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Journal articles on the topic 'Catalyseur supporté'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 May 2024

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1

Zalma, Roger, Lionel Bonneau, Jeanine Fournier, Joëlle Guignard, Françoise Borg, and Henri Pezerat. "Hydrodésazotation de l'indole sur catalyseur fer supporté sur amiante." Canadian Journal of Chemistry 65, no. 3 (March 1, 1987): 523–27. http://dx.doi.org/10.1139/v87-091.

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The aim of this study is to examine hydrodenitrogenation (HDN) of indole on asbestos catalysts (chrysotile and crocidolite) under hydrogen pressure. HDN is carried out according to two competitive pathways, either via ortho-ethylaniline or via ortho-toluidine. This reaction is assisted by increase of temperature and pressure and by pre-reduction of the asbestos. Particles of Fe0on the fibre surface are formed from the original material. Their presence plays a role in the initial breaking of the C—N bond and in the hydrogenation reaction.

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2

Bensaddik, A., B. Ernst, F. Garin, G. Maire, and A. Kiennemann. "Etude in situ par EXAFS de la réductibilité d'un catalyseur Fischer-Tropsch à base de cobalt supporté sur silice." Le Journal de Physique IV 06, no. C4 (July 1996): C4–545—C4–552. http://dx.doi.org/10.1051/jp4:1996451.

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3

Jaeger, Philippe. "Préparation de catalyseurs supportés. Preparation of supported catalysts." Sciences Géologiques. Bulletin 46, no. 1 (1993): 281–89. http://dx.doi.org/10.3406/sgeol.1993.1911.

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4

DEVYNCK, J., and F. BEDIOUI. "Catalyse électrochimique à l'aide de catalyseurs immobilisés sur support organique ou minéral." Le Journal de Physique IV 04, no. C1 (January 1994): C1–131—C1–146. http://dx.doi.org/10.1051/jp4:1994109.

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5

Bachari, Khaldoun, Rabah Bouarab, and Ouiza Chérifi. "Production d’Hydrogène via le Procédé Catalytique CH4 + CO2." Journal of Renewable Energies 4, no. 2 (December 31, 2001): 101–5. http://dx.doi.org/10.54966/jreen.v4i2.1002.

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La réaction de reformage du méthane par le CO2 en gaz de synthèse (H2, CO) a été étudiée sur catalyseurs à base de nickel, cobalt et de terres rares supportés. Les solides catalytiques ont été préparés par imprégnation sèche et caractérisés par absorption atomique et par la diffraction des rayons-X. La production d’hydrogène est remarquablement influencée par la nature de la phase métallique et des supports utilisés. L’ordre décroissent des conversions de CO2 et de CH4 ainsi que la production d’hydrogène des catalyseurs supportés sur silice est : Ru, Ni, Rh, Pt, Co. En revanche, l’activité des catalyseurs supportés sur l’alumine suit la séquence suivante : Rh , Ru, Pt.

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6

Mauret, P., P. Alphonse, and M. Ramalanjaona. "Désactivation de catalyseurs au nickel non supporté." Journal de Chimie Physique 84 (1987): 895–99. http://dx.doi.org/10.1051/jcp/1987840895.

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7

Jouve, Andrea, Stefano Cattaneo, Sofia Capelli, Marta Stucchi, Claudio Evangelisti, Alberto Villa, and Laura Prati. "CNF-Functionalization as Versatile Tool for Tuning Activity in Cellulose-Derived Product Hydrogenation." Molecules 24, no. 2 (January 16, 2019): 316. http://dx.doi.org/10.3390/molecules24020316.

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Carbon nanofibers (CNFs) have been functionalized by introducing O, N, and P containing groups in order to investigate the effect of support functionalization in Ru catalysed hydroxymethyl furfural (HMF) and levulinic acid (LA) hydrogenation. In the case of HMF, despite the fact that no effect on selectivity was observed (all the catalysts produced selectively gamma-valerolactone (GVL)), the functionalization strongly affected the activity of the reaction. O-containing and N-containing supports presented a higher activity compared to the bare support. On the contrary, in HMF hydrogenation, functionalization of the support did not have a beneficial effect on the activity of a Ru-catalysed reaction with respect to bare support and only CNFs-O behaved similarly to bare CNFs. In fact, when CNFs-N or CNFs-P were used as the supports, a lower activity was observed, as well as a change in selectivity in which the production of ethers (from the reaction with the solvent) greatly increased.

