Efficient cleavage of aryl ether C-O linkages by Rh-Ni and Ru-Ni nanoscale catalysts operating in water

被引:57
作者
Bulut, Safak [1 ]
Siankevich, Sviatlana [1 ]
van Muyden, Antoine P. [1 ]
Alexander, Duncan T. L. [2 ]
Savoglidis, Georgios [1 ]
Zhang, Jiaguang [3 ]
Hatzimanikatis, Vassily [1 ]
Yan, Ning [3 ]
Dyson, Paul J. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Interdisciplinary Ctr Electron Microscopy CIME, CH-1015 Lausanne, Switzerland
[3] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117576, Singapore
基金
瑞士国家科学基金会;
关键词
LIGNIN MODEL COMPOUNDS; BOND-DISSOCIATION ENTHALPIES; ORGANOSOLV LIGNIN; KRAFT LIGNIN; SELECTIVE HYDROGENATION; BIMETALLIC CATALYSTS; AROMATIC MONOMERS; NICKEL-CATALYST; METAL-CATALYSTS; HYDROGENOLYSIS;
D O I
10.1039/c8sc00742j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bimetallic Ru-Ni and Rh-Ni nanocatalysts coated with a phase transfer agent efficiently cleave aryl ether C-O linkages in water in the presence of hydrogen. For dimeric substrates with weaker C-O linkages, i.e. alpha-O-4 and beta-O-4 bonds, low loadings of the precious metal (Rh or Ru) in the nanocatalysts quantitatively afford monomers, whereas for the stronger 4-O-5 linkage higher amounts of the precious metal are required to achieve complete conversion. Under the optimized, relatively mild operating conditions, the C-O bonds in a range of substituted ether compounds are efficiently cleaved, and mechanistic insights into the reaction pathways are provided. This work paves the way to sustainable approaches for the hydrogenolysis of C-O bonds.
引用
收藏
页码:5530 / 5535
页数:6
相关论文
共 69 条
[31]   Recent advances in the homogeneous hydrogenation of carbon dioxide [J].
Jessop, PG ;
Joó, F ;
Tai, CC .
COORDINATION CHEMISTRY REVIEWS, 2004, 248 (21-24) :2425-2442
[32]   Transition-metal catalyzed valorization of lignin: the key to a sustainable carbon-neutral future [J].
Kaerkaes, Markus D. ;
Matsuura, Bryan S. ;
Monos, Timothy M. ;
Magallanes, Gabriel ;
Stephenson, Corey R. J. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2016, 14 (06) :1853-1914
[33]  
Kasakov S, 2015, GREEN CHEM, V17, P5079, DOI [10.1039/c5gc02160j, 10.1039/C5GC02160J]
[34]   Catalytic decomposition of phenethyl phenyl ether to aromatics over Pd-Fe bimetallic catalysts supported on ordered mesoporous carbon [J].
Kim, Jeong Kwon ;
Lee, Jong Kwon ;
Kang, Ki Hyuk ;
Lee, Jong Won ;
Song, In Kyu .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2015, 410 :184-192
[35]   Computational Study of Bond Dissociation Enthalpies for a Large Range of Native and Modified Lignins [J].
Kim, Seonah ;
Chmely, Stephen C. ;
Nimos, Mark R. ;
Bomble, Yannick J. ;
Foust, Thomas D. ;
Paton, Robert S. ;
Beckham, Gregg T. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2011, 2 (22) :2846-2852
[36]   Base promoted hydrogenolysis of lignin model compounds and organosolv lignin over metal catalysts in water [J].
Konnerth, Hannelore ;
Zhang, Jiaguang ;
Ma, Ding ;
Prechtl, Martin H. G. ;
Yan, Ning .
CHEMICAL ENGINEERING SCIENCE, 2015, 123 :155-163
[37]  
Lancefield CS, 2015, GREEN CHEM, V17, P4980, DOI [10.1039/C5GC01334H, 10.1039/c5gc01334h]
[38]   Isolation of Functionalized Phenolic Monomers through Selective Oxidation and C-O Bond Cleavage of the β-O-4 Linkages in Lignin [J].
Lancefield, Christopher S. ;
Ojo, O. Stephen ;
Tran, Fanny ;
Westwood, Nicholas J. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (01) :258-262
[39]   Catalytic roles of metals and supports on hydrodeoxygenation of lignin monomer guaiacol [J].
Lee, Cho Rim ;
Yoon, Ji Sun ;
Suh, Young-Woong ;
Choi, Jae-Wook ;
Ha, Jeong-Myeong ;
Suh, Dong Jin ;
Park, Young-Kwon .
CATALYSIS COMMUNICATIONS, 2012, 17 :54-58
[40]   Catalytic Transformation of Lignin for the Production of Chemicals and Fuels [J].
Li, Changzhi ;
Zhao, Xiaochen ;
Wang, Aiqin ;
Huber, George W. ;
Zhang, Tao .
CHEMICAL REVIEWS, 2015, 115 (21) :11559-11624