Highly dispersed ultrafine palladium nanoparticles encapsulated in a triazinyl functionalized porous organic polymer as a highly efficient catalyst for transfer hydrogenation of aldehydes was written by Yang, Jin;Yuan, Man;Xu, Dan;Zhao, Hong;Zhu, Yangyang;Fan, Menying;Zhang, Fengwei;Dong, Zhengping. And the article was included in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2018.Recommanded Product: 1777-82-8 This article mentions the following:
Fabrication of highly dispersed ultrafine noble metal nanoparticle (NMNP) based catalysts with high stability and excellent catalytic performance is a challenging issue for heterogeneous catalysis. As an alternative complement to existing solutions, herein, we designed and synthesized a stable triazinyl-pentaerythritol porous organic polymer (TP-POP) through a facile polycondensation between cyanuric chloride and pentaerythritol. The obtained TP-POP material has a three-dimensional folded structure, rich triazinyl groups, abundant hydrophobic pores and high thermal stability. Ultrafine Pd NPs with a narrow size distribution (1.4-2.8 nm) are then successfully confined in the organic pores of the TP-POP, through a reversed double solvent approach (RDSA). It is worth noting that the current strategy can effectively confine Pd NPs in the inner space of the TP-POP, and successfully avoids the agglomeration of Pd NPs as compared with the common impregnation-reduction method. The as-prepared Pd@TP-POP catalyst shows excellent catalytic activity in the reduction of 4-nitrophenol and transfer hydrogenation of aromatic aldehydes under mild conditions. The excellent performance of the Pd@TP-POP catalyst is attributed to the abundant mesopores of the TP-POP which can enhance the accessibility of the highly dispersed ultrafine Pd NP active sites that are confined in the organic pores. More importantly, the Pd@TP-POP catalyst is easily recycled and highly stable without loss of its catalytic activity even after ten reaction cycles. Therefore, this study provides a new platform for designing and fabricating stable POP materials to confine size-controlled NMNPs with superior catalytic performance for various potential catalysis applications. In the experiment, the researchers used many compounds, for example, (2,4-Dichlorophenyl)methanol (cas: 1777-82-8Recommanded Product: 1777-82-8).
(2,4-Dichlorophenyl)methanol (cas: 1777-82-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 1777-82-8
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