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8

Triki, H., H. Batis, and A. Katrib. "Propriétés acido-basiques des catalyseurs LaCrO3 supportés." Journal de Chimie Physique et de Physico-Chimie Biologique 95, no. 9 (October 1998): 2015–33. http://dx.doi.org/10.1051/jcp:1998351.

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9

Hong, Hui, Yuhui Sun, Yongjun Zhou, Emily Stephens, Markiyan Samborskyy, and Peter F. Leadlay. "Evidence for an iterative module in chain elongation on the azalomycin polyketide synthase." Beilstein Journal of Organic Chemistry 12 (October 11, 2016): 2164–72. http://dx.doi.org/10.3762/bjoc.12.206.

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The assembly-line synthases that produce bacterial polyketide natural products follow a modular paradigm in which each round of chain extension is catalysed by a different set or module of enzymes. Examples of deviation from this paradigm, in which a module catalyses either multiple extensions or none are of interest from both a mechanistic and an evolutionary viewpoint. We present evidence that in the biosynthesis of the 36-membered macrocyclic aminopolyol lactones (marginolactones) azalomycin and kanchanamycin, isolated respectively from Streptomyces malaysiensis DSM4137 and Streptomyces olivaceus Tü4018, the first extension module catalyses both the first and second cycles of polyketide chain extension. To confirm the integrity of the azl gene cluster, it was cloned intact on a bacterial artificial chromosome and transplanted into the heterologous host strain Streptomyces lividans, which does not possess the genes for marginolactone production. When furnished with 4-guanidinobutyramide, a specific precursor of the azalomycin starter unit, the recombinant S. lividans produced azalomycin, showing that the polyketide synthase genes in the sequenced cluster are sufficient to accomplish formation of the full-length polyketide chain. This provides strong support for module iteration in the azalomycin and kanchanamycin biosynthetic pathways. In contrast, re-sequencing of the gene cluster for biosynthesis of the polyketide β-lactone ebelactone in Streptomyces aburaviensis has shown that, contrary to a recently-published proposal, the ebelactone polyketide synthase faithfully follows the colinear modular paradigm.

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10

Stines-Chaumeil, Claire, François Talfournier, and Guy Branlant. "Mechanistic characterization of the MSDH (methylmalonate semialdehyde dehydrogenase) from Bacillus subtilis." Biochemical Journal 395, no. 1 (March 15, 2006): 107–15. http://dx.doi.org/10.1042/bj20051525.

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Homotetrameric MSDH (methylmalonate semialdehyde dehydrogenase) from Bacillus subtilis catalyses the NAD-dependent oxidation of MMSA (methylmalonate semialdehyde) and MSA (malonate semialdehyde) into PPCoA (propionyl-CoA) and acetyl-CoA respectively via a two-step mechanism. In the present study, a detailed mechanistic characterization of the MSDH-catalysed reaction has been carried out. The results suggest that NAD binding elicits a structural imprinting of the apoenzyme, which explains the marked lag-phase observed in the activity assay. The enzyme also exhibits a half-of-the-sites reactivity, with two subunits being active per tetramer. This result correlates well with the presence of two populations of catalytic Cys302 in both the apo- and holo-enzymes. Binding of NAD causes a decrease in reactivity of the two Cys302 residues belonging to the two active subunits and a pKapp shift from approx. 8.8 to 8.0. A study of the rate of acylation as a function of pH revealed a decrease in the pKapp of the two active Cys302 residues to approx. 5.5. Taken to-gether, these results support a sequential Cys302 activation process with a pKapp shift from approx. 8.8 in the apo-form to 8.0 in the binary complex and finally to approx. 5.5 in the ternary complex. The rate-limiting step is associated with the β-decarboxylation process which occurs on the thioacylenzyme intermediate after NADH release and before transthioesterification. These data also indicate that bicarbonate, the formation of which is enzyme-catalysed, is the end-product of the reaction.

