Ming-Chung, Hooper, Thomas J. N., Su, Ming-Der, So, Cheuk-Wai
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/160147
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Institution: Nanyang Technological University
Language: English
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Summary:The reaction of the bis(thiophosphinoyl) geminal dianion [C(PPh2S)2]2- with B2Br4(SMe2)2 in toluene afforded the diboron-carbene complex [(SPh2P)2CB]2 (2). The lability of the boron-carbene bond was found in the reaction of the sterically hindered thiophosphinoyl iminophosphoranyl geminal dianion [C(PPh2NAr)(PPh2S)]2- (Ar = 2,6-iPr2C6H3) with B2Br4(SMe2)2 in toluene to form the diboron-carbene complex 4, where one boron center bonds with two methanediides, leading to an allyl anionic-like C═B←C2- electronic structure, while another boron center is stabilized by two imino substituents. Complex 4 underwent rearrangement via a 1,2-methanediide shift in toluene at 60 °C to give the diboron-carbene complex [(SPh2P)(ArNPh2P)CB]2 (5).