Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Tomohiro Miyatake"'
Autor:
Toranosuke Tomikawa, Yuichi Kitagawa, Koki Yoshioka, Kei Murata, Tomohiro Miyatake, Yasuchika Hasegawa, Kazuyuki Ishii
Publikováno v:
Journal of Materials Chemistry C. 11:2831-2835
Using zinc-chlorin, the switching of MCPL/CPL via J-aggregation has been clearly demonstrated for the first time.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a4f7dc50c7efcad265e7c373100e2fe
https://doi.org/10.1039/d2tc04841h
https://doi.org/10.1039/d2tc04841h
Publikováno v:
Langmuir. 35:7242-7248
Controlling the supramolecular organization of pigment molecules will provide innovative materials that exhibit variable optical properties. In nature, photosynthetic systems employ chlorophyllous supramolecules in which each pigment molecule is suit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c8681b0c172b20a12ea39ec26bf6655
https://doi.org/10.1021/acs.langmuir.9b00586
https://doi.org/10.1021/acs.langmuir.9b00586
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 353:612-617
Green photosynthetic bacteria have extramembranous light-harvesting complexes called chlorosomes. Light-energy captured by bacteriochlorophyll (BChl) self-aggregates inside chlorosomes is transferred to BChl a -peptide complexes called baseplates on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15eb07246617eab3436ac5d7c753e4a5
https://doi.org/10.1016/j.jphotochem.2017.08.001
https://doi.org/10.1016/j.jphotochem.2017.08.001
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 353:654-660
Self-aggregates of zinc 31-hydroxy-chlorins were prepared in a polydimethylsiloxane (PDMS) oil. The artificial self-aggregates provided a similar chlorophyllous aggregate found in light-harvesting antennas of green photosynthetic bacteria. The zinc c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7301c4a752c86cbf1f075817742d0ceb
https://doi.org/10.1016/j.jphotochem.2017.09.012
https://doi.org/10.1016/j.jphotochem.2017.09.012
Autor:
Juan Du, Yuxin Leng, Takayoshi Kobayashi, Hitoshi Tamiaki, Tomohiro Miyatake, Xin Xing, Wei Yuan
Publikováno v:
Chemical Physics Letters. 683:154-159
By real-time vibrational spectroscopy using 6.8 fs pulses, real-time vibronic coupling in stair-like zinc chlorin aggregates was studied. Besides the observed fast excitonic relaxation, amplitudes of coherent molecular vibrations are found to be line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a57304c025a9ed2fb08917cfaed949c
https://doi.org/10.1016/j.cplett.2017.05.050
https://doi.org/10.1016/j.cplett.2017.05.050
Publikováno v:
Chemical Physics Letters. 674:38-41
A system for measuring magneto-chiral dichroism (MChD) under strong magnetic fields using a pulsed electromagnet was constructed. We succeeded in observing a relatively intense MChD signal for chiral J-aggregates of a zinc chlorin at 5 T using this m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb6503420c495b119b605a7ff1c39511
https://doi.org/10.1016/j.cplett.2017.02.033
https://doi.org/10.1016/j.cplett.2017.02.033
Publikováno v:
Tetrahedron. 73:313-321
Chlorophyll- a was chemically modified to methyl pyropheophorbides- a possessing 3,8-diethyl, 3-vinyl-8-ethyl, 3-ethyl-8-vinyl, and 3,8-divinyl groups. Analogous 3-ethyl-7-vinyl- and 3,7-divinyl-chlorins were prepared by derivatization of chlorophyll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5fb4ca86441c76c15527ef52707ef32
https://doi.org/10.1016/j.tet.2016.12.003
https://doi.org/10.1016/j.tet.2016.12.003
Publikováno v:
Tetrahedron. 72:4368-4376
Regioisomeric 3- and 8-vinylchlorins as well as 7- and 12-vinylchlorins were prepared by modifying naturally occurring chlorophylls-a and/or b. The corresponding formylchlorins were synthesized by oxidation of the 3/8-vinyl, 7-hydroxymethyl or 12-met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0e62e9a21a83b194e041fcd36808451
https://doi.org/10.1016/j.tet.2016.06.001
https://doi.org/10.1016/j.tet.2016.06.001
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:3034-3037
Wittig reaction of methyl pyropheophorbide-d possessing the 3-formyl group gave readily methyl pyropheophorbides-a bearing a variety of 3-alkenyl groups as semi-synthetic models of chlorophyll-a. The 3-substituents rotated around the C3-C3(1) bond fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f4d77ec45703b82d821985c87d8347
https://doi.org/10.1016/j.bmcl.2016.05.008
https://doi.org/10.1016/j.bmcl.2016.05.008
Publikováno v:
Tetrahedron. 72:3477-3489
Methyl 3-acyl-pyropheophorbides-a were prepared by modification of naturally occurring chlorophyll-a through Grignard or Barbier reactions of the 3-formyl group and successive Ley–Griffith or Dess–Martin oxidations of the resulting secondary alco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::235d9958d6313d0d351a9c9cf22e71b7
https://doi.org/10.1016/j.tet.2016.04.074
https://doi.org/10.1016/j.tet.2016.04.074