Liang, S., Hao, C., & Shi, Y. (2015). The Power of Single-Atom Catalysis. ChemCatChem, 7(17), 2559-2567. doi:10.1002/cctc.201500363
Liu, J. (2016). Catalysis by Supported Single Metal Atoms. ACS Catalysis, 7(1), 34-59. doi:10.1021/acscatal.6b01534
Gates, B. C., Flytzani-Stephanopoulos, M., Dixon, D. A., & Katz, A. (2017). Atomically dispersed supported metal catalysts: perspectives and suggestions for future research. Catalysis Science & Technology, 7(19), 4259-4275. doi:10.1039/c7cy00881c
[+]
Liang, S., Hao, C., & Shi, Y. (2015). The Power of Single-Atom Catalysis. ChemCatChem, 7(17), 2559-2567. doi:10.1002/cctc.201500363
Liu, J. (2016). Catalysis by Supported Single Metal Atoms. ACS Catalysis, 7(1), 34-59. doi:10.1021/acscatal.6b01534
Gates, B. C., Flytzani-Stephanopoulos, M., Dixon, D. A., & Katz, A. (2017). Atomically dispersed supported metal catalysts: perspectives and suggestions for future research. Catalysis Science & Technology, 7(19), 4259-4275. doi:10.1039/c7cy00881c
Liu, L., & Corma, A. (2018). Metal Catalysts for Heterogeneous Catalysis: From Single Atoms to Nanoclusters and Nanoparticles. Chemical Reviews, 118(10), 4981-5079. doi:10.1021/acs.chemrev.7b00776
Wang, A., Li, J., & Zhang, T. (2018). Heterogeneous single-atom catalysis. Nature Reviews Chemistry, 2(6), 65-81. doi:10.1038/s41570-018-0010-1
Parkinson, G. S. (2019). Single-Atom Catalysis: How Structure Influences Catalytic Performance. Catalysis Letters, 149(5), 1137-1146. doi:10.1007/s10562-019-02709-7
Babucci, M., Sarac Oztuna, F. E., Debefve, L. M., Boubnov, A., Bare, S. R., Gates, B. C., … Uzun, A. (2019). Atomically Dispersed Reduced Graphene Aerogel-Supported Iridium Catalyst with an Iridium Loading of 14.8 wt %. ACS Catalysis, 9(11), 9905-9913. doi:10.1021/acscatal.9b02231
Qiao, B., Wang, A., Yang, X., Allard, L. F., Jiang, Z., Cui, Y., … Zhang, T. (2011). Single-atom catalysis of CO oxidation using Pt1/FeOx. Nature Chemistry, 3(8), 634-641. doi:10.1038/nchem.1095
Duan, S., Wang, R., & Liu, J. (2018). Stability investigation of a high number density Pt1/Fe2O3 single-atom catalyst under different gas environments by HAADF-STEM. Nanotechnology, 29(20), 204002. doi:10.1088/1361-6528/aab1d2
Pinto, H., Haapasilta, V., Lokhandwala, M., Öberg, S., & Foster, A. S. (2017). Adsorption and migration of single metal atoms on the calcite (10.4) surface. Journal of Physics: Condensed Matter, 29(13), 135001. doi:10.1088/1361-648x/aa5bd9
Parkinson, G. S., Novotny, Z., Argentero, G., Schmid, M., Pavelec, J., Kosak, R., … Diebold, U. (2013). Carbon monoxide-induced adatom sintering in a Pd–Fe3O4 model catalyst. Nature Materials, 12(8), 724-728. doi:10.1038/nmat3667
Yang, X.-F., Wang, A., Qiao, B., Li, J., Liu, J., & Zhang, T. (2013). Single-Atom Catalysts: A New Frontier in Heterogeneous Catalysis. Accounts of Chemical Research, 46(8), 1740-1748. doi:10.1021/ar300361m
Cui, X., Li, W., Ryabchuk, P., Junge, K., & Beller, M. (2018). Bridging homogeneous and heterogeneous catalysis by heterogeneous single-metal-site catalysts. Nature Catalysis, 1(6), 385-397. doi:10.1038/s41929-018-0090-9
