Marilyn M. Olmstead

Bio: Marilyn M. Olmstead is an academic researcher from University of California, Davis. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 77, co-authored 762 publications receiving 24240 citations. Previous affiliations of Marilyn M. Olmstead include Yarmouk University & Durham University.

Small-bandgap endohedral metallofullerenes in high yield and purity

Abstract: The idea1 that fullerenes might be able to encapsulate atoms and molecules has been verified by the successful synthesis of a range of endohedral fullerenes, in which metallic or non-metallic species are trapped inside the carbon cage2,3,4,5,6,7,8,9,10,11,12,13. Metal-containing endohedral fullerenes have attracted particular interest as they might exhibit unusual material properties associated with charge transfer from the metal to the carbon shell. However, current synthesis methods have typical yields of less than 0.5%, and produce multiple endohedral fullerene isomers, which makes it difficult to perform detailed studies of their properties. Here we show that the introduction of small amounts of nitrogen into an electric-arc reactor allows for the efficient production of a new family of stable endohedral fullerenes encapsulating trimetallic nitride clusters, ErxSc3-xN@C80 (x = 0–3). This ‘trimetallic nitride template’ process generates milligram quantities of product containing 3–5% Sc3N@C80, which allows us to isolate the material and determine its crystal structure, and its optical and electronic properties. We find that the Sc3N moiety is encapsulated in a highly symmetric, icosahedral C80 cage, which is stabilized as a result of charge transfer between the nitride cluster and the fullerene cage. We expect that our method will provide access to a range of small-bandgap fullerene materials, whose electronic properties can be tuned by encapsulating nitride clusters containing different metals and metal mixtures.

Reactions of transition metal complexes with fullerenes (c60, c70, etc.) and related materials

Abstract: A. Lanthanum, Yttrium, and Scandium 2126 B. Hafnium, Zirconium, and Titanium 2126 C. Tantalum, Niobium, and Vanadium 2127 D. Tungsten, Molybdenum, and Chromium 2127 E. Rhenium, Technetium, and Manganese 2128 F. Osmium, Ruthenium, and Iron 2128 1. Osmylation 2128 2. Reactions with Zerovalent Compounds 2131 3. Other Addition Reactions 2133 4. Redox Reactions 2134 5. Cocrystallizations 2134 G. Iridium, Rhodium, and Cobalt 2135 1. Adduct Formation with Vaska-Type Complexes, Ir(CO)Cl(PR3)2 2135

Interaction of Curved and Flat Molecular Surfaces. The Structures of Crystalline Compounds Composed of Fullerene (C60, C60O, C70, and C120O) and Metal Octaethylporphyrin Units

Abstract: Solutions of C60, C60O, or C70 and metal complexes of octaethylporphyrin (OEPH2) yield crystals that contain both the fullerene and the porphyrin. The structures of C60·2CoII(OEP)·CHCl3, C60·2ZnII(OEP)·CHCl3, and C60O·2CoII(OEP)·CHCl3 are isomorphous and contain an ordered C60 cage surrounded by two MII(OEP) units. Although there is no covalent bond between the fullerene and porphyrin components, the separation between these units is shorter than normal van der Waals contact. Crystals of C70·CoII(OEP)·C6H6·CHCl3, C70·NiII(OEP)·C6H6·CHCl3, and C70·CuII(OEP)·C6H6·CHCl3 are also isomorphous with an ordered fullerene, but have only one porphyrin/fullerene contact. Crystalline C60·ClFeIII(OEP)·CHCl3 lacks the close face-to-face porphyrin/porphyrin contact that is common to all of the other structures reported here but retains the intimate contact between the porphyrin and the fullerene. In (C120O)·CoII(OEP)·0.6C6H6·0.4CHCl3 the fullerene dimer is enclosed by two CoII(OEP) moieties. Unfortunately disorder in th...

Aggregation-Induced Emission: Together We Shine, United We Soar!

Abstract: Ju Mei,†,‡,∥ Nelson L. C. Leung,†,‡,∥ Ryan T. K. Kwok,†,‡ Jacky W. Y. Lam,†,‡ and Ben Zhong Tang*,†,‡,§ †HKUST-Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen 518057, China ‡Department of Chemistry, HKUST Jockey Club Institute for Advanced Study, Institute of Molecular Functional Materials, Division of Biomedical Engineering, State Key Laboratory of Molecular Neuroscience, Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China Guangdong Innovative Research Team, SCUT-HKUST Joint Research Laboratory, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China

Chemical Redox Agents for Organometallic Chemistry

Abstract: 1. Advantages of Chemical Redox Agents 878 2. Disadvantages of Chemical Redox Agents 879 C. Potentials in Nonaqueous Solvents 879 D. Reversible vs Irreversible ET Reagents 879 E. Categorization of Reagent Strength 881 II. Oxidants 881 A. Inorganic 881 1. Metal and Metal Complex Oxidants 881 2. Main Group Oxidants 887 B. Organic 891 1. Radical Cations 891 2. Carbocations 893 3. Cyanocarbons and Related Electron-Rich Compounds 894

The Halogen Bond

Abstract: The halogen bond occurs when there is evidence of a net attractive interaction between an electrophilic region associated with a halogen atom in a molecular entity and a nucleophilic region in another, or the same, molecular entity. In this fairly extensive review, after a brief history of the interaction, we will provide the reader with a snapshot of where the research on the halogen bond is now, and, perhaps, where it is going. The specific advantages brought up by a design based on the use of the halogen bond will be demonstrated in quite different fields spanning from material sciences to biomolecular recognition and drug design.