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11

Carvalho, Luísa C. R., Marina J. Dias Pires, Eduarda Fernandes, and M. Manuel B. Marques. "Pd-catalysed amination on a soluble polymer support: arylation of anilines with PEG-supported aryl halides." RSC Advances 3, no. 48 (2013): 25711. http://dx.doi.org/10.1039/c3ra45177a.

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12

Mabang, Théophile, Joseph Mbadcam Ketcha, and Claudine Géron. "Préparation et caractérisation de catalyseurs au palladium supporté : monométalliques et bimétalliques." Annales de Chimie Science des Matériaux 30, no. 2 (April 28, 2005): 149–70. http://dx.doi.org/10.3166/acsm.30.149-170.

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13

Julca, Alex. "Can immigrant remittances support development finance?" Panoeconomicus 60, no. 3 (2013): 365–80. http://dx.doi.org/10.2298/pan1303365j.

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Immigrant remittances are a significant source of income and finance for developing economies, representing about three times? official development assistance and over half of foreign direct investment annually received. Major motivations to send remittances are for improving food, health, and education spending of families at home as well as for investing in entrepreneurial ventures. Economic policies to channel remittances into development finance should translate these motivations into measures to boost social investment and local and regional production, linking remittances policies to broader fiscal, financial and institutional policies. A national development bank can be a catalyser of public and private interests by supporting the scale up of remittances investment programmes and by building partnerships with regional and multilateral development institutions.

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14

van den Ancker, Tania R., and Cameron J. Love. "Polymer supported naphthalene-catalysed sodium reactions." Organic & Biomolecular Chemistry 5, no. 21 (2007): 3520. http://dx.doi.org/10.1039/b710308e.

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15

Gómez, Cecilia, Sonia Ruiz, and Miguel Yus. "Polymer supported naphthalene-catalysed lithiation reactions." Tetrahedron Letters 39, no. 11 (March 1998): 1397–400. http://dx.doi.org/10.1016/s0040-4039(97)10774-2.

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16

Gómez, Cecilia, Sonia Ruiz, and Miguel Yus. "Polymer supported arene-catalysed lithiation reactions." Tetrahedron 55, no. 22 (May 1999): 7017–26. http://dx.doi.org/10.1016/s0040-4020(99)00330-0.

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17

Harvey, Timothy G., and Trevor W. Matheson. "Hydrodenitrogenation catalysed by zeolite-supported ruthenium." Journal of the Chemical Society, Chemical Communications, no. 4 (1985): 188. http://dx.doi.org/10.1039/c39850000188.

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18

de Angelis, Alberto, Stefano Amarilli, Donatella Berti, Luciano Montanari, and Carlo Perego. "Alkylation of benzene catalysed by supported heteropolyacids." Journal of Molecular Catalysis A: Chemical 146, no. 1-2 (October 1999): 37–44. http://dx.doi.org/10.1016/s1381-1169(99)00078-3.

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19

Hernandez-Mejia, Carlos, Edwin S. Gnanakumar, Alma Olivos-Suarez, Jorge Gascon, Heather F. Greer, Wuzong Zhou, Gadi Rothenberg, and N. Raveendran Shiju. "Ru/TiO2-catalysed hydrogenation of xylose: the role of the crystal structure of the support." Catalysis Science & Technology 6, no. 2 (2016): 577–82. http://dx.doi.org/10.1039/c5cy01005e.

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20

Pell, Christopher J., and Oleg V. Ozerov. "Catalytic dehydrogenative borylation of terminal alkynes by POCOP-supported palladium complexes." Inorganic Chemistry Frontiers 2, no. 8 (2015): 720–24. http://dx.doi.org/10.1039/c5qi00074b.

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21

Li, Yi-Qun, Mei-Yun Zhou, and Xin-Ming Xu. "Cellulose Supported Tetraethylenepentamine as a Catalyst for the Knoevenagel Condensation." Journal of Chemical Research 2003, no. 3 (March 2003): 134–35. http://dx.doi.org/10.3184/030823403103173237.

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The Knoevenagel condensation of carbonyl substrates with active methylene compounds proceeds smoothly in commercial 95% ethanol and catalysed by cellulose supported tetraethylenepentamine to afford the desired products of good purity in moderate to excellent yields.

