Metal–organic framework-derived CuO catalysts for the efficient hydrogenolysis of hardwood lignin into phenolic monomers
文献情報
Qian Xu, Qiang Wang, Ling-Ping Xiao, Xiao-Ying Li, Xi Xiao, Meng-Xin Li, Meng-Ran Lin, Yu-Man Zhao, Run-Cang Sun
The selective reductive catalytic deconstruction (RCD) of lignin into phenolic monomers provides the possibility for making the full use of lignocellulose. However, the widespread use of precious metal catalysts and the harsh reaction conditions present the challenge of poor industrial utilization in the current research. Herein, we report a metal–organic framework (MOF)-derived copper oxide catalyst (CuO/c-UiO-66), which exhibits superior catalytic properties in the RCD of hardwood lignin and affords high yields (up to 42.8 wt%) of monomeric phenols via the C–O bond scission. The mechanistic reactions using lignin model compounds reveal that phenolic compounds with propyl or propanol end chains are selectively produced during the catalytic hydrogenolysis reaction. The enhanced catalytic reactivity is attributed to the synergy of acid and base sites of the catalyst, which facilitates the C–O bond cleavage process. The new insights of this study provide guidance toward the rational design of Cu-based catalysts for RCD of lignin.
関連文献
Anharmonic overtone and combination states of glycine and two model peptides examined by vibrational self-consistent field theory
Kuo Meng, Jianping Wang
DOI: 10.1039/C0CP01177K
Some measures for making halogen bonds stronger than hydrogen bonds in H2CS–HOX (X = F, Cl, and Br) complexes
Qing-Zhong Li, Bo Jing, Ran Li, Zhen-Bo Liu, Wen-Zuo Li, Feng Luan, Jian-Bo Cheng, Bao-An Gong, Jia-Zhong Sun
DOI: 10.1039/C0CP01543A
In situ surface-enhanced Raman scattering and X-ray photoelectron spectroscopic investigation of coenzyme Q10 on silver electrode
Dan Li, Da-Wei Li, Yi-Tao Long
DOI: 10.1039/C0CP01449D
Photochemistry of HI on argon and waternanoparticles: Hydronium radical generation in HI·(H2O)n
Viktoriya Poterya, Juraj Fedor, Andriy Pysanenko, Ondřej Tkáč, Jozef Lengyel, Michal Fárník
DOI: 10.1039/C0CP01518K
Wave packet calculations on the effect of the femtosecond pulse width in the time-resolved photodissociation of CH3I in the A-band
A. García-Vela, L. Bañares
DOI: 10.1039/C0CP01508C
Gas–surface energy exchange and thermal accommodation of CO2 and Ar in collisions with methyl, hydroxyl, and perfluorinated self-assembled monolayers
Jessica W. Lu, William A. Alexander, John R. Morris
DOI: 10.1039/B921893A
Photochemical induced growth and aggregation of metal nanoparticles in diode-array spectrophotometer via excited dimethyl-sulfoxide
Tomer Zidki
DOI: 10.1039/C0CP01037E
Demystifying the solvatochromic reversal in Brooker’s merocyanine dye
N. Arul Murugan, Jacob Kongsted, Zilvinas Rinkevicius, Hans Ågren
DOI: 10.1039/C0CP01014F
Rules for selectivity in oxidation processes on RuO2(110)
Núria López, Gerard Novell-Leruth
DOI: 10.1039/C0CP00176G
Visualization of oxygenreduction sites at Ptelectrodes on YSZ by means of 18Otracer incorporation: the width of the electrochemically active zone
Alexander Karl Opitz, Herbert Hutter, Jürgen Fleig
DOI: 10.1039/C0CP00309C
こちらもおすすめ
2,3-スチオエポキシマドルを取り扱う際の実験室安全事項は何ですか?
取り扱いにはPPE(プロテクティブ・パーソナル・エイド)が必要で、防ぐ手袋と保護眼鏡を着用してください。ドラフトチャンバーの使用を推奨します。漏洩した場合は、適...
BOC-S-3-アミニ-4-(4-メチオキシベンチル)-ブタン酸の代替品はありますか?
この化合物の代替品としては、BOC保護基を有さないアミノ酸やその他の保護基化合物が考えられます。また、メチオキシ基を有しない他の芳香族アミノ酸も代替品として挙げ...
Methyl 2-(chloromethyl)-3-nitrobenzoate(1218910-61-2)の代替品はありますか?
Methyl 2-(chloromethyl)-3-nitrobenzoate(1218910-61-2)の代替品としては、化学組成を変えることで効果を達成する...
(2R)-2-アミノ-N-ベンジル-3-ヒドロキシプロパナミドを含む廃棄物はどのように処理すべきですか?
(2R)-2-アミノ-N-ベンジル-3-ヒドロキシプロパナミドを含む廃棄物は、適切な廃棄物管理ガイドラインに基づき処理する必要があります。まず、廃棄物を適切に収...
6,7-二氢-咪唑並[1,2-a]ピリドイン-8(5h)-酮はどのように合成されますか?
6,7-二氢-咪唑並[1,2-a]ピリドイン-8(5h)-酮は、2-ブロモフェニルアセトインとリン酸ハロゲン化物を反応させることで合成できます。この反応は高温で...
エチル(3R)-3-ピロリジニル酢酸水和塩とは何ですか?
エチル(3R)-3-ピロリジニル酢酸水和塩は、CAS番号1332459-32-1の化合物で、(R)-乙基2-(ピロリジン-3-基)酢酸塩水和塩と呼ばれます。この...
(2S)-{[(2-メチルエチルオキシ]カルボニル}アミノ)[2-(トリアフルオロメチルフェニル]エチカシック酸の物理化学的性質は何ですか?
(2S)-{[(2-メチルエチルオキシ]カルボニル}アミノ)[2-(トリアフルオロメチルフェニル]エチカシック酸のCAS番号は1203454-45-8です。この...
2-ブロモ-1-(2-メチル-2-プロパニル)-4-ニトロベンゼンはどのように保存すればよいですか?
2-ブロモ-1-(2-メチル-2-プロパニル)-4-ニトロベンゼンは、直射日光を避けて暗所で、室温(約15℃〜25℃)、乾燥した場所に保存する必要があります。ま...
1-[(4-硝基フェニル)スルホニル]-1H-1,2,4-三唑の市場動向や研究トレンドはどうですか?
市場動向としては、1-[(4-硝基フェニル)スルホニル]-1H-1,2,4-三唑は主に農業用除草剤や合成化学製品の原料として利用されています。研究トレンドとして...
掲載誌
Journal of Materials Chemistry A

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry A are listed below. This list is neither exhaustive nor exclusive. Artificial photosynthesis Batteries Carbon dioxide conversion Catalysis Fuel cells Gas capture/separation/storage Green/sustainable materials Hydrogen generation Hydrogen storage Photocatalysis Photovoltaics Self-cleaning materials Self-healing materials Sensors Supercapacitors Thermoelectrics Water splitting Water treatment










![N-[2-(2-Pyridinyl)ethyl]-1-propanamine structure N-[2-(2-Pyridinyl)ethyl]-1-propanamine structure](https://static.chemtradehub.com/structs/554/55496-57-6-22b4.webp)



![(1R,5R)-3-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-azabicyclo[3.1.0]hexane-1-carboxylic acid structure (1R,5R)-3-{[(2-Methyl-2-propanyl)oxy]carbonyl}-3-azabicyclo[3.1.0]hexane-1-carboxylic acid structure](https://static.chemtradehub.com/structs/116/1165450-63-4-bfe1.webp)