Mitchell, S., Vorobyeva, E., & Pérez‐Ramírez, J. (2018). The Multifaceted Reactivity of Single‐Atom Heterogeneous Catalysts. Angewandte Chemie International Edition, 57(47), 15316-15329. doi:10.1002/anie.201806936
Mitchell, S., Vorobyeva, E., & Pérez‐Ramírez, J. (2018). Die facettenreiche Reaktivität heterogener Einzelatom‐Katalysatoren. Angewandte Chemie, 130(47), 15538-15552. doi:10.1002/ange.201806936
Kumar, A., Bhatti, T. M., & Goldman, A. S. (2017). Dehydrogenation of Alkanes and Aliphatic Groups by Pincer-Ligated Metal Complexes. Chemical Reviews, 117(19), 12357-12384. doi:10.1021/acs.chemrev.7b00247
Lang, R., Li, T., Matsumura, D., Miao, S., Ren, Y., Cui, Y.-T., … Zhang, T. (2016). Hydroformylation of Olefins by a Rhodium Single-Atom Catalyst with Activity Comparable to RhCl(PPh3)3. Angewandte Chemie International Edition, 55(52), 16054-16058. doi:10.1002/anie.201607885
Lang, R., Li, T., Matsumura, D., Miao, S., Ren, Y., Cui, Y.-T., … Zhang, T. (2016). Hydroformylation of Olefins by a Rhodium Single-Atom Catalyst with Activity Comparable to RhCl(PPh3)3. Angewandte Chemie, 128(52), 16288-16292. doi:10.1002/ange.201607885
Cui, X., Junge, K., Dai, X., Kreyenschulte, C., Pohl, M.-M., Wohlrab, S., … Beller, M. (2017). Synthesis of Single Atom Based Heterogeneous Platinum Catalysts: High Selectivity and Activity for Hydrosilylation Reactions. ACS Central Science, 3(6), 580-585. doi:10.1021/acscentsci.7b00105
Chen, Y., Ji, S., Sun, W., Chen, W., Dong, J., Wen, J., … Li, Y. (2018). Discovering Partially Charged Single-Atom Pt for Enhanced Anti-Markovnikov Alkene Hydrosilylation. Journal of the American Chemical Society, 140(24), 7407-7410. doi:10.1021/jacs.8b03121
Malta, G., Kondrat, S. A., Freakley, S. J., Davies, C. J., Lu, L., Dawson, S., … Hutchings, G. J. (2017). Identification of single-site gold catalysis in acetylene hydrochlorination. Science, 355(6332), 1399-1403. doi:10.1126/science.aal3439
Ye, L., Duan, X., Wu, S., Wu, T.-S., Zhao, Y., Robertson, A. W., … Tsang, S. C. E. (2019). Self- regeneration of Au/CeO2 based catalysts with enhanced activity and ultra-stability for acetylene hydrochlorination. Nature Communications, 10(1). doi:10.1038/s41467-019-08827-5
Zhang, X., Sun, Z., Wang, B., Tang, Y., Nguyen, L., Li, Y., & Tao, F. F. (2018). C–C Coupling on Single-Atom-Based Heterogeneous Catalyst. Journal of the American Chemical Society, 140(3), 954-962. doi:10.1021/jacs.7b09314
Chen, Z., Vorobyeva, E., Mitchell, S., Fako, E., Ortuño, M. A., López, N., … Pérez-Ramírez, J. (2018). A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling. Nature Nanotechnology, 13(8), 702-707. doi:10.1038/s41565-018-0167-2
Wasilke, J.-C., Obrey, S. J., Baker, R. T., & Bazan, G. C. (2005). Concurrent Tandem Catalysis. Chemical Reviews, 105(3), 1001-1020. doi:10.1021/cr020018n
Lohr, T. L., & Marks, T. J. (2015). Orthogonal tandem catalysis. Nature Chemistry, 7(6), 477-482. doi:10.1038/nchem.2262
Reuben, B., & Wittcoff, H. (1988). The SHOP process: An example of industrial creativity. Journal of Chemical Education, 65(7), 605. doi:10.1021/ed065p605
