102-24-9Relevant articles and documents
BH3 Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2 Reduction into Methanol Derivatives
Lafage, Mathieu,Pujol, Anthony,Saffon-Merceron, Nathalie,Mézailles, Nicolas
, p. 3030 - 3035 (2016)
The reaction of the geminal dianion (SCS)2- 1 with 2 equiv of BH3·SMe2 leads to the isolation and full characterization of the new organoborane [(SCS)BH2][Li(THF)2] 2, in which the C=B bond possesses ambiphilic, multiple character. Treatment of 2 with another 1 equiv of BH3·SMe2 allows the isolation of the rare cyclic diborane species [(SCS)B2H5][Li(OEt2)] 4. The electronic structures of both compounds were investigated by means of DFT calculations. Compound 4 is an efficient catalyst for the reduction of CO2 to methanol derivatives by BH3·SMe2. A TON of ca. 2800 (TOF = 127 h-1) was achieved using 0.1 mol % of 4 in THF.
A highly active phosphine-borane organocatalyst for the reduction of CO2 to methanol using hydroboranes
Courtemanche, Marc-Andre,Legare, Marc-Andre,Maron, Laurent,Fontaine, Frederic-Georges
, p. 9326 - 9329 (2013)
In this work, we report that organocatalyst 1-Bcat-2-PPh2-C 6H4 ((1); cat = catechol) acts as an ambiphilic metal-free system for the reduction of carbon dioxide in presence of hydroboranes (HBR2 = HBcat (catecholborane), HBpin (pinacolborane), 9-BBN (9-borabicyclo[3.3.1]nonane), BH3·SMe2 and BH 3·THF) to generate CH3OBR2 or (CH 3OBO)3, products that can be readily hydrolyzed to methanol. The yields can be as high as 99% with exclusive formation of CH 3OBR2 or (CH3OBO)3 with TON (turnover numbers) and TOF (turnover frequencies) reaching >2950 and 853 h-1, respectively. Furthermore, the catalyst exhibits "living" behavior: once the first loading is consumed, it resumes its activity on adding another loading of reagents.
Ph2PCH2CH2B(C8H14) and Its Formaldehyde Adduct as Catalysts for the Reduction of CO2with Hydroboranes
Ramos, Alberto,Anti?olo, Antonio,Carrillo-Hermosilla, Fernando,Fernández-Galán, Rafael
, p. 9998 - 10012 (2020)
We study two metal-free catalysts for the reduction of CO2 with four different hydroboranes and try to identify mechanistically relevant intermediate species. The catalysts are the phosphinoborane Ph2P(CH2)2BBN (1), easily accessible in a one-step synthesis from diphenyl(vinyl)phosphine and 9-borabicyclo[3.3.1]nonane (H-BBN), and its formaldehyde adduct Ph2P(CH2)2BBN(CH2O) (2), detected in the catalytic reduction of CO2 with 1 as the catalyst but properly prepared from compound 1 and p-formaldehyde. Reduction of CO2 with H-BBN gave mixtures of CH2(OBBN)2 (A) and CH3OBBN (B) using both catalysts. Stoichiometric and kinetic studies allowed us to unveil the key role played in this reaction by the formaldehyde adduct 2 and other formaldehyde-formate species, such as the polymeric BBN(CH2)2(Ph2P)(CH2O)BBN(HCO2) (3) and the bisformate macrocycle BBN(CH2)2(Ph2P)(CH2O)BBN(HCO2)BBN(HCO2) (4), whose structures were confirmed by diffractometric analysis. Reduction of CO2 with catecholborane (HBcat) led to MeOBcat (C) exclusively. Another key intermediate was identified in the reaction of 2 with the borane and CO2, this being the bisformaldehyde-formate macrocycle (HCO2){BBN(CH2)2(Ph2P)(CH2O)}2Bcat (5), which was also structurally characterized by X-ray analysis. In contrast, using pinacolborane (HBpin) as the reductant with catalysts 1 and 2 usually led to mixtures of mono-, di-, and trihydroboration products HCO2Bpin (D), CH2(OBpin)2 (E), and CH3OBpin (F). Stoichiometric studies allowed us to detect another formaldehyde-formate species, (HCO2)BBN(CH2)2(Ph2P)(CH2O)Bpin (6), which may play an important role in the catalytic reaction. Finally, only the formaldehyde adduct 2 turned out to be active in the catalytic hydroboration of CO2 using BH3·SMe2 as the reductant, yielding a mixture of two methanol-level products, [(OMe)BO]3 (G, major product) and B(OMe)3 (H, minor product). In this transformation, the Lewis adduct (BH3)Ph2P(CH2)2BBN was identified as the resting state of the catalyst, whereas an intermediate tentatively formulated as the Lewis adduct of compound 2 and BH3 was detected in solution in a stoichiometric experiment and is likely to be mechanistically relevant for the catalytic reaction.