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22

Namdeo, Ashutosh, S. M. Mahajani, and A. K. Suresh. "Palladium catalysed oxidation of glycerol—Effect of catalyst support." Journal of Molecular Catalysis A: Chemical 421 (September 2016): 45–56. http://dx.doi.org/10.1016/j.molcata.2016.05.008.

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23

Liu, Junli, John W. Crawford, and Roberto Viola. "A Theoretical Analysis of the Role of Pyrophosphate,Fructose 6-P,1-Phosphotransferase in Energy Dissipation During the Conversion of Fructose 6-Phosphate to Fructose 1,6-Bisphosphate in Plant Cells." Journal of Biological Systems 05, no. 03 (September 1997): 389–401. http://dx.doi.org/10.1142/s0218339097000242.

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A theoretical analysis of the effect of pyrophosphate,fructose 6-P,1-phosphotransferase (PFP) on energy dissipation in the conversion of fructose 6-phosphate to fructose 1,6-bisphosphate is presented. The conclusion depends sensitively on whether PFP is in equilibrium, or catalyses a net flux in the directions of gluconeogenesis or glycolysis. It is shown that the conditions under which PFP is in equilibrium are rather restricted. Furthermore, experimental evidence supports the theoretical prediction that PFP catalyses a net flux in real systems. When PFP catalyses a net glycolytic flux, the system where both PFP and PFK are active always dissipates less energy than the system where only PFK exists. However, when PFP catalyses a net flux in gluconeogenesis, the PFK-PFP system dissipates more energy than the system where only PFK exists. By comparing the theoretical work with experimental results, the evidence suggests that PFP in higher plant cells catalyses a net glycolytic flux, and its presence increases the energetic efficiency of glycolysis.

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24

Cooke, Paul R., and John R. Lindsay Smith. "Alkene epoxidation catalysed by ligand-bound supported metalloporphyrins." Tetrahedron Letters 33, no. 19 (May 1992): 2737–40. http://dx.doi.org/10.1016/s0040-4039(00)79070-8.

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25

Dell'Anna, M. M., M. Gagliardi, P. Mastrorilli, G. P. Suranna, and C. F. Nobile. "Hydrogenation reactions catalysed by a supported palladium complex." Journal of Molecular Catalysis A: Chemical 158, no. 2 (September 2000): 515–20. http://dx.doi.org/10.1016/s1381-1169(99)00445-8.

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26

Djakovitch, Laurent, Michael Wagner, and Klaus Köhler. "Amination of aryl bromides catalysed by supported palladium." Journal of Organometallic Chemistry 592, no. 2 (December 1999): 225–34. http://dx.doi.org/10.1016/s0022-328x(99)00518-5.

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27

Mastrorilli, P., A. Rizzuti, G. P. Suranna, and C. F. Nobile. "Supported rhodium catalysed hydrogenation reactions under mild conditions." Inorganica Chimica Acta 304, no. 1 (June 2000): 17–20. http://dx.doi.org/10.1016/s0020-1693(00)00054-2.

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28

Bouwkamp-Wijnoltz, A. L., W. Visscher, and J. A. R. van Veen. "Oxygen reduction catalysed by carbon supported iridium-chelates." Electrochimica Acta 39, no. 11-12 (August 1994): 1641–45. http://dx.doi.org/10.1016/0013-4686(94)85148-4.

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29

Trzeciak, A. M., J. J. Ziółkowski, Z. Jaworska-Galas, W. Migta, and J. Wrzyszcz. "Homogeneous and alumina supported rhodium complex catalysed hydrogenation." Journal of Molecular Catalysis 88, no. 1 (February 1994): 13–21. http://dx.doi.org/10.1016/0304-5102(93)e0249-g.

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30

Parnière, Alice, Pierre-Yves Blanchard, Sara Cavaliere, Nicolas Donzel, Bénédicte Prelot, Jacques Rozière, and Deborah J. Jones. "Nitrogen Plasma Modified Carbons for PEMFC with Increased Interaction with Catalyst and Ionomer." Journal of The Electrochemical Society 169, no. 4 (April 1, 2022): 044502. http://dx.doi.org/10.1149/1945-7111/ac609e.

