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Items: 1 to 20 of 84

1.

Evidence to challenge the universality of the Horiuti-Polanyi mechanism for hydrogenation in heterogeneous catalysis: origin and trend of the preference of a non-Horiuti-Polanyi mechanism.

Yang B, Gong XQ, Wang HF, Cao XM, Rooney JJ, Hu P.

J Am Chem Soc. 2013 Oct 9;135(40):15244-50. doi: 10.1021/ja408314k. Epub 2013 Sep 27.

PMID:
24032528
2.

Kinetic investigation into the chemoselective hydrogenation of α,β-unsaturated carbonyl compounds catalyzed by Ni(0) nanoparticles.

Zaramello L, Albuquerque BL, Domingos JB, Philippot K.

Dalton Trans. 2017 Apr 11;46(15):5082-5090. doi: 10.1039/c7dt00649g.

PMID:
28362451
3.

Ab initio reaction path analysis of benzene hydrogenation to cyclohexane on Pt(111).

Saeys M, Reyniers MF, Neurock M, Marin GB.

J Phys Chem B. 2005 Feb 17;109(6):2064-73.

PMID:
16851197
4.

Parahydrogen-induced polarization by pairwise replacement catalysis on Pt and Ir nanoparticles.

Zhou R, Zhao EW, Cheng W, Neal LM, Zheng H, Quiñones RE, Hagelin-Weaver HE, Bowers CR.

J Am Chem Soc. 2015 Feb 11;137(5):1938-46. doi: 10.1021/ja511476n. Epub 2015 Jan 28.

PMID:
25629434
5.

Acrolein hydrogenation on Pt(211) and Au(211) surfaces: a density functional theory study.

Yang B, Wang D, Gong XQ, Hu P.

Phys Chem Chem Phys. 2011 Dec 21;13(47):21146-52. doi: 10.1039/c1cp22512j. Epub 2011 Oct 31.

PMID:
22037592
6.

Hydrogenation of simple aromatic molecules: a computational study of the mechanism.

Zhong G, Chan B, Radom L.

J Am Chem Soc. 2007 Jan 31;129(4):924-33.

PMID:
17243829
7.

Direct Addition Mechanism during the Catalytic Hydrogenation of Olefins over Platinum Surfaces.

Dong Y, Ebrahimi M, Tillekaratne A, Zaera F.

J Phys Chem Lett. 2016 Jul 7;7(13):2439-43. doi: 10.1021/acs.jpclett.6b01103. Epub 2016 Jun 16.

PMID:
27309969
8.

Hydrogenation vs. H-D isotope scrambling during the conversion of ethylene with hydrogen/deuterium catalyzed by platinum under single-collision conditions.

Dong Y, Ebrahimi M, Tillekaratne A, Simonovis JP, Zaera F.

Phys Chem Chem Phys. 2016 Jul 28;18(28):19248-58. doi: 10.1039/c6cp04157d. Epub 2016 Jul 4.

PMID:
27373226
9.

Iridium Ziegler-type hydrogenation catalysts made from [(1,5-COD)Ir(mu-O2C8H15)](2) and AlEt3: spectroscopic and kinetic evidence for the Ir(n) species present and for nanoparticles as the fastest catalyst.

Alley WM, Hamdemir IK, Wang Q, Frenkel AI, Li L, Yang JC, Menard LD, Nuzzo RG, Ozkar S, Johnson KA, Finke RG.

Inorg Chem. 2010 Sep 6;49(17):8131-47. doi: 10.1021/ic101237c.

PMID:
20681520
10.
11.

At the frontier between heterogeneous and homogeneous catalysis: hydrogenation of olefins and alkynes with soluble iron nanoparticles.

Rangheard C, de Julián Fernández C, Phua PH, Hoorn J, Lefort L, de Vries JG.

Dalton Trans. 2010 Sep 28;39(36):8464-71. doi: 10.1039/c0dt00177e. Epub 2010 Aug 13.

PMID:
20714614
12.

Industrial Ziegler-type hydrogenation catalysts made from Co(neodecanoate)2 or Ni(2-ethylhexanoate)2 and AlEt3: evidence for nanoclusters and sub-nanocluster or larger Ziegler-nanocluster based catalysis.

Alley WM, Hamdemir IK, Wang Q, Frenkel AI, Li L, Yang JC, Menard LD, Nuzzo RG, Özkar S, Yih KH, Johnson KA, Finke RG.

Langmuir. 2011 May 17;27(10):6279-94. doi: 10.1021/la200053f. Epub 2011 Apr 11.

PMID:
21480617
13.

First Principles Calculations for Hydrogenation of Acrolein on Pd and Pt: Chemoselectivity Depends on Steric Effects on the Surface.

Tuokko S, Pihko PM, Honkala K.

Angew Chem Int Ed Engl. 2016 Jan 26;55(5):1670-4. doi: 10.1002/anie.201507631. Epub 2016 Jan 6.

PMID:
26791881
14.

Experimental and theoretical analysis of asymmetric induction in heterogeneous catalysis: diastereoselective hydrogenation of chiral alpha-hydroxyketones over Pt catalyst.

Busygin I, Taskinen A, Nieminen V, Toukoniitty E, Stillger T, Leino R, Murzin DY.

J Am Chem Soc. 2009 Apr 1;131(12):4449-62. doi: 10.1021/ja809070g.

PMID:
19260682
15.

Is it homogeneous or heterogeneous catalysis derived from [RhCp*Cl2]2? In operando XAFS, kinetic, and crucial kinetic poisoning evidence for subnanometer Rh4 cluster-based benzene hydrogenation catalysis.

Bayram E, Linehan JC, Fulton JL, Roberts JA, Szymczak NK, Smurthwaite TD, Özkar S, Balasubramanian M, Finke RG.

J Am Chem Soc. 2011 Nov 23;133(46):18889-902. doi: 10.1021/ja2073438. Epub 2011 Oct 28.

PMID:
22035197
16.

Bridging the gap between surface science and industrial catalysis.

Meunier FC.

ACS Nano. 2008 Dec 23;2(12):2441-4. doi: 10.1021/nn800787e.

PMID:
19206277
17.

Unraveling the pathway of gold(I)-catalyzed olefin hydrogenation: an ionic mechanism.

Comas-Vives A, Ujaque G.

J Am Chem Soc. 2013 Jan 30;135(4):1295-305. doi: 10.1021/ja305630z. Epub 2013 Jan 15.

PMID:
23214503
19.

The nature of the active site in heterogeneous metal catalysis.

Nørskov JK, Bligaard T, Hvolbaek B, Abild-Pedersen F, Chorkendorff I, Christensen CH.

Chem Soc Rev. 2008 Oct;37(10):2163-71. doi: 10.1039/b800260f. Epub 2008 Aug 4.

PMID:
18818819
20.

Heterogeneous catalytic hydrogenation reactions in continuous-flow reactors.

Irfan M, Glasnov TN, Kappe CO.

ChemSusChem. 2011 Mar 21;4(3):300-16. doi: 10.1002/cssc.201000354. Epub 2011 Feb 17. Review.

PMID:
21337528

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