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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, structure, and reactions of a new dimer of molybdenocene, and related bi- and tri-nuclear compounds; molecular structures of [H(η5-C5H5)2Mo(µ-σ:η5-C5H4)Mo(η5-C5H5)], [(η5-C5H5)(OC)Mo(µ-η5:σ-C5H4)Mo(CO)2(η5-C5H5)], and [{Mo(η5-C5H5)}2(µ-η5-C5H4-η5-C5H4)H3]PF6

TL;DR: In this paper, the authors described a number of new and known binuclear molybdenocene derivatives, including cis- or trans-[{Mo(η5-C5H5)H}2(µ-σ:η 5-C-5H4]2, [Mo(∆)-O-MoO3]-Mo( ∆)-MoO1]-MoO2]-H2H4]-H3]PF6] and [Mo (∆−O−MoO-3]-H4)-H
Book ChapterDOI

Influence of molybdenum and tungsten dopants on nickel catalysts for the dry reforming of methane with carbon dioxide to synthesis gas

TL;DR: In this paper, it was shown that carbide sites are formed in close proximity to nickel sites during the dry reforming over Mo/W doped Ni/Al 2 O 3, and these sites enhance the rate of carbon dioxide dissociation and thus provide more surface oxygen for reaction with the carbon formed over nickel.
Journal ArticleDOI

Mono(cyclopentadienyl)molybdenum chemistry: hydrido-, halogeno-, allylic, and butadiene derivatives of [1,2-bis(diphenylphosphino)ethane](η-cyclopentadienyl)molybdenum and related compounds

TL;DR: The trihydride [Mo(η-C5H5)(dppe)H3] reacts with butadiene giving the new compounds as discussed by the authors, which can be found in the literature.
Journal ArticleDOI

Synthesis of small nido-ferrapentaboranes; a novel borane-capped nido-diferrapentaborane

TL;DR: Pentaborane(9) reacts with [Fe(PMe3)3(η2-CH2PMe2)H] to give [2,3-{FeMe3]2}2(µ-H)B4H9] in yields of up to 1 and 22% respectively; the X-ray crystal structure of (1) shows a nido-pentaborane structure in which a BH3 fragment caps the Fe2B face as discussed by the authors.