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Vulcan XC72 carbon black, conventionally used as electrocatalyst support in proton exchange membrane fuel cells, was doped with nitrogen functionalities by exposing it to nitrogen plasma, and the effect on its morphology, structure and texture and surface properties was investigated. In particular, the strength of the interaction between the modified carbon and Nafion® ionomer was evaluated by isothermal titration calorimetry, and an enhanced exothermic effect was observed on increasing the amount of nitrogen at the Vulcan surface. The undoped and nitrogen-doped carbon blacks were catalysed with Pt nanoparticles, and the resulting materials were characterised for their electrocatalytic properties towards the oxygen reduction reaction. The electrocatalyst using nitrogen-doped supports are characterised by higher activity and stability, which is attributed to a strong Pt-support interaction promoted by the presence of the heteroatoms.

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31

AlShibane, Ihfaf, Justin S. J. Hargreaves, Andrew L. Hector, William Levason, and Andrew McFarlane. "Synthesis and methane cracking activity of a silicon nitride supported vanadium nitride nanoparticle composite." Dalton Transactions 46, no. 27 (2017): 8782–87. http://dx.doi.org/10.1039/c7dt00285h.

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32

Sedona, Francesco, Matteo Lo Cicero, Silvia Carlotto, Andrea Basagni, Mir Masoud Seyyed Fakhrabadi, Maurizio Casarin, and Mauro Sambi. "Substrate involvement in dioxygen bond dissociation catalysed by iron phthalocyanine supported on Ag(100)." Chemical Communications 54, no. 68 (2018): 9418–21. http://dx.doi.org/10.1039/c8cc04362k.

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33

ZIEGLER, Mathias, Dierk JORCKE, and Manfred SCHWEIGER. "Identification of bovine liver mitochondrial NAD+ glycohydrolase as ADP-ribosyl cyclase." Biochemical Journal 326, no. 2 (September 1, 1997): 401–5. http://dx.doi.org/10.1042/bj3260401.

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The present investigation identifies bovine liver mitochondrial NADase (NAD+ glycohydrolase) as a member of the class of bifunctional ADP-ribosyl cyclases/cyclic ADP-ribose hydrolases, known to be potential second messenger enzymes. These enzymes catalyse the synthesis and degradation of cyclic ADP-ribose, a potent intracellular calcium-mobilizing agent. The mitochondrial enzyme utilized the NAD+ analogues nicotinamide guanine dinucleotide (NGD+) and nicotinamide hypoxanthine dinucleotide (NHD+) to form fluorescent cyclic purine nucleoside diphosphoriboses. ADP-ribosyl cyclase activity was also demonstrated using 32P-labelled NAD+ as substrate. The identity of NADase and ADP-ribosyl cyclase was supported by their co-migration in SDS/polyacrylamide gels. Cyclase activity was visualized directly within the gel by detecting the formation of fluorescent cyclic IDP-ribose from NHD+. The enzyme catalysed the hydrolysis of cyclic ADP-ribose to ADP-ribose. Moreover, in the presence of nicotinamide and cyclic ADP-ribose the enzyme synthesized NAD+. Both the ADP-ribosyl cyclase and NADase activities of the enzyme were strongly inhibited by reducing agents. Treatment of the NADase with dithiothreitol caused the apparent inactivation of the enzyme. Subsequent removal of the reducing agent and addition of oxidized glutathione led to a partial recovery of enzymic activity. The results support a model for pro-oxidant-induced calcium release from mitochondria involving cyclic ADP-ribose as a specific messenger, rather than the non-enzymic modification of proteins by ADP-ribose.

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34

Suktanarak, Pattira, Sarayut Watchasit, Kantima Chitchak, Nukorn Plainpan, Kittipong Chainok, Parichatr Vanalabhpatana, Prompong Pienpinijtham, et al. "Tuning the reactivity of copper complexes supported by tridentate ligands leading to two-electron reduction of dioxygen." Dalton Transactions 47, no. 45 (2018): 16337–49. http://dx.doi.org/10.1039/c8dt03183e.

