10221-56-4Relevant articles and documents
Cobalt catalysed reduction of CO2via hydroboration
Tamang, Sem Raj,Findlater, Michael
, p. 8199 - 8203 (2018)
We report an operationally convenient reduction of CO2 to methanol via cobalt catalysed hydroboration which occurs under mild reaction conditions. Addition of NaHBEt3 to Co(acac)3 generates an active hydroboration catalyst, which is proposed to be a “Co-H” species on the basis of infrared spectroscopy. The reduction of CO2 in the presence of various boranes showed that BH3·SMe2 afforded near quantitative conversion (98% NMR yield) to methanol upon hydrolysis.
An efficient nickel catalyst for the reduction of carbon dioxide with a borane
Chakraborty, Sumit,Zhang, Jie,Krause, Jeanette A.,Guan, Hairong
, p. 8872 - 8873 (2010)
Nickel hydride with a diphosphinite-based ligand catalyzes the highly efficient reduction of CO2 with catecholborane, and the hydrolysis of the resulting methoxyboryl species produces CH3OH in good yield. The mechanism involves a nickel formate, formaldehyde, and a nickel methoxide as different reduced stages for CO2. The reaction may also be catalyzed by an air-stable nickel formate.
Cooperative bond activation and catalytic reduction of carbon dioxide at a group 13 metal center
Abdalla, Joseph A. B.,Riddlestone, Ian M.,Tirfoin, Rémi,Aldridge, Simon
, p. 5098 - 5102 (2015)
A single-component ambiphilic system capable of the cooperative activation of protic, hydridic and apolar H-X bonds across a Group 13 metal/activated β-diketiminato (Nacnac) ligand framework is reported. The hydride complex derived from the activation of H2 is shown to be a competent catalyst for the highly selective reduction of CO2 to a methanol derivative. To our knowledge, this process represents the first example of a reduction process of this type catalyzed by a molecular gallium complex. A single-component ambiphilic Group 13 system has been developed, capable of the cooperative activation of protic, hydridic, and apolar H-X bonds. The hydride complex derived from the activation of H2 catalyzes the selective transformation of CO2 to a methanol derivative, representing the first example of such a reduction process catalyzed by a molecular gallium complex.
Zinc hydridotriphenylborates supported by a neutral macrocyclic polyamine
Mukherjee, Debabrata,Wiegand, Ann-Kristin,Spaniol, Thomas P.,Okuda, Jun
, p. 6183 - 6186 (2017)
The zinc hydridotriphenylborates [(L)Zn(TMDS)][HBPh3] and [(L)ZnX][HBPh3] (L = Me4TACD, Me4[12]aneN4; TMDS = N(SiHMe2)2; X = Cl, Br, I) were synthesized by BPh3-mediated β-SiH abstraction and salt metathesis with KHBPh3, respectively. CO2 is rapidly inserted into the B-H bonds. [(L)Zn(TMDS)][HBPh3] catalyzes the hydroboration of polar substrates including CO2.
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)
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.
Efficient homogeneous catalysis in the reduction of CO2 to CO
Laitar, David S.,Mueller, Peter,Sadighi, Joseph P.
, p. 17196 - 17197 (2005)
The well-defined copper(I) boryl complex [(IPr)Cu(Bpin)] [where IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, and pin = pinacolate: 2,3-dimethyl-2,3-butanediolate] deoxygenates CO2 rapidly and quantitatively, affording CO and the borate complex [(IPr)Cu(OBpin)]. The boryl may be regenerated by treatment with the diboron compound pinB-Bpin, giving the stable byproduct pinB-O-Bpin. The use of a copper(I) alkoxide precatalyst and stoichiometric diboron reagent results in catalytic reduction of CO2, with high turnover numbers (1000 per Cu) and frequencies (100 per Cu in 1 h) depending on supporting ligand and reaction conditions. Copyright
Frustrated lewis pair inspired carbon dioxide reduction by a ruthenium tris(aminophosphine) complex
Sgro, Michael J.,Stephan, Douglas W.
