Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kazuki Urakawa"'
Publikováno v:
The Journal of Organic Chemistry. 87:3647-3651
Borocyclic radicals with highly conjugated aromatics were generated from orthoquinone-containing polycyclic aromatic compounds by trapping the photoinduced triplet state with simple boron halide under irradiation with light of appropriate wavelength.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fc63f6c274794c36420957218341cf2
https://doi.org/10.1021/acs.joc.1c02283
https://doi.org/10.1021/acs.joc.1c02283
P‐54: Development of Heat Free / Low Temperature Process High Refractive Index Materials for Display
Publikováno v:
SID Symposium Digest of Technical Papers. 53:1242-1244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30f0d1b2831766f7f52d144d61f1714a
https://doi.org/10.1002/sdtp.15731
https://doi.org/10.1002/sdtp.15731
Publikováno v:
Molecular Systems Design & Engineering. 5:757-771
Ion-pairing assemblies consisting of appropriately designed charged π-electronic species afford various functional supramolecular assemblies, including crystals and soft materials; they are formed by the anisotropic arrangement of charged π-electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7f7a417e00affa31070ec2b6e27ef62
https://doi.org/10.1039/c9me00183b
https://doi.org/10.1039/c9me00183b
Publikováno v:
Organic Letters. 22:781-785
Intramolecular aromatic C-N bond formation reactions using electron-rich aromatic tethered boron-masking N-hydroxyamide as substrate were realized. These new C-N bond formation reactions involve the in situ generation of a diaryliodonium salt by trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a166dbb7fb348bd8caec472f34dfa68d
https://doi.org/10.1021/acs.orglett.9b04076
https://doi.org/10.1021/acs.orglett.9b04076
Publikováno v:
Organic & Biomolecular Chemistry. 17:1163-1168
[38]Octaphyrin(1.1.1.1.1.1.1.1) bearing four methyl moieties at the inner nitrogen sites has been synthesized. This expanded porphyrin has helical chirality as correlated with the orientations of the inner N-methyl groups, exhibiting chiroptical prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6d9820ce1e95e186f34fbafc514177
https://doi.org/10.1039/c8ob03161d
https://doi.org/10.1039/c8ob03161d
Publikováno v:
Photosynergetic Responses in Molecules and Molecular Aggregates ISBN: 9789811554506
Ion-pairing assemblies consisting of appropriately designed oppositely charged π-electronic systems give rise to various functional supramolecular assemblies including crystals and soft materials based on the anisotropic orientation of charged speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5542a1720f6f89637b604b661644aa3e
https://doi.org/10.1007/978-981-15-5451-3_18
https://doi.org/10.1007/978-981-15-5451-3_18
Publikováno v:
Organic Letters. 20:2534-2537
α-Ketocarbenium ions derived from synthesized orthoquinone-containing polycyclic aromatic compounds were generated in the presence of Brønsted acids such as sulfuric acid, trifluoromethanesulfonic acid, and fluorosulfonic acid. The prepared α-keto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f8a984cee717e485e926980f37af947
https://doi.org/10.1021/acs.orglett.8b00682
https://doi.org/10.1021/acs.orglett.8b00682
Autor:
Michihito Takahashi, Hiroki Chisaka, Yoichiro Ijima, Kazuki Urakawa, Atsushi Yamanouchi, Dai Shiota, Katsumi Ohmori
Publikováno v:
Proceedings of the International Display Workshops. :269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beed4fa5484575bc33717d80771cdee1
https://doi.org/10.36463/idw.2021.0269
https://doi.org/10.36463/idw.2021.0269
Autor:
Toshiharu Sugawara, Kazuki Urakawa
Publikováno v:
Journal of Information Processing. 22:289-298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2da3add53d01f19bc6adf46188414e72
https://doi.org/10.2197/ipsjjip.22.289
https://doi.org/10.2197/ipsjjip.22.289
Publikováno v:
Angewandte Chemie (International ed. in English). 55(26)
Unique redox switching of orthoquinone-containing pentacyclic aromatic compounds with molecular hydrogen and oxygen in the presence of a palladium nanoparticle catalyst (SAPd) is disclosed. These molecules were predicted by in silico screening before
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6da6e8200d47816e611d2edb6ceee59d
https://pubmed.ncbi.nlm.nih.gov/27145376
https://pubmed.ncbi.nlm.nih.gov/27145376