M
Malcolm L. H. Green
Researcher at University of Oxford
Publications - 800
Citations - 32440
Malcolm L. H. Green is an academic researcher from University of Oxford. The author has contributed to research in topics: Carbon nanotube & Cyclopentadienyl complex. The author has an hindex of 82, co-authored 800 publications receiving 31121 citations. Previous affiliations of Malcolm L. H. Green include Gas Technology Institute & University of Illinois at Urbana–Champaign.
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Journal ArticleDOI
Synthesis and characterisation of the inclusion complex {(P4)2C60}
Richard E. Douthwaite,Malcolm L. H. Green,Stephen J. Heyes,Matthew J. Rosseinsky,John F. C. Turner +4 more
TL;DR: Incorporation of elemental phosphorus into hexagonal-packed C60 gives the new phase {(P4)2C60}; characterisation by powder diffraction and multinuclear solid-state NMR studies show the P4 tetrahedra occupy trigonal prismatic sites and confirm the retention of the molecular nature of the guest.
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The classification and representation of main group element compounds that feature three-center four-electron interactions
TL;DR: A means to classify and represent compounds that feature 3-center 4-electron (3c-4e) interactions in terms of the number of electrons that each atom contributes to the interaction.
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Unexpected reactions of pentafluorophenyl boron compounds with η-cyclopentadienyl(benzamidinato)zirconium derivatives
TL;DR: The compound [Zr(η-C5H5] with B(C6F5)3 in benzene or dichloromethane gave ZrIII (η)-C5 H5).
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Synthesis, Structure, and Temperature-Dependent Dynamics of Neutral Palladium Allyl Complexes of Annulated Diaminocarbenes and Their Catalytic Application for C−C and C−N Bond Formation Reactions†
TL;DR: In this paper, a bifurcated hydrogen bond between the tetrafluoroborate anions and the central imidazolinium proton (NCHN−) was found.
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Migratory insertion in N-heterocyclic carbene-containing Fe carbonyl complexes: an experimental and theoretical study.
TL;DR: DFT studies on the reactivity of [Fe(eta-C5H5)(CO)2(Me)] with PH3 and dihydroimidazole-2-ylidene (IH) have shown that CO exchange is ener getically favoured for IH, and energetically disfavoured for PH3.