Robert J. Angelici

Prof. Robert J. Angelici


Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2007 in Chemical Communications
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BZBolin Zhu
Bolin Zhu
RARobert J. Angelici
Robert J. Angelici
Bulk gold powder (∼103 nm particle size) is a highly active catalyst for the oxidative dehydrogenation of secondary amines to imines under the mild conditions of 1 atm O2 and 60–100 °C.

19 September 2003 in Chemical Communications
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Journal Article
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SMScott G. McKinley
Scott G. McKinley
RARobert J. Angelici
Robert J. Angelici
Silver (Ag+) salts adsorbed on amorphous silica or mesoporous SBA-15 extract dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-Me2DBT) from simulated, hydrotreated petroleum feedstocks.

25 August 2004 in Angewandte Chemie International Edition
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Journal Article
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PVPaul A. Vecchi
Paul A. Vecchi
Celedonio AlvarezCeledonio Alvarez
Celedonio Alvarez
AEArkady Ellern
Arkady Ellern
RARobert J. Angelici
Robert J. Angelici
ASAndrzej Sygula
Andrzej Sygula
PRPeter W. Rabideau
Peter W. Rabideau


1 March 2007 in Organometallics
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Journal Article
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BZBolin Zhu
Bolin Zhu
AEArkady Ellern
Arkady Ellern
ASAndrzej Sygula
Andrzej Sygula
RSRenata Sygula
Renata Sygula
RARobert J. Angelici
Robert J. Angelici

7 September 2012 in Catalysis Science & Technology
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Journal Article
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RARobert J. Angelici
Robert J. Angelici
Oxidative reactions that are catalysed by bulk gold consisting of ∼50 000 nm gold powder particles or gold (∼50 nm) supported on Al2O3 are reviewed. Using O2 as the oxidizing agent, bulk gold catalyzes the following types of reactions in organic solvents at 45–90 °C: (1) the conversion of amines to imines [(RCH2)2NH → RCH2NCHR], (2) the oxidation of benzyl alcohol to benzaldehyde, (3) the reaction of isocyanides with primary amines to give carbodiimides [CN–R + H2N–R′ → R′–NCN–R] and with secondary amines to give ureas , (4) the reactions of CO with primary amines to give ureas [CO + H2N–R → OC(NHR)2], and (5) the reactions of diazoalkanes with amines to give enamines . In some of these reactions, amine oxides (e.g., Me3N–O) may be used in place of O2. Mechanisms of these and related reactions are examined. These studies show that bulk, non-nanogold is capable of catalysing a variety of different reactions.