Search Results - "Carlson, Robert M."

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    Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces by Schreiner, Peter R., Chernish, Lesya V., Gunchenko, Pavel A., Tikhonchuk, Evgeniya Yu, Hausmann, Heike, Serafin, Michael, Schlecht, Sabine, Dahl, Jeremy E. P., Carlson, Robert M. K., Fokin, Andrey A.

    Published in Nature (London) (15-09-2011)
    “…Strength at length in carbon–carbon bonds The synthesis of alkane hydrocarbons containing extremely long carbon–carbon (C–C) bonds, the longest observed in…”
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    Vertical-Substrate MPCVD Epitaxial Nanodiamond Growth by Tzeng, Yan-Kai, Zhang, Jingyuan Linda, Lu, Haiyu, Ishiwata, Hitoshi, Dahl, Jeremy, Carlson, Robert M. K, Yan, Hao, Schreiner, Peter R, Vučković, Jelena, Shen, Zhi-Xun, Melosh, Nicholas, Chu, Steven

    Published in Nano letters (08-03-2017)
    “…Color center-containing nanodiamonds have many applications in quantum technologies and biology. Diamondoids, molecular-sized diamonds have been used as seeds…”
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    Sterically controlled mechanochemistry under hydrostatic pressure by Yan, Hao, Yang, Fan, Pan, Ding, Lin, Yu, Hohman, J. Nathan, Solis-Ibarra, Diego, Li, Fei Hua, Dahl, Jeremy E. P., Carlson, Robert M. K., Tkachenko, Boryslav A., Fokin, Andrey A., Schreiner, Peter R., Galli, Giulia, Mao, Wendy L., Shen, Zhi-Xun, Melosh, Nicholas A.

    Published in Nature (London) (22-02-2018)
    “…‘Molecular anvil’ molecules consisting of a compressible mechanophore and incompressible ligands react under hydrostatic pressure to produce elemental metal…”
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    Stable Alkanes Containing Very Long Carbon–Carbon Bonds by Fokin, Andrey A, Chernish, Lesya V, Gunchenko, Pavel A, Tikhonchuk, Evgeniya Yu, Hausmann, Heike, Serafin, Michael, Dahl, Jeremy E. P, Carlson, Robert M. K, Schreiner, Peter R

    Published in Journal of the American Chemical Society (22-08-2012)
    “…The metal-induced coupling of tertiary diamondoid bromides gave highly sterically congested hydrocarbon (hetero)dimers with exceptionally long central C–C…”
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    Synthesis and Transformation of Linear Adamantane Assemblies inside Carbon Nanotubes by Zhang, Jinying, Feng, Yanquan, Ishiwata, Hitoshi, Miyata, Yasumitsu, Kitaura, Ryo, Dahl, Jeremy E. P, Carlson, Robert M. K, Shinohara, Hisanori, Tománek, David

    Published in ACS nano (23-10-2012)
    “…We report the assembly and thermal transformation of linear diamondoid assemblies inside carbon nanotubes. Our calculations and observations indicate that…”
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    Evidence of Diamond Nanowires Formed inside Carbon Nanotubes from Diamantane Dicarboxylic Acid by Zhang, Jinying, Zhu, Zhen, Feng, Yanquan, Ishiwata, Hitoshi, Miyata, Yasumitsu, Kitaura, Ryo, Dahl, Jeremy E. P., Carlson, Robert M. K., Fokina, Natalie A., Schreiner, Peter R., Tománek, David, Shinohara, Hisanori

    Published in Angewandte Chemie International Edition (25-03-2013)
    “…Carbon is a girl′s best friend: Carbon‐based nanowires have been produced during thermal annealing of diamantane‐4,9‐dicarboxylic acid in carbon nanotubes…”
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    Template Synthesis of Linear-Chain Nanodiamonds Inside Carbon Nanotubes from Bridgehead-Halogenated Diamantane Precursors by Nakanishi, Yusuke, Omachi, Haruka, Fokina, Natalie A., Schreiner, Peter R., Kitaura, Ryo, Dahl, Jeremy E. P., Carlson, Robert M. K., Shinohara, Hisanori

    Published in Angewandte Chemie International Edition (07-09-2015)
    “…A simple method for the synthesis of linear‐chain diamond‐like nanomaterials, so‐called diamantane polymers, is described. This synthetic approach is primarily…”
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    London Dispersion Directs On-Surface Self-Assembly of [121]Tetramantane Molecules by Ebeling, Daniel, Šekutor, Marina, Stiefermann, Marvin, Tschakert, Jalmar, Dahl, Jeremy E. P, Carlson, Robert M. K, Schirmeisen, André, Schreiner, Peter R

    Published in ACS nano (26-09-2017)
    “…London dispersion (LD) acts between all atoms and molecules in nature, but the role of LD interactions in the self-assembly of molecular layers is still poorly…”
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    Assigning the absolute configuration of single aliphatic molecules by visual inspection by Ebeling, Daniel, Šekutor, Marina, Stiefermann, Marvin, Tschakert, Jalmar, Dahl, Jeremy E. P., Carlson, Robert M. K., Schirmeisen, André, Schreiner, Peter R.

