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Borinic acid, bis[3,5-bis(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

211636-23-6

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211636-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211636-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,6,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 211636-23:
(8*2)+(7*1)+(6*1)+(5*6)+(4*3)+(3*6)+(2*2)+(1*3)=96
96 % 10 = 6
So 211636-23-6 is a valid CAS Registry Number.

211636-23-6Downstream Products

211636-23-6Relevant academic research and scientific papers

Novel B(Ar′)2(Ar″) hetero-tri(aryl)boranes: A systematic study of Lewis acidity

Blagg, Robin J.,Simmons, Trevor R.,Hatton, Georgina R.,Courtney, James M.,Bennett, Elliot L.,Lawrence, Elliot J.,Wildgoose, Gregory G.

, p. 6032 - 6043 (2016/04/26)

A series of homo- and hetero-tri(aryl)boranes incorporating pentafluorophenyl, 3,5-bis(trifluoromethyl)phenyl, and pentachlorophenyl groups, four of which are novel species, have been studied as the acidic component of frustrated Lewis pairs for the heterolytic cleavage of H2. Under mild conditions eight of these will cleave H2; the rate of cleavage depending on both the electrophilicity of the borane and the steric bulk around the boron atom. Electrochemical studies allow comparisons of the electrophilicity with spectroscopic measurements of Lewis acidity for different series of boranes. Discrepancies in the correlation between these two types of measurements, combined with structural characterisation of each borane, reveal that the twist of the aryl rings with respect to the boron-centred trigonal plane is significant from both a steric and electronic perspective, and is an important consideration in the design of tri(aryl)boranes as Lewis acids.

Homogeneous model complexes for supported rhenia metathesis catalysts

Lai, Yu-Ying,Bornand, Marc,Chen, Peter

, p. 7558 - 7565 (2013/01/15)

A series of rhenium trioxo complexes (L-ReO3) was synthesized, characterized, and demonstrated to be active in olefin metathesis. The relationship between perrhenate (ReO4-), perrhenyl (ReO3+), and metathesis-active rhenium complexes (L-ReO3) was elucidated. Their chemical behavior can be tuned through the Lewis acid-base interaction. DFT calculations were performed for the metathesis reaction of L-ReO3 with norbornene, which demonstrates that electron-withdrawing substituents or ligands are beneficial for olefin metathesis activity. Moreover, a rhenium-alkylidene complex was synthesized, which can be activated by B(C6F5)3 to afford an active metathesis catalyst. This system can be regarded as a homogeneous model of the hypothetical species present in the heterogeneous catalytic systems. The findings from the present study are consistent with our previous gas-phase studies and constitute the elucidation of the working principles for the metathesis-active rhenium species on the surface.

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