Metal Triflates for the Production of Aromatics from Lignin

被引:81
作者
Deuss, Peter J. [1 ]
Lahive, Ciaran W. [2 ,3 ,4 ]
Lancefield, Christopher S. [2 ,3 ,4 ]
Westwood, Nicholas J. [2 ,3 ,4 ]
Kamer, Paul C. J. [2 ,3 ,4 ]
Barta, Katalin [1 ]
de Vries, Johannes G. [1 ,5 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Univ St Andrews, Biomed Sci Res Complex, St Andrews KY16 9ST, Fife, Scotland
[4] EaStCHEM, St Andrews KY16 9ST, Fife, Scotland
[5] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
基金
英国工程与自然科学研究理事会;
关键词
acidolysis; aromatics; depolymerization; lignin; metal triflates; ACID-CATALYZED DEPOLYMERIZATION; ETHANOL ORGANOSOLV PROCESS; BETA-O-4; BOND-CLEAVAGE; LEWIS-ACID; SELECTIVE OXIDATION; PHENOLIC MONOMERS; MODEL COMPOUNDS; TRIFLIC ACID; ACIDOLYSIS; CHEMICALS;
D O I
10.1002/cssc.201600831
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The depolymerization of lignin into valuable aromatic chemicals is one of the key goals towards establishing economically viable biorefineries. In this contribution we present a simple approach for converting lignin to aromatic monomers in high yields under mild reaction conditions. The methodology relies on the use of catalytic amounts of easy-to-handle metal triflates (M(OTf)(x)). Initially, we evaluated the reactivity of a broad range of metal triflates using simple lignin model compounds. More advanced lignin model compounds were also used to study the reactivity of different lignin linkages. The product aromatic monomers were either phenolic C2-acetals obtained by stabilization of the aldehyde cleavage products by reaction with ethylene glycol or methyl aromatics obtained by catalytic decarbonylation. Notably, when the method was ultimately tested on lignin, especially Fe(OTf)(3) proved very effective and the phenolic C2-acetal products were obtained in an excellent, 19.3 +/- 3.2wt% yield.
引用
收藏
页码:2974 / 2981
页数:8
相关论文
共 59 条
[1]   "Microencapsulated" and Related Catalysts for Organic Chemistry and Organic Synthesis [J].
Akiyama, Ryo ;
Kobayashi, Shu .
CHEMICAL REVIEWS, 2009, 109 (02) :594-642
[2]  
[Anonymous], 2015, ANGEW CHEM, V127, P260
[3]   Depolymerization of organosolv lignin to aromatic compounds over Cu-doped porous metal oxides [J].
Barta, Katalin ;
Warner, Genoa R. ;
Beach, Evan S. ;
Anastas, Paul T. .
GREEN CHEMISTRY, 2014, 16 (01) :191-196
[4]   Characterization of Miscanthus giganteus Lignin Isolated by Ethanol Organosolv Process under Reflux Condition [J].
Bauer, Stefan ;
Sorek, Hagit ;
Mitchell, Valerie D. ;
Ibanez, Ana B. ;
Wemmer, David E. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2012, 60 (33) :8203-8212
[5]   Conversion of Biomass into Chemicals over Metal Catalysts [J].
Besson, Michele ;
Gallezot, Pierre ;
Pinel, Catherine .
CHEMICAL REVIEWS, 2014, 114 (03) :1827-1870
[6]   Pretreatment of Miscanthus x giganteus Using the Ethanol Organosolv Process for Ethanol Production [J].
Brosse, Nicolas ;
Sannigrahi, Poulomi ;
Ragauskas, Arthur .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (18) :8328-8334
[7]   Efficient Intramolecular Hydroarylation Catalysed by BiIII Triflate [J].
Cacciuttolo, Bastien ;
Poulain-Martini, Sophie ;
Dunach, Elisabet .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 2011 (20-21) :3710-3714
[8]  
Dabral S, 2015, GREEN CHEM, V17, P4908, DOI [10.1039/C5GC00186B, 10.1039/c5gc00186b]
[9]   Alternative Monomers Based on Lignocellulose and Their Use for Polymer Production [J].
Delidovich, Irina ;
Hausoul, Peter J. C. ;
Deng, Li ;
Pfuetzenreuter, Rebecca ;
Rose, Marcus ;
Palkovits, Regina .
CHEMICAL REVIEWS, 2016, 116 (03) :1540-1599
[10]   From models to lignin: Transition metal catalysis for selective bond cleavage reactions [J].
Deuss, Peter J. ;
Barta, Katalin .
COORDINATION CHEMISTRY REVIEWS, 2016, 306 :510-532