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  • Wiley  (3)
  • 1
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Angewandte Chemie International Edition Vol. 60, No. 11 ( 2021-03-08), p. 6117-6123
    In: Angewandte Chemie International Edition, Wiley, Vol. 60, No. 11 ( 2021-03-08), p. 6117-6123
    Abstract: An anionic mechanism is used to create polymers and copolymers as confined to, or anchored to, high‐surface‐area porous nanoparticles. Linear polymers with soft and glassy chains, such as polyisoprene and polymethylmethacrylate, were produced by confined anionic polymerization in 3D networks of porous aromatic frameworks. Alternatively, multiple anions were generated on the designed frameworks which bear removal protons at selected positions, and initiate chain propagation, resulting in chains covalently connected to the 3D network. Such growth can continue outside the pores to produce polymer‐matrix nanoparticles coated with anchored chains. Sequential reactions were promoted by the living character of this anionic propagation, yielding nanoparticles that were covered by a second polymer anchored by anionic block copolymerization. The intimacy of the matrix and the grown‐in polymers was demonstrated by magnetization transfer across the interfaces in 2D 1 H‐ 13 C‐HETCOR NMR spectra.
    Type of Medium: Online Resource
    ISSN: 1433-7851 , 1521-3773
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2011836-3
    detail.hit.zdb_id: 123227-7
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2016
    In:  European Journal of Inorganic Chemistry Vol. 2016, No. 15-16 ( 2016-06), p. 2626-2633
    In: European Journal of Inorganic Chemistry, Wiley, Vol. 2016, No. 15-16 ( 2016-06), p. 2626-2633
    Abstract: The following Ag I bis(pyrazolyl)methane complexes with BF 4 – /NO 3 – as counteranions were synthesized and characterized: [Ag(L pzH )] 2 (NO 3 ) 2 ( 1 ), [Ag(L pzMe )] 2 (NO 3 ) 2 ( 2 ), [Ag(L pzH )] n (BF 4 ) n ( 3 ), and [Ag(L pzMe )] n (BF 4 ) n ( 4 ) [L pzH = bis(pyrazolyl)methane; L pzMe = bis(3,5‐dimethylpyrazolyl)methane]. These complexes were prepared to identify optimum precursors for the thermolytic deposition of metallic silver. The crystal structures of 1 and 2 show that the complexes are dinuclear and that the NO 3 – anions interact with the metals. In contrast, 3 is polymeric and the BF 4 – does not interact with the metal. When crystallizing 1 – 4 in non‐anhydrous solvents, the presence of adventitious water further reacts with 3 and 4 (but not with 1 and 2 ) to yield dinuclear complexes [Ag(L pzH )(H 2 O) 2 ] 2 (BF 4 ) 2 ( 3a ) and [Ag(L pzMe )(H 2 O) 2 ] 2 (BF 4 ) 2 ( 4a ). All of the dinuclear species 1 , 2 , 3a and 4a exhibit an argentophilic interaction with Ag ··· Ag distances in the range 3.18–2.99 Å. Thermogravimetric analysis (TGA) shows that 1 and 2 have lower decomposition temperatures (231 and 255 °C, respectively) than 3 and 4 (298 and 331 °C, respectively). 2 was further investigated as a precursor for metallic silver deposition by spin‐coating solutions (10 –3 m , THF/DMSO, 4:1), followed by annealing at 310 °C on 52100 steel substrates. According to energy‐dispersive X‐ray spectroscopy (EDS) and scanning electron microscopy (SEM) the metal deposition proceeds primarily via an island growth (Volmer–Weber) mechanism.
    Type of Medium: Online Resource
    ISSN: 1434-1948 , 1099-0682
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 1475009-0
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  • 3
    In: Angewandte Chemie, Wiley, Vol. 133, No. 11 ( 2021-03-08), p. 6182-6188
    Abstract: An anionic mechanism is used to create polymers and copolymers as confined to, or anchored to, high‐surface‐area porous nanoparticles. Linear polymers with soft and glassy chains, such as polyisoprene and polymethylmethacrylate, were produced by confined anionic polymerization in 3D networks of porous aromatic frameworks. Alternatively, multiple anions were generated on the designed frameworks which bear removal protons at selected positions, and initiate chain propagation, resulting in chains covalently connected to the 3D network. Such growth can continue outside the pores to produce polymer‐matrix nanoparticles coated with anchored chains. Sequential reactions were promoted by the living character of this anionic propagation, yielding nanoparticles that were covered by a second polymer anchored by anionic block copolymerization. The intimacy of the matrix and the grown‐in polymers was demonstrated by magnetization transfer across the interfaces in 2D 1 H‐ 13 C‐HETCOR NMR spectra.
    Type of Medium: Online Resource
    ISSN: 0044-8249 , 1521-3757
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 505868-5
    detail.hit.zdb_id: 506609-8
    detail.hit.zdb_id: 514305-6
    detail.hit.zdb_id: 505872-7
    detail.hit.zdb_id: 1479266-7
    detail.hit.zdb_id: 505867-3
    detail.hit.zdb_id: 506259-7
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