2016
DOI: 10.1002/anie.201605645
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Spontaneous Reduction of a Hydroborane To Generate a B−B Single Bond by the Use of a Lewis Pair

Abstract: The ansa-aminohydroborane 1-NMe2 -2-(BH2 )C6 H4 crystallizes in an unprecedented type of dimer containing a B-H bond activated by one FLP moiety. Upon mild heating and without the use of any catalyst, this molecule liberates one equivalent of hydrogen to generate a diborane molecule. The synthesis and structural characterization of these new compounds, as well as the kinetic monitoring of the reaction and the DFT investigation of its mechanism, are reported.

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Cited by 48 publications
(41 citation statements)
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“…Despite the reaction products being thermodynamically slightly uphill, concomitant release of H 2 by a FLP‐type process was calculated to enable favorable thermodynamics (Figure C). A similar hydrogen‐release behavior was recently reported to occur during the formation of a B−B bond from ansa ‐aminoborane 1‐BH 2 ‐2‐NMe 2 ‐C 6 H 4 …”
Section: Figuresupporting
confidence: 81%
“…Despite the reaction products being thermodynamically slightly uphill, concomitant release of H 2 by a FLP‐type process was calculated to enable favorable thermodynamics (Figure C). A similar hydrogen‐release behavior was recently reported to occur during the formation of a B−B bond from ansa ‐aminoborane 1‐BH 2 ‐2‐NMe 2 ‐C 6 H 4 …”
Section: Figuresupporting
confidence: 81%
“…Although low‐barrier boron–boron‐dehydrocoupling reactions are not unprecedented (see the example reported by Fontaine and co‐workers in ref. ), the presence of a catalyst is generally required in most known examples . In contrast, a decrease of the reaction barrier for the dehydrocoupling reaction was already observed in the case of [(RS(H)B(μ‐hpp)] 2 , which eliminates H 2 at room temperature (Scheme ) …”
Section: Resultsmentioning
confidence: 99%
“…Weller and co‐workers reported the dehydrogenative boron‐homocoupling reaction of amine‐borane at a Rh atom . Fontaine and co‐workers reported an elegant diborane(4) synthesis by thermal H 2 elimination from a diborane(6) precursor . In contrast to other known boron–boron‐dehydrocoupling reactions, no catalyst was needed in this reaction, but quite high temperatures had to be applied.…”
Section: Introductionmentioning
confidence: 99%
“…They can be regarded as boryl‐substituted boranes that react as electrophiles. Lately several spectacular results were reported with sp 3 –sp 3 ‐hybridized diborane(4) and also sp 3 –sp 3 ‐diborane(6) derivatives, but nevertheless their chemistry is still underdeveloped. Braunschweig et al.…”
Section: Introductionmentioning
confidence: 99%