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35

Stolle, Heike Lisa Kerstin Stephanie, Frank Garwe, Robert Müller, Thomas Krech, Bastian Oberleiter, Thomas Rainer, Wolfgang Fritzsche, and Achim Stolle. "Design of a scalable AuNP catalyst system for plasmon-driven photocatalysis." RSC Advances 8, no. 53 (2018): 30289–97. http://dx.doi.org/10.1039/c8ra03661f.

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36

Swennenhuis, Bert H. G., Ruifang Chen, Piet W. N. M. van Leeuwen, Johannes G. de Vries, and Paul C. J. Kamer. "Supported Chiral Monodentate Ligands in Rhodium-Catalysed Asymmetric Hydrogenation and Palladium-Catalysed Asymmetric Allylic Alkylation." European Journal of Organic Chemistry 2009, no. 33 (November 2009): 5796–803. http://dx.doi.org/10.1002/ejoc.200900911.

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37

DeMuth, Joshua C., Zhihui Song, Stephanie H. Carpenter, Theresa E. Boddie, Aleksa Radović, Tessa M. Baker, Osvaldo Gutierrez, and Michael L. Neidig. "Experimental and computational studies of the mechanism of iron-catalysed C–H activation/functionalisation with allyl electrophiles." Chemical Science 12, no. 27 (2021): 9398–407. http://dx.doi.org/10.1039/d1sc01661j.

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38

Sakirolla, Raghavendra, Yean Kee Lee, and Venkataramana Macharla. "Solid Supported Peptide Catalyst for the Synthesis of Flavanone and Azaflavanones." Mapana - Journal of Sciences 18, no. 2 (April 1, 2019): 21–28. http://dx.doi.org/10.12723/mjs.49.3.

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A variety of flavanones and azaflavanones have been synthesised from chalcones, catalysed by 30 mol% solid support proline terminal peptide, which is mildly efficient with high conversions yields and could be recycled up to three times without significant loss in its activity.Keywords: , Solid Support Peptide Catalyst, Reusable Catalyst, Cyclisation, Flavanones

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39

Primet, Michel, Mohammed El Azhar, and Michelle Guenin. "Influence of the support towards platinum catalysed 1,3-butadiene hydrogenation." Applied Catalysis 58, no. 1 (February 1990): 241–53. http://dx.doi.org/10.1016/s0166-9834(00)82293-9.

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40

Banerjee, Sudheer K., R. Shanker, and Om P. Sachdeva. "Kinetics of Pb(IV) Oxidation of Substituted Methyl Mandelates — A L.F. E. R. Study." Zeitschrift für Naturforschung B 41, no. 4 (April 1, 1986): 467–72. http://dx.doi.org/10.1515/znb-1986-0411.

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Lead tetra acetate (Pb(IV) or LTA) oxidation of the esters X -C6H4-CH(OH)-COOCH3(X = H, m-NO2, p-NO2, m-Cl, p-Cl, p-Br. p-CH3 and p-C2H5) gives corresponding keto esters. The reaction is first order in [Pb(IV)] and second order in [Ester], and is catalysed by pyridine and 2,6-lutidine. The pyridine catalysed reaction is first order each in [Pb(IV)]. [Ester] and [Pyridine]. A kinetic isotope effect is observed in oxidation of methyl m andelate for both uncatalysed reaction (kH/kD = 4.2) and pyridine catalysed reaction (kH/kD = 1.8). Activation param eters for both uncatalysed and pyridine catalysed reactions are evaluated. The results are in accord with Linear Free Energy Relationship (L.F.E.R.) and the reaction constant (ϱ = +0.75) obtained supports proton transfer in the ɑ-C-H bond rupture in the rate limiting step. The role pf pyridine in catalysis, as a ligand or as a base is discussed

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41

McAllister, Mairi I., Cédric Boulho, Liam McMillan, Lauren F. Gilpin, Sandra Wiedbrauk, Colin Brennan, and David Lennon. "The production of tyramine via the selective hydrogenation of 4-hydroxybenzyl cyanide over a carbon-supported palladium catalyst." RSC Advances 8, no. 51 (2018): 29392–99. http://dx.doi.org/10.1039/c8ra05654d.