Organocatalysts with carbon-centered activity for CO2 reduction with boranes
Yang, Yanxin,Xu, Maotong,Song, Datong
, p. 11293 - 11296 (2015)
We report two organocatalysts for CO2 hydroboration to methylborylethers, which upon hydrolysis can produce methanol. These organocatalysts feature carbon-centered reversible CO2 binding, broad borane scopes, and high catalytic activities.
Formation of a zwitterionic boronium species from the reaction of a stable carbenoid with borane: CO2 reduction
Ho, Samuel Y.-F.,So, Cheuk-Wai,Saffon-Merceron, Nathalie,Mzailles, Nicolas
, p. 2107 - 2110 (2015)
The treatment of Li2C(PPh2NMes)2 (1, Mes = 2,4,6-Me3C6H2) with hexachloroethane yielded the corresponding carbenoid 2 in good yields. The reactivity of 2 was studied with BH3·SMe2 to give a zwitterionic boronium species 4, also a stable carbenoid. Both carbenoid species were found to be excellent catalysts for the CO2 reduction by BH3·SMe2. This journal is
Reduction of CO2 to trimethoxyboroxine with BH3 in THF
Fujiwara, Koji,Yasuda, Shogo,Mizuta, Tsutomu
, p. 6692 - 6695 (2014)
Commercially available THF solutions of BH3·THF, which contain 0.5 mol % of NaBH4 as a stabilizing reagent for BH3·THF, react with 1 atm of CO2 at room temperature to form trimethoxyboroxine, (MeOBO)3, in 87% yield after 12 h. Since no reaction took place in the absence of NaBH4, NaBH4 was found to work as a promoter or catalyst for the reduction of CO2 with BH3 to the methoxy compound. A similar reaction using HCOONa in place of NaBH4 also gave (MeOBO)3 in comparable yield.
A Versatile NHC-Parent Silyliumylidene Cation for Catalytic Chemo- And Regioselective Hydroboration
Leong, Bi-Xiang,Lee, Jiawen,Li, Yan,Yang, Ming-Chung,Siu, Chi-Kit,Su, Ming-Der,So, Cheuk-Wai
, p. 17629 - 17636 (2019)
This study describes the first use of a silicon(II) complex, NHC-parent silyliumylidene cation complex [(IMe)2SiH]I (1, IMe =:C{N(Me)C(Me)}2) as a versatile catalyst in organic synthesis. Complex 1 (loading: 10 mol %) was shown to act as an efficient catalyst (reaction time: 0.08 h, yield: 94%, TOF = 113.2 h-1 reaction time: 0.17 h, yield: 98%, TOF = 58.7 h-1) for the selective reduction of CO2 with pinacolborane (HBpin) to form the primarily reduced formoxyborane [pinBOC(-O)H]. The activity is better than the currently available base-metal catalysts used for this reaction. It also catalyzed the chemo- and regioselective hydroboration of carbonyl compounds and pyridine derivatives to form borate esters and N-boryl-1,4-dihydropyridine derivatives with quantitative conversions, respectively. Mechanistic studies show that the silicon(II) center in complex 1 activated the substrates and then mediated the catalytic hydroboration. In addition, complex 1 was slightly converted into the NHC-borylsilyliumylidene complex [(IMe)2SiBpin]I (3) in the catalysis, which was also able to mediate the catalytic hydroboration.