, p. 11343 - 11345 (2012)
Frustrating ruthenium: The ruthenium complex 1 is shown to bind carbon dioxide or aldehyde in a manner similar to a frustrated Lewis pair. Compound 2 catalyzes the reduction of CO2 in the presence of pinacolborane (HBpin), yielding MeOBpin and O(Bpin)2 (see picture; Ru red, P orange, N green, O light red, C black). Copyright
Conversion of Carbon Dioxide to Methanol Using a C-H Activated Bis(imino)pyridine Molybdenum Hydroboration Catalyst
Pal, Raja,Groy, Thomas L.,Trovitch, Ryan J.
, p. 7506 - 7515 (2015)
Using a multistep synthetic pathway, a bis(imino)pyridine (or pyridine diimine, PDI) molybdenum catalyst for the selective conversion of carbon dioxide into methanol has been developed. Starting from (Ph2PPrPDI)Mo(CO), I2 addition af
Efficient Reduction of Carbon Dioxide to Methanol Equivalents Catalyzed by Two-Coordinate Amido-Germanium(II) and -Tin(II) Hydride Complexes
Hadlington, Terrance J.,Kefalidis, Christos E.,Maron, Laurent,Jones, Cameron
, p. 1853 - 1859 (2017)
The bulky amido-germanium(II) and -tin(II) hydride complexes, L?EH [E = Ge or Sn; L? = -N(Ar?) (SiPri3); Ar? = C6H2Pri{C(H)Ph2}2-4,2,6
A stable ring-expanded NHC-supported copper boryl and its reactivity towards heterocumulenes
Charman, Rex S. C.,Hall, Jonathan W.,Horsley Downie, Thomas M.,Liptrot, David J.,Lowe, John P.,Mahon, Mary F.
, p. 16336 - 16342 (2021/11/30)
Reaction of bis(pinacolato)diboron with (6-Dipp)CuOtBu generates a ring-expanded N-heterocyclic carbene supported copper(i) boryl, (6-Dipp)CuBpin. This compound showed remarkable stability and was characterised by NMR spectroscopy and X-ray crystallography. (6-Dipp)CuBpin readily dechalcogenated a range of heterocumulenes such as CO2, isocyanates and isothiocyanates to yield (6-Dipp)CuXBpin (X = O, S). In the case of CO2 catalytic reduction to CO is viable in the presence of excess bis(pinacolato)diboron. In contrast, in the case of iso(thio)cyanates, the isocyanide byproduct of dechalcogenation reacted with (6-Dipp)CuBpin to generate a copper(i) borylimidinate, (6-Dipp)CuC(NR)Bpin, which went on to react with heterocumulenes. This off-cycle reactivity gives selective access to a range of novel boron-containing heterocycles bonded to copper, but precludes catalytic reactivity.
Photo-induced thiolate catalytic activation of inert Caryl-hetero bonds for radical borylation
K?nig, Burkhard,Wang, Hua,Wang, Shun
supporting information, p. 1653 - 1665 (2021/06/17)
Substantial effort is currently being devoted to obtaining photoredox catalysts with high redox power. Yet, it remains challenging to apply the currently established methods to the activation of bonds with high bond dissociation energy and to substrates with high reduction potentials. Herein, we introduce a novel photocatalytic strategy for the activation of inert substituted arenes for aryl borylation by using thiolate as a catalyst. This catalytic system exhibits strong reducing ability and engages non-activated Caryl–F, Caryl–X, Caryl–O, Caryl–N, and Caryl–S bonds in productive radical borylation reactions, thus expanding the available aryl radical precursor scope. Despite its high reducing power, the method has a broad substrate scope and good functional-group tolerance. Spectroscopic investigations and control experiments suggest the formation of a charge-transfer complex as the key step to activate the substrates.