Fogg, D. E., & dos Santos, E. N. (2004). Tandem catalysis: a taxonomy and illustrative review. Coordination Chemistry Reviews, 248(21-24), 2365-2379. doi:10.1016/j.ccr.2004.05.012
Poe, S. L., Kobašlija, M., & McQuade, D. T. (2006). Microcapsule Enabled Multicatalyst System. Journal of the American Chemical Society, 128(49), 15586-15587. doi:10.1021/ja066476l
Lu, J., Dimroth, J., & Weck, M. (2015). Compartmentalization of Incompatible Catalytic Transformations for Tandem Catalysis. Journal of the American Chemical Society, 137(40), 12984-12989. doi:10.1021/jacs.5b07257
Abel, M.-L. (2011). Organosilanes: Adhesion Promoters and Primers. Handbook of Adhesion Technology, 237-258. doi:10.1007/978-3-642-01169-6_11
Semenov, V. V. (2011). Preparation, properties and applications of oligomeric and polymeric organosilanes. Russian Chemical Reviews, 80(4), 313-339. doi:10.1070/rc2011v080n04abeh004110
Obligacion, J. V., & Chirik, P. J. (2018). Earth-abundant transition metal catalysts for alkene hydrosilylation and hydroboration. Nature Reviews Chemistry, 2(5), 15-34. doi:10.1038/s41570-018-0001-2
Jones, J., Xiong, H., DeLaRiva, A. T., Peterson, E. J., Pham, H., Challa, S. R., … Datye, A. K. (2016). Thermally stable single-atom platinum-on-ceria catalysts via atom trapping. Science, 353(6295), 150-154. doi:10.1126/science.aaf8800
Pereira-Hernández, X. I., DeLaRiva, A., Muravev, V., Kunwar, D., Xiong, H., Sudduth, B., … Datye, A. K. (2019). Tuning Pt-CeO2 interactions by high-temperature vapor-phase synthesis for improved reducibility of lattice oxygen. Nature Communications, 10(1). doi:10.1038/s41467-019-09308-5
Speier, J. L., Zimmerman, R., & Webster, J. (1956). The Addition of Silicon Hydrides to Olefinic Double Bonds. Part I. The Use of Phenylsilane, Diphenylsilane, Phenylmethylsilane, Amylsilane and Tribromosilane. Journal of the American Chemical Society, 78(10), 2278-2281. doi:10.1021/ja01591a068
Nakajima, Y., & Shimada, S. (2015). Hydrosilylation reaction of olefins: recent advances and perspectives. RSC Advances, 5(26), 20603-20616. doi:10.1039/c4ra17281g
Meister, T. K., Riener, K., Gigler, P., Stohrer, J., Herrmann, W. A., & Kühn, F. E. (2016). Platinum Catalysis Revisited—Unraveling Principles of Catalytic Olefin Hydrosilylation. ACS Catalysis, 6(2), 1274-1284. doi:10.1021/acscatal.5b02624
Morgan, K., Goguet, A., & Hardacre, C. (2015). Metal Redispersion Strategies for Recycling of Supported Metal Catalysts: A Perspective. ACS Catalysis, 5(6), 3430-3445. doi:10.1021/acscatal.5b00535
Ono, L. K., Yuan, B., Heinrich, H., & Cuenya, B. R. (2010). Formation and Thermal Stability of Platinum Oxides on Size-Selected Platinum Nanoparticles: Support Effects. The Journal of Physical Chemistry C, 114(50), 22119-22133. doi:10.1021/jp1086703
Stein, J., Lewis, L. N., Gao, Y., & Scott, R. A. (1999). In Situ Determination of the Active Catalyst in Hydrosilylation Reactions Using Highly Reactive Pt(0) Catalyst Precursors. Journal of the American Chemical Society, 121(15), 3693-3703. doi:10.1021/ja9825377
