Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Qianggen Li"'
Publikováno v:
New Journal of Chemistry. 47:1740-1759
The methyl transfer pathway is the most favorable pathway in the polyMB cycle and the polyMB cycle is more competitive than the alkene cycle. The addition of the phosphorus atom in the FAU could improve the productivity of propene in the MTP process.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::562d98ad55ec6a82781759f2b2ff294b
https://doi.org/10.1039/d2nj04863a
https://doi.org/10.1039/d2nj04863a
Publikováno v:
Molecular Simulation. 48:495-516
We have theoretically investigated the hydrodesulphurisation (HDS) mechanism of hydrogenated thiophene over Cu–Mo-modified FAU zeolite using a two-layer ONIOM (our Own N-layered Integrated molecular Orbital and molecular Mechanics) study. The thiop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c885a1e9956a1a1f287b749f29528c5
https://doi.org/10.1080/08927022.2022.2027407
https://doi.org/10.1080/08927022.2022.2027407
Publikováno v:
International Journal of Hydrogen Energy. 46:34229-34238
Biomass-derived porous carbons are generally used as supports for metal nanoparticle (NP) stabilizations, while the strong hydrophilicity of such materials makes the as-prepared catalysts hard to be isolated after reaction, significantly affecting th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08833136a08a952be4d09e1ccec23e5a
https://doi.org/10.1016/j.ijhydene.2021.07.222
https://doi.org/10.1016/j.ijhydene.2021.07.222
Publikováno v:
Theoretical Chemistry Accounts. 141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed67c5baf119dc212731680e26709922
https://doi.org/10.1007/s00214-022-02911-8
https://doi.org/10.1007/s00214-022-02911-8
Publikováno v:
The Journal of Physical Chemistry C. 125:310-334
We have carried out a two-layer our own n-layered integrated molecular orbital and molecular mechanics (MM) study on the mechanism of ethanol to propene on H-ZSM-5 and H-FAU zeolites. The entire me...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfc3411183e4377932c9e21f6582f18f
https://doi.org/10.1021/acs.jpcc.0c07614
https://doi.org/10.1021/acs.jpcc.0c07614
Publikováno v:
New Journal of Chemistry. 45:14759-14764
Ru-based bimetallic alloy nanoparticles (NPs) have been demonstrated as efficiently catalytic sites for hydrogen evolution from ammonia borane (AB) hydrolysis, but their facile syntheses with ultrafine sizes and superior activity are still challengea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68ca8c71c0a067ae195c6dd4f9808c28
https://doi.org/10.1039/d1nj02805g
https://doi.org/10.1039/d1nj02805g
We have theoretically studied the hydrodesulphurisation (HDS) mechanism of thiophene and its hydrogenated derivatives over sulphided Co–Mo catalysts supported by four zeolites (ZSM-5, FAU, Beta, MCM-22) by a two-layer ONIOM (our Own N-layered Integ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::418b99284e1bdd6c17d9143927e93d90
We have carried out a two-layer our own n-layered integrated molecular orbital and molecular mechanics (ONIOM) study on the hydrodesulfurization (HDS) mechanism of three hydrogenated thiophene derivatives over Cu-Mo modified FAU zeolite. The thiophen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::778efbd107de5f83b638c6fb4050f025
https://doi.org/10.21203/rs.3.rs-785978/v1
https://doi.org/10.21203/rs.3.rs-785978/v1
Autor:
Xiao Yang, Qianggen Li, Ruixiang Li, Juan Tang, Haiyan Fu, Maolin Yuan, Rui Sun, Xueli Zheng, Hua Chen, Ke Xu
Publikováno v:
Organic Letters. 21:9425-9429
A simple and efficient method for the synthesis of isoquinolone and isocoumarin derivatives is reported. The method for the first time provides a one-step divergent synthesis of important isoquinol...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6790c9affdc465581a833fb28c011d0
https://doi.org/10.1021/acs.orglett.9b03638
https://doi.org/10.1021/acs.orglett.9b03638
Publikováno v:
University Chemistry. 34:108-115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b41956eeebe6fa9164940b6f919a0a4
https://doi.org/10.3866/pku.dxhx201805042
https://doi.org/10.3866/pku.dxhx201805042