TiO 2 -Modified Montmorillonite-Supported Porous Carbon-Immobilized Pd Species Nanocomposite as an Efficient Catalyst for Sonogashira Reactions.
Yuli ChenKailang SunTaojun ZhangJie ZhouYonghong LiuMinfeng ZengXiaorong RenRuokun FengZhen YangPeng ZhangBaoyi WangXing-Zhong CaoPublished in: Molecules (Basel, Switzerland) (2023)
In this study, a combination of the porous carbon (PCN), montmorillonite (MMT), and TiO 2 was synthesized into a composite immobilized Pd metal catalyst (TiO 2 -MMT/PCN@Pd) with effective synergism improvements in catalytic performance. The successful TiO 2 -pillaring modification for MMT, derivation of carbon from the biopolymer of chitosan, and immobilization of Pd species for the prepared TiO 2 -MMT/PCN@Pd 0 nanocomposites were confirmed using a combined characterization with X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N 2 adsorption-desorption isotherms, high-resolution transition electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. It was shown that the combination of PCN, MMT, and TiO 2 as a composite support for the stabilization of the Pd catalysts could synergistically improve the adsorption and catalytic properties. The resultant TiO 2 -MMT 80 /PCN 20 @Pd 0 showed a high surface area of 108.9 m 2 /g. Furthermore, it exhibited moderate to excellent activity (59-99% yield) and high stability (recyclable 19 times) in the liquid-solid catalytic reactions, such as the Sonogashira reactions of aryl halides (I, Br) with terminal alkynes in organic solutions. The positron annihilation lifetime spectroscopy (PALS) characterization sensitively detected the development of sub-nanoscale microdefects in the catalyst after long-term recycling service. This study provided direct evidence for the formation of some larger-sized microdefects during sequential recycling, which would act as leaching channels for loaded molecules, including active Pd species.
Keyphrases
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