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Search for "surface grafting" in Full Text gives 4 result(s) in Beilstein Journal of Organic Chemistry.

Radical chemistry in polymer science: an overview and recent advances

  • Zixiao Wang,
  • Feichen Cui,
  • Yang Sui and
  • Jiajun Yan

Beilstein J. Org. Chem. 2023, 19, 1580–1603, doi:10.3762/bjoc.19.116

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  • process is called Compton scattering [179]. One of the major purposes of radiation modification of polymer surfaces is grafting. The surface grafting can be simply tuned by the dose of radiation [180]. Radiation grafting on polymer surfaces is also compatible with RDRP for high density and well-defined
  • derivatives. Chemical reaction process scheme of DCP-induced crosslinking of LDPE. Scheme 16 redrawn from [126]. A probable mechanism of radical-induced hydrosilylation. Polymer surface modification by homolytic dediazonation of diazonium salts. Photoinduced polymer surface modification or surface grafting
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Published 18 Oct 2023

1,4,6,10-Tetraazaadamantanes (TAADs) with N-amino groups: synthesis and formation of boron chelates and host–guest complexes

  • Artem N. Semakin,
  • Ivan S. Golovanov,
  • Yulia V. Nelyubina and
  • Alexey Yu. Sukhorukov

Beilstein J. Org. Chem. 2022, 18, 1424–1434, doi:10.3762/bjoc.18.148

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  • Tripodal molecules are widely used as chelating ligands for transition metal catalysis [1][2][3], sensors for ions and small molecules [4][5], reagents for surface grafting [6], building blocks for the construction of supramolecular structures [7], polycyclic cage molecules [8], and porous materials [9
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Published 11 Oct 2022

Synthesis and surface grafting of a β-cyclodextrin dimer facilitating cooperative inclusion of 2,6-ANS

  • Lars W. Städe,
  • Thorbjørn T. Nielsen,
  • Laurent Duroux,
  • Reinhard Wimmer,
  • Kyoko Shimizu and
  • Kim L. Larsen

Beilstein J. Org. Chem. 2015, 11, 514–523, doi:10.3762/bjoc.11.58

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  • fluorescence spectroscopy that the inclusion of the fluorescent guest into both cavities of the β-CD dimer is maintained when grafted onto a solid surface. Keywords: 2,6-ANS; β-cyclodextrin dimer; silicon dioxide; surface grafting; total internal reflection fluorescence spectroscopy; Introduction Since the
  • functionalization. Controlled surface grafting with a well-defined β-CD dimer is, on the other hand, expected to address these issues and allow for the preparation of a homogenous surface exhibiting well-defined divalent binding sites. To meet this objective, a novel method for the facile synthesis of a β-CD dimer
  • inclusion of 2,6-ANS into both cavities of the β-CD dimer. Surface grafting The β-CD dimer was grafted onto quartz slides activated for CuAAC using an in-house method for the preparation of azidosilane monolayers (unpublished results) involving vapor deposition of 3-glycidoxypropyltrimethoxysilane (GPTMS
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Published 21 Apr 2015

Synthesis and spectroscopic properties of 4-amino-1,8-naphthalimide derivatives involving the carboxylic group: a new molecular probe for ZnO nanoparticles with unusual fluorescence features

  • Laura Bekere,
  • David Gachet,
  • Vladimir Lokshin,
  • Wladimir Marine and
  • Vladimir Khodorkovsky

Beilstein J. Org. Chem. 2013, 9, 1311–1318, doi:10.3762/bjoc.9.147

Graphical Abstract
  • intensity of the solution exhibited a four-fold enhancement. A 14 nm blue-shift was also observed (Figure 7). Fluorescence from 4 persists after several centrifugation/washing cycles (which completely remove 4 from the solvent) and the band shape does not undergo further change, thus proving the ZnO surface
  • grafting. Conclusion Derivative 4 involving both the fluorophore moiety and the carboxylic group capable of binding the ZnO surface can serve as an efficient molecular probe owing to the high sensitivity to the polarity of the surroundings. Derivative 2 can also be used when fluorescence detection at
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Published 03 Jul 2013
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