    Published in Nature communications (20-06-2018)
    “…Deciphering absolute configuration of a single molecule by direct visual inspection is the next step in compound identification, with far-reaching implications…”
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    Ultralow effective work function surfaces using diamondoid monolayers by Narasimha, Karthik Thimmavajjula, Ge, Chenhao, Fabbri, Jason D., Clay, William, Tkachenko, Boryslav A., Fokin, Andrey A., Schreiner, Peter R., Dahl, Jeremy E., Carlson, Robert M. K., Shen, Z. X., Melosh, Nicholas A.

    Published in Nature nanotechnology (01-03-2016)
    “…Air-stable monolayers of diamondoids can rival cesium's work-function-lowering ability and can dramatically increase field emission current through a radical…”
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    Spatially resolved electronic and vibronic properties of single diamondoid molecules by Wang, Yayu, Crommie, Michael F, Kioupakis, Emmanouil, Lu, Xinghua, Wegner, Daniel, Yamachika, Ryan, Dahl, Jeremy E, Carlson, Robert M. K, Louie, Steven G

    Published in Nature materials (01-01-2008)
    “…Diamondoids are a unique form of carbon nanostructure best described as hydrogen-terminated diamond molecules. Their diamond-cage structures and tetrahedral…”
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    Monochromatic Photocathodes from Graphene-Stabilized Diamondoids by Yan, Hao, Narasimha, Karthik T, Denlinger, Jonathan, Li, Fei Hua, Mo, Sung-Kwan, Hohman, J. Nathan, Dahl, Jeremy E. P, Carlson, Robert M. K, Tkachenko, Boryslav A, Fokin, Andrey A, Schreiner, Peter R, Hussain, Zahid, Shen, Zhi-Xun, Melosh, Nicholas A

    Published in Nano letters (14-02-2018)
    “…The monochromatic photoemission from diamondoid monolayers provides a new strategy to create electron sources with low energy dispersion and enables compact…”
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  14. 14

    Effects of Molecular Geometry on the Properties of Compressed Diamondoid Crystals by Yang, Fan, Lin, Yu, Baldini, Maria, Dahl, Jeremy E. P, Carlson, Robert M. K, Mao, Wendy L

    Published in The journal of physical chemistry letters (17-11-2016)
    “…Diamondoids are an intriguing group of carbon-based nanomaterials, which combine desired properties of inorganic nanomaterials and small hydrocarbon molecules…”
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    Optical response of diamond nanocrystals as a function of particle size, shape, and symmetry by Landt, Lasse, Klünder, Kathrin, Dahl, Jeremy E, Carlson, Robert M K, Möller, Thomas, Bostedt, Christoph

    Published in Physical review letters (24-07-2009)
    “…The optical spectra of hydrogen-passivated diamond clusters (diamondoids) precisely defined in size and shape have been measured in the gas phase, i.e., under…”
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    Origin of the Monochromatic Photoemission Peak in Diamondoid Monolayers by Clay, William A, Liu, Zhi, Yang, Wanli, Fabbri, Jason D, Dahl, Jeremy E, Carlson, Robert M. K, Sun, Yun, Schreiner, Peter R, Fokin, Andrey A, Tkachenko, Boryslav A, Fokina, Nataliya A, Pianetta, Piero A, Melosh, Nicholas, Shen, Zhi-Xun

    Published in Nano letters (01-01-2009)
    “…Recent photoemission experiments have discovered a highly monochromatized secondary electron peak emitted from diamondoid self-assembled monolayers on metal…”
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    Functionalized Nanodiamonds:  Triamantane and [121]Tetramantane by Schreiner, Peter R, Fokina, Natalie A, Tkachenko, Boryslav A, Hausmann, Heike, Serafin, Michael, Dahl, Jeremy E. P, Liu, Shenggao, Carlson, Robert M. K, Fokin, Andrey A

    Published in Journal of organic chemistry (01-09-2006)
    “…The selective functionalizations of the fundamental hydrogen-terminated nanodiamonds triamantane 1, as well as the most symmetrical representative of the…”
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    Selective Preparation of Diamondoid Phosphonates by Fokin, Andrey A, Yurchenko, Raisa I, Tkachenko, Boryslav A, Fokina, Natalie A, Gunawan, Maria A, Poinsot, Didier, Dahl, Jeremy E. P, Carlson, Robert M. K, Serafin, Michael, Cattey, Hélène, Hierso, Jean-Cyrille, Schreiner, Peter R

    Published in Journal of organic chemistry (06-06-2014)
    “…We present an effective sequence for the preparation of phosphonic acid derivatives of the diamondoids diamantane, triamantane, [121]tetramantane, and…”
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