2008
DOI: 10.1016/j.jorganchem.2007.10.052
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Chemical modification of poly(n-hexylsilane) – Synthesis of functional polysilanes bearing thienyl groups on the appended sila-alkyl side chains and their application in the generation and stabilization of silver nanoparticles

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Cited by 23 publications
(19 citation statements)
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“…13 In addition, we have also demonstrated that the use of functional polysilanes bearing thienyl or furyl donor groups on the appended silaÀalkyl side chains is advantageous to afford polymerÀmetal composites containing silver and palladium nanoparticles with long shelf life stability. 14,15 The passive behavior of these nanoparticles toward agglomeration in the functional polymer matrix originates from donorÀ acceptor interaction between thienyl/furyl group and the nanometal surface.…”
Section: Introductionmentioning
confidence: 99%
“…13 In addition, we have also demonstrated that the use of functional polysilanes bearing thienyl or furyl donor groups on the appended silaÀalkyl side chains is advantageous to afford polymerÀmetal composites containing silver and palladium nanoparticles with long shelf life stability. 14,15 The passive behavior of these nanoparticles toward agglomeration in the functional polymer matrix originates from donorÀ acceptor interaction between thienyl/furyl group and the nanometal surface.…”
Section: Introductionmentioning
confidence: 99%
“…To generate metal NPs using photochemical reduction, Tamai and coworkers mixed metal precursors (HAuCl 4 , AgNO 3 , or Na 2 PdCl 4 with photo-initiator (PMPS) decorated PS MS. 63 Upon irradiation by UV, oxidative decomposition of PMPS and reduction of metal ions occurred concurrently, forming hybrid metal NP-polymeric particles (Fig. 4).…”
Section: In-situ Modification Of Nanoparticlementioning
confidence: 99%
“…A few copolymer templates incorporating polysilane units [R 2 Si] n have been utilized for the synthesis of silicon‐based polymer–metal nanocomposites which exhibit excellent catalytic properties in many organic transformations, including hydrogenation, Suzuki, Sonagashira coupling, and hydrosilylation reactions 6–11. It has been shown that donor ability of the appended 2‐theinyl/2‐furyl groups on the sila‐alkyl side chains in linear polysilanes imparts better stabilization of Ag and Pd nanoparticles 12, 13. Poly(alkyl‐arylsilane)s, [R(C 6 H 4 R 1 )Si] n (R 1 = H, p ‐Me, p ‐OMe, p ‐NMe 2 ) with electron withdrawing/electron releasing substituents on the phenyl groups are found to be interesting precursors for “size controlled” synthesis of Ag and Pd nanoparticles 14.…”
Section: Introductionmentioning
confidence: 99%