Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Joshua Akhigbe"'
Autor:
Jeanette A. Krause, Derek Girouard, Martin Gouterman, Adewole O. Atoyebi, Matthias Zeller, Gamal Khalil, Joshua Akhigbe, Kimberly S. F. Lau, Lalith P. Samankumara, Dinusha Damunupola, Christian Brückner
Publikováno v:
European Journal of Organic Chemistry. 2020:475-482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e34acdd6850b25d86d95075ffd1a50
https://doi.org/10.1002/ejoc.201901727
https://doi.org/10.1002/ejoc.201901727
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 24:386-393
The platinum(II) complexes of known quinoline-annulated porphyrins were prepared and spectroscopically characterized. Their optical properties (UV-vis absorption and phosphorescence spectra and phosphorescence lifetimes) were recorded and contrasted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64b34df563af48f28363456d0b8ef7b6
https://doi.org/10.1142/s1088424619501256
https://doi.org/10.1142/s1088424619501256
Autor:
Matthias Zeller, Christian Brückner, Michael Luciano, Jiaming Ding, Damaris Thuita, Randy Hamchand, Joshua Akhigbe
Publikováno v:
The Journal of Organic Chemistry. 83:9619-9630
A novel and efficient synthetic pathway toward known meso-tetraphenylporpholactams, also applicable to the synthesis of hitherto unknown and inaccessible meso-C6F5-substituted porpholactam, is detailed (dioxochlorin → dioxochlorin urea adduct → p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5096601d1a160da8ed59a46be1f5ec
https://doi.org/10.1021/acs.joc.8b00790
https://doi.org/10.1021/acs.joc.8b00790
Autor:
Adam Meares, Subramani Swaminathan, Joshua Akhigbe, Marcin Ptaszek, Melanie A. Ehudin, Nithya Santhanam, Andrius Satraitis
Publikováno v:
The Journal of Organic Chemistry. 82:6054-6070
BODIPY-hydroporphyrin energy transfer arrays allow for development of a family of fluorophores featuring a common excitation band at 500 nm, tunable excitation band in the deep red/near-infrared window, and tunable emission. Their biomedical applicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c2b373f37b9cf508adbebf56812a68
https://doi.org/10.1021/acs.joc.7b00357
https://doi.org/10.1021/acs.joc.7b00357
Autor:
Joshua Akhigbe, Jordan A. Greco, Chirag Pancholi, Marcin Ptaszek, Robert R. Birge, Dewey Holten, Hyun Suk Kang, Zhanqian Yu, Christine Kirmaier, Nopondo N. Esemoto, David F. Bocian, Dariusz M. Niedzwiedzki, Ganga Viswanathan Bhagavathy, James R. Diers, Jamie K. Nguyen
Publikováno v:
The Journal of Physical Chemistry A. 120:379-395
Achieving tunable, intense near-infrared absorption in molecular architectures with properties suitable for solar light harvesting and biomedical studies is of fundamental interest. Herein, we report the photophysical, redox, and molecular-orbital ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::514dd1e91831cd0722d287a72d76b632
https://doi.org/10.1021/acs.jpca.5b10686
https://doi.org/10.1021/acs.jpca.5b10686
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 20:265-273
The OsO4-mediated dihydroxylation of quinoline-annulated porphyrin generates a quinoline-annulated dihydroxychlorin in a regioselective fashion. Its dihydroxypyrroline moiety, located at the opposite of the annulated pyrrole, is susceptible to the sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a09cfbfedf09eeefcac9e92de51522
https://doi.org/10.1142/s1088424616500036
https://doi.org/10.1142/s1088424616500036
Autor:
Peter L. Choyke, Joshua Akhigbe, Melissa Y. Lucero, Hisataka Kobayashi, Fusa Ogata, Tadanobu Nagaya, Daiki Fujimura, Andrius Satraitis, Ryuhei Okada, Marcin Ptaszek, Adam Meares, Yasuhiro Maruoka, Fuyuki Inagaki
Publikováno v:
Bioconjug Chem
Near infrared (NIR) fluorescent probes are attractive tools for biomedical in vivo imaging due to the relatively deeper tissue penetration and lower background autofluorescence. Activatable probes are turned on only after binding to their target, fur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35fedec18d3a4c488e300b6295a1a5e3
https://pubmed.ncbi.nlm.nih.gov/30475591
https://pubmed.ncbi.nlm.nih.gov/30475591
Autor:
Christian Brückner, Joshua Akhigbe
Publikováno v:
European Journal of Organic Chemistry. 2013:3876-3884
The group 10 metal complexes of β,β′-dioxoporphyrin monooxime 10M (M = NiII, PdII, PtII) are susceptible to a Beckmann rearrangement to produce the corresponding ring-expanded metallopyrazinoporphyrin imides 11M in good yields. These chromophores
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::934eadce51f0ac9f1e960471988ce91b
https://doi.org/10.1002/ejoc.201300274
https://doi.org/10.1002/ejoc.201300274
Autor:
Hannah M. Rhoda, Joshua Akhigbe, Victor N. Nemykin, Junichi Ogikubo, Christian Brückner, Christopher J. Ziegler, Jared R. Sabin
Publikováno v:
The journal of physical chemistry. A. 120(29)
A large set of free-base and transition-metal 5,10,15,20-tetraphenyl-substituted chlorins, bacteriochlorins, and isobacteriochlorins and their pyrrole-modified analogues were investigated by combined UV-visible spectroscopy, magnetic circular dichroi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d2ad5cc87ca0c3c90950f377c82f54
https://pubmed.ncbi.nlm.nih.gov/27400337
https://pubmed.ncbi.nlm.nih.gov/27400337
Publikováno v:
Electroanalysis. 24:1348-1355
meso-Tritolylcorrole-functionalized single-walled carbon nanotubes (TTC-SWNT) donor-acceptor (D–A) heterojunction nanocomposite film was fabricated on a polycarbonate membrane through filtration and non-covalent functionalization, providing an exce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49fc00fd9e3194dbc00f34cfd98e0361
https://doi.org/10.1002/elan.201200077
https://doi.org/10.1002/elan.201200077