C. Caputo

发表

The role of group 14 element hydrides in the activation of C-H bonds in cyclic olefins.

J. Fettinger, P. Power, Owen T. Summerscales, 2012, Journal of the American Chemical Society.

Reversible and irreversible higher-order cycloaddition reactions of polyolefins with a multiple-bonded heavier group 13 alkene analogue: contrasting the behavior of systems with π-π, π-π*, and π-n+ frontier molecular orbital symmetry.

J. Fettinger, S. Nagase, P. Power, 2012, Journal of the American Chemical Society.

Enhancing Light Absorption and Charge Transfer Efficiency in Carbon Dots through Graphitization and Core Nitrogen Doping.

J. Durrant, E. Reisner, Georgina A. M. Hutton, 2017, Angewandte Chemie.

Solar-Driven Reduction of Aqueous Protons Coupled to Selective Alcohol Oxidation with a Carbon Nitride–Molecular Ni Catalyst System

J. Durrant, B. Lotsch, V. W. Lau, 2016, Journal of the American Chemical Society.

Photocatalytic Hydrogen Production using Polymeric Carbon Nitride with a Hydrogenase and a Bioinspired Synthetic Ni Catalyst**

B. Lotsch, V. W. Lau, E. Reisner, 2014, Angewandte Chemie.

Carbon Dots as Versatile Photosensitizers for Solar-Driven Catalysis with Redox Enzymes.

E. Reisner, J. Butt, B. Reuillard, 2016, Journal of the American Chemical Society.

[NiFeSe]-hydrogenase chemistry.

E. Reisner, C. Caputo, Claire Wombwell, 2015, Accounts of chemical research.

Activation of olefins with low-valent gallium compounds under ambient conditions.

J. Fettinger, P. Power, Zhongliang Zhu, 2011, Chemical communications.

Developments in asymmetric catalysis by metal complexes of chiral chelating nitrogen-donor ligands.

N. D. Jones, C. Caputo, 2007, Dalton transactions.

Effect of Carbon Doping on CO2‐Reduction Activity of Single Cobalt Sites in Graphitic Carbon Nitride

A. Frenkel, Jiahao Huang, Lei Zhang, 2021, ChemNanoMat.

Tunable Photocatalytic Production of Syngas Using Co@C 3 N 4 and Black Phosphorus

Peipei Huang, Gonghu Li, C. Caputo, 2021 .

Carbon nitride–TiO2 hybrid modified with hydrogenase for visible light driven hydrogen production† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc02017d Click here for additional data file.

E. Reisner, Lidong Wang, C. Caputo, 2015, Chemical science.

N-heterocyclic phosphenium cations: syntheses and cycloaddition reactions.

N. D. Jones, M. Jennings, R. McDonald, 2008, Dalton transactions.

A new approach to internal Lewis pairs featuring a phosphenium acid and a pyridine base.

N. D. Jones, C. Caputo, P. Ragogna, 2010, Dalton transactions.

Addition of alkynes to digermynes: experimental insight into the reaction pathway.

P. Power, C. Caputo, P. Boyle, 2016, Dalton transactions.

Metathetical Exchange between Metal-Metal Triple Bonds.

J. Fettinger, P. Power, C. Caputo, 2020, Journal of the American Chemical Society.

Dynamic Behavior and Isomerization Equilibria of Distannenes Synthesized by Tin Hydride/Olefin Insertions: Characterization of the Elusive Monohydrido Bridged Isomer.

J. Fettinger, P. Power, M. Olmstead, 2017, Journal of the American Chemical Society.

Modular syntheses of oxazolinylamine ligands and characterization of group 10 metal complexes

N. D. Jones, M. Jennings, C. Caputo, 2007 .

Tin(II) Hydrides as Intermediates in Rearrangements of Tin(II) Alkyl Derivatives.

J. Fettinger, P. Power, M. Olmstead, 2017, Journal of the American Chemical Society.

Counterintuitive mechanisms of the addition of hydrogen and simple olefins to heavy group 13 alkene analogues.

P. Power, C. Caputo, H. Tuononen, 2013, Journal of the American Chemical Society.

Cleavage of Ge–Ge and Sn–Sn Triple Bonds in Heavy Group 14 Element Alkyne Analogues (EAriPr4)2 (E = Ge, Sn; AriPr4 = C6H3-2,6(C6H3-2,6-iPr2)2) by Reaction with Group 6 Carbonyls

J. Fettinger, P. Power, C. Caputo, 2016 .

Activation of gaseous PH3 with low coordinate diaryltetrylene compounds.

P. Power, C. Caputo, P. Ragogna, 2014, Chemical communications.

Heavier Main Group Dimetallene Reactivity: Effects of Frontier Orbital Symmetry

P. Power, C. Caputo, 2013 .

Reactions of Terphenyl-Substituted Digallene AriPr4GaGaAriPr4 (AriPr4 = C6H3-2,6-(C6H3-2,6-iPr2)2) with Transition Metal Carbonyls and Theoretical Investigation of the Mechanism of Addition

J. Fettinger, P. Power, C. Caputo, 2016 .

Solar hydrogen production using carbon quantum dots and a molecular nickel catalyst.

E. Reisner, Georgina A. M. Hutton, B. Martindale, 2015, Journal of the American Chemical Society.

Impact of vacancies on electronic properties of black phosphorus probed by STM

S. Hollen, C. Caputo, C. Flynn, 2018 .

Selective CO2 Reduction Catalyzed by Single Cobalt Sites on Carbon Nitride under Visible-Light Irradiation.

Peipei Huang, Gonghu Li, Christine A Caputo, 2018, Journal of the American Chemical Society.

Highlights from Faraday Discussion: Artificial Photosynthesis, Cambridge, UK, March 2019.

David Wakerley, Sarah Lamaison, Christine A. Caputo, 2019, Chemical communications.

Photocatalytic Hydrogen Production using Polymeric Carbon Nitride with a Hydrogenase and a Bioinspired Synthetic Ni Catalyst

B. Lotsch, V. W. Lau, E. Reisner, 2014, Angewandte Chemie.

Selective CO 2 Reduction Catalyzed by Single Cobalt Sites on Carbon Nitride under Visible-Light Irradiation

A. Frenkel, Jiahao Huang, Peipei Huang, 2018 .

Reactions of Terphenyl-Substituted Digallene AriPr4GaGaAriPr4 (AriPr4 = C6H3-2,6-(C6H3-2,6-iPr2)2) with Transition Metal Carbonyls and Theoretical Investigation of the Mechanism of Addition

J. Fettinger, P. Power, C. Caputo, 2016 .

E. Reisner, Lidong Wang, C. Caputo, 2015, Chemical science.

Counterintuitive mechanisms of the addition of hydrogen and simple olefins to heavy group 13 alkene analogues.

P. Power, C. Caputo, H. Tuononen, 2013, Journal of the American Chemical Society.

Tin(II) Hydrides as Intermediates in Rearrangements of Tin(II) Alkyl Derivatives.

J. Fettinger, P. Power, M. Olmstead, 2017, Journal of the American Chemical Society.

Synthetic approaches to artificial photosynthesis: general discussion.

Qian Wang, Chia-Yu Lin, Michael Grätzel, 2019, Faraday discussions.