Reversible Electrochemical Modulation of a Catalytic Nanosystem

被引:20
作者
della Sala, Flavio [1 ]
Chen, Jack L. -Y. [1 ]
Ranallo, Simona [2 ]
Badocco, Denis [1 ]
Pastore, Paolo [1 ]
Ricci, Francesco [2 ]
Prins, Leonard J. [1 ]
机构
[1] Univ Padua, Dept Chem Sci, Via Marzolo 1, I-35131 Padua, Italy
[2] Univ Roma Tor Vergata, Dept Chem, Via Ric Sci, I-00133 Rome, Italy
关键词
gold nanoparticles; nanocatalysis; nanozymes; supramolecular catalysis; supramolecular chemistry; ARTIFICIAL ENZYMES; GOLD NANOPARTICLES; SYSTEMS CHEMISTRY; NANOMATERIALS; METAL; MONOLAYER; PHOSPHATE; NANOZYMES;
D O I
10.1002/anie.201605309
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A catalytic system based on monolayer-functionalized gold nanoparticles (AuNPs) that can be electrochemically modulated and reversibly activated is reported. The catalytic activity relies on the presence of metal ions (Cd2+ and Cu2+), which can be complexed by the nanoparticle-bound monolayer. This activates the system towards the catalytic cleavage of 2-hydroxypropyl-p-nitrophenyl phosphate (HPNPP), which can be monitored by UV/Vis spectroscopy. It is shown that Cu2+ metal ions can be delivered to the system by applying an oxidative potential to an electrode on which Cu-0 was deposited. By exploiting the different affinity of Cd2+ and Cu2+ ions for the monolayer, it was also possible to upregulate the catalytic activity after releasing Cu2+ from an electrode into a solution containing Cd2+. Finally, it is shown that the activity of this supramolecular nanosystem can be reversibly switched on or off by oxidizing/reducing Cu/Cu2+ ions under controlled conditions.
引用
收藏
页码:10737 / 10740
页数:4
相关论文
共 26 条
[1]   Polyethylene imine derivatives ('Synzymes') accelerate phosphate transfer in the absence of metal [J].
Avenier, Frederic ;
Domingos, Josiel B. ;
Van Vliet, Liisa D. ;
Hollfelder, Florian .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (24) :7611-7619
[2]   Artificial switchable catalysts [J].
Blanco, Victor ;
Leigh, David A. ;
Marcos, Vanesa .
CHEMICAL SOCIETY REVIEWS, 2015, 44 (15) :5341-5370
[3]   In situ formation of an oxygen-evolving catalyst in neutral water containing phosphate and Co2+ [J].
Kanan, Matthew W. ;
Nocera, Daniel G. .
SCIENCE, 2008, 321 (5892) :1072-1075
[4]   Spatially Controlled Out-of-Equilibrium Host-Guest System under Electrochemical Control [J].
Krabbenborg, Sven O. ;
Veerbeek, Janneke ;
Huskens, Jurriaan .
CHEMISTRY-A EUROPEAN JOURNAL, 2015, 21 (27) :9638-9644
[5]   Catalytically Active Nanomaterials: A Promising Candidate for Artificial Enzymes [J].
Lin, Youhui ;
Ren, Jinsong ;
Qu, Xiaogang .
ACCOUNTS OF CHEMICAL RESEARCH, 2014, 47 (04) :1097-1105
[6]   Systems chemistry [J].
Ludlow, R. Frederick ;
Otto, Sijbren .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (01) :101-108
[7]   Electrochemically Mediated Atom Transfer Radical Polymerization [J].
Magenau, Andrew J. D. ;
Strandwitz, Nicholas C. ;
Gennaro, Armando ;
Matyjaszewski, Krzysztof .
SCIENCE, 2011, 332 (6025) :81-84
[8]   Progress in artificial metallonucleases [J].
Mancin, Fabrizio ;
Scrimin, Paolo ;
Tecilla, Paolo .
CHEMICAL COMMUNICATIONS, 2012, 48 (45) :5545-5559
[9]   Nanozymes: Gold-nanoparticle-based transphosphorylation catalysts [J].
Manea, F ;
Houillon, FB ;
Pasquato, L ;
Scrimin, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (45) :6165-6169
[10]  
Manea F., 2004, ANGEW CHEM INT EDIT, V116, P6291, DOI DOI 10.1002/ANGE.200460649