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The surface science of nanoparticles for catalysis: electronic and steric effects of organic ligands
Wu, Wenting; Shevchenko, Elena V., E-mail: eshevchenko@anl.gov2018
AbstractAbstract
[en] Recent studies demonstrate the important roles of surface ligands in creating metal-organic interfaces that can significantly improve both catalytic activity as well as selectivity of chemically synthetized nanoparticle (NP) catalysts. Both steric and electronic effects can be efficiently used to tune catalytic properties of the NPs. Here, we overview the recent advancements in the field of the surface science of NPs for their catalytic applications and discuss the steric and electronic effects of ligands immobilized at the NP surface on the activity and selectivity of catalytically active NPs in different catalytic reactions.
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Copyright (c) 2018 Springer Nature B.V.; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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Journal of Nanoparticle Research; ISSN 1388-0764;
; v. 20(9); p. 1-14

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[en] Data on fluoroalkylation and perfluoroalkylation methods in organic synthesis are analyzed, summarized and described systematically. The most practically important properties of compounds with fluoroalkyl substituents are illustrated. The key trends and the potential of this field of organic chemistry are considered. Electrochemical syntheses of perfluoroalkyl derivatives that are inaccessible or experimentally difficult to prepare by regular chemical techniques are presented. Particular attention is paid to processes involving organometallic compounds as well as to prospects for the development of this field of research. The bibliography includes 226 references
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Available from http://dx.doi.org/10.1070/RC2013v082n09ABEH004342; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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Russian Chemical Reviews (Print); ISSN 0036-021X;
; v. 82(9); p. 835-864

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AbstractAbstract
No abstract available
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National Academy of Sciences of Ukraine, Kyiv (Ukraine); Institute of Physics of NAS of Ukraine, Kyiv (Ukraine); Ministry of Education and Sciences of Ukraine, Kyiv (Ukraine); Fundamental Researches State Fund of Ukraine, Kyiv (Ukraine); Vasyl Stafanyk Precarpathian National University Ivano-Frankivs'k (Ukraine); 192 p; 2010; p. 261; 8. International Conference on Electronic Processes in Organic and Inorganic Materials; Ivano-Frankivsk (Ukraine); 17-22 May 2010; Available from Ukrainian INIS Centre
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AbstractAbstract
[en] Voltammograms of uranocene in benzonitrile under an Ar atmosphere were recorded in studies to measure the controlled oxidation of the compound. The results indicated that cyclooctatetraene (COT) was librated during the electrolysis, and NMR data indicated that no more than 1/3 of all the COT ligand was librated as free COT. Combination of these data led to the conclusion that oxidation produced a dimeric or cluster product cation
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Journal Article
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Journal of the American Chemical Society; v. 100(3); p. 1012-1013
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[en] Isotopically labeled compounds play an important role in chemistry, biology, and medicine. In recent years, organometallic chemistry has been utilized extensively in the development of labeled compounds. Syntheses involving the use of organoboranes have proven to be among the most versatile and effective of the new labeling methodologies. 26 refs
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Muccino, R.R. (ed.) (Hoffmann-La Roche, Inc., Nutley, NJ (USA). Chemical Research Dept.); 591 p; ISBN 0-444-42612-4;
; 1986; p. 225-230; Elsevier; Amsterdam (Netherlands); 2. International symposium on the synthesis and applications of isotopically labeled compounds; Kansas City, Missouri (USA); 3-6 Sep 1985

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[en] Published in summary form only
Original Title
Desarrollo de la quimica de los primeros elementos de la serie de los actinidos
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Instituto Nacional de Investigaciones Nucleares, Mexico City; 141 p; Dec 1986; p. 69; 6. Symposium on Nuclear Chemistry, Radiochemistry and Radiation Chemistry; Puebla, Pue (Mexico); 1-5 Dec 1986
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[en] A semiemperical model is presented to calculate diamagnetic susceptibilities of organotin compounds. Diamagnetic susceptibilities are considered to be contributed by the atoms, bonds, and bond–bond interactions. An excellent agreement between semiemperically calculated and experimental values of diamagnetic susceptibilities is reported. (AIP)
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(c) 1982 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA)
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AbstractAbstract
[en] Published data on the synthesis, structure, properties and applications of metal derivatives of tetrazoles are generalised and described systematically. Compounds based on the anionic and neutral tetrazole forms, C- and N-mono- and C,N-disubstituted tetrazoles are considered.
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Available from http://dx.doi.org/10.1070/RC2006v075n06ABEH003601; Country of input: International Atomic Energy Agency (IAEA)
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Russian Chemical Reviews (Print); ISSN 0036-021X;
; v. 75(6); p. 507-539

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[en] Data on substitution reactions at boron atoms in 10-12-vertex metallacarboranes, which are of fundamental and applied significance, are generalised. The possible mechanisms of substitution reactions and the influence of the metal fragment on substitution positions in the polyhedron are discussed.
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Available from http://dx.doi.org/10.1070/RC2004v073n05ABEH000868; Country of input: International Atomic Energy Agency (IAEA)
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Russian Chemical Reviews (Print); ISSN 0036-021X;
; v. 73(5); p. 433-453

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Serwatowski, J.
Materials of 48. Scientific Assembly of Polish Chemical Society and Association of Engineers and Technicians of Chemical2005
Materials of 48. Scientific Assembly of Polish Chemical Society and Association of Engineers and Technicians of Chemical2005
AbstractAbstract
No abstract available
Original Title
Organoborany do syntezy organicznej i metaloorganicznej
Primary Subject
Source
Polskie Towarzystwo Chemiczne, Oddzial w Poznaniu (Poland); Uniwersytet im. Adama Mickiewicza, Poznan (Poland); Politechnika Poznanska, Poznan (Poland); Instytut Chemii Bioorganicznej, PAN, Poznan (Poland); Akademia Ekonomiczna, Poznan (Poland); [p. S1-S13, W,K,P in each of S groups]; 2005; p. S1-W9; 48. Scientific Assembly of Polish Chemical Society and Association of Engineers and Technicians of Chemical Industry; 47. Zjazd Naukowy Polskiego Towarzystwa Chemicznego i Stowarzyszenia Inzynierow i Technikow Przemyslu Chemicznego; Poznan (Poland); 18-22 Sep 2005; Available at Polskie Towarzystwo Chemiczne, ul. Freta 16, Warsaw (PL); 3 refs
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