5981-10-2Relevant academic research and scientific papers
Selective catalytic hydrogenation of polycyclic aromatic hydrocarbons promoted by ruthenium nanoparticles
Bresó-Femenia, Emma,Chaudret, Bruno,Castillón, Sergio
, p. 2741 - 2751 (2015/05/27)
Ru nanoparticles stabilised by PPh3 are efficient catalysts for hydrogenation of polycyclic aromatic hydrocarbons (PAHs) containing 2-4 rings under mild reaction conditions. These compounds were partially hydrogenated with good to excellent selectivities just by optimizing the reaction conditions. The influence of the nature of substituents present in different positions of naphthalene on the selectivity of hydrogenation was also studied. Hydrogenation of products containing substituents at position 1 is slower than that of products containing substituents at position 2. In all cases, hydrogenation takes place mainly on the less substituted ring.
Facile sonochemical synthesis of carbon nanotube-supported bimetallic Pt-Rh nanoparticles for room temperature hydrogenation of arenes
Pan, Horng-Bin,Wai, Chien M.
scheme or table, p. 1649 - 1660 (2011/10/08)
Bimetallic Pt-Rh nanoparticles can be deposited uniformly on surfaces of carboxylate functionalized multi-walled carbon nanotubes (MWNTs) using a simple one-step sonochemical method. The bimetallic nanoparticle catalyst exhibits a strong synergistic effect relative to the individual Pt or Rh metal nanoparticles for catalytic hydrogenation of polycyclic aromatic hydrocarbons (PAHs), neat benzene and alkylbenzenes. Complete ring saturation of PAHs can be achieved using the bimetallic Pt-Rh/MWNTs catalyst at room temperature. This one-step synthesis technique provides a simple and rapid way of making highly active and recyclable CNT-supported monometallic and bimetallic nanocatalysts for low temperature hydrogenation reactions.
PHOTOCHEMICAL STUDIES WITH o-VINYL DIARYL ETHERS A NEW PHOTO-HETEROCYCLIZATION REACTION ?
Eberbach, Wolfgang,Hensle, Juergen
, p. 4773 - 4776 (2007/10/02)
On photoexcitation the o-vinyl diaryl ethers 10a-d are transformed into o-hydroxy stilbenes 11 which preferentially on direct irradiation are further converted affording the annulated phenanthrenes 12.
Reduction of Polycyclic Arenes by BH Boranes, III. Partial Hydrogenation: From Anthracene to Coronene
Yalpani, Mohamed,Koester, Roland
, p. 719 - 724 (2007/10/02)
Tetrapropyldiboran(6) (TPDB) katalysiert die Hydrierung polycyclischer Arene unter Wasserstoff-Druck bei bei 200 deg C.In einigen Faellen koennen sehr hohe Ausbeuten an Hydroarenen erzielt werden .Neben unterschiedlichen kleinen Mengen an Perhydroarenen bilden sich nach langer Reaktionszeit aus saemtlichen Arenen auch C-C-Spaltungsprodukte.
Regioselective Catalytic Hydrogenation of Polycyclic Aromatic Hydrocarbons under Mild Conditions
Fu, Peter P.,Lee, Hong M.,Harvey, Ronald G.
, p. 2797 - 2803 (2007/10/02)
Hydrogenation of polynuclear hydrocarbons over a palladium catalyst at low pressure and ambient temperature affords regiospecifically the corresponding K-region dihydroarenes, while analogous reactions over a platinum catalyst take place regioselectively on terminal rings to provide the related tetrahydroarenes.Hydrogenation over palladium of phenanthrene, benzanthracene, 7,12-dimethylbenzanthracene, benzpyrene, 3-methylcholanthrene, dibenzanthracene, and chrysene gave 9,10-dihydrophenanthrene, 5,6-dihydrobenzanthracene, 5,6-dihydro-7,12-dimethylbenzanthracene, 4,5-dihydrobenzopyrene, 11,12-dihydro-3-methylcholanthrene, 5,6-dihydrodibenzanthracene, and 5,6-dihydrochrysene, respectively (Table I).Hydrogenation over platinum of benzanthracene, 7-methylbenzanthracene, 12-methylbenzanthracene, 7,12-dimethylbenzanthracene, benzopyrene, chrysene, dibenzanthracene, 5,6-dihydrobenzanthracene, 5,6-dihydro-7,12-dimethylbenzanthracene, and 4,5-dihydrobenzopyrene furnished the corresponding terminal ring tetrahydroarenes (Table II).Partial hydrogenation beyond the dihydro stage in the presence of palladium was exhibited only by hydrocarbons with more than one K region.In these cases, the second stage of hydrogen addition was generally slower than the first, so that the extent of reaction was readily controllable.Hydrogenation was blocked by alkyl substitution in an otherwise susceptible ring, and regioselectivity was diminished or abolished by increased hydrogen pressure, prolonged reaction, or acidity.The mechanism of reaction over palladium is proposed to involve concerted hydrogen addition to the K region, the region of minimum bond delocalization energy, preceded by localized ? and/or ? complexes.Evidence is presented that hydrogenations over platinum do not involve initial addition to the K region followed by isomerization into the terminal ring.Instead, these reactions are suggested to involve addition of 2 mol of hydrogen via an intermediate ? complex to the terminal ring which affords the most thermodynamically favored tetrahydroarene product, i.e., that which requires the minimum amount of energy for its formation.