Sadeghmoghaddam, E., Gu, H., & Shon, Y.-S. (2012). Pd Nanoparticle-Catalyzed Isomerization vs Hydrogenation of Allyl Alcohol: Solvent-Dependent Regioselectivity. ACS Catalysis, 2(9), 1838-1845. doi:10.1021/cs300270d
Galeandro-Diamant, T., Zanota, M.-L., Sayah, R., Veyre, L., Nikitine, C., de Bellefon, C., … Thieuleux, C. (2015). Platinum nanoparticles in suspension are as efficient as Karstedt’s complex for alkene hydrosilylation. Chemical Communications, 51(90), 16194-16196. doi:10.1039/c5cc05675f
ROTH, J. F., ABELL, J. B., FANNIN, L. W., & SCHAEFER, A. R. (1970). Catalytic Dehydrogenation of Higher Normal Paraffins to Linear Olefins. Advances in Chemistry, 193-203. doi:10.1021/ba-1970-0097.ch011
Dry, M. E. (1990). The fischer-tropsch process - commercial aspects. Catalysis Today, 6(3), 183-206. doi:10.1016/0920-5861(90)85002-6
Bukur, D. B., Lang, X., Akgerman, A., & Feng, Z. (1997). Effect of Process Conditions on Olefin Selectivity during Conventional and Supercritical Fischer−Tropsch Synthesis. Industrial & Engineering Chemistry Research, 36(7), 2580-2587. doi:10.1021/ie960507b
Prieto, G., De Mello, M. I. S., Concepción, P., Murciano, R., Pergher, S. B. C., & Martı́nez, A. (2015). Cobalt-Catalyzed Fischer–Tropsch Synthesis: Chemical Nature of the Oxide Support as a Performance Descriptor. ACS Catalysis, 5(6), 3323-3335. doi:10.1021/acscatal.5b00057
Keim, W. (2013). Oligomerization of Ethylene to α-Olefins: Discovery and Development of the Shell Higher Olefin Process (SHOP). Angewandte Chemie International Edition, 52(48), 12492-12496. doi:10.1002/anie.201305308
Keim, W. (2013). Oligomerisierung von Ethen zu α-Olefinen: Erfindung und Entwicklung des Shell-Higher-Olefin-Prozesses (SHOP). Angewandte Chemie, 125(48), 12722-12726. doi:10.1002/ange.201305308
Chalk, A. J., & Harrod, J. F. (1965). Homogeneous Catalysis. II. The Mechanism of the Hydrosilation of Olefins Catalyzed by Group VIII Metal Complexes1. Journal of the American Chemical Society, 87(1), 16-21. doi:10.1021/ja01079a004
Jia, X., & Huang, Z. (2015). Conversion of alkanes to linear alkylsilanes using an iridium–iron-catalysed tandem dehydrogenation–isomerization–hydrosilylation. Nature Chemistry, 8(2), 157-161. doi:10.1038/nchem.2417
Dvořák, F., Farnesi Camellone, M., Tovt, A., Tran, N.-D., Negreiros, F. R., Vorokhta, M., … Fabris, S. (2016). Creating single-atom Pt-ceria catalysts by surface step decoration. Nature Communications, 7(1). doi:10.1038/ncomms10801
Kozlov, S. M., Viñes, F., Nilius, N., Shaikhutdinov, S., & Neyman, K. M. (2012). Absolute Surface Step Energies: Accurate Theoretical Methods Applied to Ceria Nanoislands. The Journal of Physical Chemistry Letters, 3(15), 1956-1961. doi:10.1021/jz3006942
Wodrich, M. D., Busch, M., & Corminboeuf, C. (2016). Accessing and predicting the kinetic profiles of homogeneous catalysts from volcano plots. Chemical Science, 7(9), 5723-5735. doi:10.1039/c6sc01660j
Gutiérrez-Tarriño, S., Concepción, P., & Oña-Burgos, P. (2018). Cobalt Catalysts for Alkene Hydrosilylation under Aerobic Conditions without Dry Solvents or Additives. European Journal of Inorganic Chemistry, 2018(45), 4867-4874. doi:10.1002/ejic.201801068
[-]