102 results on '"Sorribes, Iván"'
Search Results
2. From Well-Defined Clusters to Functional Materials: Molecular Engineering of Amorphous Molybdenum Sulfides for Hydrogen Evolution Electrocatalysis
3. Selective dehydrogenation of formic acid catalyzed by air‐stable cuboidal PN molybdenum sulfide clusters
4. Multifunctional Catalysis of Nanosheet Defective Molybdenum Sulfide Basal Planes for Tandem Reactions Involving Alcohols and Molecular Hydrogen
5. Base-Free Catalytic Hydrogen Production from Formic Acid Mediated by a Cubane-Type Mo3S4 Cluster Hydride
6. Disclosing the Biocide Activity of α-Ag2−2xCuxWO4 (0 ≤ x ≤ 0.16) Solid Solutions
7. Straightforward synthesis of benzimidazoles by reductive coupling of dinitroarenes with aldehydes catalyzed by a molecularly engineered molybdenum sulfide catalyst
8. Incorporation of cubane-type Mo 3S 4 molybdenum cluster sulfides in the framework of mesoporous silica
9. Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes
10. Base-Free Catalytic Hydrogen Production from Formic Acid Mediated by a Cubane-Type Mo3S4 Cluster Hydride.
11. Disclosing the Biocide Activity of α-Ag 2−2 x Cu x WO 4 (0 ≤ x ≤ 0.16) Solid Solutions.
12. Tuning the Catalytic Performance of Cobalt Nanoparticles by Tungsten Doping for Efficient and Selective Hydrogenation of Quinolines under Mild Conditions
13. Base-Free Catalytic Hydrogen Production from Formic Acid Mediated by a Cubane-Type Mo3S4Cluster Hydride
14. Unraveling a Biomass-Derived Multiphase Catalyst for the Dehydrogenative Coupling of Silanes with Alcohols under Aerobic Conditions
15. Distinctive Unimolecular Gas-Phase Reactivity of [M(en) 2] 2+ (M = Ni, Cu) Dications and Their Inclusion Complexes with the Macrocyclic Cavitand Cucurbit[8]uril
16. Nanolayered cobalt-molybdenum sulphides (Co-Mo-S) catalyse borrowing hydrogen C-S bond formation reactions of thiols or H
17. On the catalytic transfer hydrogenation of nitroarenes by a cubane-type Mo3S4 cluster hydride: disentangling the nature of the reaction mechanism
18. Palladium doping of In2O3 towards a general and selective catalytic hydrogenation of amides to amines and alcohols
19. Nanolayered cobalt–molybdenum sulphides (Co–Mo–S) catalyse borrowing hydrogen C–S bond formation reactions of thiols or H2S with alcohols
20. Effects of immigration on the Spanish labor market
21. Palladium doping of In2O3 towards a general and selective catalytic hydrogenation of amides to amines and alcohols.
22. Nanolayered Cobalt–Molybdenum Sulfides as Highly Chemo- and Regioselective Catalysts for the Hydrogenation of Quinoline Derivatives
23. Efficient and Selective N‐Methylation of Nitroarenes under Mild Reaction Conditions
24. Nanolayered Co–Mo–S Catalysts for the Chemoselective Hydrogenation of Nitroarenes
25. Chemoselective Hydrogenation of Nitroarenes Catalyzed by Molybdenum Sulphide Clusters
26. On the catalytic transfer hydrogenation of nitroarenes by a cubane-type Mo3S4 cluster hydride: disentangling the nature of the reaction mechanism.
27. Nanolayered cobalt–molybdenum sulphides (Co–Mo–S) catalyse borrowing hydrogen C–S bond formation reactions of thiols or H2S with alcohols.
28. Selective Ruthenium-Catalyzed Reductive Alkoxylation and Amination of Cyclic Imides
29. Catalytic N-Alkylation of Amines Using Carboxylic Acids and Molecular Hydrogen
30. Convenient Reductive Methylation of Amines with Carbonates at Room Temperature
31. Palladium doping of In2O3towards a general and selective catalytic hydrogenation of amides to amines and alcoholsElectronic supplementary information (ESI) available: General information, additional tables, schemes, figures, characterization data and NMR spectra of isolated products. See DOI: 10.1039/c9cy02128k
32. A Mild and Chemoselective Reduction of Nitro and Azo Compounds Catalyzed by a Well-Defined Mo3S4Cluster Bearing Diamine Ligands
33. Reduction of Nitroarenes Using CO and H2O in the Presence of a Nanostructured Cobalt Oxide/Nitrogen-Doped Graphene (NGr) Catalyst
34. Correction to “Direct Catalytic N-Alkylation of Amines with Carboxylic Acids”
35. [Cr(dmbipy)(ox)2]−: a new bis-oxalato building block for metal assembling. Crystal structures and magnetic properties of XPh4[Cr(dmbipy)(ox)2]·5H2O (X = P and As), {Ba(H2O)2[Cr(dmbipy)(ox)2]2}n·17/2nH2O and {Ag(H2O)[Cr(dmbipy)(ox)2]}n·3nH2O
36. Chiral [Mo3S4H3(diphosphine)3]+ hydrido clusters and study of the effect of the metal atom on the kinetics of proton transfer to the coordinated hydride: Mo vs W
37. Direct Catalytic N-Alkylation of Amines with Carboxylic Acids
38. General Catalytic Methylation of Amines with Formic Acid under Mild Reaction Conditions
39. Selective Methylation of Amines with Carbon Dioxide and H2
40. Selective Ruthenium-Catalyzed Reductive Alkoxylation and Amination of Cyclic Imides.
41. Chemoselective Transfer Hydrogenation to Nitroarenes Mediated by Cubane‐Type Mo3S4 Cluster Catalysts
42. General and Selective Iron-Catalyzed Transfer Hydrogenation of Nitroarenes without Base
43. Characterization of PVC-Tetraruthenated Metalloporphyrins Modified Electrodes: Application as Electrocatalyst in the Nitrite Reduction
44. [Cr(dmbipy)(ox)2]−: a new bis-oxalato building block for metal assembling. Crystal structures and magnetic properties of XPh4[Cr(dmbipy)(ox)2]·5H2O (X = P and As), {Ba(H2O)2[Cr(dmbipy)(ox)2]2}n·17/2nH2O and {Ag(H2O)[Cr(dmbipy)(ox)2]}n·3nH2O
45. A Mild and Chemoselective Reduction of Nitro and Azo Compounds Catalyzed by a Well-Defined Mo3S4 Cluster Bearing Diamine Ligands.
46. Reduction of Nitroarenes Using CO and H2O in the Presence of a Nanostructured Cobalt Oxide/Nitrogen-Doped Graphene (NGr) Catalyst.
47. Selective Methylation of Amines with Carbon Dioxide and H2.
48. Selective Methylation of Amines with Carbon Dioxide and H2.
49. Selective Methylation of Amines with Carbon Dioxide and H2.
50. Selective Methylation of Amines with Carbon Dioxide and H2.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.