Halogenated triarylboranes (BAr3) have been known for decades, however it has only been since the surge of interest in main group catalysis that their application as strong Lewis acid catalysts has been recognised. This review aims to look past the popular tris(pentafluorophenyl)borane [B(C6F5)3] to the other halogenated triarylboranes, to give a greater breadth of understanding as to how tuning the Lewis acidity of BAr3 by modifications of the aryl rings can lead to improved reactivity. In this review, a discussion on Lewis acidity determination of boranes is given, the synthesis of these boranes is discussed, and examples of how they are being used for catalysis and frustrated Lewis pair (FLP) chemistry are explained
The addition of the Grignard 3,4,5-ArFMgBr to aluminum(III) chloride in ether generates the novel tr...
Combinations of sterically encumbered Lewis acids and Lewis bases are precluded from dative bond for...
Reactive carbenes generated from diazo compounds are key intermediates for a range of organic reacti...
In the last two decades, boron-based catalysis has been gaining increasing traction in the field of ...
As main-group chemistry, in particular boron chemistry, has expanded and developed over the past 20 ...
The work described herein is concerned with Lewis acidic triarylboranes for synthetic and catalytic ...
The chemistry of Lewis acids, in particular that of triarylboranes, has received unprecedented atten...
One field of organometallic chemistry that has seen great advancements over the last 20 years is th...
The ability of halogenated triarylboranes to accept a lone pair of electrons from donor substrates r...
While the organotrifluoroborate group is commonly used as a leaving group in cross-coupling reaction...
From their inception, boron-based frustrated Lewis pairs have garnered significant scientific attent...
The focus of this thesis has been the design and synthesis of new frustrated Lewis pair (FLP) system...
This work outlines the use of Lewis acidic boranes in a variety of different reactions, mainly in th...
The metal-free catalyst tris(2,4,6-trifluorophenyl)borane has demonstrated its extensive application...
The addition of the Grignard 3,4,5-ArFMgBr to aluminum(III) chloride in ether generates the novel tr...
Combinations of sterically encumbered Lewis acids and Lewis bases are precluded from dative bond for...
Reactive carbenes generated from diazo compounds are key intermediates for a range of organic reacti...
In the last two decades, boron-based catalysis has been gaining increasing traction in the field of ...
As main-group chemistry, in particular boron chemistry, has expanded and developed over the past 20 ...
The work described herein is concerned with Lewis acidic triarylboranes for synthetic and catalytic ...
The chemistry of Lewis acids, in particular that of triarylboranes, has received unprecedented atten...
One field of organometallic chemistry that has seen great advancements over the last 20 years is th...
The ability of halogenated triarylboranes to accept a lone pair of electrons from donor substrates r...
While the organotrifluoroborate group is commonly used as a leaving group in cross-coupling reaction...
From their inception, boron-based frustrated Lewis pairs have garnered significant scientific attent...
The focus of this thesis has been the design and synthesis of new frustrated Lewis pair (FLP) system...
This work outlines the use of Lewis acidic boranes in a variety of different reactions, mainly in th...
The metal-free catalyst tris(2,4,6-trifluorophenyl)borane has demonstrated its extensive application...
The addition of the Grignard 3,4,5-ArFMgBr to aluminum(III) chloride in ether generates the novel tr...
Combinations of sterically encumbered Lewis acids and Lewis bases are precluded from dative bond for...
Reactive carbenes generated from diazo compounds are key intermediates for a range of organic reacti...