Richard D. Harcourt
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Richard D. Harcourt has a total of 60 co-authors. Here are the top co-authors by number of shared publications:
- Thomas M. Klapoetke
Department of Chemistry, Ludwig-Maximilian-University of Munich, Butenandtstr. 5-13, 81377 Munich, Germany
10 shared publications Frances L. Skrezenek
7 shared publicationsGregory D. Scholes
Department of Chemistry, The University of California, Berkeley, California 94729 1460
6 shared publicationsThomas M. Klapötke
Department of Chemistry , Ludwig-Maximilian University of Munich , Butenandstr. 5-13(D) , D-81377 Munich , Germany
6 shared publicationsKenneth P. Ghiggino
School of Chemistry, University of Melbourne, Parkville, Victoria 3052, Australia
4 shared publicationsAlison Harcourt
2 shared publications
Latest Publications
- 1 March 2018
- Published by Elsevier in Coordination Chemistry Reviews
- Vol. 358, 178-180
Oxyheme valence bond structures and the oxyheme + NO reaction
- 1 March 2018
- Published by Elsevier in Coordination Chemistry Reviews
- Vol. 358, 178-180
Oxyheme valence bond structures and the oxyheme + NO reaction
- 1 September 2017
- Published by Elsevier in Nitric Oxide
- Vol. 69, 51-55
Construction of valence bond structures for {FeNO} 7 nitrosyl heme and non-heme complexes
- 1 September 2017
- Published by Elsevier in Nitric Oxide
- Vol. 69, 51-55
Construction of valence bond structures for {FeNO} 7 nitrosyl heme and non-heme complexes
- 1 July 2016
- Published by Elsevier in Chemical Physics Letters
- Vol. 655-656, 80-85
Comments on valence-bond structures and charge-shift + recoupled-pair bonding for symmetrical 4-electron 3-centre bonding units
- 1 July 2016
- Published by Elsevier in Chemical Physics Letters
- Vol. 655-656, 80-85
Comments on valence-bond structures and charge-shift + recoupled-pair bonding for symmetrical 4-electron 3-centre bonding units
- Open Access
- 25 February 2016
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 7 (5) , 3443-3447
Comment on “A quantitative definition of hypervalency” by M. C. Durrant, Chem. Sci., 2015, 6, 6614
Consideration is given to (electronically) hypervalent increased-valence structures, which possess 2c–1e bonds, fractional 2c–2e bonds, and usually normal 2c–2e bonds. For singlet-spin electron-rich systems, increased-valence structures, with Heitler–London 2c–2e bond wavefunctions, are equivalent to resonance between non-hypervalent Kekulé and Dewar (or singlet diradical) type Lewis structures. Dewar structures are not considered in the Chem. Sci. 2015, 6, 6614 Edge article on hypervalency. Using one-electron delocalizations from lone-pair atomic orbitals into separate bonding molecular orbitals, increased-valence structures for PCl5, O3, SO4 2−, NO3 −, N2O4 and SN2 reactions are derived from the Edge-article's Kekulé-type Lewis structures, and compared with the Edge article's hypervalent structures with 2c–2e bonds. It is also shown that Durrant's method to determine the γ parameter for XAY-type systems that possess a symmetrical 3c–4e bonding unit is related to the A-atom charge density.
- 25 February 2016
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 7 (5) , 3443-3447
Open AccessComment on “A quantitative definition of hypervalency” by M. C. Durrant, Chem. Sci., 2015, 6, 6614
Consideration is given to (electronically) hypervalent increased-valence structures, which possess 2c–1e bonds, fractional 2c–2e bonds, and usually normal 2c–2e bonds. For singlet-spin electron-rich systems, increased-valence structures, with Heitler–London 2c–2e bond wavefunctions, are equivalent to resonance between non-hypervalent Kekulé and Dewar (or singlet diradical) type Lewis structures. Dewar structures are not considered in the Chem. Sci. 2015, 6, 6614 Edge article on hypervalency. Using one-electron delocalizations from lone-pair atomic orbitals into separate bonding molecular orbitals, increased-valence structures for PCl5, O3, SO4 2−, NO3 −, N2O4 and SN2 reactions are derived from the Edge-article's Kekulé-type Lewis structures, and compared with the Edge article's hypervalent structures with 2c–2e bonds. It is also shown that Durrant's method to determine the γ parameter for XAY-type systems that possess a symmetrical 3c–4e bonding unit is related to the A-atom charge density.
- 31 October 2015
- Published by Springer Nature
- p. 317-323
Some Additional Topics
- 31 October 2015
- Published by Springer Nature
- p. 313-316
A Note on Pauling “3-Electron Bonds” and Covalent-Ionic Resonance
- 31 October 2015
- Published by Springer Nature
- p. 313-316
A Note on Pauling “3-Electron Bonds” and Covalent-Ionic Resonance
- 31 October 2015
- Published by Springer Nature
- p. 299-311
Some Comparisons of Types of Wave-Funcions for 4-Eelectron 3-Centre Bonding Units
- 31 October 2015
- Published by Springer Nature
- p. 299-311
Some Comparisons of Types of Wave-Funcions for 4-Eelectron 3-Centre Bonding Units
- 31 October 2015
- Published by Springer Nature
- p. 283-297
Free-Radical and Spin-Paired Diradical Reactions
- 31 October 2015
- Published by Springer Nature
- p. 283-297
Free-Radical and Spin-Paired Diradical Reactions
- 31 October 2015
- Published by Springer Nature
- p. 269-281
Base-Displacement Reactions and Electron Conduction in Alkali Metals
- 31 October 2015
- Published by Springer Nature
- p. 269-281
Base-Displacement Reactions and Electron Conduction in Alkali Metals