钯
芳基
催化作用
化学
烯烃
碘化物
氧烷
扩展X射线吸收精细结构
X射线吸收光谱法
小角X射线散射
纳米颗粒
无机化学
光化学
有机化学
材料科学
吸收光谱法
纳米技术
烷基
光谱学
物理
散射
量子力学
光学
作者
Eloah Latocheski,Marcelo Volpatto Marques,Brunno L. Albuquerque,Thalia J. Schuh,Aline M. Signori,Daniela C. de Oliveira,T. Pal,Josiel B. Domingos
出处
期刊:Chemcatchem
[Wiley]
日期:2018-11-29
卷期号:11 (2): 684-688
被引量:8
标识
DOI:10.1002/cctc.201801817
摘要
Abstract The synthesis of small spherical palladium(II) iodide nanoparticles is reported for the first time. The formation of the particles by ligand exchange, in the presence of poly(vinyl pyrrolidone) in aqueous medium at room temperature, was investigated by in situ time‐resolved synchrotron‐based SAXS and XANES/EXAFS analysis. These new nanomaterials exhibit a double catalytic role in an aryl alkenylation chemical reaction, working without a base or ligand, in aqueous milieu. There is strong experimental evidence to suggest that the mechanism follows a single‐electron transfer (SET) pathway with the participation of iodide as a radical promoter and the palladium atoms as activator of the alkene moiety. This new protocol could evolve into a broadly applicable radical reaction for the functionalization of alkenes.
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