Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Steven H. Bergens"'
Autor:
Jinkun Liu, Octavio Martinez Perez, Dominic Lavergne, Loorthuraja Rasu, Elizabeth Murphy, Andy Galvez-Rodriguez, Steven H. Bergens
Publikováno v:
Polymers, Vol 15, Iss 16, p 3340 (2023)
To the best of our knowledge, this study reports the first direct electropolymerization of a dicyanobenzene-carbazole dye functionalized with an imidazole group to prepare redox- and photoactive porous organic polymer (POP) films in controlled amount
Externí odkaz:
https://doaj.org/article/d3c8c41d71744f39941ff1c8b5f278c1
Publikováno v:
ACS Omega, Vol 4, Iss 7, Pp 12212-12221 (2019)
Externí odkaz:
https://doaj.org/article/91746713e2ae44ddb9a52249c87fe384
Autor:
Jinkun Liu, Steven H. Bergens
Publikováno v:
ACS Applied Materials & Interfaces. 15:25624-25632
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e2ba8461b08900b4fff57e813501dca
https://doi.org/10.1021/acsami.3c04573
https://doi.org/10.1021/acsami.3c04573
Autor:
Meng-Nan Zhu, Haoqing Jiang, Bo-Wen Zhang, Minrui Gao, Peng-Fei Sui, Renfei Feng, Karthik Shankar, Steven H. Bergens, Gary J. Cheng, Jing-Li Luo
Publikováno v:
ACS Nano. 17:8705-8716
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec7be1865c31ebfcb9c70165ed9dac73
https://doi.org/10.1021/acsnano.3c01897
https://doi.org/10.1021/acsnano.3c01897
Autor:
Prabin Nepal, Suneth Kalapugama, Michael Shevlin, John R. Naber, Louis-Charles Campeau, Cristofer Pezzetta, Armando Carlone, Christopher J. Cobley, Steven H. Bergens
Publikováno v:
ACS Catalysis. 12:2034-2044
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0276def1d24d988f69c60377297bc157
https://doi.org/10.1021/acscatal.1c04983
https://doi.org/10.1021/acscatal.1c04983
Publikováno v:
ACS Applied Materials & Interfaces. 13:17745-17752
The organic carbazole-cyanobenzene push-pull dye 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene was derivatized and attached to carbon or indium-doped tin oxide (ITO) electrodes by simple diazonium electrografting. The surface-bound dye is active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb7124baf6fa290958428274c0a49fb
https://doi.org/10.1021/acsami.1c05064
https://doi.org/10.1021/acsami.1c05064
Publikováno v:
Canadian Journal of Chemistry. 99:230-235
The asymmetric imidazolium salt [Ru(dmbpy)2(bpip)](PF6)3 (bpip = 1-benzyl-3-isopropyl-1H-imidazo[4,5-f][1,10]phenanthrolinium) was prepared by a four-step synthetic route. The isotopomer labelled with 13C at the C2 position of bpip was prepared from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97327a4d33c8946add55577968c17761
https://doi.org/10.1139/cjc-2020-0397
https://doi.org/10.1139/cjc-2020-0397
Publikováno v:
ACS Omega, Vol 4, Iss 7, Pp 12212-12221 (2019)
ACS Omega
ACS Omega
A cross-linked catalyst organic framework was prepared by an alternating ring-opening olefin metathesis polymerization between dichloro{N,N′-bis({(2-diphenylphosphino)phenyl}methylidene)bicyclo[2.2.1]-hept-5-ene-2,3-diamine}ruthenium, 1,2-N-di(cis-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22316223ae2acb46cb81c23e773a4ddf
https://doi.org/10.1021/acsomega.9b01682
https://doi.org/10.1021/acsomega.9b01682
Publikováno v:
ACS Catalysis. 9:6111-6117
The catalyst system trans-Ru(H)2(1R,2R)-N,N-bis{2-[bis(3,5-dimethylphenyl)phosphino]benzyl}cyclohexane-1,2-diamine, NaOEt, in DME or THF solvent hydrogenates a series of functionalized racemic este...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa79d6f59b9a45f2f7787b4ce36f763d
https://doi.org/10.1021/acscatal.9b01037
https://doi.org/10.1021/acscatal.9b01037
Autor:
Karthik Shankar, Bin Hua, Steven H. Bergens, Meng Li, Sheng-Nian Zhang, Jing-Li Luo, Nanqi Duan, Shaochen Ding
Publikováno v:
ChemCatChem. 11:4147-4153
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0bb3a4cfa3f4dafd17853499c7b34f0
https://doi.org/10.1002/cctc.201900395
https://doi.org/10.1002/cctc.201900395