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42

Jiménez-Morales, Ignacio, Sara Cavaliere, Marc Dupont, Deborah Jones, and Jacques Rozière. "On the stability of antimony doped tin oxide supports in proton exchange membrane fuel cell and water electrolysers." Sustainable Energy & Fuels 3, no. 6 (2019): 1526–35. http://dx.doi.org/10.1039/c8se00619a.

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This study on bare and catalysed Sb–SnO₂ electrospun tubes allowed to determine the potential window for its optimal utilisation as electrocatalyst support in PEM fuel cells and water electrolysers: the stability of the oxide strongly depends on the existing surface segregation of Sb.

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43

Alesso, Elba, Rosario Torviso, Liliana Finkielsztein, Beatriz Lantaño, Graciela Moltrasio, José Aguirre, Patricia Vázquez, et al. "Dehydration of alcohols catalysed by heteropolyacids supported on silica." Journal of Chemical Research 2001, no. 12 (December 1, 2001): 508–10. http://dx.doi.org/10.3184/030823401103168884.

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44

Yu, Bin, Tuğçe Ayvalı, Zhi-Qiang Wang, Xue-Qing Gong, Abdulaziz A. Bagabas, and S. C. Edman Tsang. "Gas phase selective propylene epoxidation over La2O3-supported cubic silver nanoparticles." Catalysis Science & Technology 9, no. 13 (2019): 3435–44. http://dx.doi.org/10.1039/c9cy00567f.

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It is shown that the Ag nanocube/La₂O₃ interface catalyses gas phase oxidation of propylene to propylene oxide cooperatively with enhanced selectivity and conversion. Dioxygen is preferentially activated and dissociated by La₂O₃(001) and the active atomic oxygen over the Ag(100) facet leads to selective propylene epoxidation.

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45

Sung, David W. L., Philip Hodge, and Peter W. Stratford. "Reactions of aldehydes with diethylzinc catalysed by polymer-supported ephedrine and camphor derivatives: comparisons of enantiomeric excesses achieved with various supports: optimisation of support parameters to enable high enantiomeric excesses to be obtained †." Journal of the Chemical Society, Perkin Transactions 1, no. 11 (1999): 1463–72. http://dx.doi.org/10.1039/a901455a.

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Zhu, Ying, Jie Bai, Junzhong Wang, and Chunping Li. "Novel carbon nanofiber-supported Ni(0) nanoparticles catalyse the Heck reaction under ligand-free conditions." RSC Advances 6, no. 35 (2016): 29437–40. http://dx.doi.org/10.1039/c6ra01918h.

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Martínez, Alejandro V., Fabio Invernizzi, Alejandro Leal-Duaso, José A. Mayoral, and José I. García. "Microwave-promoted solventless Mizoroki–Heck reactions catalysed by Pd nanoparticles supported on laponite clay." RSC Advances 5, no. 14 (2015): 10102–9. http://dx.doi.org/10.1039/c4ra15418e.

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Abstract:

Palladium nanoparticles supported on laponite efficiently catalyse solventless Mizoroki–Heck reactions activated by microwaves. High yields are obtained in a few minutes and the catalyst can be efficiently recovered and reused up to thirteen times.

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Smith, D. C., and R. C. Hider. "Thiol exchange catalysed refolding of small proteins utilizing solid-phase supports." Biophysical Chemistry 31, no. 1-2 (August 1988): 21–28. http://dx.doi.org/10.1016/0301-4622(88)80004-8.

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Soares, Olívia Salomé G. P., José J. M. Órfão, and Manuel Fernando R. Pereira. "Nitrate reduction in water catalysed by Pd–Cu on different supports." Desalination 279, no. 1-3 (September 2011): 367–74. http://dx.doi.org/10.1016/j.desal.2011.06.037.

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Wang, Yu-lu, Yue-wei Zhao, and Dong-lan Ma. "Effective Solvent-Free Synthesis of A-Acylazo Compounds with Active Manganese Dioxide Catalysed by Sulfuric Acid Supported on Silica Gel." Journal of Chemical Research 2002, no. 4 (April 2002): 158–59. http://dx.doi.org/10.3184/030823402103171717.

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