Donor functionalized ruthenium N-heterocyclic carbene complexes in alcohol oxidation reactions

2014 ◽  
Vol 43 (14) ◽  
pp. 5335-5342 ◽  
Author(s):  
Abbas Raja Naziruddin ◽  
Chun-Shiuan Zhuang ◽  
Wan-Jung Lin ◽  
Wen-Shu Hwang

Ruthenium chelates bearing N^C^O-donors in bidentate or pincer coordination modes have been prepared. The ruthenium pincer complex catalyses the oxidation of alcohols to the corresponding aldehydes with yields as high as 99%.

RSC Advances ◽  
2016 ◽  
Vol 6 (82) ◽  
pp. 78403-78408 ◽  
Author(s):  
Bryan H. R. Suryanto ◽  
Chuan Zhao

Enhanced electrocatalytic oxidation of alcohols observed at multiwall carbon nanotubes following simple surface oxidation process.


RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78553-78560 ◽  
Author(s):  
Debojeet Sahu ◽  
Ana Rosa Silva ◽  
Pankaj Das

The first example of an iron(iii)-based heterogeneous catalyst for alcohol oxidation reactions in water employing molecular oxygen has been reported. Interestingly, the immobilized catalyst shows superior activity over its homogeneous counterpart.


2018 ◽  
Vol 54 (87) ◽  
pp. 12404-12407 ◽  
Author(s):  
Thantakorn Nitaya ◽  
Yi Cheng ◽  
Shanfu Lu ◽  
Kunakorn Poochinda ◽  
Kejvalee Pruksathorn ◽  
...  

Ni single atoms encapsulated in carbon nanotubes substantially enhance the activity of Pd nanoparticles for oxidation of alcohols in alkaline media.


2021 ◽  
Vol 22 (13) ◽  
pp. 6787
Author(s):  
Constantin I. Tănase ◽  
Constantin Drăghici ◽  
Miron Teodor Căproiu ◽  
Anamaria Hanganu ◽  
Gheorghe Borodi ◽  
...  

β-Ketophosphonates with pentalenofurane fragments linked to the keto group were synthesized. The bulky pentalenofurane skeleton is expected to introduce more hindrance in the prostaglandin analogues of type III, greater than that obtained with the bicyclo[3.3.0]oct(a)ene fragments of prostaglandin analogues I and II, to slow down (retard) the inactivation of the prostaglandin analogues by oxidation of 15α-OH to the 15-keto group via the 15-PGDH pathway. Their synthesis was performed by a sequence of three high yield reactions, starting from the pentalenofurane alcohols 2, oxidation of alcohols to acids 3, esterification of acids 3 to methyl esters 4 and reaction of the esters 4 with lithium salt of dimethyl methanephosphonate at low temperature. The secondary compounds 6b and 6c were formed in small amounts in the oxidation reactions of 2b and 2c, and the NMR spectroscopy showed that their structure is that of an ester of the acid with the starting alcohol. Their molecular structures were confirmed by single crystal X-ray determination method for 6c and XRPD powder method for 6b.


2021 ◽  
Author(s):  
Nicholas Wiedmaier ◽  
Hartmut Schubert ◽  
Hermann A Mayer ◽  
Lars Wesemann

The ruthenium carbene pincer complex 2 was synthesized treating the benzo annulated cycloheptatriene bisphosphine 1 with RuCl3. Addition of three equivalents of hydrogen to the carbocyclic carbene complex 2 was...


2021 ◽  
Vol 43 (2) ◽  
pp. 193-193
Author(s):  
Taiping Gao Taiping Gao ◽  
Xiaolin Ma Xiaolin Ma ◽  
Xin Li Xin Li ◽  
Qiang Xu and Yubao Wang Qiang Xu and Yubao Wang

The first mesoporous silica nanoparticles (MSNs) supported atomically precise palladium nanoclusters catalyzed alcohol oxidation reactions in water have been achieved. The catalysts was synthesized with simple impregnation method and well characterized by TEM, FT-IR, XPS anddiffuse reflectance optical spectrum and the results proved that the Pd nanoclustersimmobilized into the pores of MSNs.The as-prepared catalyst show excellent activity for the alcohol oxidation reactions with high yield under extremely mild aqueous conditions utilizes 1 atmosphere of molecular oxygen as sole oxidant. The features of clean system, gram-scale oxidation and easy recovery catalyst make this method cost effectively and environmentally benign.


Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 442
Author(s):  
Maciej Kapkowski ◽  
Anna Niemczyk-Wojdyla ◽  
Piotr Bartczak ◽  
Monika Pyrkosz Bulska ◽  
Kamila Gajcy ◽  
...  

The classical stoichiometric oxidation of alcohols is an important tool in contemporary organic chemistry. However, it still requires huge modifications in order to comply with the principles of green chemistry. The use of toxic chemicals, hazardous organic solvents, and the large amounts of toxic wastes that result from the reactions are a few examples of the problems that must be solved. Nanogold alone or conjugated with palladium were supported on different carriers (SiO2, C) and investigated in order to evaluate their catalytic potential for environmentally friendly alcohol oxidation under solvent-free and base-free conditions in the presence H2O2 as a clean oxidant. We tested different levels of Au loading (0.1–1.2% wt.) and different active catalytic site forms (monometallic Au or bimetallic Au–Pd sites). This provided new insights on how the structure of the Au-dispersions affected their catalytic performance. Importantly, the examination of the catalytic performance of the resulting catalysts was oriented toward a broad scope of alcohols, including those that are the most resistant to oxidation—the primary aliphatic alcohols. Surprisingly, the studies proved that Au/SiO2 at a level of Au loading as low as 0.1% wt. appeared to be efficient and prospective catalytic system for the green oxidation of alcohol. Most importantly, the results revealed that 0.1% Au/SiO2 might be the catalyst of choice with a wide scope of utility in the green oxidation of various structurally different alcohols as well as the non-activated aliphatic ones.


2019 ◽  
Vol 7 (18) ◽  
pp. 10918-10923 ◽  
Author(s):  
Kuanhong Cao ◽  
Xin Deng ◽  
Tian Chen ◽  
Qitao Zhang ◽  
Lei Yu

By using Se as structure-directing agent, the surface area and total mesoporous volume of polymeric carbon nitride (PCN) could be obviously enhanced. The PCN-Se material was a better support for Pd nanoparticles, which could catalyze the alcohol oxidation reaction with broad substrate scope.


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