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Malcolm L. H. Green

Bio: 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.


Papers
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Journal Article
TL;DR: In this article, the ansa-bridged compounds [M{Me 2 C(η 5 -C 5 H 4 ) 2 }(h 5 -c 5 H 5 )Cl] (M=Zr or Hf) have been synthesized and their molecular structures determined by X-ray crystallography.
Abstract: The new ansa-bridged compounds [M{Me 2 C(η 5 -C 5 H 4 ) 2 }(h 5 -C 5 H 5 )Cl] (M=Zr or Hf) have been synthesised and their molecular structures determined by X-ray crystallography. The latter is the first example of a tris(η 5 -cyclopentadienyl) derivative of hafnium

1 citations

Journal ArticleDOI
TL;DR: The crystal growth behavior and crystallography of a variety of metal halides incorporated within single walled carbon nanotubes (SWNTs) as determined by high resolution electron microscopy (HRTEM) is described in this paper.
Abstract: The crystal growth behaviour and crystallography of a variety of metal halides incorporated within single walled carbon nanotubes (SWNTs) as determined by high resolution electron microscopy (HRTEM) is described. Simple packed structures, such as the alkali halides, form related structures within SWNTs that are found to be integral atomic layers in terms of their thickness as a function of the encapsulating SWNT diameter. An enhanced HRTEM image restoration technique reveals precise data concerning lattice distortions present in these crystals. More complex structures, such as those derived from 3D complex, layered and chain halides form related crystal structures within SWNTs. In narrow SWNTs (i.e. with diameters less than ca. 1.6 nm), structures consisting of individual 1D polyhedral chains (1D-PHCs) were obtained that were derived from the corresponding bulk halides structures. In the case of infinite 3D network and layered halides, the 1D polyhedral chains form with lower co-ordinations than in the bulk. Molecular halides also intercalate into SWNTs but these do not readily form organised structures within SWNTs.

1 citations

01 Jan 1995
TL;DR: In this article, the crystal structures of the new compounds M(η-C5R5) and Zr(C5H5) have been determined, where Zr acts as a co-catalyst for the polymerisation of ethylene and propene.
Abstract: The new compounds {M(η-C5R5)[η-CPh(NSiMe3)2]]Cl2} (where R = H, M = Ti, Zr, Hf or R = Me, M = Ti or Zr), are described. The crystal structures of {M(η-C5R5)([η-CPh(NSiMe3)2]Cl2} (R = H, M = Zr or Hf) have been determined. The compound {Zr(η-C5H5)[η-CPh(NSiMe3)2]Cl2} acts as a co-catalyst for the polymerisation of ethylene and propene.

1 citations


Cited by
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Journal ArticleDOI
Sumio Iijima1, Toshinari Ichihashi1
17 Jun 1993-Nature
TL;DR: In this article, the authors reported the synthesis of abundant single-shell tubes with diameters of about one nanometre, whereas the multi-shell nanotubes are formed on the carbon cathode.
Abstract: CARBON nanotubes1 are expected to have a wide variety of interesting properties. Capillarity in open tubes has already been demonstrated2–5, while predictions regarding their electronic structure6–8 and mechanical strength9 remain to be tested. To examine the properties of these structures, one needs tubes with well defined morphologies, length, thickness and a number of concentric shells; but the normal carbon-arc synthesis10,11 yields a range of tube types. In particular, most calculations have been concerned with single-shell tubes, whereas the carbon-arc synthesis produces almost entirely multi-shell tubes. Here we report the synthesis of abundant single-shell tubes with diameters of about one nanometre. Whereas the multi-shell nanotubes are formed on the carbon cathode, these single-shell tubes grow in the gas phase. Electron diffraction from a single tube allows us to confirm the helical arrangement of carbon hexagons deduced previously for multi-shell tubes1.

8,018 citations

Journal ArticleDOI
TL;DR: The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties are equally important.
Abstract: The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties * To whom correspondence should be addressed. Phone, 404-8940292; fax, 404-894-0294; e-mail, mostafa.el-sayed@ chemistry.gatech.edu. † Case Western Reserve UniversitysMillis 2258. ‡ Phone, 216-368-5918; fax, 216-368-3006; e-mail, burda@case.edu. § Georgia Institute of Technology. 1025 Chem. Rev. 2005, 105, 1025−1102

6,852 citations

Journal ArticleDOI
01 Feb 2013-Science
TL;DR: Although not yet providing compelling mechanical strength or electrical or thermal conductivities for many applications, CNT yarns and sheets already have promising performance for applications including supercapacitors, actuators, and lightweight electromagnetic shields.
Abstract: Worldwide commercial interest in carbon nanotubes (CNTs) is reflected in a production capacity that presently exceeds several thousand tons per year. Currently, bulk CNT powders are incorporated in diverse commercial products ranging from rechargeable batteries, automotive parts, and sporting goods to boat hulls and water filters. Advances in CNT synthesis, purification, and chemical modification are enabling integration of CNTs in thin-film electronics and large-area coatings. Although not yet providing compelling mechanical strength or electrical or thermal conductivities for many applications, CNT yarns and sheets already have promising performance for applications including supercapacitors, actuators, and lightweight electromagnetic shields.

4,596 citations

Journal ArticleDOI
TL;DR: The features of nanoparticle therapeutics that distinguish them from previous anticancer therapies are highlighted, and how these features provide the potential for therapeutic effects that are not achievable with other modalities are described.
Abstract: Nanoparticles — particles in the size range 1–100 nm — are emerging as a class of therapeutics for cancer. Early clinical results suggest that nanoparticle therapeutics can show enhanced efficacy, while simultaneously reducing side effects, owing to properties such as more targeted localization in tumours and active cellular uptake. Here, we highlight the features of nanoparticle therapeutics that distinguish them from previous anticancer therapies, and describe how these features provide the potential for therapeutic effects that are not achievable with other modalities. While large numbers of preclinical studies have been published, the emphasis here is placed on preclinical and clinical studies that are likely to affect clinical investigations and their implications for advancing the treatment of patients with cancer.

3,975 citations

Journal ArticleDOI
TL;DR: Department of Materials Science, University of Patras, Greece, Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, and Dipartimento di Scienze Farmaceutiche, Universita di Trieste, Piazzale Europa 1, 34127 Triesteadays.
Abstract: Department of Materials Science, University of Patras, 26504 Rio Patras, Greece, Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vass. Constantinou Avenue, 116 35 Athens, Greece, Institut de Biologie Moleculaire et Cellulaire, UPR9021 CNRS, Immunologie et Chimie Therapeutiques, 67084 Strasbourg, France, and Dipartimento di Scienze Farmaceutiche, Universita di Trieste, Piazzale Europa 1, 34127 Trieste, Italy

3,886 citations