Polymer-coated palladium nanoparticle catalysts for Suzuki coupling reactions

被引:25
作者
Bortolotto, Tanize [1 ]
Facchinetto, Sara Elisa [1 ]
Trindade, Suelen Gauna [1 ]
Ossig, Andreia [2 ]
Petzhold, Cesar Liberato [2 ]
Vargas, Josimar [1 ]
Dorneles Rodrigues, Oscar Endrigo [1 ]
Giacomelli, Cristiano [1 ]
Schmidt, Vanessa [1 ]
机构
[1] Univ Fed Santa Maria, Dept Quim, BR-97105900 Santa Maria, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Quim, BR-91501970 Porto Alegre, RS, Brazil
关键词
Polymers; Capping agents; Palladium nanoparticles; p-Nitrophenol reduction; Suzuki-Miyaura reaction; BLOCK-COPOLYMER MICELLES; SPHERICAL POLYELECTROLYTE BRUSHES; IN-SITU GENERATION; PLATINUM NANOPARTICLES; THERMORESPONSIVE POLYMER; SHELL; HECK; SURFACTANT; CORE;
D O I
10.1016/j.jcis.2014.10.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A set of seven different palladium nanoparticle (PdNP) systems stabilized by small amounts (1.0 mg/mL) of structurally related macromolecular capping agents were comparatively tested as catalyst in p-nitrophenol (Nip) reduction and Suzuki cross-coupling reactions. The observed rate constants (k(obs)) for Nip reduction were in the range of 0.052-3.120 x 10(-2) s(-1), and the variation reflected the effects of polymer chain conformation, ionic strength and palladium-polymer complex coordination. Macromolecules featuring pendant pyridyl moieties or inverse temperature-dependent solubility were found to be unsuitable capping agents for PdNPs catalysts, despite being active. The catalytic activity in Suzuki cross-coupling reactions followed the same behavior; the most active particles in the Nip reaction also mediated the cross-coupling reaction providing the expected products in quantitative yields under relatively mild conditions after only 4 h at 50 degrees C. Experiments involving the successive addition of reactants and catalyst recovery/re-use indicated that the recycling potential was comparable to those of the standards used in this field. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:154 / 161
页数:8
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