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Boron-based stepwise dioxygen activation with 1,4,2,5-diazadiborinine.


ABSTRACT: Activation of dioxygen (O2) by 1,4,2,5-diazadiborinine 1 is reported. Two boron centers in 1 undergo a formal [4 + 2] cycloaddition with O2 at room temperature affording a bicyclo[2.2.2] molecule 2 featuring a B-O-O-B unit. Treatment of 2 with an additional equivalent of 1 leads to the cleavage of the O-O bond in 2 concomitant with the formation of two B-O bonds to yield 4 involving the extremely rare B4C2N2O2 ten-membered rings. A series of these reactions demonstrate the stepwise scission of the O[double bond, length as m-dash]O ?-bond and the O-O ?-bond of O2.

SUBMITTER: Wang B 

PROVIDER: S-EPMC6385103 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Boron-based stepwise dioxygen activation with 1,4,2,5-diazadiborinine.

Wang Baolin B   Kinjo Rei R  

Chemical science 20181211 7


Activation of dioxygen (O<sub>2</sub>) by 1,4,2,5-diazadiborinine <b>1</b> is reported. Two boron centers in <b>1</b> undergo a formal [4 + 2] cycloaddition with O<sub>2</sub> at room temperature affording a bicyclo[2.2.2] molecule <b>2</b> featuring a B-O-O-B unit. Treatment of <b>2</b> with an additional equivalent of <b>1</b> leads to the cleavage of the O-O bond in <b>2</b> concomitant with the formation of two B-O bonds to yield <b>4</b> involving the extremely rare B<sub>4</sub>C<sub>2</su  ...[more]

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