Transforming atmospheric CO2 into alternative fuels: A metal-free approach under ambient conditions
Chandra Sau, Samaresh,Bhattacharjee, Rameswar,Hota, Pradip Kumar,Vardhanapu, Pavan K.,Vijaykumar, Gonela,Govindarajan,Datta, Ayan,Mandal, Swadhin K.
, p. 1879 - 1884 (2019)
This work demonstrates the first-ever completely metal-free approach to the capture of CO2 from air followed by reduction to methoxyborane (which produces methanol on hydrolysis) or sodium formate (which produces formic acid on hydrolysis) under ambient conditions. This was accomplished using an abnormal N-heterocyclic carbene (aNHC)-borane adduct. The intermediate involved in CO2 capture (aNHC-H, HCOO, B(OH)3) was structurally characterized by single-crystal X-ray diffraction. Interestingly, the captured CO2 can be released by heating the intermediate, or by passing this compound through an ion-exchange resin. The capture of CO2 from air can even proceed in the solid state via the formation of a bicarbonate complex (aNHC-H, HCO3, B(OH)3), which was also structurally characterized. A detailed mechanism for this process is proposed based on tandem density functional theory calculations and experiments.
Lewis base activation of borane-dimethylsulfide into strongly reducing ion pairs for the transformation of carbon dioxide to methoxyboranes
Légaré, Marc-André,Courtemanche, Marc-André,Fontaine, Frédéric-Georges
, p. 11362 - 11365 (2014)
The hydroboration of carbon dioxide into methoxyboranes by borane-dimethylsulfide using different base catalysts is described. A non-nucleophilic proton sponge is found to be the most active catalyst, with TOF reaching 64 h-1 at 80°C, and is acting via the activation of BH3·SMe2 into a boronium-borohydride ion pair. the Partner Organisations 2014.
Acetate-catalyzed hydroboration of CO2 for the selective formation of methanol-equivalent products
Dagorne, Samuel,Dos Santos, Jo?o H. Z.,Jacques, Béatrice,López, Carlos Silva,Nieto Faza, Olalla,Schrekker, Henri S.,Sokolovicz, Yuri C. A.,Specklin, David
, p. 2407 - 2414 (2020/05/13)
The present study details the use of the acetate anion, an inexpensive and robust anion, as a CO2 hydroboration catalyst for the selective formation, in most cases, of methanol-equivalent borane products. Thus, upon heating (90 °C, PhBr), tetrabutylammonium, sodium and potassium acetate (1, 2 and 3, respectively) effectively catalyze CO2 hydroboration by pinacolborane (pinB-H) to afford CO2 reduction products HOCOBpin (A), pinBOCH2OBpin (B) and methoxyborane (C). In most cases, high selectivity for product C with higher borane loading and longer reaction time with a TON of up to 970 was observed. The reduction catalysis remains efficient at low catalyst loading (down to 0.1 mol%) and may also be performed under solvent-free conditions using salt 1 as a catalyst, reflecting the excellent robustness and stability of the acetate anion. In control experiments, a 1/1 1/pinB-H mixture was found to react fast with CO2 at room temperature to produce formate species [pinB(O2CH)(OAc)][N(nBu)4] (5) through CO2 insertion into the B-H bond. DFT calculations were also performed to gain insight into the acetate-mediated CO2 hydroboration catalysis, which further supported the crucial role of acetate as a Lewis base in CO2 functionalization catalysis by pinB-H. The DFT-estimated mechanism is in line with experimental data and rationalizes the formation of the most thermodynamically stable reduction product C through acetate catalysis.
